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1.
Chemphyschem ; 19(21): 2938-2946, 2018 11 05.
Artículo en Inglés | MEDLINE | ID: mdl-30238613

RESUMEN

A new Zn-N4 -Schiff base L=((±)-trans-N,N'-Bis(2-aminobenzylidene)-1,2-diaminocyclohexane) complex was synthesized and fully characterized, showing an unexpected self-assembled double-stranded helicate structure. The X-ray crystal analysis of the Zn2 L2 complex ((C40 H44 N8 Zn2 ,CH2 Cl2 , a=14.2375(3) Å, b=16.7976(4) Å, c=16.1613(4) Å, monoclinic, P21 /n, Z=4) shows a centrosymmetrical structure in which zinc atoms are in distorted tetrahedral environments, revealing an M- (R, R) left-handed helicity in its asymmetric unit. However, it was observed that this dinuclear complex is thermodynamically unstable in the presence of small water amounts and undergoes demetallation into free N4-Schiff base ligand and ZnO nanoparticles. This hydrolysis process was thoroughly identified and monitored through detailed 1 H NMR, DOSY NMR analysis. The reaction mechanism of this demetallation event was elucidated by using the DFT method, involving an activation energy smaller than 13 kcal/mol. Besides, a theoretical mechanism of the demetallation process is given for the first time.

2.
J Mol Recognit ; 30(4)2017 04.
Artículo en Inglés | MEDLINE | ID: mdl-27885729

RESUMEN

New biosourced chiral cross-linkers were reported for the first time in the synthesis of methyltestosterone (MT) chiral molecularly imprinted polymers (cMIPs). Isosorbide and isomannide, known as 1,4:3,6-dianhydrohexitols, were selected as starting diols. The cMIPs were synthesized following a noncovalent approach via thermal radical polymerization and monitored by Raman spectroscopy. These cross-linkers were fully characterized by 1 H and 13 C nuclear magnetic resonance (NMR) spectroscopy and high-resolution mass spectrometry. The cross-polarization magic angle spinning 13 C NMR, Fourier transform infrared spectroscopy, scanning electron microscopy, and specific surface areas following the Brunauer-Emmett-Teller (BET) method were used to characterize the cMIPs. The effect of stereochemistry of cross-linkers on the reactivity of polymerization, morphology, and adsorption-recognition properties of the MIP was evaluated. The results showed that the cMIP exhibited an obvious improvement in terms of rebinding capacity for MT as compared with the nonimprinted polymer (NIP). The highest binding capacity was observed for cMIP-Is (27.298 mg g-1 ) for high concentrations (500 mg L-1 ). However, the isomannide homologue cMIP-Im showed higher recovery-up to 65% and capacity for low concentrations (15 mg L-1 ). The experimental data were properly fitted by the Freundlich adsorption isothermal model.


Asunto(s)
Impresión Molecular/métodos , Polímeros/síntesis química , Metiltestosterona/metabolismo , Microscopía Electrónica de Rastreo , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Polímeros/química , Polímeros/metabolismo , Extracción en Fase Sólida , Espectroscopía Infrarroja por Transformada de Fourier , Espectrometría Raman , Estereoisomerismo
3.
J Environ Manage ; 183: 175-181, 2016 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-27591843

RESUMEN

The objective of the present study was to assess the influence of extreme pH and redox potential (Eh) conditions on phosphorus (P) retention within the surface sludge deposit layer of a vertical flow constructed wetland (VFCW) where phosphorus was captured by FeCl3 injection. Series of 27 successive batch leaching tests were conducted under acidic, alkaline or reductive conditions using a representative sludge sample taken from an 8-year old VFCW plant. Experiments were followed by monitoring the pH and Eh variations and analysing the releases of P and other selected elements into the solutions. The sludge material was also analyzed before and after leaching, using solution (31)P NMR spectroscopy and sequential chemical extractions, in order to evaluate dissolutions of both organic and inorganic P-bearing species and their respective contributions to P release. The correlations between the monitored variables were analyzed and visualized through principal components analyses (PCA). Results showed a very good stability of P retention in the sludge deposit and a relatively good acid-buffering capacity of the sludge, revealing that the risk of accidental P release into the environment would be extremely low during the real plant operation.


