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Determination of arbidol in human plasma by LC-ESI-MS

机译:LC-ESI-MS测定人血浆中的阿比多尔

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摘要

A sensitive, specific and accurate method for determination of arbidol in human plasma was developed. Arbidol and internal standard were extracted from plasma samples by liquid-liquid extraction with diethyl ether. The chromatographic separation was accomplished on a Shiseido C_(18) 3mum analytical column (100 mm x 2.0 mm i.d.) at a flow rate of 0.3 mL/rnin isocratically. Detection was performed on a single quadrupole mass spectrometer by selected ion monitoring (SIM) mode via electrospray ionization (ESI) source. The method had a chromatographic run time of 6 min and a good linear relationship over the range 1-1000 ng/mL. The limit of quantitation for arbidol in plasma was 1 ng/mL. The intra-day and inter-day precision (R.S.D.%) was lower than 7% and accuracy ranged from 95 to 105%. The proposed method enables unambiguous identification and quantification of arbidol in vivo and has been successfully applied to study the pharmacokinetics of arbidol in healthy male Chinese volunteers.
机译:建立了一种灵敏,特异性和准确的测定人血浆中阿比多尔的方法。通过用乙醚进行液-液萃取从血浆样品中萃取出阿比多尔和内标物。色谱分离是在Shiseido C_(18)3毫米分析柱(100 mm x 2.0 mm i.d.)上进行的,等度流速为0.3 mL / mL。通过电喷雾电离(ESI)源,通过选定的离子监测(SIM)模式在单个四极质谱仪上进行检测。该方法的色谱运行时间为6分钟,并且在1-1000 ng / mL范围内具有良好的线性关系。血浆中阿比多尔的定量限为1 ng / mL。日内和日间精度(R.S.D.%)低于7%,精度范围为95%至105%。所提出的方法能够在体内明确鉴定和定量阿比多尔,并已成功地用于研究阿比多尔在健康的中国男性志愿者中的药代动力学。

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