Department of Ophthalmology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan.
Department of Legal Medicine, Showa University School of Medicine, Japan.
Rapid Commun Mass Spectrom. 2019 Dec 30;33(24):1906-1914. doi: 10.1002/rcm.8531.
We developed a new high-throughput method to analyze tegafur (FT) and 5-fluorouracil (5-FU) in tear and plasma samples using hydrophilic interaction liquid chromatography (HILIC)/tandem mass spectrometry (MS/MS).
The tear samples (10 μL) spiked with FT, 5-FU, and 5-chlorouracil (internal standard) were diluted using 40 μL of 2 M ammonium acetate and 250 μL of acetonitrile with 2% formic acid; 20 μL of plasma spiked with the two drugs and internal standard was diluted with 80 μL of 2 M ammonium acetate and 500 μL of acetonitrile with 2% formic acid. After centrifugation, the clear supernatant extract (15 μL) was directly injected into the HILIC/MS/MS instrument, and each drug was separated on a Unison UK-Amino column (50 mm × 3 mm i.d., 3 μm particle size) with a linear gradient elution system composed of 10 mM ammonium acetate (pH 6.8) and acetonitrile at a flow rate of 0.7 mL/min. We performed quantification by multiple reaction monitoring (MRM) with negative-ion atmospheric-pressure chemical ionization.
Distinct peaks were observed for the drugs on each MRM channel within 2 min. The regression equations showed good linearity within the range 0.04-4.0 μg/mL for the tear and plasma samples with detection limits at 0.02-0.04 μg/mL. Recoveries for target analytes (FT and 5-FU) for the tear and plasma samples were in the 94-128% and 94-104% ranges, respectively. The intra- and inter-day coefficients of variation for the two drugs were lower than 10.8%. The accuracies of quantitation were 97-115% for both samples.
We established a high-throughput, reproducible, and practical procedure for analyzing FT and 5-FU in human tear and plasma samples using HILIC/MS/MS analysis with an aminopropyl-bonded mixed-mode separation column. This method can be applied to the high-throughput routines used in clinical analyses.
我们开发了一种新的高通量方法,使用亲水相互作用液相色谱(HILIC)/串联质谱(MS/MS)分析泪液和血浆样品中的替加氟(FT)和 5-氟尿嘧啶(5-FU)。
在泪液样品(10μL)中加入 FT、5-FU 和 5-氯尿嘧啶(内标),用 40μL 的 2M 乙酸铵和 250μL 的乙腈(含 2%甲酸)稀释;向 20μL 的血浆中加入两种药物和内标,用 80μL 的 2M 乙酸铵和 500μL 的乙腈(含 2%甲酸)稀释。离心后,直接将澄清的上清液(15μL)注入 HILIC/MS/MS 仪器,用 Unison UK-Amino 柱(50mm×3mm id,3μm 粒径)分离各药物,线性梯度洗脱系统由 10mM 乙酸铵(pH 6.8)和乙腈组成,流速为 0.7mL/min。我们通过负离子大气压化学电离的多反应监测(MRM)进行定量。
在每个 MRM 通道内,药物在 2 分钟内显示出明显的峰。泪液和血浆样品的回归方程在 0.04-4.0μg/mL 范围内具有良好的线性,检测限在 0.02-0.04μg/mL。泪液和血浆样品中目标分析物(FT 和 5-FU)的回收率分别在 94-128%和 94-104%范围内。两种药物的日内和日间变异系数均低于 10.8%。定量的准确度在两种样品中均为 97-115%。
我们使用氨基丙基键合混合模式分离柱的 HILIC/MS/MS 分析,建立了一种高通量、重现性好、实用的分析人泪液和血浆样品中 FT 和 5-FU 的方法。该方法可应用于临床分析中的高通量常规。