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		<title>IJMS: Material Sciences and Nanotechnology</title>
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	<title>IJMS, Vol. 13, Pages 1658-1669: Preparation of TiO2 Nanocrystallite Powders Coated with 9 mol% ZnO for Cosmetic Applications in Sunscreens</title>
	<link>http://www.mdpi.com/1422-0067/13/2/1658/</link>
	<description>The preparation of TiO2 nanocrystallite powders coated with and without 9 mol% ZnO has been studied for cosmetic applications in sunscreens by a co-precipitation process using TiCl4 and Zn(NO3)2·6H2O as starting materials. XRD results show that the phases of anatase TiO2 and rutile TiO2 coexist for precursor powders without added ZnO (T-0Z) and calcined at 523 to 973 K for 2 h. When the T-0Z precursor powders are calcined at 1273 K for 2 h, only the rutile TiO2 appears. In addition, when the TiO2 precursor powders contain 9 mol% ZnO (T-9Z) are calcined at 873 to 973 K for 2 h, the crystallized samples are composed of the major phase of rutile TiO2 and the minor phases of anatase TiO2 and Zn2Ti3O8. The analyses of UV/VIS/NIR spectra reveal that the absorption of the T-9Z precursor powders after being calcined has a red-shift effect in the UV range with increasing calcination temperature. Therefore, the TiO2 nanocrystallite powders coated with 9 mol% ZnO can be used as the attenuate agent in the UV-A region for cosmetic applications in sunscreens.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/2/1658/</guid>
	<pubDate>Fri, 03 Feb 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2012-02-03</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1658</prism:startingPage>
		<prism:endingPage>1669</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Preparation of TiO2 Nanocrystallite Powders Coated with 9 mol% ZnO for Cosmetic Applications in Sunscreens</dc:title>
	<dc:date>2012-02-03</dc:date>
	<dc:identifier>doi: 10.3390/ijms13021658</dc:identifier>
		<dc:creator>Horng-Huey Ko</dc:creator>
		<dc:creator>Hui-Ting Chen</dc:creator>
		<dc:creator>Feng-Ling Yen</dc:creator>
		<dc:creator>Wan-Chen Lu</dc:creator>
		<dc:creator>Chih-Wei Kuo</dc:creator>
		<dc:creator>Moo-Chin Wang</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
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	<item rdf:about="http://www.mdpi.com/1422-0067/13/2/1612/">
	<title>IJMS, Vol. 13, Pages 1612-1619: Tetrachloridocuprates(II)—Synthesis and Electron Paramagnetic Resonance (EPR) Spectroscopy</title>
	<link>http://www.mdpi.com/1422-0067/13/2/1612/</link>
	<description>Ionic liquids (ILs) on the basis of metal containing anions and/or cations are of interest for a variety of technical applications e.g., synthesis of particles, magnetic or thermochromic materials. We present the synthesis and the results of electron paramagnetic resonance (EPR) spectroscopic analyses of a series of some new potential ionic liquids based on tetrachloridocuprates(II), [CuCl4]2−, with different sterically demanding cations: hexadecyltrimethylammonium 1, tetradecyltrimethylammonium 2, tetrabutylammonium 3 and benzyltriethylammonium 4. The cations in the new compounds were used to achieve a reasonable separation of the paramagnetic Cu(II) ions for EPR spectroscopy. The EPR hyperfine structure was not resolved. This is due to the exchange broadening, resulting from still incomplete separation of the paramagnetic Cu(II) centers. Nevertheless, the principal values of the electron Zeemann tensor (g║ and g┴) of the complexes could be determined. Even though the solid substances show slightly different colors, the UV/Vis spectra are nearly identical, indicating structural changes of the tetrachloridocuprate moieties between solid state and solution. The complexes have a promising potential e.g., as high temperature ionic liquids, as precursors for the formation of copper chloride particles or as catalytic paramagnetic ionic liquids.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/2/1612/</guid>
	<pubDate>Thu, 02 Feb 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2012-02-02</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1612</prism:startingPage>
		<prism:endingPage>1619</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Tetrachloridocuprates(II)—Synthesis and Electron Paramagnetic Resonance (EPR) Spectroscopy</dc:title>
	<dc:date>2012-02-02</dc:date>
	<dc:identifier>doi: 10.3390/ijms13021612</dc:identifier>
		<dc:creator>Alette Winter</dc:creator>
		<dc:creator>André Zabel</dc:creator>
		<dc:creator>Peter Strauch</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/13/1/1109/">
	<title>IJMS, Vol. 13, Pages 1109-1125: The Effect of Temozolomide/Poly(lactide-co-glycolide) (PLGA)/Nano-Hydroxyapatite Microspheres on Glioma U87 Cells Behavior</title>
	<link>http://www.mdpi.com/1422-0067/13/1/1109/</link>
	<description>In this study, we investigated the effects of temozolomide (TMZ)/Poly (lactide-co-glycolide)(PLGA)/nano-hydroxyapatite microspheres on the behavior of U87 glioma cells. The microspheres were fabricated by the “Solid/Water/Oil” method, and they were characterized by using X-Ray diffraction, scanning electron microscopy and differential scanning calorimetry. The proliferation, apoptosis and invasion of glioma cells were evaluated by MTT, flow cytometry assay and Transwell assay. The presence of the key invasive gene, αVβ3 integrin, was detected by the RT-PCR and Western blot method. It was found that the temozolomide/PLGA/nano-hydroxyapatite microspheres have a significantly diminished initial burst of drug release, compared to the TMZ laden PLGA microspheres. Our results suggest they can significantly inhibit the proliferation and invasion of glioma cells, and induce their apoptosis. Additionally, αVβ3 integrin was also reduced by the microspheres. These data suggest that by inhibiting the biological behavior of glioma cells in vitro, the newly designed temozolomide/PLGA/nano-hydroxyapatite microspheres, as controlled drug release carriers, have promising potential in treating glioma.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/1/1109/</guid>
	<pubDate>Thu, 19 Jan 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2012-01-19</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1109</prism:startingPage>
		<prism:endingPage>1125</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>The Effect of Temozolomide/Poly(lactide-co-glycolide) (PLGA)/Nano-Hydroxyapatite Microspheres on Glioma U87 Cells Behavior</dc:title>
	<dc:date>2012-01-19</dc:date>
	<dc:identifier>doi: 10.3390/ijms13011109</dc:identifier>
		<dc:creator>Dongyong Zhang</dc:creator>
		<dc:creator>Ang Tian</dc:creator>
		<dc:creator>Xiangxin Xue</dc:creator>
		<dc:creator>Mei Wang</dc:creator>
		<dc:creator>Bo Qiu</dc:creator>
		<dc:creator>Anhua Wu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/13/1/1095/">
	<title>IJMS, Vol. 13, Pages 1095-1108: Local Mechanical Stimulation of Mardin-Darby Canine Kidney Cell Sheets on Temperature-Responsive Hydrogel</title>
	<link>http://www.mdpi.com/1422-0067/13/1/1095/</link>
	<description>Collective motion of cell sheets plays a role not only in development and repair, but also in devastating diseases such as cancer. However, unlike single-cell motility, collective motion of cell sheets involves complex cell-cell communication during migration; therefore, its mechanism is largely unknown. To elucidate propagation of signaling transduced by cell-cell interaction, we designed a hydrogel substrate that can cause local mechanical stretching of cell sheets. Poly (N-isopropyl acrylamide) (PNIPAAm) hydrogel is a temperature-responsive polymer gel whose volume changes isotropically in response to temperature changes below 37 °C. We designed a combined hydrogel substrate consisting of collagen-immobilized PNIPAAm as the local stimulation side and polyacrylamide (PAAm) as the non-stimulation side to assess propagation of mechanical transduction. Mardin-Darby canine kidney (MDCK) cells adhered to the collagen-immobilized PNIPAAm gel increased it area and were flattened as the gel swelled with temperature decrease. E-cadherin in these cells became undetectable in some domains, and actin stress fibers were more clearly observed at the cell base. In contrast, E-cadherin in cells adhered to the collagen-immobilized PAAm side was equally stained as that in cells adhered to the collagen-immobilized PAAm side even after temperature decrease. ERK1/2 MAPK activation of cells on the non-stimulated substrate occurred after partial stretching of the cell sheet suggesting the propagation of signaling. These results indicate that a change in the balance of mechanical tension induced by partial stretching of cell sheets leads to activation and propagation of the cell signaling.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/1/1095/</guid>
	<pubDate>Thu, 19 Jan 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2012-01-19</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1095</prism:startingPage>
		<prism:endingPage>1108</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Local Mechanical Stimulation of Mardin-Darby Canine Kidney Cell Sheets on Temperature-Responsive Hydrogel</dc:title>
	<dc:date>2012-01-19</dc:date>
	<dc:identifier>doi: 10.3390/ijms13011095</dc:identifier>
		<dc:creator>Ichiro Harada</dc:creator>
		<dc:creator>Shunpei Yanagisawa</dc:creator>
		<dc:creator>Katsuhiko Iwasaki</dc:creator>
		<dc:creator>Chong-Su Cho</dc:creator>
		<dc:creator>Toshihiro Akaike</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/13/1/918/">
	<title>IJMS, Vol. 13, Pages 918-928: Characterization of Electrosynthesized Conjugated Polymer-Carbon Nanotube Composite: Optical Nonlinearity and Electrical Property</title>
	<link>http://www.mdpi.com/1422-0067/13/1/918/</link>
	<description>The effects of multi-walled carbon nanotube (MWNT) concentration on the structural, optical and electrical properties of conjugated polymer-carbon nanotube composite are discussed. Multi-walled carbon nanotube-polypyrrole nanocomposites were synthesized by electrochemical polymerization of monomers in the presence of different amounts of MWNTs using sodium dodecylbenzensulfonate (SDBS) as surfactant at room temperature and normal pressure. Field emission scanning electron microscopy (FESEM) indicates that the polymer is wrapped around the nanotubes. Measurement of the nonlinear refractive indices (n2) and the nonlinear absorption (β) of the samples with different MWNT concentrations measurements were performed by a single Z-scan method using continuous wave (CW) laser beam excitation wavelength of λ = 532 nm. The results show that both nonlinear optical parameters increased with increasing the concentration of MWNTs. The third order nonlinear susceptibilities were also calculated and found to follow the same trend as n2 and β. In addition, the conductivity of the composite film was found to increase rapidly with the increase in the MWNT concentration.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/1/918/</guid>
	<pubDate>Mon, 16 Jan 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2012-01-16</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>918</prism:startingPage>
		<prism:endingPage>928</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Characterization of Electrosynthesized Conjugated Polymer-Carbon Nanotube Composite: Optical Nonlinearity and Electrical Property</dc:title>
	<dc:date>2012-01-16</dc:date>
	<dc:identifier>doi: 10.3390/ijms13010918</dc:identifier>
		<dc:creator>Afarin Bahrami</dc:creator>
		<dc:creator>Zainal Abidin Talib</dc:creator>
		<dc:creator>Esmaeil Shahriari</dc:creator>
		<dc:creator>Wan Mahmood Mat Yunus</dc:creator>
		<dc:creator>Anuar Kasim</dc:creator>
		<dc:creator>Kasra Behzad</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/13/1/516/">
	<title>IJMS, Vol. 13, Pages 516-533: Biodegradable Nanoparticles of mPEG-PLGA-PLL Triblock Copolymers as Novel Non-Viral Vectors for Improving siRNA Delivery and Gene Silencing </title>
	<link>http://www.mdpi.com/1422-0067/13/1/516/</link>
	<description>Degradation of mRNA by RNA interference is one of the most powerful and specific mechanisms for gene silencing. However, insufficient cellular uptake and poor stability have limited its usefulness. Here, we report efficient delivery of siRNA via the use of biodegradable nanoparticles (NPs) made from monomethoxypoly(ethylene glycol)-poly(lactic-co-glycolic acid)-poly-l-lysine (mPEG-PLGA-PLL) triblock copolymers. Various physicochemical properties of mPEG-PLGA-PLL NPs, including morphology, size, surface charge, siRNA encapsulation efficiency, and in vitro release profile of siRNA from NPs, were characterized by scanning electron microscope, particle size and zeta potential analyzer, and high performance liquid chromatography. The levels of siRNA uptake and targeted gene inhibition were detected in human lung cancer SPC-A1-GFP cells stably expressing green fluorescent protein. Examination of the cultured SPC-A1-GFP cells with fluorescent microscope and flow cytometry showed NPs loading Cy3-labeled siRNA had much higher intracellular siRNA delivery efficiencies than siRNA alone and Lipofectamine-siRNA complexes. The gene silencing efficiency of mPEG-PLGA-PLL NPs was higher than that of commercially available transfecting agent Lipofectamine while showing no cytotoxicity. Thus, the current study demonstrates that biodegradable NPs of mPEG-PLGA-PLL triblock copolymers can be potentially applied as novel non-viral vectors for improving siRNA delivery and gene silencing.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/1/516/</guid>
