首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of bifendate in human plasma by HPLC-MS and bioequivalence on bifendate pills in healthy volunteers.
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Determination of bifendate in human plasma by HPLC-MS and bioequivalence on bifendate pills in healthy volunteers.

机译:通过HPLC-MS测定人体血浆中的联苯菊酯,并在健康志愿者中测定联苯菊酯药丸的生物等效性。

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摘要

A sensitive and specific method for the determination of bifendate in human plasma was developed, based on high-performance liquid chromatography (HPLC)-mass spectrometry (MS). The samples were extracted from plasma with diethyl ether, followed by separation and evaporation after addition of internal standard diazepam. The residue was reconstituted in methanol and injected into the HPLC-MS. Chromatography was performed on an Inertsil ODS column with a mobile phase consisting of methanol-distilled water (70/30, v/v) at a flow rate of 0.3 mL/min. Quantitative analysis was achieved by MS detection, using a mass spectrometer equipped with an electrospray ionization interface (ESI) and operated in selected ion monitoring (SIM) and positive-ionization mode using target ions at m/z 419 for bifendate and m/z 285 for internal standard, respectively. The linearity was confirmed in the concentration range of 2-200 ng/mL in human plasma and the precision of this assay was not more than 6.79% over the entire concentration range. The method was sensitive and repeatable enough to be used in pharmacokinetic and bioavailability studies.
机译:基于高效液相色谱(HPLC)-质谱(MS),开发了一种灵敏而特异性的测定人血浆中联苯双酯的方法。用乙醚从血浆中提取样品,然后在添加内标地西epa之后分离和蒸发。将残余物在甲醇中重构,并注入HPLC-MS中。在Inertsil ODS色谱柱上进行色谱分离,流动相由甲醇蒸馏水(70/30,v / v)组成,流速为0.3 mL / min。使用配备电喷雾电离接口(ESI)并在选定离子监测(SIM)和正电离模式下运行的质谱仪通过质谱检测实现定量分析,使用目标离子在m / z 419处有联苯二酸盐和m / z 285分别用于内部标准。在人血浆中2-200 ng / mL的浓度范围内证实了线性,并且该测定的精度在整个浓度范围内不超过6.79%。该方法灵敏且可重复,足以用于药代动力学和生物利用度研究。

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