Search

In this study, grape marc waste from Negroamaro (a South of Italy vine variety) winery production was used to prepare biosorbents for Hg(II) removal in aqueous media. A green approach was used to develop a proper biosorbent through two different grape marc washing procedures. In particular, the common chloridric acid and the greener citric acid were evaluated. The biosorbent prepared using citric acid as a washing agent (GM-CA) gave similar results to the biosorbent washed with HCl (GM-HCl) with a maximum adsorption capacity of 36.39 mg g-1. Isothermal studies revealed heterogeneous physical adsorption of Hg(II) on the biosorbents. Moreover, FTIR analysis of the grape marc-based biosorbent without and with Hg(II) confirmed ionic interactions in the biosorbent that fit with a pseudo-second-order kinetic model. Furthermore, no significant adsorption on the biosorbent was observed when two other heavy metals, copper(II) and nickel(II), previously studied for similar sorbents, were considered. Finally, the reusability of GM-CA biosorbent was also demonstrated over three cycles. Thus, the green preparation approach used in this work can be considered suitable for developing grape marc-based biosorbents.

Methylene blue (MB) is a dye hazardous pollutant widely used in several industrial processes that represents a relevant source of water pollution. Thus, the research of new systems to avoid their environmental dispersion represents an important goal. In this work, an efficient and sustainable nanocomposite material based on green gold nanoparticles for MB water remediation was developed. Starting from the reducing and stabilizing properties of some compounds naturally present in Lambrusco winery waste (grape marc) extracts, green gold nanoparticles (GM-AuNPs) were synthesized and deposited on a supporting membrane to create an easy and stable system for water MB decontamination. GM-AuNPs, with a specific plasmonic band at 535 nm, and the modified membrane were first characterized by UV–vis spectroscopy, X-ray diffraction (XRD), and electron microscopy. Transmission electron microscopy analysis revealed the presence of two breeds of crystalline shapes, triangular platelets and round-shaped penta-twinned nanoparticles, respectively. The crystalline nature of GM-AuNPs was also confirmed from XRD analysis. The photocatalytic performance of the modified membrane was evaluated under natural sunlight radiation, obtaining a complete disappearance of MB (100%) in 116 min. The photocatalytic process was described from a pseudo-first-order kinetic with a rate constant (k) equal to 0.044 ± 0.010 min−1. The modified membrane demonstrated high stability since it was reused up to 20 cycles, without any treatment for 3 months, maintaining the same performance. The GM-AuNPs-based membrane was also tested with other water pollutants (methyl orange, 4-nitrophenol, and rhodamine B), revealing a high selectivity towards MB. Finally, the photocatalytic performance of GM-AuNPs-based membrane was also evaluated in real samples by using tap and pond water spiked with MB, obtaining a removal % of 99.6 ± 1.2% and 98.8 ± 1.9%, respectively. [ABSTRACT FROM AUTHOR]

Pyracantha is a genus of wild perennial shrubs native in an area extending from Southwest Europe to Southeast Asia, and it is used in traditional medicine for the diuretic, cardiac, and tonic properties of its fruits, which can also be cooked to make jellies, jams, and sauces. This work aims to study and compare the antioxidant activity and the phenolic and anthocyanin composition of three varieties of Pyracantha coccinea: Red Column (PCR), Orange Glow (PCO), and Soleil d'Or (PCS), and one of Pyracantha angustifolia: Orange glow (PAO), collected from the spontaneous flora of the Mediterranean region (Southern Italy). Two different extraction processes were tested using methanol and an aqueous methanol solution (80% MeOH) to evaluate the polyphenolic content and antioxidant activity of freeze-dried berries. The highest total phenolic content was found in PCR and PAO berries (174.21 ± 0.149 and 168.01 ± 0.691 mg of gallic acid equivalent per gram of dry matter, respectively) extracted with an aqueous methanol solution (80% MeOH). Polyphenolic extracts analyzed by HPLC-DAD-ESI/MS confirmed the presence of rutin, quercetin hexose, neoeriocitrin, procyanidin B, and resveratrol. Moreover, the total antioxidant activity of the berries' extracts was measured by comparing two different spectrophotometric methods (ABTS and DPPH), showing that the varieties with the highest total phenolic content, PCR and PAO, also had the highest scavenging activity. Finally, a suitable extraction process was chosen for the evaluation of the anthocyanins' composition of all frozen berries, and in all MS spectra of Pyracantha varieties, two ionic species at 449 m/z attributable to two cyanidin derivatives were found. [ABSTRACT FROM AUTHOR]

l-Kynurenine (l-Kyn) is an endogenous metabolite produced in the catabolic route of l-Tryptophan (l-Trp), and it is a potential biomarker of several immunological disorders. Thus, the development of a fast and cheap technology for the specific detection of l-Kyn in biological fluids is of great relevance, especially considering its recent correlation with SARS-CoV-2 disease progression. Herein, a disposable screen-printed electrode based on a molecularly imprinted polymer (MIP) has been constructed: the o-Phenylenediamine monomer, in the presence of l-Kyn as a template with a molar ratio of monomer/template of 1/4, has been electropolymerized on the surface of a screen-printed carbon electrode (SPCE). The optimized kyn-MIP-SPCE has been characterized via cyclic voltammetry (CV), using [Fe(CN)6)]3−/4− as a redox probe and a scanning electron microscopy (SEM) technique. After the optimization of various experimental parameters, such as the number of CV electropolymerization cycles, urine pretreatment, electrochemical measurement method and incubation period, l-Kyn has been detected in standard solutions via square wave voltammetry (SWV) with a linear range between 10 and 100 μM (R2 = 0.9924). The MIP-SPCE device allowed l-Kyn detection in human urine in a linear range of 10–1000 μM (R2 = 0.9902) with LOD and LOQ values of 1.5 and 5 µM, respectively. Finally, a high selectivity factor α (5.1) was calculated for l-Kyn toward l-Trp. Moreover, the Imprinting Factor obtained for l-Kyn was about seventeen times higher than the IF calculated for l-Trp. The developed disposable sensing system demonstrated its potential application in the biomedical field. [ABSTRACT FROM AUTHOR]

In this work, we developed a novel approach to purify [11C]Raclopride ([11C]RAC), an important positron emission tomography radiotracer, based on tailored shape-recognition polymers, with the aim to substitute single-pass HPLC purification with an in-flow trap & release process. Molecular imprinting technology (MIT) applied to solid phase extraction (MISPE) was investigated to develop a setting able to selectively extract [11C]RAC in a mixture containing a high amount of its precursor, (S)-O-Des-Methyl-Raclopride (DM-RAC). Two imprinted polymers selective for unlabeled RAC and DM-RAC were synthesized through a radical polymerization at 65 °C using methacrylic acid and trimethylolpropane trimethacrylate in the presence of template molecule (RAC or DM-RAC). The prepared polymer was characterized by scanning electron microscopy and Fourier transform infrared spectroscopy and tested in MISPE experiments. The polymers were used in testing conditions, revealing a high retention capacity of RAC-MISPE to retain RAC either in the presence of similar concentrations of RAC and DM-RAC precursor (96.9%, RSD 6.6%) and in the presence of a large excess of precursor (90%, RSD 4.6%) in the loading solution. Starting from these promising results, preliminary studies for selective purification of [11C]Raclopride using this RAC-MISPE were performed and, while generally confirming the selectivity capacity of the polymer, revealed challenging applicability to the current synthetic process, mainly due to high backpressures and long elution times. [ABSTRACT FROM AUTHOR]