	<pubDate>Wed, 04 Jan 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2012-01-04</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>516</prism:startingPage>
		<prism:endingPage>533</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Biodegradable Nanoparticles of mPEG-PLGA-PLL Triblock Copolymers as Novel Non-Viral Vectors for Improving siRNA Delivery and Gene Silencing </dc:title>
	<dc:date>2012-01-04</dc:date>
	<dc:identifier>doi: 10.3390/ijms13010516</dc:identifier>
		<dc:creator>Jing Du</dc:creator>
		<dc:creator>Ying Sun</dc:creator>
		<dc:creator>Qiu-Sheng Shi</dc:creator>
		<dc:creator>Pei-Feng Liu</dc:creator>
		<dc:creator>Ming-Jie Zhu</dc:creator>
		<dc:creator>Chun-Hui Wang</dc:creator>
		<dc:creator>Lian-Fang Du</dc:creator>
		<dc:creator>You-Rong Duan</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/13/1/453/">
	<title>IJMS, Vol. 13, Pages 453-465: Force Measurement Enabling Precise Analysis by Dynamic Force Spectroscopy</title>
	<link>http://www.mdpi.com/1422-0067/13/1/453/</link>
	<description>Dynamic force spectroscopy (DFS) makes it possible to investigate specific interactions between two molecules such as ligand-receptor pairs at the single-molecule level. In the DFS method based on the Bell-Evans model, the unbinding force applied to a molecular bond is increased at a constant rate, and the force required to rupture the molecular bond is measured. By analyzing the relationship between the modal rupture force and the logarithm of the loading rate, microscopic potential barrier landscapes and the lifetimes of bonds can be obtained. However, the results obtained, for example, in the case of streptavidin/biotin complexes, have differed among previous studies and some results have been inconsistent with theoretical predictions. In this study, using an atomic force microscopy technique that enables the precise analysis of molecular interactions on the basis of DFS, we investigated the effect of the sampling rate on DFS analysis. The shape of rupture force histograms, for example, was significantly deformed at a sampling rate of 1 kHz in comparison with that of histograms obtained at 100 kHz, indicating the fundamental importance of ensuring suitable experimental conditions for further advances in the DFS method.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/1/453/</guid>
	<pubDate>Thu, 29 Dec 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-12-29</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>453</prism:startingPage>
		<prism:endingPage>465</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Force Measurement Enabling Precise Analysis by Dynamic Force Spectroscopy</dc:title>
	<dc:date>2011-12-29</dc:date>
	<dc:identifier>doi: 10.3390/ijms13010453</dc:identifier>
		<dc:creator>Atsushi Taninaka</dc:creator>
		<dc:creator>Yuuichi Hirano</dc:creator>
		<dc:creator>Osamu Takeuchi</dc:creator>
		<dc:creator>Hidemi Shigekawa</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/13/1/302/">
	<title>IJMS, Vol. 13, Pages 302-315: Photocatalytic Degradation of p-Cresol by Zinc Oxide under UV Irradiation</title>
	<link>http://www.mdpi.com/1422-0067/13/1/302/</link>
	<description>Photocatalytic degradation of p-cresol was carried out using ZnO under UV irradiation. The amount of photocatalyst, concentration of p-cresol and pH were studied as variables. The residual concentration and mineralization of p-cresol was monitored using a UV-visible spectrophotometer and total organic carbon (TOC) analyzer, respectively. The intermediates were detected by ultra high pressure liquid chromatography (UPLC). The highest photodegradation of p-cresol was observed at 2.5 g/L of ZnO and 100 ppm of p-cresol. P-cresol photocatalytic degradation was favorable in the pH range of 6–9. The detected intermediates were 4-hydroxy-benzaldehyde and 4-methyl-1,2-benzodiol. TOC studies show that 93% of total organic carbon was removed from solution during irradiation time. Reusability shows no significant reduction in photocatalytic performance in photodegrading p-cresol.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/1/302/</guid>
	<pubDate>Tue, 27 Dec 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-12-27</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>302</prism:startingPage>
		<prism:endingPage>315</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Photocatalytic Degradation of p-Cresol by Zinc Oxide under UV Irradiation</dc:title>
	<dc:date>2011-12-27</dc:date>
	<dc:identifier>doi: 10.3390/ijms13010302</dc:identifier>
		<dc:creator>Yadollah Abdollahi</dc:creator>
		<dc:creator>Abdul Halim Abdullah</dc:creator>
		<dc:creator>Zulkarnain Zainal</dc:creator>
		<dc:creator>Nor Azah Yusof</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/13/1/180/">
	<title>IJMS, Vol. 13, Pages 180-186: The Effect of Hydrogen Content on Ballistic Transport Behaviors in the Ni-Nb-Zr-H Glassy Alloys</title>
	<link>http://www.mdpi.com/1422-0067/13/1/180/</link>
	<description>The electronic transport behaviors of (Ni0.39Nb0.25Zr0.35)100−xHx (0 ≤ x &lt; 23.5) glassy alloys with subnanostructural icosahedral Zr5Nb5Ni3 clusters have been studied as a function of hydrogen content. These alloys show semiconducting, electric current-induced voltage (Coulomb) oscillation and ballistic transport behaviors. Coulomb oscillation and ballistic transport occur at hydrogen contents between 6.7 and 13.5 at% and between 13.5 and 21.2 at%, respectively. These results suggest that the localization effect of hydrogen in the clusters plays an important role in various electron transport phenomena.</description>
	
	<guid>http://www.mdpi.com/1422-0067/13/1/180/</guid>
	<pubDate>Fri, 23 Dec 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-12-23</prism:publicationDate>
	<prism:volume>13</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>180</prism:startingPage>
		<prism:endingPage>186</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>The Effect of Hydrogen Content on Ballistic Transport Behaviors in the Ni-Nb-Zr-H Glassy Alloys</dc:title>
	<dc:date>2011-12-23</dc:date>
	<dc:identifier>doi: 10.3390/ijms13010180</dc:identifier>
		<dc:creator>Mikio Fukuhara</dc:creator>
		<dc:creator>Yoshimasa Umemori</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/12/9031/">
	<title>IJMS, Vol. 12, Pages 9031-9056: Enhanced Immunomodulatory Activity of Gelatin-Encapsulated Rubus coreanus Miquel Nanoparticles</title>
	<link>http://www.mdpi.com/1422-0067/12/12/9031/</link>
	<description>The aim of this work was to investigate the immunomodulatory activities of Rubus coreanus Miquel extract-loaded gelatin nanoparticles. The mean size of the produced nanoparticles was 143 ± 18 nm with a bandwidth of 76 nm in the size distribution and a maximum size of ~200 nm, which allows effective nanoparticle uptake by cells. Confocal imaging confirmed this, since the nanoparticles were internalized within 30 min and heterogeneously distributed throughout the cell. Zeta-potential measurements showed that from pH = 5 onwards, the nanoparticles were highly negatively charged, which prevents agglomeration to clusters by electrostatic repulsion. This was confirmed by TEM imaging, which showed a well dispersed colloidal solution. The encapsulation efficiency was nearly 60%, which is higher than for other components encapsulated in gelatin nanoparticles. Measurements of immune modulation in immune cells showed a significant effect by the crude extract, which was only topped by the nanoparticles containing the extract. Proliferation of B-, T- and NK cells was notably enhanced by Rubus coreanus-gelatin nanoparticles and in general ~2–3 times higher than control and on average ~2 times higher than ferulic acid. R. coreanus-gelatin nanoparticles induced cytokine secretion (IL-6 and TNF-α) from B- and T-cells on average at a ~2–3 times higher rate compared with the extract and ferulic acid. In vivo immunomodulatory activity in mice fed with R. coreanus-gelatin nanoparticles at 1 mL/g body weight showed a ~5 times higher antibody production compared to control, a ~1.3 times higher production compared to the extract only, and a ~1.6 times higher production compared to ferulic acid. Overall, our results suggest that gelatin nanoparticles represent an excellent transport vehicle for Rubus coreanus extract and extracts from other plants generally used in traditional Asian medicine. Such nanoparticles ensure a high local concentration that results in enhancement of immune cell activities, including proliferation, cytokine secretion, and antibody production.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/12/9031/</guid>
	<pubDate>Wed, 07 Dec 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-12-07</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>12</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>9031</prism:startingPage>
		<prism:endingPage>9056</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Enhanced Immunomodulatory Activity of Gelatin-Encapsulated Rubus coreanus Miquel Nanoparticles</dc:title>
	<dc:date>2011-12-07</dc:date>
	<dc:identifier>doi: 10.3390/ijms12129031</dc:identifier>
		<dc:creator>Yong Chang Seo</dc:creator>
		<dc:creator>Woon Yong Choi</dc:creator>
		<dc:creator>Choon Geun Lee</dc:creator>
		<dc:creator>Seon Woo Cha</dc:creator>
		<dc:creator>Young Ock Kim</dc:creator>
		<dc:creator>Jin-Chul Kim</dc:creator>
		<dc:creator>Gregor P. C. Drummen</dc:creator>
		<dc:creator>Hyeon Yong Lee</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/12/9009/">
	<title>IJMS, Vol. 12, Pages 9009-9030: Mechanobiology of Platelets: Techniques to Study the Role of Fluid Flow and Platelet Retraction Forces at the Micro- and Nano-Scale</title>
	<link>http://www.mdpi.com/1422-0067/12/12/9009/</link>
	<description>Coagulation involves a complex set of events that are important in maintaining hemostasis. Biochemical interactions are classically known to regulate the hemostatic process, but recent evidence has revealed that mechanical interactions between platelets and their surroundings can also play a substantial role. Investigations into platelet mechanobiology have been challenging however, due to the small dimensions of platelets and their glycoprotein receptors. Platelet researchers have recently turned to microfabricated devices to control these physical, nanometer-scale interactions with a higher degree of precision. These approaches have enabled exciting, new insights into the molecular and biomechanical factors that affect platelets in clot formation. In this review, we highlight the new tools used to understand platelet mechanobiology and the roles of adhesion, shear flow, and retraction forces in clot formation.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/12/9009/</guid>
	<pubDate>Wed, 07 Dec 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-12-07</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>12</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>9009</prism:startingPage>
		<prism:endingPage>9030</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Mechanobiology of Platelets: Techniques to Study the Role of Fluid Flow and Platelet Retraction Forces at the Micro- and Nano-Scale</dc:title>
	<dc:date>2011-12-07</dc:date>
	<dc:identifier>doi: 10.3390/ijms12129009</dc:identifier>
		<dc:creator>Shirin Feghhi</dc:creator>
		<dc:creator>Nathan J. Sniadecki</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/12/8596/">
	<title>IJMS, Vol. 12, Pages 8596-8609: Approaches to Manipulating the Dimensionality and Physicochemical Properties of Common Cellular Scaffolds</title>
	<link>http://www.mdpi.com/1422-0067/12/12/8596/</link>
	<description>A major hurdle in studying biological systems and administering effective tissue engineered therapies is the lack of suitable cell culture models that replicate the dynamic nature of cell-microenvironment interactions. Advances in the field of surface chemistry and polymer science have allowed researchers to develop novel methodologies to manipulate materials to be extrinsically tunable. Usage of such materials in modeling tissues in vitro has offered valuable insights into numerous cellular processes including motility, invasion, and alterations in cell morphology. Here, we discuss novel techniques devised to more closely mimic cell-tissue interactions and to study cell response to distinct physico-chemical changes in biomaterials, with an emphasis on the manipulation of collagen scaffolds. The benefits and pitfalls associated with using collagen are discussed in the context of strategies proposed to control the engineered microenvironment. Tunable systems such as these offer the ability to alter individual features of the microenvironment in vitro, with the promise that the molecular basis of mechanotransduction in vivo may be laid out in future.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/12/8596/</guid>
