Protection of hepatic cell damage and antimicrobial evaluation of chitosan-catechin conjugate
The chitosan-catechin conjugate was developed by free radical-induced conjugating reaction, and its protection ability against hydrogen peroxide-induced hepatic damage in human normal Chang liver cells and antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA) and foodborn...
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Published in | Applied biological chemistry Vol. 56; no. 6; pp. 701 - 707 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.12.2013
Springer Nature B.V 한국응용생명화학회 |
Subjects | |
Online Access | Get full text |
ISSN | 1738-2203 2468-0834 2234-344X 2468-0842 |
DOI | 10.1007/s13765-013-3168-8 |
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Summary: | The chitosan-catechin conjugate was developed by free radical-induced conjugating reaction, and its protection ability against hydrogen peroxide-induced hepatic damage in human normal Chang liver cells and antimicrobial activity against methicillin-resistant
Staphylococcus aureus
(MRSA) and foodborne pathogens were investigated. Treatment of hydrogen peroxide (650 μM) on Chang liver cells decreased cell viability up to 59.38% compared to the non-treatment group; however, cotreatment of the chitosan-catechin conjugate increased cell viability up to 76.90% at 200 μg/mL, and the protection ability was significantly higher than the unmodified chitosan (
p
<0.05). The chitosan-catechin conjugate significantly (
p
<0.05) inhibited the formation of intracellular reactive oxygen species and lipid peroxidation in Chang liver cells. Moreover, the chitosan-catechin conjugate increased glutathione levels in normal condition as well as under oxidative stress by hydrogen peroxide. Additionally, the chitosan-catechin conjugate showed increased antimicrobial activity against MRSA and foodborne pathogens as compared to those of the unmodified chitosan. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 G704-000111.2013.56.6.017 |
ISSN: | 1738-2203 2468-0834 2234-344X 2468-0842 |
DOI: | 10.1007/s13765-013-3168-8 |