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提高鞣花酸生物利用度的策略:从天然或半合成衍生物到基于创新载体的纳米技术方法。

Strategies to improve ellagic acid bioavailability: from natural or semisynthetic derivatives to nanotechnological approaches based on innovative carriers.

机构信息

Department of Systems Medicine, University of Rome Tor Vergata, Via Montpellier 1 00133, Rome, Italy.

出版信息

Nanotechnology. 2020 Sep 18;31(38):382001. doi: 10.1088/1361-6528/ab912c. Epub 2020 May 7.

DOI:10.1088/1361-6528/ab912c
PMID:32380485
Abstract

Ellagic acid (EA) is a polyphenolic compound whose dietary consumption is mainly associated with the intake of red fruits, including pomegranates, strawberries, blackberries, blackcurrants, raspberries, grapes or dried fruits, like walnuts and almonds. A number of studies indicate that EA exerts health-beneficial effects against several chronic pathologies associated with oxidative damage, including different kinds of cancer, cardiovascular and neurodegenerative diseases. Furthermore, EA possesses wound-healing properties, antibacterial and antiviral effects, and acts as a systemic antioxidant. However, clinical applications of this polyphenol have been hampered and prevented by its poor water solubility (9.7 ± 3.2 μg ml in water) and pharmacokinetic profile (limited absorption rate and plasma half-life <1 h after ingestion of pomegranate juice), properties due to the chemical nature of the organic heterotetracyclic compound. Little has been reported on efficient strategies to enhance EA poor oral bioavailability, including chemical structure modifications, encapsulation within nano-microspheres to be used as carriers, and molecular dispersion in polymer matrices. In this review we summarize the experimental approaches investigated so far in order to improve EA pharmacokinetics, supporting the hypothesis that enhancement in EA solubility is a feasible route for increasing its oral absorption.

摘要

鞣花酸(EA)是一种多酚化合物,其膳食摄入量主要与摄入红色水果有关,包括石榴、草莓、黑莓、黑加仑、覆盆子、葡萄或干水果,如核桃和杏仁。许多研究表明,EA 对几种与氧化损伤有关的慢性疾病具有有益的健康作用,包括各种癌症、心血管疾病和神经退行性疾病。此外,EA 具有伤口愈合、抗菌和抗病毒作用,并作为一种全身性抗氧化剂。然而,由于这种多酚的化学性质为有机杂四环化合物,其较差的水溶性(水中为 9.7±3.2μg/ml)和药代动力学特征(石榴汁摄入后吸收率有限,血浆半衰期<1 小时)阻碍并阻止了其临床应用。关于提高 EA 口服生物利用度的有效策略的报道很少,包括化学结构修饰、封装在纳米微球中用作载体,以及在聚合物基质中的分子分散。在这篇综述中,我们总结了迄今为止为改善 EA 药代动力学而研究的实验方法,支持了提高 EA 溶解度是增加其口服吸收的可行途径的假设。

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