Asunto(s)
Fósforo/análisis , Aguas del Alcantarillado/química , Eliminación de Residuos Líquidos/métodos , Humedales , Cloruros , Compuestos Férricos , Francia , Concentración de Iones de Hidrógeno , Espectroscopía de Resonancia Magnética
4.
Environ Sci Technol ; 49(8): 4903-10, 2015 Apr 21.
Artículo en Inglés | MEDLINE | ID: mdl-25710195

RESUMEN

This study was conducted to determine phosphorus (P) species captured in a vertical-flow constructed wetland (VFCW) system combining a trickling filter followed by FeCl3 injection for phosphate coagulation. Suspended solids (SS) thus formed accumulated over time at the VFCW surface and transformed into a sludge deposit layer, which was shown to concentrate most of the P captured in the system. In order to investigate the effect of aging on P species, representative SS and sludge samples were taken from a wastewater treatment plant that had been in operation for 8 years and analyzed using P fractionation, solution (31)P NMR spectroscopy, and P and Fe K-edge XANES spectroscopy. A partial mineralization of organic matter was shown by comparing organic carbon contents of SS and sludge materials. Chemical fractionations combined with P and Fe K-edge XANES spectroscopy showed that P was predominantly bound to iron within both samples in the form of ferric phosphate, rather than adsorbed onto ferric oxyhydroxide. Calcium-bound P was more significantly observed in sludge than in SS, suggesting that aging induced the recombination of part of the organic and iron-bound P species into calcium-bound forms, as a possible consequence of the partial mineralization of organic matter.


Asunto(s)
Fósforo/análisis , Fósforo/química , Eliminación de Residuos Líquidos/métodos , Humedales , Adsorción , Calcio/química , Fraccionamiento Químico , Diseño de Equipo , Filtración/instrumentación , Hierro/química , Fosfatos/química , Aguas del Alcantarillado/química , Aguas Residuales , Espectroscopía de Absorción de Rayos X
5.
Molecules ; 20(10): 18128-43, 2015 Oct 05.
Artículo en Inglés | MEDLINE | ID: mdl-26445040

RESUMEN

A phytochemical investigation of Diplotaxis virgata D.C. and D. erucoides (L.) D.C. (Brassicaceae) offered to the isolation of two new flavonoids isorhamnetin-3-O-α-l-glucopyranoside (1) and rhamnetin-3,3'-di-O-ß-d-glucopyranoside (2), respectively. Their structures have been elucidated from the extended spectroscopic methods, including 1D- and 2D-NMR, UV and mass spectrometry analysis and by comparison with literature data. The fatty acid composition of the hexane extracts of the two species was also investigated by using GC-MS. The antioxidant activity of ethanol, ethyl acetate, n-butanol extracts and the isolated compounds from the two species was evaluated using DPPH and ABTS⁺ scavenging assays. All the tested samples showed an efficient radical scavenging ability, with IC50 values ranging from 16-40 µg/mL for the DPPH and from 17-44 µg/mL for the ABTS⁺ assays. In addition, the antibacterial activity of the prepared extracts and compounds 1 and 2, determined by well diffusion agar method against two Gram positive and five Gram negative bacteria, was evaluated and the results showed significant effects against all strains used.


