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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Interaction of glycyrrhetinic acid, furosemide and hydrochlorothiazide with bovine serum albumin and their displacement interactions: capillary electrophoresis and fluorescence quenching study.
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Interaction of glycyrrhetinic acid, furosemide and hydrochlorothiazide with bovine serum albumin and their displacement interactions: capillary electrophoresis and fluorescence quenching study.

机译:甘草次酸,速尿和氢氯噻嗪与牛血清白蛋白的相互作用及其置换相互作用:毛细管电泳和荧光猝灭研究。

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摘要

Licorice is the most widely used crude drug in traditional Chinese medicine. Glycyrrhetinic acid (GA) is the metabolite of glycyrrhizic acid, which is the main bioactive ingredient of licorice. In this work, capillary electrophoresis-frontal analysis (CE-FA) was applied to study the binding of bovine serum albumin with GA and two diuretics: furosemide (FU) and hydrochlorothiazide (HZ). The binding parameters of GA were determined by Scatchard analysis, which showed that there are two kinds of binding sites in bovine serum albumin for GA. However, the results showed that the CE-FA method was not suitable for the interaction study of FU and HZ. Therefore, utracentrifugation-CE was used to probe the binding characteristic of these two drugs and the results showed only one kind of binding site for them under the studied conditions. Displacement interactions between these drugs were also investigated by utracentrifugation-CE method and the results showed that GA hardly displaces HZ while it can slightly displace FU and FU can slightly displace HZ. For comparison, the binding of these drugs was also studied by the fluorescence quenching method and the data were processed by the Stern-Volmer quenching equation. Results showed that the binding constants were basically consistent for two methods for all drugs studied. The number of binding sites on one protein molecule was well consistent for FU and HZ while it was quite different for GA.
机译:甘草是中药中使用最广泛的原料药。甘草次酸(GA)是甘草酸的代谢产物,甘草酸是甘草的主要生物活性成分。在这项工作中,毛细管电泳-前沿分析(CE-FA)用于研究牛血清白蛋白与GA和两种利尿剂的结合:速尿(FU)和氢氯噻嗪(HZ)。通过Scatchard分析确定了GA的结合参数,表明牛血清白蛋白中有两种结合位点。然而,结果表明,CE-FA方法不适合用于FU和HZ的相互作用研究。因此,使用超速离心-CE来检测这两种药物的结合特性,结果表明在所研究的条件下,这两种药物仅具有一种结合位点。还通过超速离心-CE法研究了这些药物之间的置换相互作用,结果表明,GA几乎不能置换HZ,而它可以稍微置换FU,FU可以稍微置换HZ。为了进行比较,还通过荧光猝灭法研究了这些药物的结合,并通过Stern-Volmer猝灭方程对数据进行了处理。结果表明,对于所有研究的药物,两种方法的结合常数基本一致。一个蛋白质分子上的结合位点数目对于FU和HZ而言是非常一致的,而对于GA则完全不同。

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