Search Results (22)

Beryllium (Be) is one of the most toxic non-radioactive elements on the periodic table, and its presence or intake can negatively impact both the environment and human health. Classified as a carcinogen, Be is dangerous even at trace concentrations, stressing the necessity of developing reliable methods for quantifying it at very low levels. Spectrometric techniques for quantifying Be vary in sensitivity and applicability, with inductively coupled plasma mass spectrometry (ICP-MS) being the most sensitive for ultra-trace analysis. Flame atomic absorption spectrometry (FAAS) is suitable for higher Be concentrations, but preconcentration techniques can significantly lower detection limits. Electrothermal atomic absorption spectrometry (ETAAS) provides enhanced sensitivity for low-level Be quantification, further optimized using pyrolytically coated graphite tubes and chemical modifiers such as Mg(NO₃)₂ or Pd(NO₃)₂. Effective separation and preconcentration techniques are essential for reliable Be quantification in complex matrices. Liquid-liquid extraction (LLE), including single-drop microextraction (SDME) and dispersive liquid-liquid microextraction (DLLME), have evolved to reduce the use of hazardous solvents. When combined with ETAAS, surfactant-assisted DLLME using agents like cetylpyridinium ammonium bromide (CPAB) and dioctyl sodium sulfosuccinate (AOT) achieves preconcentration factors of approximately 25, reducing LOD to 1 ng/L. Vesicle-mediated DLLME coupled with ETAAS further enhances sensitivity, allowing detection limits as low as 0.01 ng/L in seawater. Cloud-point extraction (CPE), often employing Triton X-114, facilitates Be extraction using complexing agents or nanomaterials like graphene oxide. These advancements are critical for accurately quantifying Be at ultra-trace levels in diverse environmental and biological samples, overcoming challenges posed by low analyte concentrations and matrix interferences. Full article

Medicinal plants contain a wide range of bioactive compounds including antioxidants. Thus, the evaluation of the antioxidant capacity of medicinal plant extracts used in phytotherapy is of practical interest. Water extracts from 11 plants obtained by sonication for 30 min were studied by cyclic voltammetry at bare glassy carbon electrode (GCE) and GCE modified with a mixture of 1 mg mL⁻¹ CeO₂ and SnO₂ nanoparticles (NPs) dispersed in 0.10 mM cetylpyridinium bromide. A two-step chronoamperometric approach (at 400 and 900 mV for 75 s each one) was developed to estimate the antioxidant capacity of medicinal plant extracts. A strong and very strong correlation level was obtained between the antioxidant capacity and total phenolic contents or antioxidant capacity toward 2,2-diphenyl-1-picrylhydrazyl (DPPH^•). Full article

The relevance of active research lies in the need to develop new technologies to improve drug delivery methods for the effective treatment of wound healing. Additionally, the potential application of organogels in other areas of biomedicine, such as creating medical patches with controlled drug delivery, indicates a wide range of possibilities for using this technology. This study focuses on developing controlled drug delivery systems using organogels as carriers for ceftriaxone and ofloxacin. By selecting optimal formulations, organogels were created to immobilize the drugs, facilitating their effective and sustained release. The swelling behavior of the hydrogels was studied, showing a swelling coefficient between 16 and 32%, indicating their ability to absorb liquid relative to their weight. Drug release studies demonstrated that ceftriaxone was released 1.8 times slower than ofloxacin, ensuring a more controlled delivery. Microbiological tests confirmed that the organogels containing ofloxacin exhibited antimicrobial activity against Escherichia coli, Bacillus subtilis, and Staphylococcus aureus. However, it was a challenge to estimate activity for the model antibiotic ceftriaxone due to bacterial resistance to it. Organogel poly(vinyl alcohol) (PVA)-DMSO–alginate modifications with surfactant cetylpyridinium bromide led to the formation of a polyelectrolyte complex on the interphase, allowing further enhanced the prolonged release of the drugs. The research identified that the optimal compositions for sustained drug release were organogels with compositions PVA (10%)-PVP (1%) DMSO (50%) and PVA (10%)-DMSO (50%) formulations, illustrating the transparent nature of these organogels making them suitable for ophthalmological application. Various organogels compositions (PVA-DMSO, PVA-poly(vinylpyrrolidone)-DMSO, PVA-DMSO–alginate, PVA-DMSO-PLGA, PVA-DMSO–drug–surfactant) loaded with ceftriaxone, ofloxacin, and surfactant were prepared and characterized, highlighting their potential use in antibiotic patches for wound healing. These organogels illustrate promising results for localized treatment of infections in wounds, cuts, burns, and other skin lesions. Full article

