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Sensitive liquid chromatography/tandem mass spectrometry method for the determination of two novel highly lipophilic anti-cancer drug candidates in rat plasma and tissues

机译:灵敏液相色谱/串联质谱法测定大鼠血浆和组织中的两种新型高亲脂性抗癌候选药物

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摘要

A simple and sensitive liquid chromatography/electrospray ionization tandem mass spectrometry (LC–ESI-MS/MS) method was developed and validated for determination of two highly lipophilic anti-cancer drug candidates, LG1980, and GH501, in rat plasma and tissues (liver, kidney and femur bones).LG1980 and GH501 were extracted from rat plasma and tissue homogenates using liquid–liquid extraction. The method provided a linear range of 1.0–200.0 ng/mL for GH501 in plasma and LG1980 in plasma and liver. For both analytes in other tissue homogenates the linear range was 2.0–400.0 ng/mL. The method was validated with precision within 15% relative standard deviation (RSD), accuracy within 15% relative error (RE) and a consistent recovery. This method has been successfully applied in two preclinical studies for LG1980 and GH501 to determine their concentrations in rat plasma, liver, kidney and bone over 24 h after intravenous injection of compounds.
机译:开发了一种简单而灵敏的液相色谱/电喷雾串联质谱(LC-ESI-MS / MS)方法,并已用于确定大鼠血浆和组织中两种高度亲脂性抗癌药物LG1980和GH501的验证。 (肾和股骨)。LG1980和GH501使用液-液萃取法从大鼠血浆和组织匀浆中提取。该方法为血浆中的GH501和血浆和肝脏中的LG1980提供了1.0–200.0 ng / mL的线性范围。对于其他组织匀浆中的两种分析物,线性范围为2.0–400.0 ng / mL。该方法的相对精度在15%相对标准偏差(RSD)之内,精度在15%相对误差(RE)之内,并且回收率稳定。该方法已成功用于LG1980和GH501的两项临床前研究中,以确定在静脉注射化合物后24小时内它们在大鼠血浆,肝,肾和骨骼中的浓度。

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