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A novel voltammetric sensor was constructed by modifying a glassy carbon electrode with a composite material consisting of platinum–nickel-doped tin oxide and carbon black (PtNiSnO2-CB/GCE), enabling highly sensitive differential pulse voltammetry (DPV) determination of trazodone HCl (TRZ). The DPV experimental parameters, including the composition of the supporting electrolyte and instrumental settings, were carefully optimized to achieve maximum analytical efficiency. Within the linear range of 1–10 µM, quantification of TRZ molecules could be performed without the preconcentration step. When applying a 60 s accumulation time (in the range 0.02–0.2 µM of TRZ), the detection limit reached 4.1 nM (1.67 mg L−1), indicating superior sensitivity compared to previously reported voltammetric techniques. The method demonstrated good reproducibility, with a relative standard deviation of 4.3% for 10 repeated measurements at 0.06 µM TRZ. The developed sensor exhibits excellent stability, simplicity of fabrication, and operational convenience. Its practical applicability was confirmed by the successful analysis of molecules of TRZ in diverse sample types, including pharmaceutical products, urine, plasma, river water, and artificial gastric and intestinal fluids, with recovery rates between 97.7% and 104.2%. Flow injection analysis (FIA) with amperometric detection was also performed for TRZ molecule determination.

For the first time, a new composite voltammetric sensor based on yttria-stabilized zirconia doped with neodymium-carbon black-Nafion glassy carbon electrode (YSZNd-CB-Nafion/GCE) for the determination of metoprolol (MET) has been developed. The instrumental parameters and supporting electrolyte were optimized. For 105 s accumulation time, linearity was achieved in the range of 0.01 to 0.2 µM. The limit of detection (for 105 s accumulation time) was equal to 2.9 nM (2 µg/L), and was the best result in comparison to other voltametric sensors. The reproducibility of the metoprolol signal presented as relative standard deviation (RSD) was equal to 1.9% (n = 7). Additionally, our electrode is characterized by high stability, is easy to use, and has a short preparation time. The proposed sensor was found useful for MET determination in plasma and urine, as well as for pharmaceutical samples, with a good recovery parameter (96–108%). Flow injection analysis (FIA) with amperometric detection was also performed for MET determination. The recovery was calculated and was in the range 101–103%, suggesting that the proposed material may be applied in flow injection analysis.

A specific feature of mushrooms (including those of the genus Pleurotus) is their natural ability to absorb and accumulate many chemical substances present in their immediate environment, which makes them an excellent natural sorption material. Hence, fruiting bodies of mushrooms have been recognized for years as excellent indicators of the environment, reflecting its current state. Nevertheless, mushrooms can accumulate both health-promoting substances, such as bioelements, and toxic substances, such as heavy metals and organic compounds, including bisphenol A® (BPA). This organic chemical compound in the phenol group, although it has been withdrawn in the EU since 2010, is widely present in the environment around us. In the present experiment, we aimed to determine the effect of adding BPA to liquid media for in vitro cultures of Pleurotus spp. The biomass increases were determined. Moreover, the degrees of adsorption and desorption of BPA from the obtained freeze-dried biomass in two different environments (neutral and acidic) were determined as a function of time. This is the first study to determine the bioavailability of adsorbed BPA in obtained biomass by extracting the mycelium into artificial digestive juices in a model digestive system. BPA was added to the liquid Oddoux medium in the following amounts: 0.01, 0.5, and 0.5 g/250 mL of medium. The amounts of adsorbed and desorbed BPA were determined by flow injection analysis (FIA) with amperometric detection. The addition of BPA to the substrate reduced the biomass growth in each of the discussed cases. BPA adsorption by the mycelium occurred at over 90% and depended on the morphology of the mushroom (structure, surface development, and pore size). BPA desorption depended on the pH of the environment and the desorption time. Mushrooms are an excellent natural remedial material, but BPA is extracted into artificial digestive juices; therefore, consuming mushrooms from industrialized areas may have health consequences for our bodies.