Fomitiporia species have aroused the interest of numerous investigations that reveal their biological activity and medicinal potential. The present investigation shows the antioxidant, anticancer, and immunomodulatory activity of acidic polysaccharides obtained from the fungus Fomitiporia chilensis. The acidic polysaccharides were obtained for acidic precipitation with 2% O-N-cetylpyridinium bromide. Chemical analysis was performed using FT-IR and GC-MS methods. The antioxidant capacity of acidic polysaccharides from F. chilensis was evaluated by scavenging free radicals with an ABTS assay. Macrophage proliferation and cytokine production assays were used to determine the immunomodulatory capacity of the polysaccharides. Anti-tumor and cytotoxicity activity was evaluated with an MTT assay in the U-937, HTC-116, and HGF-1 cell lines. The effect of polysaccharides on the cell cycle of the HCT-116 cell line was determined for flow cytometry. Fourier Transform-infrared characterization revealed characteristic absorption peaks for polysaccharides, whereas the GC-MS analysis detected three peaks corresponding to D-galactose, galacturonic acid, and D-glucose. The secreted TNF-α concentration was increased when the cell was treated with 2 mg mL⁻¹ polysaccharides, whereas the IL-6 concentration was increased with all of the evaluated polysaccharide concentrations. A cell cycle analysis of HTC-116 treated with polysaccharides evidenced that the acidic polysaccharides from F. chilensis induce an increase in the G0/G1 cell cycle phase, increasing the apoptotic cell percentage. Results from a proteomic analysis suggest that some of the molecular mechanisms involved in their antioxidant and cellular detoxifying effects and justify their traditional use in heart diseases. Proteomic data are available through ProteomeXchange under identifier PXD048361. The study on acidic polysaccharides from F. chilensis has unveiled their diverse biological activities, including antioxidant, anticancer, and immunomodulatory effects. These findings underscore the promising therapeutic applications of acidic polysaccharides from F. chilensis, warranting further pharmaceutical and medicinal research exploration. Full article

Two new surfactant sensors were developed by synthesizing Pt-doped acid-activated multi-walled carbon nanotubes (Pt@MWCNTs). Two different ionophores using Pt@MWCNTs, a new plasticizer, and (a) cationic surfactant 1,3-dihexadecyl-1H-benzo[d]imidazol-3-ium-DHBI (Pt@MWCNT-DHBI ionophore) and (b) anionic surfactant dodecylbenzenesulfonate-DBS (Pt@MWCNT-DBS ionophore) composites were successfully synthesized and characterized. Both surfactant sensors showed a response to anionic surfactants (dodecylsulfate (SDS) and DBS) and cationic surfactants (cetylpyridinium chloride (CPC) and hexadecyltrimethylammonium bromide (CTAB)). The Pt@MWCNT-DBS sensor showed lower sensitivity than expected with the sub-Nernstian response of ≈23 mV/decade of activity for CPC and CTAB and ≈33 mV/decade of activity for SDS and DBS. The Pt@MWCNT-DHBI surfactant sensor had superior response properties, including a Nernstian response to SDS (59.1 mV/decade) and a near-Nernstian response to DBS (57.5 mV/decade), with linear response regions for both anionic surfactants down to ≈2 × 10⁻⁶ M. The Pt@MWCNT-DHBI was also useful in critical micellar concentration (CMC) detection. Common anions showed very low interferences with the sensor. The sensor was successfully employed for the potentiometric titration of a technical grade cationic surfactant with good recoveries. The content of cationic surfactants was measured in six samples of complex commercial detergents. The Pt@MWCNT-DHBI surfactant sensor showed good agreement with the ISE surfactant sensor and classical two-phase titration and could be used as an analytical tool in quality control. Full article

