用高效率液态色谱法测定人体血浆中的特氨酸,用质谱检测器测定

Q3 Pharmacology, Toxicology and Pharmaceutics Drug Development and Registration Pub Date : 2021-05-29 DOI:10.33380/2305-2066-2021-10-2-120-127
A. V. Aleshina, T. N. Komarov, O. A. Archakova, D. S. Shchelgacheva, N. S. Bagaeva, V. V. Davydanova, A. Y. Savchenko, I. Shohin
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引用次数: 1

摘要

介绍。氨甲环酸是外科和妇科创伤后止血最常用的药物之一。测定该化合物最常用的分析方法是反相高效液相色谱法。然而,由于其化学结构,这种化合物属于所谓的难保留化合物。有必要开发一种分析方法,以最短的时间和资源成本,不使用专门的色谱柱,测定人血浆中的氨甲环酸。的目标。本研究的目的是建立高效液相色谱-串联质谱法(HPLC-MS/MS)测定人血浆中氨甲环酸的药代动力学研究方法。材料和方法。高效液相色谱-质谱联用法测定血浆中氨甲环酸。样品采用乙腈蛋白沉淀法处理。结果和讨论。通过选择性、矩阵效应、校准曲线、准确度、精密度、回收率、定量下限、结转效应和稳定性等参数对该方法进行验证。结论。建立了HPLC-MS/MS法测定人血浆中氨甲环酸的方法,并进行了验证。血浆样品在100.00 ~ 15000.00 ng/ml浓度范围内呈线性。该方法可用于血浆中氨甲环酸的药代动力学和生物等效性研究。
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Определение транексамовой кислоты в плазме крови человека методом высокоэффективной жидкостной хроматографии с масс-спектрометрическим детектированием
Introduction. Tranexamic acid is one of the most common drugs used to stop bleeding after trauma, in surgery and gynecology. The most common analytical method for the determination of this compound is reversed-phase high-performance liquid chromatography (HPLC). However, this compound belongs to the group of so-called poorly retained compounds due to its chemical structure. It is necessary to develop an analytical method that will allow the determination of tranexamic acid in human blood plasma with the least time, resource costs and without the use of specialized columns. Aim. The aim of this study is to develop a method for tranexamic acid in human plasma by high performance liquid chromatography with tandem mass-spectrometry (HPLC-MS/MS) for pharmacokinetic studies. Materials and methods. Determination of tranexamic acid in plasma by HPLC-MS/MS. The samples were processed by acetonitrile protein precipitation. Results and discussion. This method was validated by next parameters: selectivity, matrix effect, calibration curve, accuracy, precision, recovery, lower limit of quantification, carry-over effect and stability. Conclusion. The method of the determination of tranexamic acid in human plasma was developed and validated by HPLC-MS/MS. The linearity in plasma sample was achieved in the concentration range of 100.00–15000.00 ng/ml. Method could be applied to tranexamic acid determination in plasma for pharmacokinetics and bioequivalence studies.
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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