生物标志物在天然药物代谢动力学研究中的应用

V. Kosman, N. Faustova, M. V. Karlina, V. Makarov, M. Makarova
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引用次数: 1

摘要

天然药品因其药理功效和相对安全性而被广泛使用。这类药物的化学组成通常是复杂的,它们可以由杂多聚物或含有肽、多糖和其他内源性和/或在活生物体中快速代谢的化合物的混合物来表示。传统的、以色谱为基础的评价这类药物的方法通常不适用。天然来源的药物的药代动力学可以通过基于评估这些药物的生物作用和药效学特性的方法来研究,其中包括确定生物标记物(biomarker)水平。本研究的目的是总结生物标志物在药代动力学研究中使用的累积实验数据,如一些天然来源的药物所示。材料和方法。作者研究了从褐藻中提取的岩藻聚糖,以及从绿海胆的生殖腺中分离出的生物活性化合物复合物和糖肽。通过体外/离体实验建立试验混合物浓度与潜在生物标志物活性/浓度之间的相关性。实验显示生物标志物在使用研究产品前后在血浆或血清(体外)和全血(离体)中的浓度,以评估生物标志物反应的特异性、校准(线性)范围及其天然浓度。分析方法基于显色(光学)抗Xa因子活性(AXA)测定,动力学法测定二肽基肽酶4和乳酸脱氢酶活性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of Biomarkers in Pharmacokinetics Studies of Medicinal Products of Natural Origin
Medicinal products of natural origin are widely used by virtue of their pharmacological efficacy and relative safety. Chemical composition of such medicines is usually complex, they may be represented by heteropolymers or mixtures containing peptides, polysaccharides, and other compounds which are endogenous and/or rapidly metabolised in a living organism. Conventional, chromatography-based approaches to evaluation of such medicines are often not applicable. Pharmacokinetics of medicinal products of natural origin may be studied by methods based on assessment of biological action and pharmacodynamic properties of such medicines, which involves determination of biological marker (biomarker) levels. The aim of the study was to summarise the accumulated experimental data on the use of biomarkers in pharmacokinetics studies as illustrated by a few medicinal products of natural origin. Material and methods. The authors studied fucoidan from Fucus vesiculosus, as well as a complex of bioactive compounds and a glycopeptide—both isolated from gonads of green sea urchins (Strongylocentrotus droebachiensis). In vitro / ex vivo experiments were used to establish correlation between the concentrations of the test mixtures and the activity/ concentration of potential biomarkers. Experiments showing the biomarker concentration in plasma or serum (in vitro) and whole blood (ex vivo) before and after spiking with the studied products were performed in order to assess specificity, calibration (linear) range of the biomarker response, and its native concentration. The analytical procedures were based on the chromogenic (optical) anti-factor Xa activity (AXA) assay, and determination of dipeptidyl peptidase 4 and lactate dehydrogenase activity by kinetic
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