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高效液相色谱-串联质谱法测定血浆中氯法拉滨与氟达拉滨浓度

英文原题:Quantification of Clofarabine and Fludarabine in Plasma by High-Performance Liquid Chromatography-Tandem Mass Spectrometry.

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Quantification of Clofarabine and Fludarabine in Plasma by High-Performance Liquid Chromatography-Tandem Mass Spectrometry.

PubMed 2024/01/01(内容时间) Methods Mol Biol

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中文摘要

异基因造血细胞移植(allo-HCT)可能治愈许多高危血液系统恶性肿瘤及骨髓衰竭综合征患者。allo-HCT虽可高度有效,但也会出现明显的骨髓预处理方案相关毒性,以及免疫重建不良导致的感染等并发症。本章介绍氯法拉滨和氟达拉滨血浆浓度测定方法,以支持临床试验确定最佳治疗浓度范围,在提高疗效的同时减少变异及预处理方案相关不良事件和毒性。相同考虑也适用于将氟达拉滨作为CAR-T(CAR-T)细胞治疗淋巴清除方案组成部分的患者。治疗结局差异的原因之一可能是淋巴清除期间氟达拉滨血药浓度存在差异。本章介绍一种高效液相色谱-串联质谱(HPLC-MS/MS)方法,可同时测量两种药物。将以甲醇配制的氘代内标加入血浆样本,使用溶剂提取氯法拉滨和氟达拉滨;随后通过反相色谱柱分离,并采用正离子模式进行质谱分析。所述方法快速、准确且灵敏,可用于快速监测血浆药物浓度并及时调整剂量。

展开英文摘要原文

Allogeneic hematopoietic cell transplantation (allo-HCT) is a potentially curative therapeutic treatment for many patients with high-risk hematologic malignancies and bone marrow failure syndromes. While allo-HCT can be highly effective, it is met with significant bone marrow conditioning regimen-related toxicities and complications such as infections related to poor immune reconstitution.

This chapter describes the measurement of clofarabine and fludarabine concentrations to support clinical trials whose goal is to determine the optimal therapeutic ranges in order to maximize effectiveness while minimizing variability and regimen-related adverse events and toxicities.

Moreover, the same holds true for patients receiving fludarabine as part of their lymphodepleting chemotherapy for chimeric antigen receptor T-cells (CAR T-cells). It is believed that one of the causes of variable outcomes after CAR T-cell therapy is lymphodepletion due to the variable fludarabine concentrations.

This chapter describes a HPLC-MS/MS method to measure both compounds simultaneously. Clofarabine and fludarabine are extracted with solvent from plasma by the addition of deuterated internal standards prepared in methanol. Chromatographic separation is attained using a reversed-phase column followed by mass spectrometry which is performed in the positive ion mode.

Herein, the described method to quantify both compounds in plasma is fast, accurate, and sensitive and allows for rapid drug concentration monitoring and timely dose adjustments.

论文信息

作者
Schofield RC、Scordo M、Shah G、Carlow DC
第一作者单位
Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.United States
通讯作者单位
Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA. carlowd@mskcc.org.United States
文献类型
美国 NIH 院内研究
期刊
Methods in molecular biology (Clifton, N.J.)2024
原文标识
PubMed 38036821 · DOI 10.1007/978-1-0716-3541-4_17