INFLUENCE OF QUERCETIN ON THE BINDING OF TIGECYCLINE TO HUMAN SERUM ALBUMIN

Emina Mrkalić, Marina Ćendić Serafinović, Ratomir M. Jelić, Stefana Stojanović, Miroslav Sovrlić
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Abstract

Serum albumin is the major soluble protein in the circulatory system of humans. The metabolism of drugs, their distribution, free concentration, and efficacy depend on the drug-serum albumin interaction [1]. Accordingly, it is important to study the interactions of drugs with serum albumin, which determines the pharmacology and pharmacodynamics of drugs. Quercetin (QUE), a natural polyphenol widely distributed in many plant foods, such as fruits, vegetables, nuts, seeds, grains, and tea [2], bind to serum albumin [3]. Tigecycline (TGC), is a tetracycline antibiotic widely used in the treatment of bacterial infections [4]. This study aimed to investigate the binding properties of TGC to HSA in the presence of QUE, under physiological conditions, by fluorescence spectroscopy.
槲皮素对替加环素与人血清白蛋白结合的影响
血清白蛋白是人体循环系统中主要的可溶性蛋白。药物的代谢、分布、游离浓度和疗效取决于药物与血清白蛋白的相互作用[1]。因此,研究药物与血清白蛋白的相互作用决定了药物的药理学和药效学,具有重要的意义。槲皮素(Quercetin, QUE)是一种天然多酚,广泛存在于水果、蔬菜、坚果、种子、谷物和茶叶等多种植物性食物中[2],可与血清白蛋白结合[3]。替加环素(TGC)是一种广泛用于治疗细菌感染的四环素类抗生素[4]。本研究旨在通过荧光光谱研究生理条件下QUE存在下TGC与HSA的结合特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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