Worldwide, mushrooms belonging to the Pleurotus spp. such as P. citrinopileatus, P. djamor, and P. pulmonarius are highly valued not only for their taste and aroma but also for their health-promoting properties. These species are rich in bioelements, vitamins, and above all, compounds that exhibit immunostimulatory activity. Therefore, in this study, we aimed to determine the effect of the supplementation of culture media using inorganic Mg and Zn salts. This is the first study to establish the bioavailability of the selected elements (Mg and Zn) and anions (Cl−, SO42−) from the enriched biomass by means of the extraction of lyophilized mycelium into artificial digestive juices. The following salts were added to the liquid Oddoux medium: ZnSO4·7H2O, ZnCl2, MgSO4·7H2O or MgCl2·6H2O. The bioelements, anions and organic compounds in the obtained biomass were determined. The addition of Zn and Mg salts to the media increased the production of biomass by 30% and increased the bioaccumulation of the inorganic salts. Maintaining in vitro cultures under optimized and controlled conditions produced mycelium with a better composition and health properties than otherwise. Such enriched biomass may be classified as potential functional foods, aiding in overcoming deficiencies of elements and organic compounds with biological activity in humans.

A novel composite voltammetric biosensor has been developed for the first time, utilizing a glassy carbon electrode modified with yttria-stabilized zirconia doped with titanium dioxide and carbon black (YSZTiO2-CB/GCE), specifically designed for the detection of trimetazidine (TMZ). The measurement conditions, including both the supporting electrolyte and instrumental settings, were optimized to enhance performance. In the concentration range of 0.5 to 7 µM, it is not necessary to use preconcentration time for the determination of TMZ. The limit of detection (for 60 s of preconcentration time) was equal to 5.5 nM (1.87 ng mL−1), outperforming other voltammetric methods in terms of sensitivity. The reproducibility of the trimetazidine signal (with a concentration of 0.05 µM) exhibited a relative standard deviation (RSD) of 3.3% over 10 measurements. Additionally, our biosensor is characterized by excellent stability, ease of use, and straightforward preparation. The proposed biosensor and method have proven effective in analyzing TMZ in a variety of matrices, including urine, blood plasma, pharmaceutical formulations, as well as gastric and intestinal fluids, yielding recovery rates ranging from 97.7 to 102.3%.

This study evaluated the influence of gamma-polyglutamic acid (γ-PGA) on the heavy metal sorption efficiency of three edible mushroom species—Pleurotus ostreatus, Agaricus bisporus, and Boletus edulis—exposed to cadmium (Cd), lead (Pb), and their mixtures (in a 1:1 ratio). The experiment presented an innovative approach—combining the natural sorption properties of mushrooms with the addition of γ-PGA, which has strong chelating properties. Sorption assays were performed using escalating γ-PGA concentrations (1, 2, and 5 mL to 250 mL of liquid medium), with data analyzed via generalized linear models employing a gamma distribution and a log link function. Results revealed that sorption efficiency was highest at the lowest γ-PGA concentration and decreased significantly with increasing γ-PGA levels across all species and metal treatments. Notably, P. ostreatus and A. bisporus demonstrated superior and more stable sorption capacities relative to B. edulis, which exhibited greater variability. These findings suggest that while edible mushrooms are effective biosorbents for heavy metals, higher γ-PGA concentrations may inhibit metal uptake by chelating metals in solution and reducing their bioavailability. Additionally, γ-PGA at 1 mM markedly enhanced antimicrobial activity against Salmonella enteritidis and Escherichia coli (with a 20% increase in growth inhibition zone compared to the control group) in mushroom cultures and when applied independently. This dual functionality underscores the potential of γ-PGA–mushroom systems for bioremediation and food safety applications, highlighting the need for the careful optimization of γ-PGA concentration to maximize biosorption efficacy and antimicrobial benefits.

The use of substrates supplemented with minerals is a promising strategy for increasing the nutraceutical value of Pleurotus spp. The current research was performed to analyze the effect of substrate supplementation with magnesium (Mg) salts on the Mg content, biomass, and chemical composition of pink oyster mushroom (Pleurotus djamor) fruiting bodies. Before inoculation, substrate was supplemented with MgCl2 × 6 H2O and MgSO4, both salts were applied at three concentrations: 210, 420, and 4200 mg of Mg per 2 kg of substrate. The harvest period included three flushes. Substrate supplementation with 4200 mg of Mg caused the most significant decrease in mushroom productivity, of about 28% for both Mg salts. The dry matter content in fruiting bodies was significantly lower in the treatment in which 210 mg of Mg was applied as MgSO4 in comparison to the control. Supplementation effectively increased the Mg content in fruiting bodies of P. djamor by 19–85% depending on the treatment, and significantly affected the level of remaining bioelements and anions. One hundred grams of pink oyster fruiting bodies, supplemented with Mg salts, provides more than 20% of the Mg dietary value recommended by the Food and Drug Administration (FDA); thus, supplementation can be an effective technique for producing mushrooms that are rich in dietary Mg. Although P. djamor grown in supplemented substrate showed lower productivity, this was evident only in the fresh weight because the differences in dry weight were negligible. Mg supplementation increased the antioxidant activity of the fruiting bodies, phenolic compounds, and some amino acids, including L-tryptophan, and vitamins (thiamine and l-ascorbic acid).

