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Keywords = polydopamine shell

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15 pages, 3889 KB  
Article
Stable Gold@Polydopamine@ssDNA Bioconjugates for Highly Efficient Detection of Tumor-Related mRNA in Living Cells
by Senhao Hu, Wenjing Wang, Yu Zou, Chunmei Li, Hongyan Zou, Chengzhi Huang and Lei Zhan
Molecules 2025, 30(17), 3551; https://doi.org/10.3390/molecules30173551 - 29 Aug 2025
Viewed by 885
Abstract
The development of low-background, facile, and robust fluorescent nanoprobes for imaging and monitoring of intracellular mRNA changes remains a great challenge. Taking advantage of the high fluorescence quenching efficiency of core-shell gold@polydopamine (Au@PDA) nanocomposites and Ca2+-promoting DNA adsorption stability, a simple [...] Read more.
The development of low-background, facile, and robust fluorescent nanoprobes for imaging and monitoring of intracellular mRNA changes remains a great challenge. Taking advantage of the high fluorescence quenching efficiency of core-shell gold@polydopamine (Au@PDA) nanocomposites and Ca2+-promoting DNA adsorption stability, a simple and universal bioconjugate strategy was designed to a construct fluorescent nanoprobe for highly efficient tumor-related mRNA imaging. The fluorescence of Cy5-labeled DNA was quenched up to 92.38% by the AuNP and PDA via nanometal surface energy transfer (NSET) and photoinduced electron transfer (PET), respectively. TK1 mRNA, a biomarker of tumor growth, initiates hybridization and results in fluorescence recovery, which built the foundation for identifying the expression level changes in living cells. More importantly, three kinds of tumor-related mRNA (TK1 mRNA, GalNAc-T mRNA, and C-myc mRNA) can be detected simultaneously with different fluorophore-modified recognition sequences, which can avoid false positive signals and improve the reliability of cancer diagnostic, holding great promise for cancer diagnosis, prognosis, and therapy. Full article
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19 pages, 2374 KB  
Article
Magnetothermal Energy Conversion of Polydopamine-Coated Iron Oxide Ferrogels Under High-Frequency Rotating Magnetic Fields
by Jakub Musiał, Artur Jędrzak, Rafał Bielas and Andrzej Skumiel
Energies 2025, 18(16), 4291; https://doi.org/10.3390/en18164291 - 12 Aug 2025
Viewed by 494
Abstract
This study provides a comparison between magnetic-to-thermal energy conversion efficiency in liquid and gel phases under high-frequency magnetic fields. Magnetite cores (11 ± 2 nm) were tested as water-based ferrofluids and as 5 wt% agar ferrogels, both with and without a biocompatible polydopamine [...] Read more.
This study provides a comparison between magnetic-to-thermal energy conversion efficiency in liquid and gel phases under high-frequency magnetic fields. Magnetite cores (11 ± 2 nm) were tested as water-based ferrofluids and as 5 wt% agar ferrogels, both with and without a biocompatible polydopamine (PDA) shell. A custom two-phase coil switched between rotating (RMF) and alternating (AMF) modes, enabling phase- and coating-dependent effects to be measured at identical field strengths and frequencies (100–300 kHz, 1–4 kA/m). Across all conditions, RMF generated 1.7–2.1 times more specific loss power (SLP) than AMF, and moving from the liquid to the gel phase reduced SLP by 5–8%, indicating that heating is controlled by Néel relaxation with negligible Brownian contribution. SLP rose with magnetic-field amplitude according to a power law, while hysteretic losses remained minimal. PDA improved colloidal stability and biocompatibility without harming the heating performance, lowering SLP by <17%. Within Brezovich limits, the system still exceeded therapeutic hyperthermia thresholds. Thus, in this iron-oxide/PDA system, neither medium viscosity nor the PDA shell’s non-magnetic mass significantly affects thermal energy output, an important finding for translating laboratory calorimetry data into reliable, application-oriented modelling for magnetic hyperthermia. Full article
(This article belongs to the Section J: Thermal Management)
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14 pages, 6399 KB  
Article
Core–Shell CoS2/FeS2 Heterojunction Encapsulated in N-Doped Carbon Nanocubes Derived from Coordination Polymers for Electrocatalytic Alkaline Water/Seawater Splitting
by Xiaoyin Zhang, Yan Liu, Zihan Zeng, Yan Zou, Wanzhen Wang, Jing Zhang, Jing Wang, Xiangfeng Kong and Xiangmin Meng
Polymers 2025, 17(12), 1701; https://doi.org/10.3390/polym17121701 - 19 Jun 2025
Viewed by 666
Abstract
Utilizing renewable energy for green hydrogen production via electrolyzed seawater is a promising technology for the future. However, undesired chlorine evolution and the corrosive nature of seawater are crucial challenges for direct seawater splitting technology. In this work, heterojunctions of CoS2/FeS [...] Read more.
