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Int J Biol Macromol ; 161: 1440-1446, 2020 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-32781126

RESUMO

This study presents a novel fully enzymatic process for the controlled depolymerisation of fungal and shrimp chitosan, and their subsequent use in the synthesis of lignin cross-linked chitosan (CTS) hydrogels. Cellobiosehydrolase (CBH) was used to depolymerize CTS resulting in decrease in average molecular weight (Mw) of shrimp CTS from 140 kDa and degree of deacetylation (DD %) from 91.3% to an average MW of 15 kDa and 16% DD. Similarly, fungal chitosan average molecular weight decreased from 92 kDa and the degree of deacetylation (DD) of 48.3% to 12 kDa and a DD of 13%. The depolymerized CTS were completely soluble in water and miscible with lignosulfonates without encountering the usual problem of formation of flocs. Introduction of laccase into a lignosulfonate-chitosan mixture resulted in the oxidation and generation of lignin reactive phenoxyl radicals that cross-linked with CTS-NH2 reactive groups resulting in the increase of Mw from 20 kDa to >500 kDa and viscosity from 20 mPa to >500 mPa. This resulted in the formation of stable lignin-cross-linked hydrogels with elongation at break of 111% and tensile strength of 7 mPa. The produced functional hydrogels have potential application in food and biomedical industries as e.g. as oxygen barriers in packaging or as functional wound dressing or tissue engineering platforms.


Assuntos
Quitosana/química , Hidrogéis/síntese química , Lignina/química , Celulose 1,4-beta-Celobiosidase/química , Técnicas de Química Sintética , Reagentes de Ligações Cruzadas/química , Sequestradores de Radicais Livres/química , Hidrogéis/química , Hidrólise , Lacase/química , Fenômenos Mecânicos , Solubilidade , Espectroscopia de Infravermelho com Transformada de Fourier
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