Asunto(s)
Antibacterianos/química , Antioxidantes/química , Brassicaceae/química , Flavonoides/química , Hexanos/química , Extractos Vegetales/análisis , Antibacterianos/farmacología , Antioxidantes/farmacología , Brassicaceae/clasificación , Flavonoides/farmacología , Depuradores de Radicales Libres/química , Depuradores de Radicales Libres/farmacología , Bacterias Gramnegativas/efectos de los fármacos , Bacterias Grampositivas/efectos de los fármacos , Hexanos/farmacología , Estructura Molecular , Fitoquímicos/química , Fitoquímicos/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Túnez
6.
Sci Rep ; 13(1): 17733, 2023 10 18.
Artículo en Inglés | MEDLINE | ID: mdl-37853114

RESUMEN

Lactate accumulation and acidification in tumours are a cancer hallmark associated with the Warburg effect. Lactic acidosis correlates with cancer malignancy, and the benefit it offers to tumours has been the subject of numerous hypotheses. Strikingly, lactic acidosis enhances cancer cell survival to environmental glucose depletion by repressing high-rate glycolysis and lactic fermentation, and promoting an oxidative metabolism involving reactivated respiration. We used real-time NMR to evaluate how cytosolic lactate accumulation up to 40 mM and acidification up to pH 6.5 individually impact glucose consumption, lactate production and pyruvate evolution in isolated cytosols. We used a reductive cell-free system (CFS) to specifically study cytosolic metabolism independently of other Warburg-regulatory mechanisms found in the cell. We assessed the impact of lactate and acidification on the Warburg metabolism of cancer cytosols, and whether this effect extended to different cytosolic phenotypes of lactic fermentation and cancer. We observed that moderate acidification, independently of lactate concentration, drastically reduces the glucose consumption rate and halts lactate production in different lactic fermentation phenotypes. In parallel, for Warburg-type CFS lactate supplementation induces pyruvate accumulation at control pH, and can maintain a higher cytosolic pyruvate pool at low pH. Altogether, we demonstrate that intracellular acidification accounts for the direct repression of lactic fermentation by the Warburg-associated lactic acidosis.


Asunto(s)
Acidosis Láctica , Neoplasias , Humanos , Ácido Láctico/metabolismo , Acidosis Láctica/metabolismo , Fermentación , Sistema Libre de Células/metabolismo , Glucólisis , Neoplasias/patología , Piruvatos/metabolismo , Glucosa/metabolismo , Concentración de Iones de Hidrógeno
7.
Anal Chem ; 84(10): 4481-8, 2012 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-22497552

RESUMEN

The preparation of steroid-based molecularly imprinted polymers (MIPs) based upon noncovalent interaction is particularly suited for selective capture of steroid hormones in biological and environmental samples. The success of this method lies in the optimization of the interaction between steroids (template) and methacrylic acid (functional monomer) in the prepolymerization mixture. NMR techniques coupled with DFT calculations were used to evaluate the capacity of the methacrylic acid to bind a steroid for future applications. The androstane derivative steroids considered in the present study have two functional groups at C(3) and C(17), which may interact with the methacrylic acid. These can be hydroxyl or ketone groups. Experimental results show that the steroids can be divided in three groups corresponding to the ketone type at C(3), the H-bond strength increasing with the number of double bonds. DFT calculations are in very good agreement with experimental results, showing increasing binding energy from no bonds, a single bond, and two double bond steroids. For steroids holding a hydroxyl group the binding energy obtained in the solvent model is comparable to the binding energy of single bond ketone steroids.

8.
Chem Commun (Camb) ; 51(21): 4458-61, 2015 Mar 14.
Artículo en Inglés | MEDLINE | ID: mdl-25679473

RESUMEN

We report the first synthesis of a methylene blue (MB) phosphoramidite derivative suitable for DNA solid-phase synthesis. The electrochemical and optical properties of the resulting MB modified oligonucleotides were confirmed. This new molecule is an important breakthrough in the design of new probes labelled with MB.


Asunto(s)
Azul de Metileno/química , Oligonucleótidos/química , Compuestos Organofosforados/química , Técnicas Electroquímicas , Oligonucleótidos/síntesis química , Técnicas de Síntesis en Fase Sólida
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