Utilizing renewable energy for green hydrogen production via electrolyzed seawater is a promising technology for the future. However, undesired chlorine evolution and the corrosive nature of seawater are crucial challenges for direct seawater splitting technology. In this work, heterojunctions of CoS2/FeS2 encapsulated in N-doped carbon nanocubes (denoted as CoS2/FeS2@NC) were designed by proposing the synchronous pyrolysis and vulcanization of polydopamine-coated coordination polymers. Such a synthetic strategy was demonstrated to be effective in increasing the favorable exposure of active sites, moderately regulating electronic structure, and remarkably facilitating charge transfer due to the controllable generation of unique core–shell structures with suitable carbon shells, leading to the excellent bifunctional electrocatalytic performance and enhanced stability of electrocatalysts. As a result, CoS2/FeS2@NC can be revealed as a superior water splitting catalyst, possessing a small voltage of 1.75 V and requiring 100.0 mA cm−2 in 1 M KOH alkaline solution and 1.80 V for alkaline seawater media, with satisfactory long-term stability. This work presents fresh strategies for designing core–shell heterostructures and developing green technology for hydrogen production. Full article
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13 pages, 2158 KB  
Article
A Smart Nanoprobe for Visually Investigating the Activation Effect of Cyclical DOX Release on the p53 Pathway and Pathway-Related Molecules
by Ping Sun, Chunlei Gao, Zhe Chen, Siyu Wang, Gang Li, Mingming Luan and Yaoguang Wang
Biosensors 2025, 15(6), 383; https://doi.org/10.3390/bios15060383 - 13 Jun 2025
Viewed by 681
Abstract
Developing appropriate methods for real-time in situ investigation of how drugs influence signaling pathways and related biomolecules holds enormous potential for helping to provide an understanding of how anticancer drugs exert their effects. Herein, we report a smart nanoprobe, PDA-MB (DOX)-Pep, constructed on [...] Read more.
Developing appropriate methods for real-time in situ investigation of how drugs influence signaling pathways and related biomolecules holds enormous potential for helping to provide an understanding of how anticancer drugs exert their effects. Herein, we report a smart nanoprobe, PDA-MB (DOX)-Pep, constructed on the basis of polydopamine nanoparticles (PDA NPs) modified with a dense shell of molecular beacon (MB) with embedded doxorubicin (DOX) and peptide, which can respond specifically to miRNA-34a and Caspase-3 targets. Intracellular experiments demonstrated that, in comparison to the control nanoprobe PDA-MB-Pep, the smart nanoprobe could selectively respond to miRNA-34a, facilitating the release of the embedded DOX. The released DOX subsequently activated the p53 pathway, which further upregulated miRNA-34a expression, leading to additional DOX release. This initiated a cyclical process involving the probe’s response to miRNA-34a, DOX release, p53 activation, and miRNA-34a upregulation, ultimately enhancing cell apoptosis and increasing Caspase-3 expression. The designed smart nanoprobe offers a visual approach to explore how anticancer drugs influence signaling pathways and related molecules at the cellular level. Full article
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23 pages, 6067 KB  
Article
Preparation and Application of Core–Shell Nanocarbon-Based Slow-Release Foliar Fertilizer
by Ting Zhang, Xinheng Chen, Hongtao Gu, Huayi Chen, Kaichun Huang, Jinjin Wang, Huijuan Xu, Yulong Zhang and Wenyan Li
Nanomaterials 2025, 15(7), 565; https://doi.org/10.3390/nano15070565 - 7 Apr 2025
Cited by 1 | Viewed by 1565
Abstract
The application of nanotechnology offers a promising solution to improve fertilizer utilization efficiency by mitigating the losses and volatilization of conventional fertilizers, contributing to sustainable agriculture. In this study, a core–shell nanocarbon-based slow-release foliar fertilizer (CN@mSiO2-NH2@Urea@PDA) was synthesized using [...] Read more.
