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1.
Int J Biol Macromol ; 163: 801-816, 2020 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-32652152

RESUMEN

In this study, the new N, N, O tridentate donor water soluble isoniazid based biopolymer Schiff base ligand and their Co (II), Cu (II), Zn (II) metal complexes were prepared. The compounds were designed for potential biological application such as antibacterial, antifungal, anti-inflammatory, total antioxidant, antidiabetic and DNA binding studies. The synthesized compounds were illuminated in different light sources of various spectra were used to explore the functional groups of Biopolymer derivatives. Thermal degradation, thermal stability and percentage of mass loss for the prepared compounds were investigated through thermo gravimetric and differential thermal (TGA-DTA) analyses. Crystalline structure of synthesized biopolymer derivatives were explored by X-ray diffraction (XRD) studies, the crystallinity of chitosan is gradually decreased after the Schiff base and complex formation. Surface morphology and structures of the prepared compounds were examined using SEM analysis. The magnetic moment and magnetism of the metal complexes were studied using Vibrating-sample magnetometer (VSM). Antidiabetic studies of Biopolymer Schiff base and metal complexes were carried out by α-amylose inhibitory method. DNA nuclease activities of synthesized metal complexes were investigated by Ultra-Violet (UV) and viscometry methods. The Cu (II) complexes showed better DNA binding results than Co (II) and Zn (II) complexes.


Asunto(s)
Quitosano/análogos & derivados , Cobalto/química , Complejos de Coordinación/química , Cobre/química , Isoniazida/química , Bases de Schiff/química , Zinc/química , Antibacterianos/química , Antibacterianos/farmacología , Antifúngicos/química , Antifúngicos/farmacología , Antioxidantes/química , Antioxidantes/farmacología , Fenómenos Químicos , Técnicas de Química Sintética , Quitosano/química , Desoxirribonucleasas/química , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/farmacología , Ligandos , Porosidad , Solubilidad , Espectroscopía Infrarroja por Transformada de Fourier , Análisis Espectral , Termogravimetría , Difracción de Rayos X , alfa-Amilasas/química
2.
Int J Biol Macromol ; 152: 873-883, 2020 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-32112839

RESUMEN

A biocomposite film composed of biopolymers chitosan (CS), gelatin (GE) and allantoin (AT) was fabricated by solution casting technique. The functional group interaction of the biocomposite films was inspected through the Attenuated total reflectance Fourier transform spectrometer (ATR-FTIR). The morphological changes and crystallinity of biocomposite films with varied ratios of chitosan/gelatin (CS/GE) and allantoin were examined under Scanning electron microscope (SEM) and X-ray diffractometer (XRD). The water-absorbing capacity was found enhanced by an increase in the chitosan ratio. The biocomposite films exhibit good antioxidant, anti-inflammatory properties. The biocomposite films also display enhanced stability with steady degradation under the PBS medium. The biocomposite films reveal improved antibacterial activity against Escherichia coli (E.coli) and Staphylococcus aureus (S.aureus). Blood compatibility studies explore the non-hemolytic nature. The in vitro cytotoxicity by MTT assay shows excellent biocompatibility. The fibroblast adhesion on the biocomposite film displays enhanced proliferation and viability. These significant biological properties of biocomposite film make it an appropriate candidate for wound dressing application.


Asunto(s)
Alantoína/química , Vendajes , Materiales Biocompatibles/química , Materiales Biocompatibles/farmacología , Quitosano/química , Gelatina/química , Cicatrización de Heridas/efectos de los fármacos , Animales , Antibacterianos/química , Antibacterianos/farmacología , Antiinflamatorios/química , Antiinflamatorios/farmacología , Adhesión Celular/efectos de los fármacos , Línea Celular , Supervivencia Celular/efectos de los fármacos , Depuradores de Radicales Libres/química , Depuradores de Radicales Libres/farmacología , Ensayo de Materiales , Fenómenos Mecánicos , Ratones
3.
RSC Adv ; 10(31): 18259-18279, 2020 May 10.
Artículo en Inglés | MEDLINE | ID: mdl-35692624