Voltammetric sensors based on CeO₂, SnO_2, CeO₂·Fe₂O₃ nanoparticles (NPs) and MnO₂ nanorods (NRs) were developed for the quantification of various organic substances. Surfactant media were applied as dispersive agents for metal oxide nanomaterials, providing a high stability of the dispersions after sonication and a decrease in the NPs’ size, as well as the preconcentration of the target analytes at the sensor surface due to the hydrophobic interactions between the surfactant and the analyte molecules. Natural phenolics (quercetin, rutin, gallic acid, taxifolin, eugenol, vanillin, and hesperidin), propyl gallate, α-lipoic acid, and synthetic food colorants (tartrazine, brilliant blue FCF, and sudan I) were studied as analytes. The effect of the nature and concentration of the surfactant on the target analyte response was evaluated. Cationic surfactants (cetylpyridinium (CPB) or cetyltriphenylphosphonium bromides (CTPPB)) showed the best effect for the majority of the analytes. Wide linear dynamic ranges and low detection limits were obtained and were improved vs. reported to date. The simultaneous quantification of tartrazine and brilliant blue FCF was achieved with a high selectivity. The practical applicability of the sensors was shown on the real samples and was validated by comparison to independent methods. Full article

Chelating agents’ application for well stimulation is gaining more and more interest, as they can perform under harsh conditions. However, the mutual influence of surfactants and chelating agents on the wettability alteration of hydrophobic carbonate rock under conditions of high-temperature well stimulation is relatively unexplored. This paper aims to study interfacial processes on the surface of hydrophobic rock in the presence of the EDTA-based chelating agent and surfactants of different classes. Cationic (cetyltrimethylammonium bromide, CTAB, and cetylpyridinium bromide, CPB), anionic (sodium dodecyl sulfate, SDS), and amhoteric (alkyldimethyl aminooxide, AO) surfactants were studied. Wettability alteration of model hydrophobic rock was studied under conditions specific to well stimulation. It was shown that chelating agent (CA) alone and its mixture with SDS could not lead to sufficient wettability alteration. CTAB, CPB, and AO were able to change the wettability effectively. A synergistic effect between CA and these surfactants was observed and a possible mechanism was proposed. AO was selected as the most promising surfactant. The influence of surfactant on the CA’s dissolution capacity towards carbonate rock was investigated; dissolution capacity strongly depends on wettability alteration. Finally, the effect of CA, AO, and their mixture on the wettability of aged reservoir rock was studied and the absence of negative effects was proven. Full article

Tartrazine and brilliant blue FCF are synthetic dyes used in the food, cosmetic and pharmaceutical industries. The individual and/or simultaneous control of their concentrations is required due to dose-dependent negative health effects. Therefore, the paper presents experimental results related to the development of a sensing platform for the electrochemical detection of tartrazine and brilliant blue FCF based on a glassy carbon electrode (GCE) modified with MnO₂ nanorods, using anodic differential pulse voltammetry. Homogeneous and stable suspensions of MnO₂ nanorods have been obtained involving cetylpyridinium bromide solution as a cationic surfactant. The MnO₂ nanorods-modified electrode showed a 7.9-fold increase in the electroactive surface area and a 72-fold decrease in the electron transfer resistance. The developed sensor allowed the simultaneous quantification of dyes for two linear domains: in the ranges of 0.10–2.5 and 2.5–15 μM for tartrazine and 0.25–2.5 and 2.5–15 μM for brilliant blue FCF with detection limits of 43 and 41 nM, respectively. High selectivity of the sensor response in the presence of typical interference agents (inorganic ions, saccharides, ascorbic and sorbic acids), other food dyes (riboflavin, indigo carmine, and sunset yellow), and vanillin has been achieved. The sensor has been tested by analyzing soft and isotonic sports drinks and the determined concentrations were close to those obtained involving the chromatography technique. Full article