The application of nanotechnology offers a promising solution to improve fertilizer utilization efficiency by mitigating the losses and volatilization of conventional fertilizers, contributing to sustainable agriculture. In this study, a core–shell nanocarbon-based slow-release foliar fertilizer (CN@mSiO2-NH2@Urea@PDA) was synthesized using nanocarbon (CN) as the core, amino-functionalized mesoporous silica (mSiO2-NH2) as the shell, and polydopamine (PDA) as the coating layer. BET analysis revealed a 3.5-fold and 1.9-fold reduction in material porosity after PDA encapsulation, confirming successful synthesis. The controlled-release performance was enhanced, with a 24% decrease in the release rate and a prolonged nutrient delivery duration. Hydrophobicity tests demonstrated a 20° increase in the contact angle, indicating improved adhesion. Seed germination assays validated biosafety, while field trials showed a 69.94% increase in the choy sum (Brassica rapa) yield, 21.64% higher nitrogen utilization efficiency, and 22.21% reduced nitrogen loss. The foliar application increased the plant nitrogen use efficiency by 18.37%. These findings highlight the potential of CN@mSiO2-NH2@Urea@PDA as an advanced foliar fertilizer, providing a strategic approach to promote nanomaterial applications in agriculture and enhance the acceptance of functional fertilizers among farmers. Full article
(This article belongs to the Special Issue Development and Evaluation of Nanomaterials for Agriculture)
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11 pages, 2176 KB  
Article
Sustainable Photocatalytic Reduction of Maleic Acid: Enhancing CuxO/ZnO Stability with Polydopamine
by Francesca Coccia, Andrea Mascitti, Giorgia Rastelli, Nicola d’Alessandro and Lucia Tonucci
Appl. Sci. 2025, 15(3), 1631; https://doi.org/10.3390/app15031631 - 6 Feb 2025
Cited by 1 | Viewed by 1141
Abstract
The development of effective photocatalysts for environmental applications is still a critical aspect of green chemistry. This study explores copper oxide (CuxO) catalysts supported on titanium dioxide (TiO2) and zinc oxide (ZnO) for the photocatalytic reduction of maleic acid [...] Read more.
The development of effective photocatalysts for environmental applications is still a critical aspect of green chemistry. This study explores copper oxide (CuxO) catalysts supported on titanium dioxide (TiO2) and zinc oxide (ZnO) for the photocatalytic reduction of maleic acid to succinic acid under ultraviolet (UV) light in water. The main goal was to evaluate the performance of CuO/ZnO compared to CuO/TiO2 in photoreduction. In order to improve the efficiency of the first catalyst, an environmentally friendly synthesis, assisted by polydopamine (PDA), was tested, obtaining the Cu2O/ZnO-PDA catalyst. The results showed that CuO/TiO2 exhibited the highest activity for maleic acid reduction, obtaining a succinic acid yield and a selectivity of 32% after 24 h of reaction time, but comparable results could be reached even with Cu2O/ZnO-PDA increasing the reaction time. Furthermore, the addition of sodium ascorbate as a co-catalyst in the reaction mixture allowed us to overtake the previous results, leading to a succinic acid yield of 61% and a selectivity of 67%. These findings suggest that the PDA shell can be a solution for CuxO photodegradation, making Cu2O/ZnO-PDA an alternative to the toxic CuO/TiO2. Full article
(This article belongs to the Section Chemical and Molecular Sciences)
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26 pages, 4876 KB  
Article
Microfluidic-Assisted Silk Nanoparticles Co-Loaded with Epirubicin and Copper Sulphide: A Synergistic Photothermal–Photodynamic Chemotherapy Against Breast Cancer
by Zijian Gao, Muhamad Hawari Mansor, Faith Howard, Jordan MacInnes, Xiubo Zhao and Munitta Muthana
Nanomaterials 2025, 15(3), 221; https://doi.org/10.3390/nano15030221 - 30 Jan 2025
Cited by 3 | Viewed by 1704
Abstract
Phototherapy, including photodynamic therapy (PDT) and photothermal therapy (PTT), has emerged as a promising non-invasive cancer treatment, addressing issues like drug resistance and systemic toxicity common in conventional breast cancer therapies. Recent research has shown that copper sulphide (CuS) nanoparticles and polydopamine (PDA) [...] Read more.