	<pubDate>Tue, 29 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-11-29</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>12</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>8596</prism:startingPage>
		<prism:endingPage>8609</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Approaches to Manipulating the Dimensionality and Physicochemical Properties of Common Cellular Scaffolds</dc:title>
	<dc:date>2011-11-29</dc:date>
	<dc:identifier>doi: 10.3390/ijms12128596</dc:identifier>
		<dc:creator>Saumendra Bajpai</dc:creator>
		<dc:creator>Na Young Kim</dc:creator>
		<dc:creator>Cynthia A. Reinhart-King</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/11/8217/">
	<title>IJMS, Vol. 12, Pages 8217-8244: Cell-Biomaterial Mechanical Interaction in the Framework of Tissue Engineering: Insights, Computational Modeling and Perspectives</title>
	<link>http://www.mdpi.com/1422-0067/12/11/8217/</link>
	<description>Tissue engineering is an emerging field of research which combines the use of cell-seeded biomaterials both in vitro and/or in vivo with the aim of promoting new tissue formation or regeneration. In this context, how cells colonize and interact with the biomaterial is critical in order to get a functional tissue engineering product. Cell-biomaterial interaction is referred to here as the phenomenon involved in adherent cells attachment to the biomaterial surface, and their related cell functions such as growth, differentiation, migration or apoptosis. This process is inherently complex in nature involving many physico-chemical events which take place at different scales ranging from molecular to cell body (organelle) levels. Moreover, it has been demonstrated that the mechanical environment at the cell-biomaterial location may play an important role in the subsequent cell function, which remains to be elucidated. In this paper, the state-of-the-art research in the physics and mechanics of cell-biomaterial interaction is reviewed with an emphasis on focal adhesions. The paper is focused on the different models developed at different scales available to simulate certain features of cell-biomaterial interaction. A proper understanding of cell-biomaterial interaction, as well as the development of predictive models in this sense, may add some light in tissue engineering and regenerative medicine fields.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/11/8217/</guid>
	<pubDate>Mon, 21 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-11-21</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>8217</prism:startingPage>
		<prism:endingPage>8244</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Cell-Biomaterial Mechanical Interaction in the Framework of Tissue Engineering: Insights, Computational Modeling and Perspectives</dc:title>
	<dc:date>2011-11-21</dc:date>
	<dc:identifier>doi: 10.3390/ijms12118217</dc:identifier>
		<dc:creator>Jose A. Sanz-Herrera</dc:creator>
		<dc:creator>Esther Reina-Romo</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/11/7662/">
	<title>IJMS, Vol. 12, Pages 7662-7691: Bioengineering Embryonic Stem Cell Microenvironments for the Study of Breast Cancer</title>
	<link>http://www.mdpi.com/1422-0067/12/11/7662/</link>
	<description>Breast cancer is the most prevalent disease amongst women worldwide and metastasis is the main cause of death due to breast cancer. Metastatic breast cancer cells and embryonic stem (ES) cells display similar characteristics. However, unlike metastatic breast cancer cells, ES cells are nonmalignant. Furthermore, embryonic microenvironments have the potential to convert metastatic breast cancer cells into a less invasive phenotype. The creation of in vitro embryonic microenvironments will enable better understanding of ES cell-breast cancer cell interactions, help elucidate tumorigenesis, and lead to the restriction of breast cancer metastasis. In this article, we will present the characteristics of breast cancer cells and ES cells as well as their microenvironments, importance of embryonic microenvironments in inhibiting tumorigenesis, convergence of tumorigenic and embryonic signaling pathways, and state of the art in bioengineering embryonic microenvironments for breast cancer research. Additionally, the potential application of bioengineered embryonic microenvironments for the prevention and treatment of invasive breast cancer will be discussed.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/11/7662/</guid>
	<pubDate>Tue, 08 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-11-08</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>7662</prism:startingPage>
		<prism:endingPage>7691</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Bioengineering Embryonic Stem Cell Microenvironments for the Study of Breast Cancer</dc:title>
	<dc:date>2011-11-08</dc:date>
	<dc:identifier>doi: 10.3390/ijms12117662</dc:identifier>
		<dc:creator>Nurazhani Abdul Raof</dc:creator>
		<dc:creator>Bridget M. Mooney</dc:creator>
		<dc:creator>Yubing Xie</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/11/7438/">
	<title>IJMS, Vol. 12, Pages 7438-7444: Novel Ionic Liquid with Both Lewis and Brønsted Acid Sites for Michael Addition</title>
	<link>http://www.mdpi.com/1422-0067/12/11/7438/</link>
	<description>Ionic liquid with both Lewis and Brønsted acid sites has been synthesized and its catalytic activities for Michael addition were carefully studied. The novel ionic liquid was stable to water and could be used in aqueous solution. The molar ratio of the Lewis and Brønsted acid sites could be adjusted to match different reactions. The results showed that the novel ionic liquid was very efficient for Michael addition with good to excellent yields within several min. Operational simplicity, high stability to water and air, small amount used, low cost of the catalyst used, high yields, chemoselectivity, applicability to large-scale reactions and reusability are the key features of this methodology, which indicated that this novel ionic liquid also holds great potential for environmentally friendly processes.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/11/7438/</guid>
	<pubDate>Fri, 28 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-10-28</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7438</prism:startingPage>
		<prism:endingPage>7444</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Novel Ionic Liquid with Both Lewis and Brønsted Acid Sites for Michael Addition</dc:title>
	<dc:date>2011-10-28</dc:date>
	<dc:identifier>doi: 10.3390/ijms12117438</dc:identifier>
		<dc:creator>Xiaoyue Jiang</dc:creator>
		<dc:creator>Weidong Ye</dc:creator>
		<dc:creator>Xiaohua Song</dc:creator>
		<dc:creator>Wenxin Ma</dc:creator>
		<dc:creator>Xuejun Lao</dc:creator>
		<dc:creator>Runpu Shen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/11/7410/">
	<title>IJMS, Vol. 12, Pages 7410-7423: A Sandwich Electrochemical Immunosensor Using Magnetic DNA Nanoprobes for Carcinoembryonic Antigen</title>
	<link>http://www.mdpi.com/1422-0067/12/11/7410/</link>
	<description>A novel magnetic nanoparticle-based electrochemical immunoassay of carcinoembryonic antigen (CEA) was designed as a model using CEA antibody-functionalized magnetic beads [DNA/Fe3O4/ZrO2; Fe3O4 (core)/ZrO2 (shell) nano particles (ZMPs)] as immunosensing probes. To design the immunoassay, the CEA antibody and O-phenylenediamine (OPD) were initially immobilized on a chitosan/nano gold composite membrane on a glassy carbon electrode (GCE/CS-nano Au), which was used for CEA recognition. Then, horseradish peroxidase (HRP)-labeled anti-CEA antibodies (HRP-CEA Ab2) were bound to the surface of the synthesized magnetic ZMP nanoparticles as signal tag. Thus, the sandwich-type immune complex could be formed between secondary antibody (Ab2) modified DNA/ZMPs nanochains tagged by HRP and GCE/CS-nano Au. Unlike conventional nanoparticle-based electrochemical immunoassays, the recognition elements of this immunoassay included both electron mediators and enzyme labels, which obviously simplifies the electrochemical measurement process. The sandwich-type immunoassay format was used for online formation of the immunocomplex of CEA captured in the detection cell with an external magnet. The electrochemical signals derived from HRP during the reduction of H2O2 with OPD as electron mediator were measured. The method displayed a high sensitivity for CEA detection in the range of 0.008–200 ng/mL, with a detection limit of 5 pg/mL (estimated at a signal-to-noise ratio of 3). The precision, reproducibility, and stability of the immunoassay were good. The use of the assay was evaluated with clinical serum samples, and the results were in excellent accordance with those obtained using the standard enzyme-linked immunosorbent assay (ELISA) method. Thus, the magnetic nanoparticle-based assay format is a promising approach for clinical applications, and it could be further developed for the detection of other biomarkers in cancer diagnosis.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/11/7410/</guid>
	<pubDate>Fri, 28 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-10-28</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7410</prism:startingPage>
		<prism:endingPage>7423</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>A Sandwich Electrochemical Immunosensor Using Magnetic DNA Nanoprobes for Carcinoembryonic Antigen</dc:title>
	<dc:date>2011-10-28</dc:date>
	<dc:identifier>doi: 10.3390/ijms12117410</dc:identifier>
		<dc:creator>Ning Gan</dc:creator>
		<dc:creator>Liyong Jia</dc:creator>
		<dc:creator>Lei Zheng</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/11/7360/">
	<title>IJMS, Vol. 12, Pages 7360-7400: Review of Crystalline Structures of Some Selected Homologous Series of Rod-Like Molecules Capable of Forming Liquid Crystalline Phases</title>
	<link>http://www.mdpi.com/1422-0067/12/11/7360/</link>
	<description>The crystal structures of four homologous series of rod-like molecules are reviewed, two of which form hydrogen bonds and two with a symmetric chemical constitution. Many of the compounds investigated turn into liquid crystalline phases upon temperature increase. It is of valuable interest to know possible conformations and possible packing arrangements as prerequisites to model liquid crystalline structures. The hydrogen bonds of homologous series of pure 4-(ω-hydroxyalkyloxy)-4′-hydroxybiphenyl (HnHBP, n the alkyloxy tail length) are realized through head to tail arrangements of the hydroxyl groups and crystallize except one compound in chiral space groups without the molecules containing any asymmetric carbon. The hydrogen bonds of the homologous series of 4-substituted benzoic acids with various lengths of the tail provide dimers through strong polar bonding of adjacent carboxyl groups and thus provide the stiff part of a mesogenic unit prerequisite for liquid crystalline phases. The homologous series of dialkanoyloxybiphenyls (BP-n, n = 1, 19), of which nine compounds could be crystallized, show liquid crystalline behavior for longer alkane chain lengths, despite the high mobility of the alkane chain ends already detectable in the crystal phase. A single molecule, half a molecule or two half molecules form the asymmetric unit in a centrosymmetric space group. The homologous series of 1,4-terephthalidene-bis-N-(4′-n-alkylaniline) (TBAA-n) exhibit a large variety of packing arrangements in the crystalline state, with or without relying on the symmetry center within the molecules.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/11/7360/</guid>
	<pubDate>Fri, 28 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-10-28</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>7360</prism:startingPage>
		<prism:endingPage>7400</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Review of Crystalline Structures of Some Selected Homologous Series of Rod-Like Molecules Capable of Forming Liquid Crystalline Phases</dc:title>
	<dc:date>2011-10-28</dc:date>
	<dc:identifier>doi: 10.3390/ijms12117360</dc:identifier>
		<dc:creator>Peter Zugenmaier</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/11/7286/">
	<title>IJMS, Vol. 12, Pages 7286-7300: Chitosan Fibers Modified with HAp/β–TCP Nanoparticles</title>
	<link>http://www.mdpi.com/1422-0067/12/11/7286/</link>
