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采用 LC-MS/MS 法测定人外周血单个核细胞内的氟达拉滨三磷酸。

Determination of intracellular fludarabine triphosphate in human peripheral blood mononuclear cells by LC-MS/MS.

机构信息

Drug Research Unit, Department of Clinical Pharmacy, University of California at San Francisco, San Francisco, CA 94143, USA.

出版信息

J Pharm Biomed Anal. 2013 Dec;86:198-203. doi: 10.1016/j.jpba.2013.08.007. Epub 2013 Aug 23.

Abstract

Fludarabine is a nucleoside analog routinely used in conditioning regimens of pediatric allogeneic stem cell transplantation to promote stem cell engraftment. In children, it remains a challenge to accurately and precisely quantify the active intracellular triphosphate species of fludarabine in vivo, primarily due to limitations on blood volume and inadequate assay sensitivity. Here we report a liquid chromatography tandem mass spectrometry (LC-MS/MS) method for determination of fludarabine triphosphate in human peripheral blood mononuclear cells (PBMC). PBMC (∼5 million cells) were collected and lysed in 1mL 70% methanol containing 1.2mM tris buffer (pH 7.4). The lysate (80μL) was mixed with internal standard (2-chloro-adenosine triphosphate, 150ng/mL, 20μL) and injected onto an API5000 LC-MS/MS system. Separation was achieved on a hypercarb column (100mm×2.1mm, 3μm) eluted with 100mM ammonium acetate (pH 9.8) and acetonitrile in a gradient mode at a flow rate of 0.4mL/min. Multiple reactions monitoring (MRM) and electrospray ionization in negative mode (ESI(-)) were used for detection. The ion pairs 524.0/158.6 for the drug and 540.0/158.8 for the IS were selected for quantification and 524.0/425.7 used for confirmation. Retention time was 3.0 and 3.4min for fludarabine triphosphate and the IS, respectively. The concentration range for the calibration curve was 1.52-76nM. Our method is simple, fast, and has been successfully applied in a clinical dose-concentration study in children to quantify intracellular fludarabine in low volume clinical samples. The median concentration was 1.03 and 3.19pmole/million PBMC at trough and peak time points, respectively. Fludarabine triphosphate is degraded in water within hours but relatively stable in 70% methanol-tris (1.2mM, pH 7.4). One limitation is that the hypercarb column takes a longer time to equilibrate than conventional reverse phase columns, and peaks become broad and distorted if the column is not washed and stored properly.

摘要

氟达拉滨是一种核苷类似物,常用于儿科异基因干细胞移植的预处理方案中,以促进干细胞植入。在儿童中,准确、精确地量化体内氟达拉滨的活性细胞内三磷酸形式仍然是一个挑战,主要是由于血量有限和检测灵敏度不足。在这里,我们报告了一种用于测定人外周血单个核细胞(PBMC)中氟达拉滨三磷酸的液相色谱串联质谱(LC-MS/MS)方法。收集约 500 万个 PBMC 细胞,在 1ml 含 1.2mM 三羟甲基氨基甲烷缓冲液(pH7.4)的 70%甲醇中裂解。裂解液(80μL)与内标(2-氯-腺苷三磷酸,150ng/mL,20μL)混合,注入到 API5000 LC-MS/MS 系统中。在 Hypercarb 柱(100mm×2.1mm,3μm)上以 100mM 乙酸铵(pH9.8)和乙腈的梯度模式在 0.4mL/min 的流速下进行分离。采用多反应监测(MRM)和电喷雾电离在负离子模式(ESI(-))下进行检测。选择药物的离子对 524.0/158.6 和 IS 的离子对 540.0/158.8 进行定量,524.0/425.7 用于确证。氟达拉滨三磷酸和 IS 的保留时间分别为 3.0 和 3.4min。校准曲线的浓度范围为 1.52-76nM。我们的方法简单、快速,并已成功应用于儿童临床剂量-浓度研究中,以定量低体积临床样本中的细胞内氟达拉滨。在谷值和峰值时间点,中位数浓度分别为 1.03 和 3.19pmole/百万 PBMC。氟达拉滨三磷酸在水中数小时内降解,但在 70%甲醇-三羟甲基氨基甲烷(1.2mM,pH7.4)中相对稳定。一个限制是 Hypercarb 柱的平衡时间比常规反相柱长,如果柱不适当清洗和储存,峰会变宽和变形。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c8f/3835489/b2166dcc81ee/nihms520281f1.jpg

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本文引用的文献

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Physiologically based pharmacokinetic (PBPK) modeling in children.儿童生理药代动力学(PBPK)建模。
Clin Pharmacol Ther. 2012 Jul;92(1):40-9. doi: 10.1038/clpt.2012.64. Epub 2012 Jun 6.
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