Phototherapy, including photodynamic therapy (PDT) and photothermal therapy (PTT), has emerged as a promising non-invasive cancer treatment, addressing issues like drug resistance and systemic toxicity common in conventional breast cancer therapies. Recent research has shown that copper sulphide (CuS) nanoparticles and polydopamine (PDA) exhibit exceptional photothermal conversion efficiency under 808 nm near-infrared (NIR) laser irradiation, making them valuable for cancer phototherapy. However, the effectiveness of PDT is limited in hypoxic tumour environments, which are common in many breast cancer types, due to its reliance on local oxygen levels. Moreover, single-modality approaches, including phototherapy, often prove insufficient for complete tumour elimination, despite their therapeutic strength. In this paper, a microfluidic-assisted approach was used to create multifunctional silk-based nanoparticles (SFNPs) encapsulating the chemotherapeutic drug Epirubicin (EPI), the PTT/PDT agent CuS, and the heat-activated, oxygen-independent alkyl radical generator AIPH for combined chemotherapy, PTT, and PDT, with a polydopamine (PDA) coating for enhanced photothermal effects and surface-bound folic acid (FA) for targeted delivery in breast cancer treatment. The synthesised CuS-EPI-AIPH@SF-PDA-FA nanoparticles achieved a controlled size of 378 nm, strong NIR absorption, and high photothermal conversion efficiency. Under 808 nm NIR irradiation, these nanoparticles selectively triggered the release of alkyl radicals and EPI, improving intracellular drug levels and effectively killing various breast cancer cell lines while demonstrating low toxicity to non-cancerous cells. We demonstrate that novel core–shell CuS-EPI-AIPH@SF-PDA-FA NPs have been successfully designed as a multifunctional nanoplatform integrating PTT, PDT, and chemotherapy for targeted, synergistic breast cancer treatment. Full article
(This article belongs to the Special Issue Emerging Nanoscale Materials for Cancer Diagnosis and Therapy)
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20 pages, 25267 KB  
Article
Cu-ZnO Embedded in a Polydopamine Shell for the Generation of Antibacterial Surgical Face Masks
by Nicola d’Alessandro, Francesca Coccia, Luca Agostino Vitali, Giorgia Rastelli, Amedeo Cinosi, Andrea Mascitti and Lucia Tonucci
Molecules 2024, 29(18), 4512; https://doi.org/10.3390/molecules29184512 - 23 Sep 2024
Cited by 3 | Viewed by 1701
Abstract
A new easy protocol to functionalize the middle layer of commercial surgical face masks (FMs) with Zn and Cu oxides is proposed in order to obtain antibacterial personal protective equipment. Zinc and copper oxides were synthesized embedded in a polydopamine (PDA) shell as [...] Read more.