Synthetic colorants, in particular tartrazine and brilliant blue FCF, are widely used in food chemistry and technology although they can give negative health effects of various severities. Therefore, sensitive, selective, simple, and reliable methods for the quantification of these dyes are required. A glassy carbon electrode (GCE) modified with manganese dioxide nanorods (MnO₂ NR) dispersed in cetylpyridinium bromide gives a sensitive response to tartrazine and brilliant blue FCF in mixtures. Electrode modification provides a 7.9-fold increase in the electroactive surface area and a 72-fold decrease in electron transfer resistance. Simultaneous voltammetric quantification of colorants was performed in phosphate buffer pH 7.0 in differential pulse mode. The linear dynamic ranges of 0.10–2.5 and 2.5–15 µM of tartrazine and 0.25–2.5 and 2.5–15 µM of brilliant blue FCF were obtained with the limits of detection of 43 and 41 nM, respectively. The advantage of the sensor developed is the high selectivity of response in the presence of typical interferences (inorganic ions, saccharides, ascorbic and sorbic acids) and other food colorants (riboflavin, indigo carmine, and sunset yellow). The practical applicability of the approach is shown in soft and isotonic sports drinks and is validated by comparison to chromatography. Full article

In this manuscript, the application of cetyltrimethylammonium bromide (CTAB) and cetylpyridinium chloride (CPC) for the removal of Naphthol Green B (NGB) as a synthetic effluent has been studied. The solubilization of NGB by a single and mixed micellar system using Triton X-100 (TX-100) as a nonionic surfactant has been performed to establish both the extent of the partitioning (k_x) of NGB and ultimately their respective Gibbs free energies ΔG_p as well. An applied methodology, micellar-enhanced ultrafiltration (MEUF), has also been studied in different micellar media of cationic surfactants by variation in some selective parameters, such as the concentration of surfactant, electrolyte, pressure, pH, and RPM to obtain optimum conditions. The results have been analyzed by a UV/visible double beam spectrophotometer. ΔG_p was found to be −39.65 kJ/mol and −47.94 kJ/mol by CTAB and CPC, respectively, in the presence of a nonionic surfactant. The maximum value of Gibbs free energy (ΔG_p) of the partition was obtained by CPC. The values of the rejection coefficient (R%) and permeate flux (J) are also calculated. A maximum removal of 99.77% and 98.53% by CTAB and CPC, respectively, was obtained. It has been observed that both of the surfactants are strong candidates for NGB removal. Full article

Indigo carmine is a widely used colorant in the food and pharmaceutical industry a high concentration of which can lead to a wide range of negative effects on human health. Therefore, colorant contents have to be strictly controlled. SeO₂-nanoparticle-modified glassy carbon electrodes (GCE) have been developed as a voltammetric sensor for indigo carmine. Various types and concentrations of surfactants have been used as reagents for the stabilization of SeO₂ nanoparticle dispersions and as electrode surface co-modifiers. An amount of 1.0 mM cationic cetylpyridinium bromide (CPB) provides the best response of the indigo carmine on the modified electrode. The electrodes were characterized by cyclic voltammetry, chronoamperometry, and electrochemical impedance spectroscopy (EIS). SeO₂ nanoparticle–CPB-modified electrodes show 4.2-fold higher electroactive area vs. GCE as well as a dramatic 5043-fold decrease in the electron transfer resistance indicating effectivity of the modifier developed. The surface-controlled electrooxidation of indigo carmine proceeds irreversibly (α_a = 0.46) with the participation of two electrons and two protons. A linear dynamic range of 0.025–1.0 and 1.0–10 µM of indigo carmine were obtained with the detection and quantification limits of 4.3 and 14.3 nM, respectively. The practical applicability of the sensor was successfully shown on the pharmaceutical dosage forms. Full article

A new sorbent cetylpyridinium bromide/polyvinylchloride (CPB/PVC) was prepared and tested to extract rare earth elements (REEs) from their chloride solutions. It was identified by FTIR, TGA, SEM, EDX, and XRD. The impact of various factors such as pH, RE ion initial concentration, contacting time, and dose amount via sorption process was inspected. The optimum pH was 6.0, and the equilibrium contact time was reached at 60 min at 25 °C. The prepared adsorbent (CPB/PVC) uptake capacity was 182.6 mg/g. The adsorption of RE ions onto the CPB/PVC sorbent was found to fit the Langmuir isotherm as well as pseudo-second-order models well. In addition, the thermodynamic parameters of RE ion sorption were found to be exothermic and spontaneous. The desorption of RE ions from the loaded CPB/PVC sorbent was investigated. It was observed that the optimum desorption was achieved at 1.0 M HCl for 60 min contact time at ambient room temperature and a 1:60 solid: liquid phase ratio (S:L). As a result, the prepared CPB/PVC sorbent was recognized as a competitor sorbent for REEs. Full article

