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采用高效液相色谱-光电二极管阵列检测法同时定量检测达沙替尼、尼洛替尼、博舒替尼和帕纳替尼。

Simultaneous quantification of dasatinib, nilotinib, bosutinib, and ponatinib using high-performance liquid chromatography-Photodiode array detection.

机构信息

Division of Pharmaceutical Care Sciences, Center for Social Pharmacy and Pharmaceutical Care Sciences, Keio University Faculty of Pharmacy, Tokyo, Japan.

Division of Pharmaceutical Care Sciences, Keio University Graduate School of Pharmaceutical Sciences, Tokyo, Japan.

出版信息

J Clin Lab Anal. 2022 Aug;36(8):e24598. doi: 10.1002/jcla.24598. Epub 2022 Jul 12.

Abstract

BACKGROUND

Dasatinib, nilotinib, and bosutinib, second-generation tyrosine kinase inhibitors (TKIs), and ponatinib, a third-generation TKI, are approved pharmaceuticals used in the treatment of chronic myeloid leukemia (CML). Although liquid chromatography-tandem mass spectrometry assays for simultaneous quantification of the four TKIs in human serum have been reported in the literature, a high-performance liquid chromatography (HPLC) assay that simultaneously quantifies these compounds has not yet been developed. This study aims to establish and validate an efficient HPLC analytical method using a photodiode array (PDA) detector for the simultaneous quantification of the four TKIs.

METHODS

Calibration standards were prepared by serial dilution of serum samples containing the four TKIs, followed by solid-phase extraction. The four TKIs were eluted in order within 10 min using a binary HPLC gradient system.

RESULTS

The calibration ranges were 2-500 ng/ml for dasatinib, 100-5000 ng/ml for nilotinib, and 10-500 ng/ml for bosutinib and ponatinib. Intra-day and inter-day precision and accuracy values were found to be in accordance with the U.S. Food and Drug Administration guidelines. The recovery rates were 92.9%-96.0%, 80.7%-86.1%, 91.6%-99.0%, and 86.4%-92.6% for dasatinib, nilotinib, bosutinib, and ponatinib, respectively.

CONCLUSION

To the best of our knowledge, this is the first report of an HPLC-PDA analytical method that allows efficient simultaneous quantification of the four TKIs in the serum of patients with CML. We believe that the method developed herein can improve the efficiency of therapeutic drug monitoring in patients with CML in clinical practice.

摘要

背景

达沙替尼、尼洛替尼和博舒替尼是第二代酪氨酸激酶抑制剂(TKI),而泊那替尼是第三代 TKI,均已被批准用于治疗慢性髓性白血病(CML)。尽管文献中已经报道了用于同时定量检测人血清中四种 TKI 的液相色谱-串联质谱分析方法,但尚未开发出同时定量检测这些化合物的高效液相色谱(HPLC)分析方法。本研究旨在建立和验证一种使用光电二极管阵列(PDA)检测器同时定量检测四种 TKI 的高效 HPLC 分析方法。

方法

通过将含有四种 TKI 的血清样品进行连续稀释并进行固相萃取来制备校准标准品。使用二元 HPLC 梯度系统,四种 TKI 在 10 分钟内按顺序洗脱。

结果

达沙替尼的校准范围为 2-500ng/ml,尼洛替尼为 100-5000ng/ml,博舒替尼和泊那替尼为 10-500ng/ml。日内和日间精密度和准确度值符合美国食品和药物管理局的指南。达沙替尼、尼洛替尼、博舒替尼和泊那替尼的回收率分别为 92.9%-96.0%、80.7%-86.1%、91.6%-99.0%和 86.4%-92.6%。

结论

据我们所知,这是首次报道 HPLC-PDA 分析方法可高效同时定量检测 CML 患者血清中的四种 TKI。我们相信,本文所开发的方法可以提高 CML 患者临床治疗药物监测的效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b8/9396206/7ee7c30d4564/JCLA-36-e24598-g001.jpg

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