Wu Yuling, Lee Jean W, Uy Lennie, Abosaleem Bassam, Gunn Han, Ma Mark, DeSilva Binodh
Pharmacokinetics and Drug Metabolism, Amgen Inc., Thousand Oaks, CA 91320, USA.
J Pharm Biomed Anal. 2009 Jul 12;49(5):1203-12. doi: 10.1016/j.jpba.2009.03.002. Epub 2009 Mar 20.
A commercial kit assay of tartrate-resistant acid phosphatase (TRACP 5b) used for the diagnosis of bone resorption was modified with a 'Fit-For-Purpose' approach for drug development of anti-resorptive therapeutics. The modifications included changing the standard matrix from buffer to serum, using a consistent bulk reference material to prepare standards and quality controls (QC), and adding sample controls (SC) prepared from authentic sample pools. Method validation experiments were conducted for: inter- and intra-assay accuracy and precision, establishment of SC, range finding of different population groups, selectivity tests, parallelism and stability. The analytical range was 1.00-10.0 U/L and the total errors of lower limit of quantification (LLOQ) and upper limit of quantification (ULOQ) validation samples were 8% and 21%, respectively. Data of range finding experiment showed that serum samples should be collected in tubes instead of bags. Selectivity results showed accurate spike recovery among the majority of test samples from target populations. Samples were demonstrated to be stable for up to four freeze/thaw cycles and for 24 months at -70+/-10 degrees C. Our results show that the modified TRACP 5b method is reliable for the quantification of TRACP 5b in human serum samples to support clinical trials of bone resorptive effect reflected by TRACP 5b activities. The method was robust with similar assay performance characteristics shown in three bioanalytical laboratories.
一种用于骨吸收诊断的酒石酸抗性酸性磷酸酶(TRACP 5b)商业试剂盒检测方法,采用了“适用目的”方法进行抗吸收治疗药物的研发。修改内容包括将标准基质从缓冲液改为血清,使用一致的大量参考物质制备标准品和质量控制品(QC),并添加由真实样本库制备的样本对照(SC)。进行了方法验证实验,包括批间和批内准确性与精密度、SC的建立、不同人群组的范围确定、选择性测试、平行性和稳定性。分析范围为1.00 - 10.0 U/L,定量下限(LLOQ)和定量上限(ULOQ)验证样品的总误差分别为8%和21%。范围确定实验数据表明,血清样本应收集在试管而非采血管中。选择性结果显示,大多数来自目标人群的测试样品中加标回收率准确。样品在高达四个冻融循环以及在-70±10摄氏度下24个月内均表现稳定。我们的结果表明,改良后的TRACP 5b方法对于定量人血清样本中的TRACP 5b是可靠的,可支持通过TRACP 5b活性反映的骨吸收效应的临床试验。该方法具有稳健性,在三个生物分析实验室中表现出相似的检测性能特征。