	<description>This paper describes a method for preparing chitosan fibers modified with hydroxyapatite (HAp), tricalcium phosphate (β-TCP), and HAp/β-TCP nanoparticles. Fiber-grade chitosan derived from the northern shrimp (Pandalus borealis) and nanoparticles of tricalcium phosphate (β-TCP) and hydroxyapatite (HAp) suspended in a diluted chitosan solution were used in the investigation. Diluted chitosan solution containing nanoparticles of Hap/β-TCP was introduced to a 5.16 wt% solution of chitosan in 3.0 wt% acetic acid. The properties of the spinning solutions were examined. Chitosan fibers modified with nanoparticles of HAp/β-TCP were characterized by a level of tenacity and calcium content one hundred times higher than that of regular chitosan fibers.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/11/7286/</guid>
	<pubDate>Tue, 25 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-10-25</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7286</prism:startingPage>
		<prism:endingPage>7300</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Chitosan Fibers Modified with HAp/β–TCP Nanoparticles</dc:title>
	<dc:date>2011-10-25</dc:date>
	<dc:identifier>doi: 10.3390/ijms12117286</dc:identifier>
		<dc:creator>Dariusz Wawro</dc:creator>
		<dc:creator>Luciano Pighinelli</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/10/7238/">
	<title>IJMS, Vol. 12, Pages 7238-7249: Use of Oligonucleotides Carrying Photolabile Groups for the Control of the Deposition of Nanoparticles in Surfaces and Nanoparticle Association</title>
	<link>http://www.mdpi.com/1422-0067/12/10/7238/</link>
	<description>An oligodeoxynucleotide hairpin containing a photolabile 2-nitrobenzyl group in the loop and terminated with a thiol function was prepared. The photocleavage of such a hairpin on gold yields a surface activated with a single stranded oligonucleotide which can be utilised to direct the assembly of nanoparticles conjugated with a complementary strand. Analysis of photocleaved surfaces gives nanoparticle coverage one order of magnitude higher than nonphotocleaved surfaces. This illustrates the ability of photocleavable hairpins to direct the assembly of nanomaterials on conducting materials. The conjugation of the photocleavable hairpin to a gold nanoparticle allows the observation of intermolecular interactions between hairpins linked in different nanoparticles, by comparing the thermal dissociations of a hairpin-nanoparticle conjugates at 260 nm and 520 nm. We have also shown that it is possible to permanently alter the physiochemical properties of DNA-nanoparticles by the introduction of a photocleavable group. Indeed for the first time it has been shown that by exposure to UV light the disassembly of nanoparticle aggregates can be induced.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/10/7238/</guid>
	<pubDate>Mon, 24 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-10-24</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>10</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7238</prism:startingPage>
		<prism:endingPage>7249</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Use of Oligonucleotides Carrying Photolabile Groups for the Control of the Deposition of Nanoparticles in Surfaces and Nanoparticle Association</dc:title>
	<dc:date>2011-10-24</dc:date>
	<dc:identifier>doi: 10.3390/ijms12107238</dc:identifier>
		<dc:creator>Brendan Manning</dc:creator>
		<dc:creator>Ramon Eritja</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/10/7186/">
	<title>IJMS, Vol. 12, Pages 7186-7198: Metal Complexes of Diisopropylthiourea: Synthesis, Characterization and Antibacterial Studies</title>
	<link>http://www.mdpi.com/1422-0067/12/10/7186/</link>
	<description>Co(II), Cu(II), Zn(II) and Fe(III) complexes of diisopropylthiourea have been synthesized and characterized by elemental analyses, molar conductivity, magnetic susceptibility, FTIR and electronic spectroscopy. The compounds are non-electrolytes in solution and spectroscopic data of the complexes are consistent with 4-coordinate geometry for the metal(II) complexes and six coordinate octahedral for Fe(III) complex. The complexes were screened for their antibacterial activities against six bacteria: Escherichia coli, Pseudomonas auriginosa, Klebsiella pneumoniae, Bacillus cereus, Staphylococcus aureus and Bacillus pumilus. The complexes showed varied antibacterial activities and their minimum inhibitory concentrations (MICs) were determined.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/10/7186/</guid>
	<pubDate>Fri, 21 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-10-21</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>10</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7186</prism:startingPage>
		<prism:endingPage>7198</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Metal Complexes of Diisopropylthiourea: Synthesis, Characterization and Antibacterial Studies</dc:title>
	<dc:date>2011-10-21</dc:date>
	<dc:identifier>doi: 10.3390/ijms12107186</dc:identifier>
		<dc:creator>Peter A. Ajibade</dc:creator>
		<dc:creator>Nonkululeko H. Zulu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/10/6597/">
	<title>IJMS, Vol. 12, Pages 6597-6618: Crystallization Study and Comparative in Vitro–in Vivo Hydrolysis of PLA Reinforcement Ligament</title>
	<link>http://www.mdpi.com/1422-0067/12/10/6597/</link>
	<description>In the present work, the crystallization behavior and in vitro–in vivo hydrolysis rates of PLA absorbable reinforcement ligaments used in orthopaedics for the repair and reinforcement of articulation instabilities were studied. Tensile strength tests showed that this reinforcement ligament has similar mechanical properties to Fascia Latta, which is an allograft sourced from the ilio-tibial band of the human body. The PLA reinforcement ligament is a semicrystalline material with a glass transition temperature around 61 °C and a melting point of ~178 °C. Dynamic crystallization revealed that, although the crystallization rates of the material are slow, they are faster than the often-reported PLA crystallization rates. Mass loss and molecular weight reduction measurements showed that in vitro hydrolysis at 50 °C initially takes place at a slow rate, which gets progressively higher after 30–40 days. As found from SEM micrographs, deterioration of the PLA fibers begins during this time. Furthermore, as found from in vivo hydrolysis in the human body, the PLA reinforcement ligament is fully biocompatible and after 6 months of implantation is completely covered with flesh. However, the observed hydrolysis rate from in vivo studies was slow due to high molecular weight and degree of crystallinity.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/10/6597/</guid>
	<pubDate>Mon, 10 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-10-10</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>10</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6597</prism:startingPage>
		<prism:endingPage>6618</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Crystallization Study and Comparative in Vitro–in Vivo Hydrolysis of PLA Reinforcement Ligament</dc:title>
	<dc:date>2011-10-10</dc:date>
	<dc:identifier>doi: 10.3390/ijms12106597</dc:identifier>
		<dc:creator>Theodore Beslikas</dc:creator>
		<dc:creator>Ioannis Gigis</dc:creator>
		<dc:creator>Vasilios Goulios</dc:creator>
		<dc:creator>John Christoforides</dc:creator>
		<dc:creator>George Z. Papageorgiou</dc:creator>
		<dc:creator>Dimitrios N. Bikiaris</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/10/6397/">
	<title>IJMS, Vol. 12, Pages 6397-6406: Mössbauer Spectroscopy and X-ray Diffraction Study of 57Fe-Labeled Tetrachloroferrate(III)-Based Magnetic Ionic Liquids</title>
	<link>http://www.mdpi.com/1422-0067/12/10/6397/</link>
	<description>Four 57Fe-labeled tetrachloroferrates(III) of organic cations (1-butyl-3-methyl-imidazolium, 1-allyl-3-methylimidazolium, 1-methyl-1-propylpyrrolidinium, tetraphenyl­phosphonium) were examined by temperature-dependent Mössbauer spectroscopy. The hyperfine and dynamic parameters of the iron(III) site were determined. Single crystal X-ray diffraction data of [Ph4P][FeCl4] were collected at four temperatures (295, 223, 173, and 123 K), and the dynamics of the iron atom inferred from the Mössbauer data and the single crystal Ui,j parameters have been compared.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/10/6397/</guid>
	<pubDate>Mon, 26 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-26</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>10</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6397</prism:startingPage>
		<prism:endingPage>6406</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Mössbauer Spectroscopy and X-ray Diffraction Study of 57Fe-Labeled Tetrachloroferrate(III)-Based Magnetic Ionic Liquids</dc:title>
	<dc:date>2011-09-26</dc:date>
	<dc:identifier>doi: 10.3390/ijms12106397</dc:identifier>
		<dc:creator>Rolfe H. Herber</dc:creator>
		<dc:creator>Israel Nowik</dc:creator>
		<dc:creator>Mirco E. Kostner</dc:creator>
		<dc:creator>Volker Kahlenberg</dc:creator>
		<dc:creator>Christoph Kreutz</dc:creator>
		<dc:creator>Gerhard Laus</dc:creator>
		<dc:creator>Herwig Schottenberger</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/6346/">
	<title>IJMS, Vol. 12, Pages 6346-6356: Fabrication and Characterization of Gelatin Stabilized Silver Nanoparticles under UV-Light</title>
	<link>http://www.mdpi.com/1422-0067/12/9/6346/</link>
	<description>Silver nanoparticles (Ag-NPs) were successfully synthesized using the UV irradiation of aqueous solutions containing AgNO3 and gelatin as a silver source and stabilizer, respectively. The UV irradiation times influence the particles’ diameter of the Ag-NPs, as evidenced from surface plasmon resonance (SPR) bands and transmission electron microscopy (TEM) images. When the UV irradiation time was increased, the mean size of particles continuously decreased as a result of photoinduced Ag-NPs fragmentation. Based on X-ray diffraction (XRD), the UV-irradiated Ag-NPs were a face-centered cubic (fcc) single crystal without any impurity. This study reveals that the UV irradiation-mediated method is a green chemistry and promising route for the synthesis of stable Ag-NPs for several applications (e.g., medical and surgical devices). The important advantages of this method are that it is cheap, easy, and free of toxic materials.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/6346/</guid>
	<pubDate>Fri, 23 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-23</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6346</prism:startingPage>
		<prism:endingPage>6356</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Fabrication and Characterization of Gelatin Stabilized Silver Nanoparticles under UV-Light</dc:title>
	<dc:date>2011-09-23</dc:date>
	<dc:identifier>doi: 10.3390/ijms12096346</dc:identifier>
		<dc:creator>Majid Darroudi</dc:creator>
		<dc:creator>Mansor B. Ahmad</dc:creator>
		<dc:creator>Ali Khorsand Zak</dc:creator>
		<dc:creator>Reza Zamiri</dc:creator>
		<dc:creator>Mohammad Hakimi</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/6320/">
	<title>IJMS, Vol. 12, Pages 6320-6328: Effect of Low Concentration Sn Doping on Optical Properties of CdS Films Grown by CBD Technique</title>
	<link>http://www.mdpi.com/1422-0067/12/9/6320/</link>
	<description>Thin and transparent films of doped cadmium sulfide (CdS) were obtained on commercial glass substrates by Chemical Bath Deposition (CBD) technique. The films were doped with low concentration of Sn, and annealed in air at 300 °C for 45 min. The morphological characterization of the films with different amounts of dopant was made using SEM and EDAX analysis. Optical properties of the films were evaluated by measuring transmittance using the UV-vis spectrophotometer. A comparison of the results revealed that lower concentration of Sn doping improves transmittance of CdS films and makes them suitable for application as window layer of CdTe/CIGS solar cells.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/6320/</guid>
	<pubDate>Fri, 23 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-23</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6320</prism:startingPage>
		<prism:endingPage>6328</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Effect of Low Concentration Sn Doping on Optical Properties of CdS Films Grown by CBD Technique</dc:title>
	<dc:date>2011-09-23</dc:date>
	<dc:identifier>doi: 10.3390/ijms12096320</dc:identifier>
		<dc:creator>Atefeh Jafari</dc:creator>
		<dc:creator>Azmi Zakaria</dc:creator>
		<dc:creator>Zahid Rizwan</dc:creator>
		<dc:creator>Mohd Sabri Mohd Ghazali</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/6267/">
	<title>IJMS, Vol. 12, Pages 6267-6280: Nanoparticles and Neurotoxicity</title>
	<link>http://www.mdpi.com/1422-0067/12/9/6267/</link>
