Bioanalytical Department, Integrated Product Development, Dr. Reddy's Laboratories Ltd, Bachupalli, Hyderabad 500 072, India.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Apr 15;878(13-14):981-6. doi: 10.1016/j.jchromb.2010.02.028. Epub 2010 Mar 3.
A highly sensitive, specific and evaporation free SPE extraction, LC-MS/MS method has been developed for the estimation of trospium in human plasma using trospium-d8 as an internal standard (IS). The analyte was separated using isocratic mobile phase on reverse phase column and analyzed by MS/MS in the multiple reaction monitoring mode using the respective [M(+)] cations, m/z 392-164 for trospium and m/z 400-172 for the IS. The total run time was 3.50 min and the elution of trospium and trospium-d8 (IS) occurred at 2.8 min. The developed method was validated in human plasma with a lower limit of quantification of 0.05 ng/mL. A linear response function was established for the range of concentrations 0.05-10 ng/mL (r>0.998) for trospium in human plasma. The intra- and inter-day precision values for trospium met the acceptance as per FDA guidelines. Trospium was stable in the battery of stability studies viz., bench-top, auto-sampler, dry extracts and freeze/thaw cycles. The developed assay method was applied to an oral pharmacokinetic study in humans.
已经开发出一种高灵敏度、高特异性且无蒸发的 SPE 提取、LC-MS/MS 方法,用于使用 trospium-d8 作为内标 (IS) 来估算人血浆中的 trospium。使用等度流动相在反相柱上分离分析物,并通过 MS/MS 在多重反应监测模式下使用各自的 [M(+)] 阳离子,m/z 392-164 用于 trospium 和 m/z 400-172 用于 IS 进行分析。总运行时间为 3.50 分钟,trospium 和 trospium-d8 (IS) 的洗脱时间为 2.8 分钟。该方法在人血浆中进行了验证,定量下限为 0.05 ng/mL。已经建立了 trospium 在人血浆中的浓度范围为 0.05-10 ng/mL(r>0.998)的线性响应函数。根据 FDA 指南,trospium 的日内和日间精密度值符合要求。在一系列稳定性研究中,trospium 稳定,包括台式、自动进样器、干提取物和冻融循环。所开发的测定方法已应用于人体口服药代动力学研究。