首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Concurrent determination of topotecan and model permeability markers (atenolol, antipyrine, propranolol and furosemide) by reversed phase liquid chromatography: Utility in Caco-2 intestinal absorption studies
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Concurrent determination of topotecan and model permeability markers (atenolol, antipyrine, propranolol and furosemide) by reversed phase liquid chromatography: Utility in Caco-2 intestinal absorption studies

机译:反相液相色谱法同时测定拓扑替康和模型通透性标志物(阿替洛尔,安替比林,普萘洛尔和速尿):在Caco-2肠吸收研究中的用途

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摘要

A simple, sensitive, specific and high-resolution reversed-phase liquid chromatographic method utilizing ultraviolet detection has been developed and validated for simultaneous determination of topotecan and four intestinal permeability markers (atenolol, antipyrine, propranolol and furosemide) as suggested by US-FDA. Chromatography was carried out on C-18 column with mobile phase comprising water (pH 3.0) and acetonitrile gradient pumped at a flow rate of I ml min(-1). The validation parameters included specificity, accuracy, precision, sensitivity and stability studies. Topotecan, an anti-cancer drug widely used in metastatic carcinoma, is a P-glycoprotein substrate having oral bioavailability of 30% with large inter-patient variability. The present method was successfully applied for demonstrating P-gp mediated transport of topotecan and its inhibition using verapamil in Caco-2 cell monolayer. The method can be used in identification of novel P-gp inhibitors for topotecan and estimating the contribution of P-gp in affecting oral bioavailability of topotecan. The other applications of method include its use in validation of Caco-2 monolayer assay for getting biowaiver based on Biopharmaceutic Classification System and its extrapolation to in situ and/or in vivo studies. (c) 2007 Elsevier B.V. All rights reserved.
机译:已开发出一种简单,灵敏,特异且高分辨率的利用紫外检测的反相液相色谱方法,并经验证可同时测定拓扑替康和四种肠道通透性标志物(阿替洛尔,安替比林,普萘洛尔和速尿),如美国食品和药物管理局所建议。色谱法在C-18色谱柱上进行,流动相包括水(pH 3.0)和乙腈梯度泵,流速为1 ml min(-1)。验证参数包括特异性,准确性,精密度,敏感性和稳定性研究。托泊替康是一种广泛用于转移癌的抗癌药物,是一种P-糖蛋白底物,口服生物利用度为30%,患者之间的差异较大。本方法已成功用于证明P-gp介导的拓扑替康的转运及其在Caco-2细胞单层中使用维拉帕米的抑制作用。该方法可用于鉴定拓扑替康的新型P-gp抑制剂,并估计P-gp在影响拓扑替康的口服生物利用度中的作用。该方法的其他应用包括基于生物制药分类系统用于验证Caco-2单层测定是否获得生物豁免以及将其外推至原位和/或体内研究。 (c)2007 Elsevier B.V.保留所有权利。

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