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用于人血浆中利福平定量分析的快速简便的液相色谱-串联质谱法

Fast and Simple LC-MS/MS Method for Rifampicin Quantification in Human Plasma.

作者信息

Temova Rakuša Žane, Roškar Robert, Klančar Andrejc Anita, Trdan Lušin Tina, Faganeli Nataša, Grabnar Iztok, Mrhar Aleš, Kristl Albin, Trontelj Jurij

机构信息

University of Ljubljana, Faculty of Pharmacy, Ljubljana, Slovenia.

Valdoltra Orthopaedic Hospital, Ankaran, Slovenia.

出版信息

Int J Anal Chem. 2019 Feb 3;2019:4848236. doi: 10.1155/2019/4848236. eCollection 2019.

Abstract

A simple, fast, and cost-effective LC-MS/MS method for quantification of rifampicin in human plasma was developed and fully validated. The plasma samples containing rifampicin and isotopically labelled internal standard rifampicin D8, were cleaned up using a Captiva ND Lipids filtration plate. Chromatographic separation was achieved on an 1290 Infinity liquid chromatograph coupled to 6460 Triple Quadrupole operated in positive mode on a core-shell Kinetex C18 column (50 × 2.1 mm, 2.6 m) by gradient elution using 0.1% formic acid in water and acetonitrile as a mobile phase. The proposed method is the fastest method published by now, both in terms of sample preparation (approximately one minute per sample) and chromatographic analysis (total run time 2.4 min). Another key benefit is the outstanding sensitivity and wide analytical range (5-40000 g/L) with good linearity, accuracy, and precision. The method showed almost complete recovery (92%) and absence of any significant matrix effect as demonstrated by uniform responses from QC samples prepared in blood plasma from 6 volunteers (RSD <5%). The proposed method was successfully applied to rifampicin quantification in 340 patients' plasma samples, thus demonstrating its suitability for both therapeutic drug monitoring and pharmacokinetic analysis.

摘要

建立并全面验证了一种简单、快速且经济高效的液相色谱-串联质谱法,用于定量测定人血浆中的利福平。含有利福平和同位素标记内标利福平D8的血浆样品,使用Captiva ND脂质过滤板进行净化处理。在1290 Infinity液相色谱仪与6460三重四极杆联用仪上进行色谱分离,该联用仪在核壳型Kinetex C18柱(50×2.1 mm,2.6μm)上以正模式运行,采用水和乙腈中含0.1%甲酸的流动相进行梯度洗脱。所提出的方法是目前已发表的最快方法,无论是在样品制备方面(每个样品约1分钟)还是色谱分析方面(总运行时间2.4分钟)。另一个关键优势是具有出色的灵敏度和宽分析范围(5 - 40000μg/L),线性、准确度和精密度良好。该方法显示几乎完全回收(92%),并且如6名志愿者血浆中制备的质控样品的一致响应所示(相对标准偏差<5%),不存在任何显著的基质效应。所提出的方法成功应用于340例患者血浆样品中利福平的定量测定,从而证明了其适用于治疗药物监测和药代动力学分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83dc/6377990/8a058e3bd598/IJAC2019-4848236.001.jpg

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