Raw Ca-based montmorillonite (MMT) was treated by H₂SO₄, calcination and organic compounds (hexadecyltrimethyl ammonium bromide (HTAB), cetylpyridinium chloride (CPC) and chitosan (CTS)), respectively. The modified montmorillonites were characterized by different methods and their adsorption performances for three mycotoxins (Aflatoxin B1 (AFB1), zearalenone (ZEA) and deoxynivalenol (DON)) were evaluated at pH = 2.8 and 8.0, respectively. The results indicate that surfactants (CPC and HTAB) intercalation is the most efficient modification, which obviously improves the adsorption performance of montmorillonite for mycotoxins, with adsorption efficiency of above 90% for AFB1 and ZEA whether under acid or alkaline conditions, due to the increase in basal spacing and the improvement of hydrophobicity. Moreover, the adsorption efficiencies of AFB1 and ZEA over CPC-modified montmorillonite (CPC-AMMT-3) coexisting with vitamin B6 or lysine are still at a high level (all above 94%). All modified montmorillonites, however, have low adsorption efficiency for DON, with somewhat spherical molecular geometry. Full article

C-Phycocyanin (PC) and B-phycoerythrin (PE) are light-harvesting water-soluble phycobiliproteins from microalgae that belong mainly to the cyanobaceria and rhodhophytes families. Different methods have been developed for PC and PE extraction and purification from microalgae, and offer a high potential for their use as additives in sectors such as food and cosmetics. However, the main limitations of using these dyes are the sensitivity of their environmental factors, such as light fastness, temperature, and pH. We successfully employed safe lamellar nanoclays such as montmorillonite (M) and Laponite (L) for phycobiliproteins stabilization, as we did before with other natural dyes. We obtained a wide color gamut from blues to pink by combining four different factors under synthesis conditions: three dye concentrations; two laminar nanoclay sizes; a two nanoclay surface modifiers combination with cetylpyridinium bromide (CPB) and a coupling agent (3-Aminopropyl) triethoxysilane. The experimental conditions were defined according to a multilevel factorial design of experiment (DOE) to study the factors interacting in the final hybrid pigment characteristics. In both M and L, the d001 distance (nm) increased due to PC and PE adsorption. The best conditions to increase the basal space depend on the nanoclay structure, and it is better to use the surfactant for M, and silane modification for L. In addition, optical and thermal PE and PC properties significantly improved. We show the optimal synthesis conditions to increase PC and PE adsorption using the high dye concentration, with surfactant and silane depending on the nanoclay. The hybrid pigments from these phycobiliproteins offer the opportunity to perform several industrial applications, including in polymer additives, cosmetics, and packaging. Full article

Diclofenac (DC) and ibuprofen (IBU) are widely prescribed non-steroidal anti-inflammatory drugs, the consumption of which has rapidly increased in recent years. The biodegradability of pharmaceuticals is negligible and their removal efficiency by wastewater treatment is very low. Therefore, the beidelitte (BEI) as unique nanomaterial was modified by the following different surfactants: cetylpyridinium (CP), benzalkonium (BA) and tetradecyltrimethylammonium (TD) bromides. Organobeidellites were tested as potential nanosorbents for analgesics. The organobeidellites were characterized using X-ray powder diffraction (XRD), Infrared spectroscopy (IR), Thermogravimetry and differential thermal analysis (TG/DTA) and scanning microscopy (SEM). The equilibrium concentrations of analgesics in solution were determined using UV-VIS spectroscopy. The intercalation of surfactants into BEI structure was confirmed both using XRD analysis due to an increase in basal spacing from 1.53 to 2.01 nm for BEI_BA and IR by decreasing in the intensities of bands related to the adsorbed water. SEM proved successful in the uploading of surfactants by a rougher and eroded organobeidellite surface. TG/DTA evaluated the decrease in dehydration/dehydroxylation temperatures due to higher hydrophobicity. The Sorption experiments demonstrated a sufficient sorption ability for IBU (55–86%) and an excellent ability for DC (over 90%). The maximum adsorption capacity was found for BEI_BA-DC (49.02 mg·g⁻¹). The adsorption according to surfactant type follows the order BEI_BA > BEI_TD > BEI_CP. Full article