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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 >Quantitative determination of zidovudine diaryl phosphate triester pro-drugs in rat plasma by high-performance liquid chromatography-electrospray ionization tandem mass spectrometry.
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Quantitative determination of zidovudine diaryl phosphate triester pro-drugs in rat plasma by high-performance liquid chromatography-electrospray ionization tandem mass spectrometry.

机译:高效液相色谱-电喷雾串联质谱法定量测定齐多夫定磷酸二芳基酯三酯前药在大鼠血浆中的含量。

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摘要

A rapid, simple, and sensitive high-performance liquid chromatography/electrospray ionization tandem mass spectrometry (HPLC/ESI-MS/MS) method was developed and validated for quantitative analysis of 3'-azido-3'-deoxythymidine (zidovudine, AZT) diaryl phosphate triester pro-drugs, in rat plasma using 2',3'-dideoxy-2'3'-didehydrothymidine (d4T) as internal standard (IS). The analytes were extracted from rat plasma with methanol after protein precipitation. The compounds were separated by HPLC with gradient elution (on a Shim-pack VP-ODS C(18) analytical column using a mobile phase of methanol/10mM ammonium acetate). All the analytes were detected in positive ion mode using multiple reaction monitoring (MRM). The method was validated and the specificity, linearity, lower limit of quantitation (LLOQ), precision, accuracy, recoveries and stability were determined. LLOQs were 10ngmL(-1) for M1, M2, M3, M4, and M5, respectively. Correlation coefficient (r) values for the linear range of 10-10,000ngmL(-1) were greater than 0.999 for all the analytes. The intra-day and inter-day precision and accuracy were higher than 7.13%. The relative and absolute recovery was above 72% and no matrix effects were observed for all the analytes. This validated method provides a modern, rapid, and robust procedure for the pharmacokinetic studies of the pro-drugs after intravenous administration to rats. Some important results of AZT diaryl phosphate triester pro-drugs concerning chemical effect on pharmacokinetic performance are also studied.
机译:建立了快速,简单,灵敏的高效液相色谱/电喷雾电离串联质谱(HPLC / ESI-MS / MS)方法,并验证了3'-叠氮基3'-脱氧胸苷(zidovudine,AZT)的定量分析方法磷酸二芳基三酯前药,在大鼠血浆中使用2',3'-二脱氧-2'3'-二氢胸苷(d4T)作为内标(IS)。蛋白质沉淀后,用甲醇从大鼠血浆中提取分析物。通过梯度洗脱(通过Shim-pack VP-ODS C(18)分析柱,使用甲醇/ 10mM乙酸铵的流动相,通过HPLC分离化合物)。使用多反应监测(MRM)以阳离子模式检测所有分析物。验证了该方法的有效性,并确定了特异性,线性,定量下限(LLOQ),精密度,准确性,回收率和稳定性。 M1,M2,M3,M4和M5的LLOQ分别为10ngmL(-1)。对于所有分析物,线性范围为10-10,000ngmL(-1)的相关系数(r)值均大于0.999。日内和日间精度和准确度均高于7.13%。相对和绝对回收率均高于72%,并且所有分析物均未观察到基质效应。这种经过验证的方法为大鼠静脉内给药后的前药的药代动力学研究提供了一种现代,快速且可靠的方法。还研究了AZT磷酸二芳基酯三酯前药在化学动力学上对药代动力学性能的一些重要结果。

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