	<description>Humans are exposed to nanoparticles (NPs; diameter &lt; 100 nm) from ambient air and certain workplaces. There are two main types of NPs; combustion-derived NPs (e.g., particulate matters, diesel exhaust particles, welding fumes) and manufactured or engineered NPs (e.g., titanium dioxide, carbon black, carbon nanotubes, silver, zinc oxide, copper oxide). Recently, there have been increasing reports indicating that inhaled NPs can reach the brain and may be associated with neurodegeneration. It is necessary to evaluate the potential toxic effects of NPs on brain because most of the neurobehavioral disorders may be of environmental origin. This review highlights studies on both combustion-derived NP- and manufactured or engineered NP-induced neuroinflammation, oxidative stress, and gene expression, as well as the possible mechanism of these effects in animal models and in humans.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/6267/</guid>
	<pubDate>Fri, 23 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-23</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>6267</prism:startingPage>
		<prism:endingPage>6280</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Nanoparticles and Neurotoxicity</dc:title>
	<dc:date>2011-09-23</dc:date>
	<dc:identifier>doi: 10.3390/ijms12096267</dc:identifier>
		<dc:creator>Tin-Tin Win-Shwe</dc:creator>
		<dc:creator>Hidekazu Fujimaki</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/6240/">
	<title>IJMS, Vol. 12, Pages 6240-6254: Preparation and Scintillating Properties of Sol-Gel Eu3+, Tb3+ Co-Doped Lu2O3 Nanopowders</title>
	<link>http://www.mdpi.com/1422-0067/12/9/6240/</link>
	<description>Nanocrystalline Eu3+, Tb3+ co-doped Lu2O3 powders with a maximum size of 25.5 nm were prepared by the sol-gel process, using lutetium, europium and terbium nitrates as precursors, and ethanol as a solvent. Differential thermal analysis (DTA) and infrared spectroscopy (IR) were used to study the chemical changes during the xerogel annealing. After the sol evaporation at 100 °C, the formed gel was annealed from 300 to 900 °C for 30 min under a rich O2 atmosphere, and the yielded product was analyzed by X-ray diffraction (XRD) to characterize the microstructural behavior and confirm the crystalline structure. The results showed that Lu2O3 nanopowders start to crystallize at 400 °C and that the crystallite size increases along with the annealing temperature. A transmission electron microscopy (TEM) study of samples annealed at 700 and 900 °C was carried out in order to analyze the microstructure, as well as the size, of crystallites. Finally, in regard to scintillating properties, Eu3+ dopant (5 mol%), Tb3+ codoped Lu2O3 exhibited a typical red emission at 611 nm (Do→7F2), furthermore, the effect of Tb3+ molar content (0.01, 0.015 and 0.02% mol) on the Eu3+ radioluminiscence was analyzed and it was found that the higher emission intensity corresponds to the lower Tb3+ content.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/6240/</guid>
	<pubDate>Fri, 23 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-23</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6240</prism:startingPage>
		<prism:endingPage>6254</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Preparation and Scintillating Properties of Sol-Gel Eu3+, Tb3+ Co-Doped Lu2O3 Nanopowders</dc:title>
	<dc:date>2011-09-23</dc:date>
	<dc:identifier>doi: 10.3390/ijms12096240</dc:identifier>
		<dc:creator>Ángel de Jesús Morales Ramírez</dc:creator>
		<dc:creator>Antonieta García Murillo</dc:creator>
		<dc:creator>Felipe de Jesús Carrillo Romo</dc:creator>
		<dc:creator>Margarita García Hernández</dc:creator>
		<dc:creator>Joel Moreno Palmerin</dc:creator>
		<dc:creator>Rosario Ruiz Guerrero</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/6176/">
	<title>IJMS, Vol. 12, Pages 6176-6193: Optical Properties of Some New Azo Photoisomerizable Bismaleimide Derivatives</title>
	<link>http://www.mdpi.com/1422-0067/12/9/6176/</link>
	<description>Novel polythioetherimides bearing azobenzene moieties were synthesized from azobismaleimides and bis-2-mercaptoethylether. Kinetics of trans-cis photoisomerization and of thermal conversion of cis to trans isomeric forms were investigated in both polymer solution and poly(methyl methacrylate) doped films using electronic absorption spectroscopy. Thermal recovery kinetics is well described by a two-exponential relation both in solution and polymer matrix, while that of low molecular weight azobismaleimide fit a first-order equation. The photoinduced cis-trans isomerization by visible light of azobenzene chromophores was examined in solution and in polymer films. The rate of photoinduced recovery was very high for azobismaleimides.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/6176/</guid>
	<pubDate>Wed, 21 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-21</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6176</prism:startingPage>
		<prism:endingPage>6193</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Optical Properties of Some New Azo Photoisomerizable Bismaleimide Derivatives</dc:title>
	<dc:date>2011-09-21</dc:date>
	<dc:identifier>doi: 10.3390/ijms12096176</dc:identifier>
		<dc:creator>Anton Airinei</dc:creator>
		<dc:creator>Nicusor Fifere</dc:creator>
		<dc:creator>Mihaela Homocianu</dc:creator>
		<dc:creator>Constantin Gaina</dc:creator>
		<dc:creator>Viorica Gaina</dc:creator>
		<dc:creator>Bogdan C. Simionescu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/6040/">
	<title>IJMS, Vol. 12, Pages 6040-6050: Comparison of In Situ Polymerization and Solution-Dispersion Techniques in the Preparation of Polyimide/Montmorillonite (MMT) Nanocomposites</title>
	<link>http://www.mdpi.com/1422-0067/12/9/6040/</link>
	<description>In this paper, Polyimide/Montmorillonite Nanocomposites (PI/MMT NCs), based on aromatic diamine (4-Aminophenyl sulfone) (APS) and aromatic dianhydride (3,3',4,4'-benzophenonetetracarboxylic dianhydride) (BTDA) were prepared using in situ polymerization and solution-dispersion techniques. The prepared PI/MMT NCs films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM) and thermogravimetric analysis (TGA). The XRD results showed that at the content of 1.0 wt % Organo Montmorillonite (OMMT) for two techniques and 3.0 wt % OMMT for the in situ polymerization technique, the OMMT was well-intercalated, exfoliated and dispersed into polyimide matrix. The OMMT agglomerated when its amount exceeded 10 wt % and 3.0 wt % for solution-dispersion and in situ polymerization techniques respectively. These results were confirmed by the TEM images of the prepared PI/MMT NCs. The TGA thermograms indicated that thermal stability of prepared PI/MMT NCs were increased with the increase of loading that, the effect is higher for the samples prepared by in situ polymerization technique.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/6040/</guid>
	<pubDate>Mon, 19 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-19</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6040</prism:startingPage>
		<prism:endingPage>6050</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Comparison of In Situ Polymerization and Solution-Dispersion Techniques in the Preparation of Polyimide/Montmorillonite (MMT) Nanocomposites</dc:title>
	<dc:date>2011-09-19</dc:date>
	<dc:identifier>doi: 10.3390/ijms12096040</dc:identifier>
		<dc:creator>Mansor Bin Ahmad</dc:creator>
		<dc:creator>Yadollah Gharayebi</dc:creator>
		<dc:creator>Mohd. Sapuan Salit</dc:creator>
		<dc:creator>Mohd. Zobir Hussein</dc:creator>
		<dc:creator>Kamyar Shameli</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/5853/">
	<title>IJMS, Vol. 12, Pages 5853-5861: Enzymatic Cross-Linking of Alkali Extracted Arabinoxylans: Gel Rheological and Structural Characteristics</title>
	<link>http://www.mdpi.com/1422-0067/12/9/5853/</link>
	<description>Ferulated arabinoxylans were alkali-extracted from wheat bran at different incubation times (0.0, 0.5, 1.0, 1.5 and 2.0 h). Wheat bran ferulated arabinoxylans (WBAX) arabinose-to-xylose ratio, ferulic acid content, intrinsic viscosity and viscosimetric molecular weight values decreased as the incubation time of extraction increased. WBAX enzymatic cross-linking capability was affected by incubation time while an increase in WBAX concentration from 5 to 6% (w/v) favored gelation. The WBAX gels formed presented a macroporous structure with mesh size ranging from 40 to 119 nm and hardness values varying from 1.7 to 5 N.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/5853/</guid>
	<pubDate>Fri, 09 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-09</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5853</prism:startingPage>
		<prism:endingPage>5861</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Enzymatic Cross-Linking of Alkali Extracted Arabinoxylans: Gel Rheological and Structural Characteristics</dc:title>
	<dc:date>2011-09-09</dc:date>
	<dc:identifier>doi: 10.3390/ijms12095853</dc:identifier>
		<dc:creator>Claudia M. Berlanga-Reyes</dc:creator>
		<dc:creator>Elizabeth Carvajal-Millan</dc:creator>
		<dc:creator>Jaime Lizardi-Mendoza</dc:creator>
		<dc:creator>Alma R. Islas-Rubio</dc:creator>
		<dc:creator>Agustin Rascón-Chu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/5762/">
	<title>IJMS, Vol. 12, Pages 5762-5781: Automatic Defect Detection for TFT-LCD Array Process Using Quasiconformal Kernel Support Vector Data Description</title>
	<link>http://www.mdpi.com/1422-0067/12/9/5762/</link>
	<description>Defect detection has been considered an efficient way to increase the yield rate of panels in thin film transistor liquid crystal display (TFT-LCD) manufacturing. In this study we focus on the array process since it is the first and key process in TFT-LCD manufacturing. Various defects occur in the array process, and some of them could cause great damage to the LCD panels. Thus, how to design a method that can robustly detect defects from the images captured from the surface of LCD panels has become crucial. Previously, support vector data description (SVDD) has been successfully applied to LCD defect detection. However, its generalization performance is limited. In this paper, we propose a novel one-class machine learning method, called quasiconformal kernel SVDD (QK-SVDD) to address this issue. The QK-SVDD can significantly improve generalization performance of the traditional SVDD by introducing the quasiconformal transformation into a predefined kernel. Experimental results, carried out on real LCD images provided by an LCD manufacturer in Taiwan, indicate that the proposed QK-SVDD not only obtains a high defect detection rate of 96%, but also greatly improves generalization performance of SVDD. The improvement has shown to be over 30%. In addition, results also show that the QK-SVDD defect detector is able to accomplish the task of defect detection on an LCD image within 60 ms.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/5762/</guid>
	<pubDate>Fri, 09 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-09-09</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5762</prism:startingPage>
		<prism:endingPage>5781</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Automatic Defect Detection for TFT-LCD Array Process Using Quasiconformal Kernel Support Vector Data Description</dc:title>
	<dc:date>2011-09-09</dc:date>
	<dc:identifier>doi: 10.3390/ijms12095762</dc:identifier>
		<dc:creator>Yi-Hung Liu</dc:creator>
		<dc:creator>Yan-Jen Chen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/5565/">
	<title>IJMS, Vol. 12, Pages 5565-5576: New Dye-Sensitized Solar Cells Obtained from Extracted Bracts of Bougainvillea Glabra and Spectabilis Betalain Pigments by Different Purification Processes</title>
	<link>http://www.mdpi.com/1422-0067/12/9/5565/</link>
	<description>The performance of a new dye-sensitized solar cell (DSSC) based in a natural dye extracted from the Bougainvillea spectabilis’ bracts, is reported. The performance of this solar cell was compared with cells prepared using extract of the Bougainvillea glabra and mixture of both extracts; in both cases the pigments were betalains, obtained from Reddish-purple extract. These dyes were purified to different extents and used for the construction of solar cells that were electrically characterized. The materials were characterized using FTIR and UV-Vis. Solar cells were assembled using TiO2 thin film on indium tin oxide (ITO)-coated glass; a mesoporous film was sensitized with the Bougainvillea extracts. The obtained solar energy conversion efficiency was of 0.48% with a current density JSC of 2.29 mA/cm2 using an irradiation of 100 mW/cm2 at 25 °C.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/5565/</guid>
	<pubDate>Tue, 30 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-30</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5565</prism:startingPage>
		<prism:endingPage>5576</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>New Dye-Sensitized Solar Cells Obtained from Extracted Bracts of Bougainvillea Glabra and Spectabilis Betalain Pigments by Different Purification Processes</dc:title>
	<dc:date>2011-08-30</dc:date>
	<dc:identifier>doi: 10.3390/ijms12095565</dc:identifier>
