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首页> 外文期刊>Therapeutic Drug Monitoring >Development and validation of a high-throughput assay for quantification of the proliferation inhibitor ABT-578 using LC/LC-MS/MS in blood and tissue samples.
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Development and validation of a high-throughput assay for quantification of the proliferation inhibitor ABT-578 using LC/LC-MS/MS in blood and tissue samples.

机译:开发并验证了使用LC / LC-MS / MS对血液和组织样品中增殖抑制剂ABT-578进行定量的高通量分析方法。

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We report here a specific, automated LC/LC-MS/MS assay for the quantification of ABT-578 in human and rabbit blood and rabbit tissues for drug-eluting stent development. After protein precipitation, samples were injected into the HPLC system and extracted online using a high flow of 5 mL/min. The extracts were then backflushed onto the analytic column. The [M+Na] of ABT-578 (m/z 988.6-->369.4) and its internal standard sirolimus (m/z 936.5-->409.3) were monitored. Extraction and analysis took 4 minutes. The assay was validated following the US Food & Drug Administration guidelines. Linearity was 0.025-25 ng/mL for most matrices. In human blood, interday accuracies were 81.8% (at 0.025 ng/mL), 91.0% (1 ng/mL), and 99.5% (50 ng/mL), and interday precisions were 10.7% (0.025 ng/mL), 3.0% (1 ng/mL), and 1.8% (50 ng/mL).
机译:我们在这里报告了一种特定的,自动化的LC / LC-MS / MS分析方法,用于量化人和兔血液以及兔组织中用于药物洗脱支架开发的ABT-578。蛋白质沉淀后,将样品注入HPLC系统,并以5 mL / min的高流速在线提取。然后将提取物反吹到分析柱上。监测了ABT-578的[M + Na](m / z 988.6-> 369.4)及其内标西罗莫司(m / z 936.5-> 409.3)。提取和分析花费了4分钟。该测定方法已按照美国食品药品监督管理局的指南进行了验证。大多数基质的线性为0.025-25 ng / mL。在人类血液中,日间准确度为81.8%(0.025 ng / mL),91.0%(1 ng / mL)和99.5%(50 ng / mL),日间精密度为10.7%(0.025 ng / mL),3.0 %(1 ng / mL)和1.8%(50 ng / mL)。

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