一个模拟化疗药物的药代动力学模型,用于评估软琼脂菌落形成分析系统中的药物效应。

M Malmberg, H K Slocum, Y M Rustum
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引用次数: 3

摘要

菌落形成分析系统是体外药物评价的重要组成部分。如果能在模拟临床条件下进行体外药物细胞毒性研究,将是有益的。我们已经开发了一种单个菌落形成测定系统,可以在琼脂糖细胞镀后,在药物存在的情况下,在连续和/或短期暴露的条件下,监测和定量单个菌落的生长。在这篇简短的报告中,我们在琼脂糖中建立了四种药物的药代动力学特征,即胞嘧啶阿拉伯糖(araC)、阿霉素(Dox)、5-氟尿嘧啶(5-FUra)和5-氟-2'-脱氧尿苷(FdUrd),模拟了这些药物在体内静脉注射时的药代动力学特征。结果表明,在琼脂糖中短期处理是可行的,药物的洗涤过程在44小时内降低了药物浓度3-4 log。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A model for mimicking the pharmacokinetics of chemotherapy drugs for evaluation of drug effects in a soft agar colony formation assay system.

Colony formation assay systems are an important part of in vitro drug evaluation. It would be useful if the in vitro drug cytotoxicity could be carried out under conditions mimicking those employed clinically. We have developed an individual colony formation assay system that would allow monitoring and quantitation of the growth of individual colonies (9) in the presence of the drug under conditions of continuous and/or short-term exposure, after plating of the cells in the agarose. In this brief report, we established the pharmacokinetic profile of four drugs, cytosine arabinoside (araC), Doxorubicin (Dox), 5-fluorouracil (5-FUra) and 5-fluoro-2'-deoxyuridine (FdUrd) in agarose mimicking those that are achieved when these agents were administered in vivo as an i.v. push. The results show that short-term treatment in agarose is possible and that the washing procedure of the drugs decreased the drug concentrations 3-4 logs over 44 hours.

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