		<dc:creator>Angel Ramon Hernandez-Martinez</dc:creator>
		<dc:creator>Miriam Estevez</dc:creator>
		<dc:creator>Susana Vargas</dc:creator>
		<dc:creator>Fracisco Quintanilla</dc:creator>
		<dc:creator>Rogelio Rodriguez</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/9/5538/">
	<title>IJMS, Vol. 12, Pages 5538-5551: ZnS, CdS and HgS Nanoparticles via Alkyl-Phenyl Dithiocarbamate Complexes as Single Source Precursors</title>
	<link>http://www.mdpi.com/1422-0067/12/9/5538/</link>
	<description>The synthesis of II-VI semiconductor nanoparticles obtained by the thermolysis of certain group 12 metal complexes as precursors is reported. Thermogravimetric analysis of the single source precursors showed sharp decomposition leading to their respective metal sulfides. The structural and optical properties of the prepared nanoparticles were characterized by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) UV-Vis and photoluminescence spectroscopy. The X-ray diffraction pattern showed that the prepared ZnS nanoparticles have a cubic sphalerite structure; the CdS indicates a hexagonal phase and the HgS show the presence of metacinnabar phase. The TEM image demonstrates that the ZnS nanoparticles are dot-shaped, the CdS and the HgS clearly showed a rice and spherical morphology respectively. The UV-Vis spectra exhibited a blue-shift with respect to that of the bulk samples which is attributed to the quantum size effect. The band gap of the samples have been calculated from absorption spectra and werefound to be about 4.33 eV (286 nm), 2.91 eV (426 nm) and 4.27 eV (290 nm) for the ZnS, CdS and HgS samples respectively.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/9/5538/</guid>
	<pubDate>Mon, 29 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-29</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5538</prism:startingPage>
		<prism:endingPage>5551</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>ZnS, CdS and HgS Nanoparticles via Alkyl-Phenyl Dithiocarbamate Complexes as Single Source Precursors</dc:title>
	<dc:date>2011-08-29</dc:date>
	<dc:identifier>doi: 10.3390/ijms12095538</dc:identifier>
		<dc:creator>Damian C. Onwudiwe</dc:creator>
		<dc:creator>Peter A. Ajibade</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/8/5422/">
	<title>IJMS, Vol. 12, Pages 5422-5427: Preparation and Microcosmic Structural Analysis of Recording Coating on Inkjet Printing Media</title>
	<link>http://www.mdpi.com/1422-0067/12/8/5422/</link>
	<description>Preparation of recording coating on inkjet printing (RC-IJP) media was proposed. The microstructure and roughness of RC-IJP was analyzed by scanning electron microscopy (SEM) and atomic force microscope (AFM). The surface infiltration process of RC-IJP was studied by a liquid infiltration instrument. The distribution of C, O and Si composites on recording coating surface is analyzed by energy dispersive spectrum (EDS). The transmission electron microscopy (TEM) analysis showed that the nanoscale silica could be dissolved uniformly in water. Finally, the print color is shown clearly by the preparative recording coating.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/8/5422/</guid>
	<pubDate>Tue, 23 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-23</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Communication</prism:section>
	<prism:startingPage>5422</prism:startingPage>
		<prism:endingPage>5427</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Preparation and Microcosmic Structural Analysis of Recording Coating on Inkjet Printing Media</dc:title>
	<dc:date>2011-08-23</dc:date>
	<dc:identifier>doi: 10.3390/ijms12085422</dc:identifier>
		<dc:creator>Bo Jiang</dc:creator>
		<dc:creator>Weiyan Liu</dc:creator>
		<dc:creator>Yongping Bai</dc:creator>
		<dc:creator>Yudong Huang</dc:creator>
		<dc:creator>Li Liu</dc:creator>
		<dc:creator>Jianping Han</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/8/5352/">
	<title>IJMS, Vol. 12, Pages 5352-5372: Structure and Dynamics of Reentrant Nematics: Any Open Questions after Almost 40 Years?</title>
	<link>http://www.mdpi.com/1422-0067/12/8/5352/</link>
	<description>Liquid crystals have attracted enormous interest because of the variety of their phases and richness of their application. The interplay of general physical symmetries and specific molecular features generates a myriad of different phenomena. A surprising behavior of liquid crystals is the reentrancy of phases as temperature, pressure, or concentration are varied. Here, we review the main experimental facts and the different theoretical scenarios that have guided the understanding of bulk reentrant nematics. Recently, some computer simulations of a system confined to nanoscopic scales have found new dynamical features of the reentrant nematic phase. We discuss this prediction in relation with the available experimental evidence on reentrant nematics and with the dynamics of liquids in strongly confined environments.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/8/5352/</guid>
	<pubDate>Mon, 22 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-22</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>5352</prism:startingPage>
		<prism:endingPage>5372</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Structure and Dynamics of Reentrant Nematics: Any Open Questions after Almost 40 Years?</dc:title>
	<dc:date>2011-08-22</dc:date>
	<dc:identifier>doi: 10.3390/ijms12085352</dc:identifier>
		<dc:creator>Marco G. Mazza</dc:creator>
		<dc:creator>Martin Schoen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/8/5330/">
	<title>IJMS, Vol. 12, Pages 5330-5338: Effect of Filler Size and Temperature on Packing Stress and Viscosity of Resin-composites</title>
	<link>http://www.mdpi.com/1422-0067/12/8/5330/</link>
	<description>The objective of this study was to investigate the effect of filler size on the packing stress and viscosity of uncured resin-composite at 23 °C and 37 °C. A precision instrument used was designed upon the penetrometer principle. Eight resin-composite materials were tested. Packing-stress ranged from 2.60 to 0.43 MPa and viscosity ranged from 2.88 to 0.02 MPa.s at 23 °C. Values for both properties were reduced significantly at 37 °C. Statistical analysis, by ANOVA and post hoc methods, were carried out to check any significant differences between materials tested (P &lt; 0.05). Conclusions: Filler size and distribution will affect the viscosity and packing of resin-composites during cavity placement.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/8/5330/</guid>
	<pubDate>Thu, 18 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-18</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5330</prism:startingPage>
		<prism:endingPage>5338</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Effect of Filler Size and Temperature on Packing Stress and Viscosity of Resin-composites</dc:title>
	<dc:date>2011-08-18</dc:date>
	<dc:identifier>doi: 10.3390/ijms12085330</dc:identifier>
		<dc:creator>Haitham Elbishari</dc:creator>
		<dc:creator>Julian Satterthwaite</dc:creator>
		<dc:creator>Nick Silikas</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/8/5039/">
	<title>IJMS, Vol. 12, Pages 5039-5051: Potential Antibacterial Activity of Carvacrol-Loaded Poly(DL-lactide-co-glycolide) (PLGA) Nanoparticles against Microbial Biofilm</title>
	<link>http://www.mdpi.com/1422-0067/12/8/5039/</link>
	<description>The ability to form biofilms contributes significantly to the pathogenesis of many microbial infections, including a variety of ocular diseases often associated with the biofilm formation on foreign materials. Carvacrol (Car.) is an important component of essential oils and recently has attracted much attention pursuant to its ability to promote microbial biofilm disruption. In the present study Car. has been encapsulated in poly(DL-lactide-co-glycolide (PLGA) nanocapsules in order to obtain a suitable drug delivery system that could represent a starting point for developing new therapeutic strategies against biofilm-associated infections, such as improving the drug effect by associating an antimicrobial agent with a biofilm viscoelasticity modifier.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/8/5039/</guid>
	<pubDate>Mon, 08 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-08</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5039</prism:startingPage>
		<prism:endingPage>5051</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Potential Antibacterial Activity of Carvacrol-Loaded Poly(DL-lactide-co-glycolide) (PLGA) Nanoparticles against Microbial Biofilm</dc:title>
	<dc:date>2011-08-08</dc:date>
	<dc:identifier>doi: 10.3390/ijms12085039</dc:identifier>
		<dc:creator>Antonio Iannitelli</dc:creator>
		<dc:creator>Rossella Grande</dc:creator>
		<dc:creator>Antonio Di Stefano</dc:creator>
		<dc:creator>Mara Di Giulio</dc:creator>
		<dc:creator>Piera Sozio</dc:creator>
		<dc:creator>Lucinda Janete Bessa</dc:creator>
		<dc:creator>Sara Laserra</dc:creator>
		<dc:creator>Cecilia Paolini</dc:creator>
		<dc:creator>Feliciano Protasi</dc:creator>
		<dc:creator>Luigina Cellini</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/8/5031/">
	<title>IJMS, Vol. 12, Pages 5031-5038: Comparative Clinical Study of Bactigras and Telfa AMD for Skin Graft Donor-Site Dressing</title>
	<link>http://www.mdpi.com/1422-0067/12/8/5031/</link>
	<description>The Bactigras® paraffin tulle coated with chlorhexidine is normally used for the treatment of donor-site wounds in burn patients who received split-thickness skin grafts in several centers. It has some disadvantages, such as adhesion to wound surfaces and pain from the irritation caused by this dressing. The Telfa AMD®, a non-adherent wound dressing which consists of absorbent cotton fibers impregnated with polyhexamethylene biguanide enclosed in a sleeve of thermoplastic polymers, is a new option for donor-site wound care which causes less adherence to the wound. The purpose of this study was to compare clinical efficacy of these two dressings for the management of donor-site wounds. Thirty-two patients who received split-thickness skin grafts by donor site harvesting from the thigh were enrolled in this study and randomized into two groups receiving either the Bactigras® or the Telfa AMD® wound treatment. Re-epithelialization, pain, infection and cost-effectiveness analyses were compared between both groups. The results showed that there was no significant difference in age, area of donor sites or length of hospital stays between the groups (p &gt; 0.05). However, the day of re-epithelialization (≥90%) was significantly shorter in patients treated with the Telfa AMD® compared to the Bactigras® group (14.00 ± 3.05 vs. 9.25 ± 1.88 days for Bactigras® and Telfa AMD® groups, respectively, p &lt; 0.001). The average pain score was also significantly lower in the Telfa AMD® group (1.57 ± 0.55 vs. 4.70 ± 1.16, p &lt; 0.001). There was no difference in the cost of treatment between the groups (4.64 ± 1.97 vs. 5.72 ± 2.54 USD, p = 0.19). This study indicated that the Telfa AMD® was an effective dressing for the treatment of donor-site wounds.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/8/5031/</guid>
	<pubDate>Mon, 08 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-08</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5031</prism:startingPage>
		<prism:endingPage>5038</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Comparative Clinical Study of Bactigras and Telfa AMD for Skin Graft Donor-Site Dressing</dc:title>
	<dc:date>2011-08-08</dc:date>
	<dc:identifier>doi: 10.3390/ijms12085031</dc:identifier>
		<dc:creator>Pornprom Muangman</dc:creator>
		<dc:creator>Sooksan Nitimonton</dc:creator>
		<dc:creator>Pornanong Aramwit</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/8/4923/">
	<title>IJMS, Vol. 12, Pages 4923-4945: The Langmuir-Blodgett Technique as a Tool for Homeotropic Alignment of Fluorinated Liquid Crystals Mixed with Arachidic Acid</title>
	<link>http://www.mdpi.com/1422-0067/12/8/4923/</link>
	<description>Some fluoro-substituted liquid crystals mixed with arachidic acid in monolayers formed at air-liquid (Langmuir films) and air-solid substrate (Langmuir-Blodgett films) interfaces were investigated. Molecular organization in Langmuir films was determined on the basis of the analysis of the shape of the surface pressure-mean molecular area isotherm and observations made by means of a Brewster angle microscope. It was found that in the compression process the liquid crystal molecules are pushed out towards the top of the first monolayer being in direct contact with the subphase. Langmuir films were transferred onto the quartz substrates at various surface pressures and mono- and multilayered Langmuir-Blodgett films were obtained. The films were characterized using electronic absorption measurements. The conditions for obtaining the homeotropic orientation of the liquid crystal molecules were determined.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/8/4923/</guid>