RESUMEN

This study focused on the synthesis, photocatalytic degradation of organic dyes and biological activity of novel N, N, O-donor tridentate water soluble 4-hydroxy benzohydrazide-grafted biopolymer Schiff base Cu(ii) complexes. The eco-friendly catalysts were designed for potential application in the degradation of organic dyes. The photocatalytic degradation of methylene blue was investigated with various irradiation times (30, 60, 90 and 120 min), catalytic dosages (5, 10, 15 and 20 mg) and pH (3, 7 and 12). The as-prepared compounds were characterised via various techniques including FT-IR and FT-NMR spectroscopy; TGA-DTA, XRD, SEM-EDAX; ESR and UV-vis spectroscopy; photoluminescence, magnetic moment, and conductivity measurements; and elemental and thermal analysis. The crystallinity of the Schiff base ligands, chitosan, and their Cu(ii) complexes was analysed via X-ray diffraction (XRD) studies. The XRD patterns revealed that the polymer chitosan was more crystalline than the Schiff base ligands and their complexes. The surface morphological analysis by scanning electron microscopy (SEM) revealed that the Cu(ii) complexes were amorphous in nature compared to chitosan and the ligands. The anti-inflammatory and anti-diabetic studies of the biopolymer Cu(ii) complexes were performed using the albumin denaturation technique and McCue and Shetty method, respectively. The as-synthesized 4-hydroxy benzohydrazide-grafted O-carboxymethyl chitosan Schiff base ligands and their Cu(ii) complexes showed a good anti-inflammatory and antidiabetic effect. The photocatalytic activity proved that the aryl-substituted complex was more efficient than the aliphatic-substituted complex.

4.
Int J Biol Macromol ; 136: 738-754, 2019 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-31220500

RESUMEN

Water soluble hydrazide based O-carboxymethyl chitosan Schiff base ligands have been prepared from chitosan and a mixture of benzoic acidhydrazide with ß-diketone by carboxymethylation using mono chloroaceticacid (MCA) through in-situ reaction. The degree of deacetylation of chitosan was determined by elemental analysis and potentiometric titration. Schiff base ligands and the functional groups were characterised by FT-IR, 1H, and 13C NMR spectroscopic techniques. The crystallinity of ligands and complexes was evaluated by X-ray powder diffraction (XRD) studies. Thermal stability of all the synthesized compounds was investigated by thermo gravimetric analysis and differential thermal analysis (TGA-DTA) which revealed the presence of metal oxide (CuO) residue to elevate the temperature to >500 °C. Filed emission scanning electron microscopic (FESEM) analysis revealed that Cu (II) complexes were more amorphous in nature than chitosan and Schiff base ligands. Vibrating sample magnetometer (VSM) studies reported that the d9 configuration of the metal complex was paramagnetic in nature and the geometry of the complex was square pyramidal. The antimicrobial activity of the synthesized hydrazide Cu (II) complexes was characterised by agar plate method, anti-inflammatory study was characterised by egg albumin denaturation technique and total antioxidant activity was characterised by phosphomolybdenum method.


Asunto(s)
Quitosano/análogos & derivados , Complejos de Coordinación/síntesis química , Complejos de Coordinación/farmacología , Cobre/química , Hidrazinas/química , Agua/química , Albúminas/química , Antibacterianos/síntesis química , Antibacterianos/química , Antibacterianos/farmacología , Antiinflamatorios/síntesis química , Antiinflamatorios/química , Antiinflamatorios/farmacología , Antifúngicos/síntesis química , Antifúngicos/química , Antifúngicos/farmacología , Antioxidantes/síntesis química , Antioxidantes/química , Antioxidantes/farmacología , Técnicas de Química Sintética , Quitosano/química , Complejos de Coordinación/química , Ligandos , Nitrógeno/química , Oxígeno/química , Desnaturalización Proteica/efectos de los fármacos , Bases de Schiff/química , Solubilidad
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