EA3035 Clinique et Expérimentale de Médicaments Anticancereux, Institut Claudius Regaud, 31052 Toulouse, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Mar 1;878(7-8):645-52. doi: 10.1016/j.jchromb.2010.01.019. Epub 2010 Jan 25.
Topetecan is an important anti-cancer drug that has recently become available as an oral formulation. In order to study its intestinal absorption in vitro and a potential drug-drug interaction with the anti-emetic ondansetron, a sensitive and accurate method for the analysis of topotecan in biological media was required. We developed a liquid-liquid extraction method at pH 7.0-7.5 with a recovery of 85% and which took into account the complex chemical behaviour of topotecan related to the lactone opening and the keto-enol tautomerism. This enabled us to validate a new specific and sensitive LC-MS method of analysis, with satisfactory inter- and intra-day repeatability and accuracy. The method was applied to a study of topotecan uptake in rat everted gut sacs that showed that, despite being a P-glycoprotein substrate like topotecan, ondansetron did not interfere with topotecan uptake.
拓扑替康是一种重要的抗癌药物,最近已作为口服制剂上市。为了研究其在体外的肠道吸收以及与止吐药昂丹司琼的潜在药物相互作用,需要建立一种用于生物介质中拓扑替康分析的灵敏、准确的方法。我们开发了一种在 pH 值 7.0-7.5 下进行的液-液萃取方法,回收率为 85%,并考虑了与内酯开环和酮-烯醇互变异构有关的拓扑替康的复杂化学行为。这使我们能够验证一种新的特异性和灵敏性的 LC-MS 分析方法,该方法具有令人满意的日间和日内重复性和准确性。该方法应用于大鼠外翻肠囊对拓扑替康摄取的研究表明,尽管昂丹司琼与拓扑替康一样是 P-糖蛋白的底物,但它并不干扰拓扑替康的摄取。