	<pubDate>Wed, 03 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-03</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4923</prism:startingPage>
		<prism:endingPage>4945</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>The Langmuir-Blodgett Technique as a Tool for Homeotropic Alignment of Fluorinated Liquid Crystals Mixed with Arachidic Acid</dc:title>
	<dc:date>2011-08-03</dc:date>
	<dc:identifier>doi: 10.3390/ijms12084923</dc:identifier>
		<dc:creator>Anna Modlińska</dc:creator>
		<dc:creator>Danuta Bauman</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/8/4872/">
	<title>IJMS, Vol. 12, Pages 4872-4884: Green Synthesis and Characterization of Silver/Chitosan/Polyethylene Glycol Nanocomposites without any Reducing Agent</title>
	<link>http://www.mdpi.com/1422-0067/12/8/4872/</link>
	<description>This paper presents the green synthesis of silver nanoparticles (Ag NPs) in aqueous medium. This method was performed by reducing AgNO3 in different stirring times of reaction at a moderate temperature using green agents, chitosan (Cts) and polyethylene glycol (PEG). In this work, silver nitrate (AgNO3) was used as the silver precursor while Cts and PEG were used as the solid support and polymeric stabilizer. The properties of Ag/Cts/PEG nanocomposites (NCs) were studied under different stirring times of reaction. The developed Ag/Cts/PEG NCs were then characterized by the ultraviolet-visible (UV-Vis) spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/8/4872/</guid>
	<pubDate>Tue, 02 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-08-02</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4872</prism:startingPage>
		<prism:endingPage>4884</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Green Synthesis and Characterization of Silver/Chitosan/Polyethylene Glycol Nanocomposites without any Reducing Agent</dc:title>
	<dc:date>2011-08-02</dc:date>
	<dc:identifier>doi: 10.3390/ijms12084872</dc:identifier>
		<dc:creator>Mansor Bin Ahmad</dc:creator>
		<dc:creator>Mei Yen Tay</dc:creator>
		<dc:creator>Kamyar Shameli</dc:creator>
		<dc:creator>Mohd Zobir Hussein</dc:creator>
		<dc:creator>Jenn Jye Lim</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/7/4735/">
	<title>IJMS, Vol. 12, Pages 4735-4744: Antifungal Activity of Denture Soft Lining Material Modified by Silver Nanoparticles—A Pilot Study</title>
	<link>http://www.mdpi.com/1422-0067/12/7/4735/</link>
	<description>Soft liner materials in oral cavity environments are easily colonized both by fungi and dental plaque. These factors are the cause of mucosal infections. The microorganism that most frequently colonizes soft liner materials is Candida albicans. Colonization occurs on the surface of materials and within materials. A solution to this problem might involve modification of soft liner materials with silver nanoparticles (AgNPs). In this article, we present results showing the antifungal efficacy of silicone soft lining materials modified with AgNPs. The modification process was conducted by dissolving both material components (base and catalyst) in a colloidal solution of AgNPs and evaporating the solvent. Composites with various AgNP concentrations (10, 20, 40, 80, 120 and 200 ppm) were examined. The in vitro antifungal efficacy (AFE) of composite samples was 16.3% to 52.5%.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/7/4735/</guid>
	<pubDate>Fri, 22 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-07-22</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4735</prism:startingPage>
		<prism:endingPage>4744</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Antifungal Activity of Denture Soft Lining Material Modified by Silver Nanoparticles—A Pilot Study</dc:title>
	<dc:date>2011-07-22</dc:date>
	<dc:identifier>doi: 10.3390/ijms12074735</dc:identifier>
		<dc:creator>Grzegorz Chladek</dc:creator>
		<dc:creator>Anna Mertas</dc:creator>
		<dc:creator>Izabela Barszczewska-Rybarek</dc:creator>
		<dc:creator>Teresa Nalewajek</dc:creator>
		<dc:creator>Jarosław Żmudzki</dc:creator>
		<dc:creator>Wojciech Król</dc:creator>
		<dc:creator>Jan Łukaszczyk</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/7/4488/">
	<title>IJMS, Vol. 12, Pages 4488-4503: Steady State–Hopf Mode Interactions at the Onset of Electroconvection in the Nematic Liquid Crystal Phase V</title>
	<link>http://www.mdpi.com/1422-0067/12/7/4488/</link>
	<description>We report on a new mode interaction found in electroconvection experiments on the nematic liquid crystal mixture Phase V in planar geometry. The mode interaction (codimension two) point occurs at a critical value of the frequency of the driving AC voltage. For frequencies below this value the primary pattern-forming instability at the onset voltage is an oblique stationary instability involving oblique rolls, and above this value it is an oscillatory instability giving rise to normal traveling rolls (oriented perpendicular to and traveling in the director direction). The transition has been confirmed by measuring the roll angle and the dominant frequency of the time series, as both quantities exhibit a discontinuous jump across zero when the AC frequency is varied near threshold. The globally coupled system of Ginzburg–Landau equations that qualitatively describe this mode interaction is constructed, and the resulting normal form, in which slow spatial variations of the mode amplitudes are ignored, is analyzed. This analysis shows that the Ginzburg–Landau system provides the adequate theoretical description for the experimentally observed phenomenon. The experimentally observed patterns at and higher above the onset allow us to narrow down the range of the parameters in the normal form.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/7/4488/</guid>
	<pubDate>Wed, 13 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-07-13</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4488</prism:startingPage>
		<prism:endingPage>4503</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Steady State–Hopf Mode Interactions at the Onset of Electroconvection in the Nematic Liquid Crystal Phase V</dc:title>
	<dc:date>2011-07-13</dc:date>
	<dc:identifier>doi: 10.3390/ijms12074488</dc:identifier>
		<dc:creator>Gyanu Acharya</dc:creator>
		<dc:creator>Gerhard Dangelmayr</dc:creator>
		<dc:creator>James Gleeson</dc:creator>
		<dc:creator>Iuliana Oprea</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/7/4414/">
	<title>IJMS, Vol. 12, Pages 4414-4434: Isoniazid Proliposome Powders for Inhalation—Preparation, Characterization and Cell Culture Studies</title>
	<link>http://www.mdpi.com/1422-0067/12/7/4414/</link>
	<description>The aims of this study were to develop proliposome powders containing isoniazid (INH) in a dry powder aerosol form. INH-proliposome powders were prepared by a spray drying method. Proliposome physicochemical properties were determined using cascade impactor, X-ray diffraction and differential scanning calorimetry. The toxicity of proliposomes to respiratory-associated cell lines and its potential to provoke immunological responses from alveolar macrophages (AM) were determined. Free INH and INH-proliposome bioactivities were tested in vitro and in AM infected with Mycobacterium bovis (M. bovis). Aerosolization properties of INH-proliposome powders at 60 L/min, the powders showed mass median aerodynamic diameters of 2.99–4.92 mm, with fine particle fractions (aerosolized particles less than 4.4 µm) of 15–35%. Encapsulation of INH was 18–30%. Proliposome formulations containing INH to mannitol ratios of 4:6 and 6:4 exhibited the greatest overlapping peak between the drug and mannitol. INH-proliposomes were evidently nontoxic to respiratory-associated cells, and did not activate AM to produce inflammatory mediators—including interleukin-1b (IL-1b), tumor necrosis factor-a (TNF-a), and nitric oxide—at a toxic level. The efficacy of INH-proliposome against AM infected with M. bovis was significantly higher than that of free INH (p &lt; 0.05). INH-proliposomes are potential candidates for an alternative tuberculosis treatment.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/7/4414/</guid>
	<pubDate>Thu, 07 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-07-07</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4414</prism:startingPage>
		<prism:endingPage>4434</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Isoniazid Proliposome Powders for Inhalation—Preparation, Characterization and Cell Culture Studies</dc:title>
	<dc:date>2011-07-07</dc:date>
	<dc:identifier>doi: 10.3390/ijms12074414</dc:identifier>
		<dc:creator>Wipaporn Rojanarat</dc:creator>
		<dc:creator>Narumon Changsan</dc:creator>
		<dc:creator>Ekawat Tawithong</dc:creator>
		<dc:creator>Sirirat Pinsuwan</dc:creator>
		<dc:creator>Hak-Kim Chan</dc:creator>
		<dc:creator>Teerapol Srichana</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/7/4365/">
	<title>IJMS, Vol. 12, Pages 4365-4377: Novel Recovery of Nano-Structured Ceria (CeO2) from Ce(III)-Benzoxazine Dimer Complexes via Thermal Decomposition</title>
	<link>http://www.mdpi.com/1422-0067/12/7/4365/</link>
	<description>N,N-bis(2-hydroxybenzyl)alkylamines, benzoxazine dimers, are the major product produced from benzoxazine monomers on mono-functional phenol by the one  step ring opening reaction. Due to the metal responsive property of benzoxazine dimers, in this present work, N,N-bis(5-methyl-2-hydroxybenzyl)methylamine (MMD), N,N-bis (5-ethyl-2-hydroxybenzyl)methylamine (EMD), and N,N-bis(5-methoxy-2-hydroxybenzyl) methyl amine (MeMD), are considered as novel ligands for rare earth metal ion, such as cerium(III) ion. The complex formed when the clear and colorless solutions of cerium nitrate and benzoxazine dimers were mixed, results in a brown colored solution. The metal-ligand ratios determined by the molar ratio and the Job’s methods were found to be in a ratio of 1:6. To clarify the evidence of the complex formation mechanism, the interactions among protons in benzoxazine dimers both prior to and after the formation of complexes were determined by means of 1H-NMR, 2D-NMR and a computational simulation. The single phase ceria (CeO2) was successfully prepared by thermal decomposition of the Ce(III)-benzoxazine dimer complexes at 600 °C for 2 h, was then characterized using XRD. In addition, the ceria powder investigated by TEM is spherical with an average diameter of 20 nm.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/7/4365/</guid>
	<pubDate>Tue, 05 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-07-05</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4365</prism:startingPage>
		<prism:endingPage>4377</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Novel Recovery of Nano-Structured Ceria (CeO2) from Ce(III)-Benzoxazine Dimer Complexes via Thermal Decomposition</dc:title>
	<dc:date>2011-07-05</dc:date>
	<dc:identifier>doi: 10.3390/ijms12074365</dc:identifier>
		<dc:creator>Chatchai Veranitisagul</dc:creator>
		<dc:creator>Attaphon Kaewvilai</dc:creator>
		<dc:creator>Sarawut Sangngern</dc:creator>
		<dc:creator>Worawat Wattanathana</dc:creator>
		<dc:creator>Songwut Suramitr</dc:creator>
		<dc:creator>Nattamon Koonsaeng</dc:creator>
		<dc:creator>Apirat Laobuthee</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/7/4294/">
	<title>IJMS, Vol. 12, Pages 4294-4314: Controlled Delivery of Gentamicin Using Poly(3-hydroxybutyrate) Microspheres</title>
	<link>http://www.mdpi.com/1422-0067/12/7/4294/</link>
	<description>Poly(3-hydroxybutyrate), P(3HB), produced from Bacillus cereus SPV using a simple glucose feeding strategy was used to fabricate P(3HB) microspheres using a solid-in-oil-water (s/o/w) technique. For this study, several parameters such as polymer concentration, surfactant and stirring rates were varied in order to determine their effect on microsphere characteristics. The average size of the microspheres was in the range of 2 µm to 1.54 µm with specific surface areas varying between 9.60 m2/g and 6.05 m2/g. Low stirring speed of 300 rpm produced slightly larger microspheres when compared to the smaller microspheres produced when the stirring velocity was increased to 800 rpm. The surface morphology of the microspheres after solvent evaporation appeared smooth when observed under SEM. Gentamicin was encapsulated within these P(3HB) microspheres and the release kinetics from the microspheres exhibiting the highest encapsulation efficiency, which was 48%, was investigated. The in vitro release of gentamicin was bimodal, an initial burst release was observed followed by a diffusion mediated sustained release. Biodegradable P(3HB) microspheres developed in this research has shown high potential to be used in various biomedical applications.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/7/4294/</guid>
	<pubDate>Mon, 04 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-07-04</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4294</prism:startingPage>