A new easy protocol to functionalize the middle layer of commercial surgical face masks (FMs) with Zn and Cu oxides is proposed in order to obtain antibacterial personal protective equipment. Zinc and copper oxides were synthesized embedded in a polydopamine (PDA) shell as potential antibacterial agents; they were analyzed by XRD and TEM, revealing, in all the cases, the formation of metal oxide nanoparticles (NPs). PDA is a natural polymer appreciated for its simple and rapid synthesis, biocompatibility, and high functionalization; it is used in this work as an organic matrix that, in addition to stabilizing NPs, also acts as a diluent in the functionalization step, decreasing the metal loading on the polypropylene (PP) surface. The functionalized middle layers of the FMs were characterized by SEM, XRD, FTIR, and TXRF and tested in their bacterial-growth-inhibiting effect against Klebsiella pneumoniae and Staphylococcus aureus. Among all functionalizing agents, Cu2O-doped-ZnO NPs enclosed in PDA shell, prepared by an ultrasound-assisted method, showed the best antibacterial effect, even at low metal loading, without changing the hydrophobicity of the FM. This approach offers a sustainable solution by prolonging FM lifespan and reducing material waste. Full article
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13 pages, 4836 KB  
Article
Bioinspired Fabrication of an Insensitive Ammonium Perchlorate Core–Shell Composite with Polydopamine Coating
by Yafeng Huang, Xuan Tian, Jinfei Wang, Kejun Zhong, Yuan Chen, Chenglong Li and Pengxiang Jia
Polymers 2024, 16(8), 1069; https://doi.org/10.3390/polym16081069 - 11 Apr 2024
Cited by 3 | Viewed by 1754
Abstract
In this research, an ammonium perchlorate/polydopamine (AP/PDA) core–shell composite was prepared in a non-aqueous solution to reduce the mechanical sensitivity of ammonium perchlorate (AP). The result showed that the AP/PDA core–shell composite could be successfully constructed in ethyl acetate solution with an AP [...] Read more.
In this research, an ammonium perchlorate/polydopamine (AP/PDA) core–shell composite was prepared in a non-aqueous solution to reduce the mechanical sensitivity of ammonium perchlorate (AP). The result showed that the AP/PDA core–shell composite could be successfully constructed in ethyl acetate solution with an AP recovery rate that reached 86%. The mechanical sensitivity of the obtained AP/PDA core–shell composite was significantly reduced with a PDA content of only 0.76%. The DSC and TG also indicated that the coating of PDA showed catalytic activity in the thermal decomposition of AP with a lower decomposition temperature and a decreased Ea value of AP. Thus, this study proposed a simple strategy for achieving a good balanced between harnessing the energy and ensuring the safety of ammonium perchlorate by significantly reducing its mechanical sensitivity by using a very low polydopamine coating layer content, and this shows great potential for the design and fabrication of insensitive energetic composites for use in propellants. Full article
(This article belongs to the Section Biobased and Biodegradable Polymers)
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12 pages, 5167 KB  
Article
Fluorinated Polydopamine Shell Decorated Fillers in Polytetrafluoroethylene Composite for Achieving Highly Reduced Coefficient of Thermal Expansion
by Yuanying Yu, Xiao Chen, Dajun Hou, Jingjing Zhou, Pengchao Zhang, Jie Shen and Jing Zhou
Polymers 2024, 16(7), 987; https://doi.org/10.3390/polym16070987 - 4 Apr 2024
Cited by 1 | Viewed by 1707
Abstract
The noticeable difference in the coefficient of thermal expansion (CTE) for polytetrafluoroethylene (PTFE) coatings and copper substrates is a major challenge for thermal debonding of the copper-clad laminate (CCL) in high-frequency communications. Theoretically, ceramic fillers with low CTEs in the coating can effectively [...] Read more.
