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一种使用高效液相色谱-串联质谱法和铯离子加合物测定免疫抑制药物的新方法。

A new approach for the determination of immunosuppressive drugs using HPLC-MS/MS and Cs+ adducts.

作者信息

Kaiser Patricia, Akerboom Theodorus, Wood William Graham, Reinauer Hans

机构信息

Reference Laboratory, Instand e.V., Düsseldorf, Germany.

出版信息

Ger Med Sci. 2006 Jan 18;4:Doc01.

Abstract

In this study a new principle of measurement in LC-MS/MS (liquid chromatography mass spectrometry) for determination of the immunosuppressive drugs sirolimus, everolimus, tacrolimus, and cyclosporin A has been introduced by using the Cs(+) ion as the product ion in the multiple reaction monitoring mode (MRM). Separation of the immunosuppressive agents was achieved using a phenyl-hexyl-RP column together with a ternary gradient elution profile, consisting of water, methanol and acetonitrile combined with 0.1% v/v formic acid and 0.1 mmol/l Cs+. Quantification was performed using cyclosporin D, ascomycin and 32-desmethoxy-rapamycin as internal standards. The inter-run precision of this new method, expressed as the coefficient of variation, was 2.57% for sirolimus, 2.11% for everolimus, 2.31% for tacrolimus and 2.11% for cyclosporin A.

摘要

在本研究中,引入了一种用于液相色谱 - 串联质谱法(LC-MS/MS)测定免疫抑制药物西罗莫司、依维莫司、他克莫司和环孢素A的新测量原理,即在多反应监测模式(MRM)中使用Cs(+)离子作为产物离子。使用苯基己基反相柱以及由水、甲醇和乙腈组成的三元梯度洗脱曲线,并加入0.1% v/v甲酸和0.1 mmol/l Cs+,实现了免疫抑制剂的分离。使用环孢素D、子囊霉素和32-去甲氧基雷帕霉素作为内标进行定量。该新方法的批间精密度以变异系数表示,西罗莫司为2.57%,依维莫司为2.11%,他克莫司为2.31%,环孢素A为2.11%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9d0/2703222/a696e2daaa22/GMS-04-01-t-001.jpg

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