		<prism:endingPage>4314</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Controlled Delivery of Gentamicin Using Poly(3-hydroxybutyrate) Microspheres</dc:title>
	<dc:date>2011-07-04</dc:date>
	<dc:identifier>doi: 10.3390/ijms12074294</dc:identifier>
		<dc:creator>Lydia Francis</dc:creator>
		<dc:creator>Decheng Meng</dc:creator>
		<dc:creator>Jonathan Knowles</dc:creator>
		<dc:creator>Tajalli Keshavarz</dc:creator>
		<dc:creator>Aldo R. Boccaccini</dc:creator>
		<dc:creator>Ipsita Roy</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/7/4282/">
	<title>IJMS, Vol. 12, Pages 4282-4293: Preparation and Characterization of Catalase-Loaded Solid Lipid Nanoparticles Protecting Enzyme against Proteolysis</title>
	<link>http://www.mdpi.com/1422-0067/12/7/4282/</link>
	<description>Catalase-loaded solid lipid nanoparticles (SLNs) were prepared by the double emulsion method (w/o/w) and solvent evaporation techniques, using acetone/methylene chloride (1:1) as an organic solvent, lecithin and triglyceride as oil phase and Poloxmer 188 as a surfactant. The optimized SLN was prepared by lecithin: triglyceride ratio (5%), 20-second + 30-second sonication, and 2% Poloxmer 188. The mean particle size of SLN was 296.0 ± 7.0 nm, polydispersity index range and zeta potential were 0.322–0.354 and −36.4 ± 0.6, respectively, and the encapsulation efficiency reached its maximum of 77.9 ± 1.56. Catalase distributed between the solid lipid and inner aqueous phase and gradually released from Poloxmer coated SLNs up to 20% within 20 h. Catalase-loaded SLN remained at 30% of H2O2-degrading activity after being incubated with Proteinase K for 24 h, while free catalase lost activity within 1 h.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/7/4282/</guid>
	<pubDate>Mon, 04 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-07-04</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4282</prism:startingPage>
		<prism:endingPage>4293</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Preparation and Characterization of Catalase-Loaded Solid Lipid Nanoparticles Protecting Enzyme against Proteolysis</dc:title>
	<dc:date>2011-07-04</dc:date>
	<dc:identifier>doi: 10.3390/ijms12074282</dc:identifier>
		<dc:creator>Ce Qi</dc:creator>
		<dc:creator>Yan Chen</dc:creator>
		<dc:creator>Qing-Zhe Jing</dc:creator>
		<dc:creator>Xing-Guo Wang</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/7/4250/">
	<title>IJMS, Vol. 12, Pages 4250-4270: Biodegradable Metals for Cardiovascular Stent Application: Interests and New Opportunities</title>
	<link>http://www.mdpi.com/1422-0067/12/7/4250/</link>
	<description>During the last decade, biodegradable metallic stents have been developed and investigated as alternatives for the currently-used permanent cardiovascular stents. Degradable metallic materials could potentially replace corrosion-resistant metals currently used for stent application as it has been shown that the role of stenting is temporary and limited to a period of 6–12 months after implantation during which arterial remodeling and healing occur. Although corrosion is generally considered as a failure in metallurgy, the corrodibility of certain metals can be an advantage for their application as degradable implants. The candidate materials for such application should have mechanical properties ideally close to those of 316L stainless steel which is the gold standard material for stent application in order to provide mechanical support to diseased arteries. Non-toxicity of the metal itself and its degradation products is another requirement as the material is absorbed by blood and cells. Based on the mentioned requirements, iron-based and magnesium-based alloys have been the investigated candidates for biodegradable stents. This article reviews the recent developments in the design and evaluation of metallic materials for biodegradable stents. It also introduces the new metallurgical processes which could be applied for the production of metallic biodegradable stents and their effect on the properties of the produced metals.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/7/4250/</guid>
	<pubDate>Wed, 29 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-06-29</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>4250</prism:startingPage>
		<prism:endingPage>4270</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Biodegradable Metals for Cardiovascular Stent Application: Interests and New Opportunities</dc:title>
	<dc:date>2011-06-29</dc:date>
	<dc:identifier>doi: 10.3390/ijms12074250</dc:identifier>
		<dc:creator>Maryam Moravej</dc:creator>
		<dc:creator>Diego Mantovani</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/6/4009/">
	<title>IJMS, Vol. 12, Pages 4009-4020: Synthesis of Cross-Linked Chitosan and Application to Adsorption and Speciation of Se (VI) and Se (IV) in Environmental Water Samples by Inductively Coupled Plasma Optical Emission Spectrometry</title>
	<link>http://www.mdpi.com/1422-0067/12/6/4009/</link>
	<description>A new type of cross-linked chitosan was synthesized with Diethylene Triamine (DCCTS). The adsorption of Se (VI) on DCCTS was studied. The effect factors on adsorption and the adsorption mechanism were considered. The results indicated that the DCCTS could concentrate and separate Se (IV) at pH = 3.6; the maximum adsorption efficiency was 94%, the adsorption equilibrium time was 30 min; the maximum adsorption capacity was 42.7 mg/g; the adsorption fitted Langmuir equation. A novel method for speciation of Se (VI) and Se (IV) in environmental water samples has been developed using DCCTS as adsorbent and ICP–OES as determination means. The detection limit of this method was 12 ng/L, the relatively standard deviation was 4.5% and the recovery was 99%~104%.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/6/4009/</guid>
	<pubDate>Tue, 14 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-06-14</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4009</prism:startingPage>
		<prism:endingPage>4020</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Synthesis of Cross-Linked Chitosan and Application to Adsorption and Speciation of Se (VI) and Se (IV) in Environmental Water Samples by Inductively Coupled Plasma Optical Emission Spectrometry</dc:title>
	<dc:date>2011-06-14</dc:date>
	<dc:identifier>doi: 10.3390/ijms12064009</dc:identifier>
		<dc:creator>Jun Dai</dc:creator>
		<dc:creator>Feng Lian Ren</dc:creator>
		<dc:creator>Chun Yuan Tao</dc:creator>
		<dc:creator>Yang Bai</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/6/3857/">
	<title>IJMS, Vol. 12, Pages 3857-3870: Structural Characterization of Poly-L-lactic Acid (PLLA) and Poly(glycolic acid)(PGA) Oligomers</title>
	<link>http://www.mdpi.com/1422-0067/12/6/3857/</link>
	<description>Structural characterization of poly-L-lactic acid (PLLA) and poly(glycolic acid) (PGA) oligomers containing three units was carried out with an atomistic approach. Oligomer structures were first optimized through quantum chemical calculations, using density functional theory (DFT); rotational barriers concerning dihedral angles along the chain were then investigated. Diffusion coefficients of L-lactic acid and glycolic acid in pure water were estimated through molecular dynamic (MD) simulations. Monomer structures were obtained with quantum chemical computation in implicit water using DFT method; atomic charges were fitted with Restrained Electrostatic Potentials (RESP) formalism, starting from electrostatic potentials calculated with quantum chemistry. MD simulations were carried out in explicit water, in order to take into account solvent presence</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/6/3857/</guid>
	<pubDate>Fri, 10 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-06-10</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>3857</prism:startingPage>
		<prism:endingPage>3870</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Structural Characterization of Poly-L-lactic Acid (PLLA) and Poly(glycolic acid)(PGA) Oligomers</dc:title>
	<dc:date>2011-06-10</dc:date>
	<dc:identifier>doi: 10.3390/ijms12063857</dc:identifier>
		<dc:creator>Tommaso Casalini</dc:creator>
		<dc:creator>Filippo Rossi</dc:creator>
		<dc:creator>Marco Santoro</dc:creator>
		<dc:creator>Giuseppe Perale</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/6/3821/">
	<title>IJMS, Vol. 12, Pages 3821-3830: Synthesis of Brushite Particles in Reverse Microemulsions of the Biosurfactant Surfactin</title>
	<link>http://www.mdpi.com/1422-0067/12/6/3821/</link>
	<description>In this study the “green chemistry” use of the biosurfactant surfactin for the synthesis of calcium phosphate using the reverse microemulsion technique was demonstrated. Calcium phosphates are bioactive materials that are a major constituent of human teeth and bone tissue. A reverse microemulsion technique with surfactin was used to produce nanocrystalline brushite particles. Structural diversity (analyzed by SEM and TEM) resulted from different water to surfactin ratios (W/S; 250, 500, 1000 and 40,000). The particle sizes were found to be in the 16–200 nm range. Morphological variety was observed in the as-synthesized microemulsions, which consisted of nanospheres (~16 nm in diameter) and needle-like (8–14 nm in diameter and 80–100 nm in length) noncalcinated particles. However, the calcinated products included nanospheres (50–200 nm in diameter), oval (~300 nm in diameter) and nanorod (200–400 nm in length) particles. FTIR and XRD analysis confirmed the formation of brushite nanoparticles in the as-synthesized products, while calcium pyrophosphate was produced after calcination. These results indicate that the reverse microemulsion technique using surfactin is a green process suitable for the synthesis of nanoparticles.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/6/3821/</guid>
	<pubDate>Thu, 09 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-06-09</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>3821</prism:startingPage>
		<prism:endingPage>3830</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Synthesis of Brushite Particles in Reverse Microemulsions of the Biosurfactant Surfactin</dc:title>
	<dc:date>2011-06-09</dc:date>
	<dc:identifier>doi: 10.3390/ijms12063821</dc:identifier>
		<dc:creator>Jyoti Prakash Maity</dc:creator>
		<dc:creator>Tz-Jiun Lin</dc:creator>
		<dc:creator>Henry Pai-Heng Cheng</dc:creator>
		<dc:creator>Chien-Yen Chen</dc:creator>
		<dc:creator>A. Satyanarayana Reddy</dc:creator>
		<dc:creator>Shashi B. Atla</dc:creator>
		<dc:creator>Young-Fo Chang</dc:creator>
		<dc:creator>Hau-Ren Chen</dc:creator>
		<dc:creator>Chien-Cheng Chen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1422-0067/12/6/3810/">
	<title>IJMS, Vol. 12, Pages 3810-3820: Screen-Printed Carbon Electrodes Modified with Cobalt Phthalocyanine for Selective Sulfur Detection in Cosmetic Products</title>
	<link>http://www.mdpi.com/1422-0067/12/6/3810/</link>
	<description>Cobalt phthalocyanine (CoPc) films were deposited on the surface of a screen-printed carbon electrode using a simple drop coating method. The cyclic voltammogram of the resulting CoPc modified screen-printed electrode (CoPc/SPE) prepared under optimum conditions shows a well-behaved redox couple due to the (CoI/CoII) system. The CoPc/SPE surface demonstrates excellent electrochemical activity towards the oxidation of sulfur in a 0.01 mol·L−1 NaOH. A linear calibration curve with the detection limit (DL, S/N = 3) of 0.325 mg·L−1 was achieved by CoPc/SPE coupled with flow injection analysis of the sulfur concentration ranging from 4 to 1120 mg·L−1. The precision of the system response was evaluated (3.60% and 3.52% RSD for 12 repeated injections), in the range of 64 and 480 mg·L−1 sulfur. The applicability of the method was successfully demonstrated in a real sample analysis of sulfur in anti-acne creams, and good recovery was obtained. The CoPc/SPE displayed several advantages in sulfur determination including easy fabrication, high stability, and low cost.</description>
	
	<guid>http://www.mdpi.com/1422-0067/12/6/3810/</guid>
	<pubDate>Thu, 09 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>International Journal of Molecular Sciences</prism:publicationName>
	<prism:publicationDate>2011-06-09</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>3810</prism:startingPage>
		<prism:endingPage>3820</prism:endingPage>
		<prism:issn>1422-0067</prism:issn>
	
	<dc:title>Screen-Printed Carbon Electrodes Modified with Cobalt Phthalocyanine for Selective Sulfur Detection in Cosmetic Products</dc:title>
	<dc:date>2011-06-09</dc:date>
	<dc:identifier>doi: 10.3390/ijms12063810</dc:identifier>
		<dc:creator>Pei-Yen Chen</dc:creator>
		<dc:creator>Chin-Hsiang Luo</dc:creator>
		<dc:creator>Mei-Chin Chen</dc:creator>
		<dc:creator>Feng-Jie Tsai</dc:creator>
		<dc:creator>Nai-Fang Chang</dc:creator>
		<dc:creator>Ying Shih</dc:creator>
	
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