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采用稳定同位素标记内标物的液相色谱-串联质谱法微量分析人血浆中的西那卡塞。

Micromethod for quantification of cinacalcet in human plasma by liquid chromatography-tandem mass spectrometry using a stable isotope-labeled internal standard.

机构信息

Clinical Pathology Laboratory Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.

出版信息

Ther Drug Monit. 2013 Feb;35(1):112-7. doi: 10.1097/FTD.0b013e318278dc69.

Abstract

BACKGROUND

Cinacalcet hydrochloride is a calcimimetic agent indicated for the treatment of secondary hyperparathyroidism in dialysis-dependent patients with chronic kidney disease. In the context of a pharmacokinetic (PK)/pharmacodynamic study of cinacalcet in dialysis-dependent chronic kidney disease children with secondary hyperparathyroidism, we describe the development and validation of a new, rapid, simple, and economical liquid chromatography-tandem mass spectrometry (LC-MS/MS) micromethod for quantifying cinacalcet plasma concentrations.

METHODS

Cinacalcet was analyzed in 50-μL plasma samples over a wide range of concentrations (0.1-100 ng/mL) by LC-MS/MS after protein precipitation and addition of deuterated cinacalcet as the internal standard. Cinacalcet was quantified using selective reaction monitoring of the specific transition m/z 358.1 > 155.1, with the 361.1 > 158.1 transition used for the internal standard. The suitability of the assay for clinical PK studies was evaluated using data from a pilot PK study in a pediatric patient.

RESULTS

The overall turnaround time for the assay was 20 minutes. The lower limit of quantification of the method was 0.1 ng/mL. Intraassay imprecision and inaccuracy for quality control samples ranged from 2.8% to 9% and 100% to 102%, respectively. Interassay imprecision and inaccuracy ranged from 6.9% to 8.5% and 99% to 103%, respectively. The overall recovery ranged from 90% to 106%. No ion suppression due to matrix effects was found with different preanalytical conditions, such as hemolysis, lipemia, and hyperuricemia.

CONCLUSIONS

This LC-MS/MS micromethod provides high specificity, precision, and accuracy for rapid quantification of cinacalcet plasma concentrations, and it is suitable for application in pediatric PK studies; it also has potential for use in the establishment of target ranges and ultimately routine therapeutic drug monitoring to optimize cinacalcet dosing.

摘要

背景

盐酸西那卡塞是一种拟钙剂,用于治疗患有慢性肾脏病的透析依赖型患者的继发性甲状旁腺功能亢进症。在一项针对透析依赖型慢性肾脏病继发性甲状旁腺功能亢进症儿童的西那卡塞药代动力学(PK)/药效学研究中,我们描述了一种新的、快速、简单且经济的液相色谱-串联质谱(LC-MS/MS)微方法的开发和验证,用于定量检测西那卡塞的血浆浓度。

方法

通过 LC-MS/MS 分析 50μL 血浆样品中的西那卡塞,范围为 0.1-100ng/mL,采用蛋白沉淀法,加入氘代西那卡塞作为内标。使用特定的过渡 m/z 358.1 > 155.1 的选择性反应监测对西那卡塞进行定量,使用 361.1 > 158.1 过渡对内部标准进行定量。使用儿科患者的 PK 研究初步数据评估该测定方法用于临床 PK 研究的适用性。

结果

该测定方法的总周转时间为 20 分钟。该方法的定量下限为 0.1ng/mL。质控样品的日内精密度和准确度的范围分别为 2.8%-9%和 100%-102%。日间精密度和准确度的范围分别为 6.9%-8.5%和 99%-103%。总体回收率为 90%-106%。在不同的预处理条件下,如溶血、脂血和高尿酸血症,未发现由于基质效应引起的离子抑制。

结论

该 LC-MS/MS 微方法可快速定量检测西那卡塞的血浆浓度,具有高特异性、精密度和准确度,适用于儿科 PK 研究;它也有可能用于建立目标范围,最终常规治疗药物监测以优化西那卡塞的剂量。

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