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人血浆中西那卡塞一步沉淀法LC-MS/MS测定方法的建立与验证

Development and validation of an LC-MS/MS method by one-step precipitation for cinacalcet in human plasma.

作者信息

Lu Haoyang, Guo Tingting, Huang Shanqing, Li Yuandan, Wen Yuguan, Shang Dewei, Wen Xin

机构信息

Department of Pharmacy, The Affiliated Brain Hospital of Guangzhou Medical University, No.36, Mingxin Road, Guangzhou 510370, China.

Department of Nephrology, Zhujiang Hospital, Southern Medical University, No. 253, Industrial Avenue, Guangzhou 501280, China.

出版信息

Heliyon. 2023 Jun 12;9(6):e17230. doi: 10.1016/j.heliyon.2023.e17230. eCollection 2023 Jun.

Abstract

A sensitive, convenient, rapid and economic liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed to determine cinacalcet concentration in human plasma. A stable isotope cinacalcet (cinacalcet-D) was selected as internal standard and the analytes were extracted from plasma samples by a one-step precipitation procedure. Chromatography separation was conducted on an Eclipse Plus C18 column by gradient elution with mobile phase of methanol-water-ammonium formate system at a constant flow rate of 0.6 mL/min. Mass spectrometric detection was conducted by multiple reaction monitoring using positive electrospray ionization. Cinacalcet concentrations in human plasma were determined over the concentration range of 0.1-50 ng/mL. The accuracies of lower limit of quantification (LLOQ) and quality control samples were all within the range of 85-115%, and the inter- and intra-batch precisions (%) were all within 15%. The average extraction recovery rates were 95.67-102.88%, and the quantification was not interfered by the matrix components. The validated method was successfully applied to determined cinacalcet concentrations in human plasma from secondary hyperparathyroidism patients.

摘要

建立了一种灵敏、便捷、快速且经济的液相色谱-串联质谱(LC-MS/MS)法,用于测定人血浆中西那卡塞的浓度。选择稳定同位素西那卡塞(西那卡塞-D)作为内标,采用一步沉淀法从血浆样品中提取分析物。在Eclipse Plus C18柱上进行色谱分离,以甲醇-水-甲酸铵体系为流动相进行梯度洗脱,流速恒定为0.6 mL/min。采用正电喷雾电离,通过多反应监测进行质谱检测。测定人血浆中西那卡塞浓度的范围为0.1 - 50 ng/mL。定量下限(LLOQ)和质量控制样品的准确度均在85 - 115%范围内,批间和批内精密度(%)均在15%以内。平均提取回收率为95.67 - 102.88%,定量不受基质成分干扰。该验证方法成功应用于测定继发性甲状旁腺功能亢进患者人血浆中西那卡塞的浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea3/10285229/cb6b268da8c4/gr1.jpg

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