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首页> 外文期刊>Journal of materials science >The inhibition of collagenase induced degradation of collagen by the galloyl-containing polyphenols tannic acid, epigallocatechin gallate and epicatechin gallate
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The inhibition of collagenase induced degradation of collagen by the galloyl-containing polyphenols tannic acid, epigallocatechin gallate and epicatechin gallate

机译:含没食子酰基的多酚鞣酸,表没食子儿茶素没食子酸酯和表儿茶素没食子酸酯对胶原酶的抑制作用

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摘要

Collagen based cosmetic fillers require repeat treatments due to collagenase derived degradation of the filler in the intradermal injection site. The objective of this study was to investigate the inhibition of this degradation by the galloyl-containing compounds tannic acid, epigallocatechin gallate (EGCG), epicatechin gallate (ECG) and gallic acid (GA). A gel permeation chromatography assay was developed to quantitate the collagenase induced reductions in collagen molecular weight. The binding of the compounds to collagen was measured using HPLC. The stabilization of collagen was measured using Differential Scanning Calorimetry (DSC). Tannic acid, EGCG and ECG (but not GA) were found to strongly inhibit collagen degradation at concentrations in the low micromolar range. The compounds bound strongly to collagen and stabilized collagen. It is concluded that tannic acid, EGCG and ECG bind to collagen via extensive hydrogen bonding augmented by some hydrophobic interactions and prevent the free access of collagenase to active sites on the collagen chains.
机译:基于胶原蛋白的化妆品填充剂由于在皮内注射部位中胶原酶衍生的填充剂降解而需要重复处理。这项研究的目的是研究含没食子酰基的化合物鞣酸,表没食子儿茶素没食子酸酯(EGCG),表儿茶素没食子酸酯(ECG)和没食子酸(GA)对这种降解的抑制作用。开发了凝胶渗透色谱分析法以定量胶原酶诱导的胶原蛋白分子量的减少。使用HPLC测量化合物与胶原的结合。使用差示扫描量热法(DSC)测量胶原的稳定性。发现单宁酸,EGCG和ECG(而非GA)在低微摩尔浓度范围内能强烈抑制胶原蛋白降解。这些化合物与胶原蛋白牢固结合并稳定了胶原蛋白。结论是单宁酸,EGCG和ECG通过广泛的氢键结合到胶原蛋白上,而氢键由于一些疏水相互作用而增强,并阻止胶原酶自由进入胶原蛋白链上的活性位点。

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  • 来源
    《Journal of materials science 》 |2010年第5期| P.1435-1443| 共9页
  • 作者单位

    Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC V6T 1Z3, Canada;

    Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC V6T 1Z3, Canada;

    Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC V6T 1Z3, Canada;

    Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC V6T 1Z3, Canada;

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