The noticeable difference in the coefficient of thermal expansion (CTE) for polytetrafluoroethylene (PTFE) coatings and copper substrates is a major challenge for thermal debonding of the copper-clad laminate (CCL) in high-frequency communications. Theoretically, ceramic fillers with low CTEs in the coating can effectively reduce the gap, and there remains a trade-off between the dispersibility of fillers and the interfacial interactions with the polymeric matrix. Here, we propose a novel approach to prepare a pentafluorobenzoyl chloride (PFBC)-modified polydopamine (PDA) shell on silica particles by using amidation. Such modified particles perform excellent dispersion and exhibit diminished interfacial gaps in the PTFE matrix, which highly reduces CTE to 77 ppm/°C, accounting for only 48.1% of the neat coating. Moreover, the composite exhibits enhanced mechanical strength and toughness, and consequently suppresses thermal debonding in CCL under high-temperature conditions. Therefore, results present a promising potential for its use in the next-generation CCL of high-frequency communication devices. Full article
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31 pages, 9263 KB  
Article
Bubble Wrap-like Carbon-Coated Rattle-Type silica@silicon Nanoparticles as Hybrid Anode Materials for Lithium-Ion Batteries via Surface-Protected Etching
by Angelica Martino, Jiyun Jeon, Hyun-Ho Park, Hochun Lee and Chang-Seop Lee
Batteries 2024, 10(2), 53; https://doi.org/10.3390/batteries10020053 - 1 Feb 2024
Cited by 2 | Viewed by 4722
Abstract
Severe volumetric expansion (~400%) limits practical application of silicon nanoparticles as anode materials for next-generation lithium-ion batteries (LIBs). Here, we describe the fabrication and characterization of a conformal polydopamine carbon shell encapsulating rattle-type silica@silicon nanoparticles (PDA–PEI@PVP–SiO2@Si) with a tunable void structure [...] Read more.
Severe volumetric expansion (~400%) limits practical application of silicon nanoparticles as anode materials for next-generation lithium-ion batteries (LIBs). Here, we describe the fabrication and characterization of a conformal polydopamine carbon shell encapsulating rattle-type silica@silicon nanoparticles (PDA–PEI@PVP–SiO2@Si) with a tunable void structure using a dual template strategy with TEOS and (3-aminopropyl)triethoxysilane (APTES) pretreated with polyvinylpyrrolidone (PVP K30) as SiO2 sacrificial template via a modified Stöber process. Polyethylene imine (PEI) crosslinking facilitated the construction of an interconnected three-dimensional bubble wrap-like carbon matrix structure through hydrothermal treatment, pyrolysis, and subsequent surface-protected etching. The composite anode material delivered satisfactory capacities of 539 mAh g−1 after 100 cycles at 0.1 A g−1, 512.76 mAh g−1 after 200 cycles at 1 A g−1, and 453 mAh g−1 rate performance at 5 A g−1, respectively. The electrochemical performance of PDA–PEI@PVP–SiO2@Si was attributed to the rattle-type structure providing void space for Si volume expansion, PVP K30-pretreated APTES/TEOS SiO2 seeds via catalyst-free, hydrothermal-assisted Stöber protecting Si/C spheres upon etching, carbon coating strategy increasing Si conductivity while stabilizing the solid electrolyte interface (SEI), and PEI carbon crosslinks providing continuous conductive pathways across the electrode structure. The present work describes a promising strategy to synthesize tunable yolk shell C@void@Si composite anode materials for high power/energy-density LIBs applications. Full article
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25 pages, 7410 KB  
Article
Microfluidic-Assisted ZIF-Silk-Polydopamine Nanoparticles as Promising Drug Carriers for Breast Cancer Therapy
by Zijian Gao, Muhamad Hawari Mansor, Natalie Winder, Secil Demiral, Jordan Maclnnes, Xiubo Zhao and Munitta Muthana
Pharmaceutics 2023, 15(7), 1811; https://doi.org/10.3390/pharmaceutics15071811 - 24 Jun 2023
Cited by 13 | Viewed by 3744
Abstract
Metal–organic frameworks (MOFs) are heralded as potential nanoplatforms for biomedical applications. Zeolitic imidazolate framework-8 (ZIF-8), as one of the most well known MOFs, has been widely applied as a drug delivery carrier for cancer therapy. However, the application of ZIF-8 nanoparticles as a [...] Read more.
