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提高绿茶表没食子儿茶素没食子酸酯在水溶液中的稳定性和生物利用度的简单方法:实验与理论表征

Simple Approach to Enhance Green Tea Epigallocatechin Gallate Stability in Aqueous Solutions and Bioavailability: Experimental and Theoretical Characterizations.

作者信息

Secretan Philippe-Henri, Thirion Olivier, Sadou Yayé Hassane, Damy Thibaud, Astier Alain, Paul Muriel, Do Bernard

机构信息

Matériaux et Santé, Université Paris-Saclay, 92296 Châtenay-Malabry, France.

Department of Pharmacy, Hôpitaux Universitaires Henri Mondor, AP-HP, 94000 Créteil, France.

出版信息

Pharmaceuticals (Basel). 2021 Nov 30;14(12):1242. doi: 10.3390/ph14121242.

DOI:10.3390/ph14121242
PMID:34959643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8706847/
Abstract

Because of its antioxidant, antimutagenic, and anti-infectious properties, epigallocatechin gallate (EGCG) is the most interesting compound among the green tea catechins polyphenols. However, its health effects are inconclusive due to its very low bioavailability, largely due to a particular instability that does not allow EGCG to reach the potency required for clinical developments. Over the last decade, many efforts have been made to improve the stability and bioavailability of EGCG using complex delivery systems such as nanotechnology, but these efforts have not been successful and easy to translate to industrial use. To meet the needs of a large-scale clinical trial requiring EGCG in a concentrated solution to anticipate swallowing impairments, we developed an EGCG-based aqueous solution in the simplest way while trying to circumvent EGCG instability. The solution was thoroughly characterized to sort out the unexpected stability outcome by combining experimental (HPLC-UV-mass spectrometry and infrared spectroscopy) and computational (density functional theory) studies. Against all odds, the EGCG-sucrose complex under certain conditions may have prevented EGCG from degradation in aqueous media. Indeed, in agreement with the ICH guidelines, the formulated solution was shown to be stable up to at least 24 months under 2-8 °C and at ambient temperature. Furthermore, considerable improvement in bioavailability in rats, against EGCG powder formulated in hard-gel capsules, was shown after gavage. Thus, the proposed formulation may provide an easily implementable platform to administer EGCG in the context of clinical development.

摘要

由于表没食子儿茶素没食子酸酯(EGCG)具有抗氧化、抗诱变和抗感染特性,它是绿茶儿茶素多酚中最具吸引力的化合物。然而,由于其生物利用度极低,其健康效应尚无定论,这主要是由于一种特殊的不稳定性,使得EGCG无法达到临床开发所需的效力。在过去十年中,人们通过纳米技术等复杂递送系统来提高EGCG的稳定性和生物利用度,但这些努力并未成功,也难以转化为工业应用。为满足大规模临床试验的需求,该试验需要浓缩溶液形式的EGCG以应对吞咽障碍,我们以最简单的方式开发了一种基于EGCG的水溶液,同时试图规避EGCG的不稳定性。通过结合实验(高效液相色谱-紫外-质谱联用和红外光谱)和计算(密度泛函理论)研究,对该溶液进行了全面表征,以梳理出意外的稳定性结果。出乎意料的是,在某些条件下,EGCG-蔗糖复合物可能防止了EGCG在水性介质中降解。事实上,根据国际人用药品注册技术协调会(ICH)指南,所配制的溶液在2-8℃和室温下至少24个月内显示稳定。此外,经口灌胃后,与硬胶囊剂型的EGCG粉末相比,大鼠体内的生物利用度有了显著提高。因此,所提出的制剂可能为临床开发背景下EGCG的给药提供一个易于实施的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/ebfb15af18a7/pharmaceuticals-14-01242-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/52999c474cd6/pharmaceuticals-14-01242-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/ab751b1f9a0c/pharmaceuticals-14-01242-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/769faea8d23a/pharmaceuticals-14-01242-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/c0b4795f1897/pharmaceuticals-14-01242-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/84dc5fa5efac/pharmaceuticals-14-01242-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/12f966b07fb0/pharmaceuticals-14-01242-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/16ad2963d98a/pharmaceuticals-14-01242-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/ebfb15af18a7/pharmaceuticals-14-01242-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/52999c474cd6/pharmaceuticals-14-01242-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/ab751b1f9a0c/pharmaceuticals-14-01242-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/769faea8d23a/pharmaceuticals-14-01242-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/c0b4795f1897/pharmaceuticals-14-01242-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/84dc5fa5efac/pharmaceuticals-14-01242-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/12f966b07fb0/pharmaceuticals-14-01242-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/16ad2963d98a/pharmaceuticals-14-01242-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/881e/8706847/ebfb15af18a7/pharmaceuticals-14-01242-g008.jpg

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