Dong Xiaona, Meng Zhiyun, Jin Jide, Gu Ruolan, Dou Guifang
State Key Laboratory of Drug Metabolism and Pharmacokinetics, Laboratory of Hematological Pharmacology, Beijing Institute of Transfusion Medicine, 27, Taiping Road, Haidian District, Beijing 100850, PR China.
Laboratory of Experimental Hematology, Beijing Institute of Radiation Medicine, 27, Taiping Road, Beijing 100850, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Sep 15;1063:204-213. doi: 10.1016/j.jchromb.2017.08.030. Epub 2017 Aug 24.
Recombinant Neorudin (EPR-hirudin, EH), a novel, low-bleeding anticoagulant fusion protein, has been developed as an inactive prodrug that is converted to an active metabolite, hirudin variant 2-Lys47 (HV2), at the thrombus site and is undergoing Phase I clinical trials in China. The goal of our present research was to establish a novel ultra-performance liquid chromatography/tandem mass spectrometry (UPLC-MS/MS) method for simultaneously quantifying EH and HV2 in human serum. Furthermore, the method was used in clinical pharmacokinetic study after validation. The stock and dilute working solutions were dissolved in methanol/water (1/1, v/v) to avoid their adsorption. The internal standard (IS) used, had a similar structure to that of EH. The serum sample pretreatment involved protein precipitation with methanol. The volume ratio of the precipitating solvent to the serum sample was 3:1 (300μL methanol: 100μL serum sample). The chromatographic separation was performed using a 300Å C18 column using a multi-step gradient with a mobile phase consisting of acetonitrile:water containing 0.1% formic acid. The detection was carried out using an ESI source in the positive multiple reaction monitoring (MRM) mode. The within and between run precision were in the range of 3.5%-10.3% for EH and 3.3%-8.8% for HV2, and the accuracy of both EH and HV2 was between -4.6% and 2.1%. The extraction recoveries and matrix effect at three quality control (QC) levels for EH and HV2 were satisfactory. The stabilities of EH and HV2 during the storage, preparation, and analysis were confirmed, and the carryover also proved to be acceptable. This technique was efficiently used in Phase I clinical pharmacokinetic trials of EH following intravenous administration of 0.2mg/kg to healthy volunteers.
重组水蛭素(EPR-水蛭素,EH)是一种新型、低出血风险的抗凝融合蛋白,它被开发为一种无活性的前药,在血栓部位转化为活性代谢产物水蛭素变体2-Lys47(HV2),目前正在中国进行I期临床试验。我们当前研究的目标是建立一种新型超高效液相色谱/串联质谱(UPLC-MS/MS)方法,用于同时定量人血清中的EH和HV2。此外,该方法经验证后用于临床药代动力学研究。储备液和稀释工作液溶解于甲醇/水(1/1,v/v)中以避免吸附。所使用的内标(IS)与EH结构相似。血清样品预处理采用甲醇沉淀蛋白。沉淀溶剂与血清样品的体积比为3:1(300μL甲醇:100μL血清样品)。色谱分离使用300Å C18柱,采用多步梯度洗脱,流动相为含0.1%甲酸的乙腈:水。检测采用电喷雾离子源正离子多反应监测(MRM)模式。EH的批内和批间精密度在3.5%-10.3%范围内,HV2在3.3%-8.8%范围内,EH和HV2的准确度均在-4.6%至2.1%之间。EH和HV2在三个质量控制(QC)水平下的提取回收率和基质效应均令人满意。确认了EH和HV2在储存、制备和分析过程中的稳定性,且残留也被证明是可接受的。该技术有效地应用于对健康志愿者静脉注射0.2mg/kg EH后的I期临床药代动力学试验。