Metal–organic frameworks (MOFs) are heralded as potential nanoplatforms for biomedical applications. Zeolitic imidazolate framework-8 (ZIF-8), as one of the most well known MOFs, has been widely applied as a drug delivery carrier for cancer therapy. However, the application of ZIF-8 nanoparticles as a therapeutic agent has been hindered by the challenge of how to control the release behaviour of anti-cancer zinc ions to cancer cells. In this paper, we designed microfluidic-assisted core-shell ZIF-8 nanoparticles modified with silk fibroin (SF) and polydopamine (PDA) for sustained release of zinc ions and curcumin (CUR) and tested these in vitro in various human breast cancer cells. We report that microfluidic rapid mixing is an efficient method to precisely control the proportion of ZIF-8, SF, PDA, and CUR in the nanoparticles by simply adjusting total flow rates (from 1 to 50 mL/min) and flow rate ratios. Owing to sufficient and rapid mixing during microfluidic-assisted nanoprecipitation, our designer CUR@ZIF-SF-PDA nanoparticles had a desired particle size of 170 nm with a narrow size distribution (PDI: 0.08), which is much smaller than nanoparticles produced using traditional magnetic stirrer mixing method (over 1000 nm). Moreover, a properly coated SF layer successfully enhanced the capability of ZIF-8 as a reservoir of zinc ions. Meanwhile, the self-etching reaction between ZIF-8 and PDA naturally induced a pH-responsive release of zinc ions and CUR to a therapeutic level in the MDA-MB-231, SK-BR-3, and MCF-7 breast cancer cell lines, resulting in a high cellular uptake efficiency, cytotoxicity, and cell cycle arrest. More importantly, the high biocompatibility of designed CUR@ZIF-SF-PDA nanoparticles remained low in cytotoxicity on AD-293 non-cancer cells. We demonstrate the potential of prepared CUR@ZIF-SF-PDA nanoparticles as promising carriers for the controlled release of CUR and zinc ions in breast cancer therapy. Full article
(This article belongs to the Special Issue Nanocarriers for Cancer Therapy and Diagnosis, 2nd Edition)
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38 pages, 7916 KB  
Review
The Convenience of Polydopamine in Designing SERS Biosensors with a Sustainable Prospect for Medical Application
by Lulu Tian, Cong Chen, Jing Gong, Qi Han, Yujia Shi, Meiqi Li, Liang Cheng, Lin Wang and Biao Dong
Sensors 2023, 23(10), 4641; https://doi.org/10.3390/s23104641 - 10 May 2023
Cited by 10 | Viewed by 4974
Abstract
Polydopamine (PDA) is a multifunctional biomimetic material that is friendly to biological organisms and the environment, and surface-enhanced Raman scattering (SERS) sensors have the potential to be reused. Inspired by these two factors, this review summarizes examples of PDA-modified materials at the micron [...] Read more.
Polydopamine (PDA) is a multifunctional biomimetic material that is friendly to biological organisms and the environment, and surface-enhanced Raman scattering (SERS) sensors have the potential to be reused. Inspired by these two factors, this review summarizes examples of PDA-modified materials at the micron or nanoscale to provide suggestions for designing intelligent and sustainable SERS biosensors that can quickly and accurately monitor disease progression. Undoubtedly, PDA is a kind of double-sided adhesive, introducing various desired metals, Raman signal molecules, recognition components, and diverse sensing platforms to enhance the sensitivity, specificity, repeatability, and practicality of SERS sensors. Particularly, core-shell and chain-like structures could be constructed by PDA facilely, and then combined with microfluidic chips, microarrays, and lateral flow assays to provide excellent references. In addition, PDA membranes with special patterns, and hydrophobic and strong mechanical properties can be used as independent platforms to carry SERS substances. As an organic semiconductor material capable of facilitating charge transfer, PDA may possess the potential for chemical enhancement in SERS. In-depth research on the properties of PDA will be helpful for the development of multi-mode sensing and the integration of diagnosis and treatment. Full article
(This article belongs to the Special Issue Feature Papers in Section Biosensors 2023)
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15 pages, 3118 KB  
Article
Polydopamine-Coated Alginate Microgels: Process Optimization and In Vitro Validation
by Iriczalli Cruz-Maya, Simona Zuppolini, Mauro Zarrelli, Elisabetta Mazzotta, Anna Borriello, Cosimino Malitesta and Vincenzo Guarino
J. Funct. Biomater. 2023, 14(1), 2; https://doi.org/10.3390/jfb14010002 - 20 Dec 2022
Cited by 5 | Viewed by 3591
Abstract
In the last decade, alginate-based microgels have gained relevant interest as three-dimensional analogues of extracellular matrix, being able to support cell growth and functions. In this study, core-shell microgels were fabricated by self-polymerization of dopamine (DA) molecules under mild oxidation and in situ [...] Read more.