The aim of the investigations was to use, for the first time, zirconia nanopowders stabilized with yttria (YSZ) and rare element oxides (YSZ-Nd, YSZ-Gd) for removal of humic acids (HA) from aqueous solutions. Nanopowders were synthesized by means of hydrothermal crystallization and characterized using scanning electron microscope (SEM) with energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) methods and analysis of zeta potential. The adsorption processes analysis was carried out in a series of experiments depending on: initial concentration of humic acids, contact time, pH and mass of the used adsorbent. It was found, that the YSZ-Nd exhibits strong and much higher effectiveness of HA adsorption than YSZ and YSZ-Gd. The HA adsorption rate reached 96.8% for YSZ-Nd dosage of 100 mg, pH 4, and 15 min reaction time and for HA initial concentration equal to 25 mg/L. According to the Langmuir model simulation, the maximum adsorption capacity of HA on YSZ-Nd at pH 4 was calculated to be 2.95 mg/g. Changes in the FT-IR spectra of YSZ-Nd confirmed humic acids’ adsorption on the tested nanopowders, by the presence of additional bands representing carboxylic, alcohol, carbonyl and amino groups in humic acid structure. These functional groups could represent humic acids binding on the YSZ, YSZ-Nd or YSZ-Gd surfaces.

A novel voltammetric sensor was constructed by modifying a glassy carbon electrode with a composite material consisting of platinum–nickel-doped tin oxide and carbon black (PtNiSnO[sub.2]-CB/GCE), enabling highly sensitive differential pulse voltammetry (DPV) determination of trazodone HCl (TRZ). The DPV experimental parameters, including the composition of the supporting electrolyte and instrumental settings, were carefully optimized to achieve maximum analytical efficiency. Within the linear range of 1–10 µM, quantification of TRZ molecules could be performed without the preconcentration step. When applying a 60 s accumulation time (in the range 0.02–0.2 µM of TRZ), the detection limit reached 4.1 nM (1.67 mg L[sup.−1]), indicating superior sensitivity compared to previously reported voltammetric techniques. The method demonstrated good reproducibility, with a relative standard deviation of 4.3% for 10 repeated measurements at 0.06 µM TRZ. The developed sensor exhibits excellent stability, simplicity of fabrication, and operational convenience. Its practical applicability was confirmed by the successful analysis of molecules of TRZ in diverse sample types, including pharmaceutical products, urine, plasma, river water, and artificial gastric and intestinal fluids, with recovery rates between 97.7% and 104.2%. Flow injection analysis (FIA) with amperometric detection was also performed for TRZ molecule determination.

A novel voltammetric sensor was constructed by modifying a glassy carbon electrode with a composite material consisting of platinum-nickel-doped tin oxide and carbon black (PtNiSnO -CB/GCE), enabling highly sensitive differential pulse voltammetry (DPV) determination of trazodone HCl (TRZ). The DPV experimental parameters, including the composition of the supporting electrolyte and instrumental settings, were carefully optimized to achieve maximum analytical efficiency. Within the linear range of 1-10 µM, quantification of TRZ molecules could be performed without the preconcentration step. When applying a 60 s accumulation time (in the range 0.02-0.2 µM of TRZ), the detection limit reached 4.1 nM (1.67 mg L ), indicating superior sensitivity compared to previously reported voltammetric techniques. The method demonstrated good reproducibility, with a relative standard deviation of 4.3% for 10 repeated measurements at 0.06 µM TRZ. The developed sensor exhibits excellent stability, simplicity of fabrication, and operational convenience. Its practical applicability was confirmed by the successful analysis of molecules of TRZ in diverse sample types, including pharmaceutical products, urine, plasma, river water, and artificial gastric and intestinal fluids, with recovery rates between 97.7% and 104.2%. Flow injection analysis (FIA) with amperometric detection was also performed for TRZ molecule determination.