In the last decade, alginate-based microgels have gained relevant interest as three-dimensional analogues of extracellular matrix, being able to support cell growth and functions. In this study, core-shell microgels were fabricated by self-polymerization of dopamine (DA) molecules under mild oxidation and in situ precipitation of polydopamine (PDA) onto alginate microbeads, processed by electro fluid dynamic atomization. Morphological (optical, SEM) and chemical analyses (ATR-FTIR, XPS) confirmed the presence of PDA macromolecules, distributed onto the microgel surface. Nanoindentation tests also indicated that the PDA coating can influence the biomechanical properties of the microgel surfaces—i.e., σmaxALG = 0.45 mN vs. σmaxALG@PDA = 0.30 mN—thus improving the interface with hMSCs as confirmed by in vitro tests; in particular, protein adsorption and viability tests show a significant increase in adhesion and cell proliferation, strictly related to the presence of PDA. Hence, we concluded that PDA coating contributes to the formation of a friendly interface able to efficiently support cells’ activities. In this perspective, core-shell microgels may be suggested as a novel symmetric 3D model to study in vitro cell interactions. Full article
(This article belongs to the Special Issue State-of-the-Art Functional Biomaterials in Italy)
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15 pages, 4685 KB  
Article
Tribological Properties of Polydopamine-Modified Ag as Lubricant Oil Additives
by Yanxin Zhang, Jun Cheng, Changfeng Lu, Hao Chen, Guoxin Xie, Lin Zhang and Jianbin Luo
Lubricants 2022, 10(12), 343; https://doi.org/10.3390/lubricants10120343 - 1 Dec 2022
Cited by 3 | Viewed by 2857
Abstract
Nanoparticles agglomerate easily because of their high surface energy, which seriously reduces their tribological properties as lubricant additives. In this work, the core-shell nanoparticles Ag@polydopamine (PDA) were successfully prepared by the self-oxidation of dopamine hydrochloride on the surface of Ag nanoparticles and the [...] Read more.
Nanoparticles agglomerate easily because of their high surface energy, which seriously reduces their tribological properties as lubricant additives. In this work, the core-shell nanoparticles Ag@polydopamine (PDA) were successfully prepared by the self-oxidation of dopamine hydrochloride on the surface of Ag nanoparticles and the dispersion of Ag nanoparticles in PAO6 was improved to promote anti-wear behaviors. The tribological properties of Ag@PDA nanocomposites as additives in poly alpha olefin (PAO) oil were studied under different concentrations, pressure and speed conditions by UMT-5 tribometer. It was demonstrated that the strong electrostatic repulsion of the PDA structure made the Ag nanoparticles better dispersed in PAO oil, thus playing a better lubricating role. When the concentration of the modified nanoparticles was 0.25 wt%, the friction coefficient of the lubricating oil decreased by 18.67% and no obvious wear was observed on the friction pair surface. When the Ag@PDA content was higher than 0.25 wt%, the tribological performance of the lubricating oil was weakened, which may be due to excessive Ag@PDA acting as an abrasive on the friction surface, thereby increasing friction and wear. The friction coefficient of the lubricating oil containing Ag@PDA decreased with the increase in load, but hardly changed with the increase in frequency. Full article
(This article belongs to the Special Issue State-of-the-Art of Tribology in China)
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