Kehler Jonathan, Akella Neha, Citerone David, Szapacs Matthew
Platform Technology & Science, Drug Metabolism & Pharmacokinetics, GlaxoSmithKline Pharmaceuticals, 709 Swedeland Road, King of Prussia, PA 19406, USA.
Bioanalysis. 2011 Oct;3(20):2283-90. doi: 10.4155/bio.11.231.
Dried blood spot (DBS) sampling has recently gained popularity in the bioanalysis community for quantitation of small molecules. Since the pharmaceutical industry continues to increase investment in biopharmaceuticals, DBS technologies were investigated to determine if immunoassay and/or LC-MS/MS techniques would be amenable for quantitation of a large protein therapeutic (>70 kDa).
Methods were successfully qualified for the protein therapeutic utilizing DBS technology. DBS methods in rat blood were qualified for this therapeutic protein using either immunoassay or enzymatic digestion directly off the DBS card followed by UHPLC-MS/MS separation and detection. Both qualifications were carried out in accordance with current acceptable practices defined by international acceptance criteria. Card selection was critical to both DBS methods.
The advantages gained by DBS technology can successfully be applied to the quantitative assessment of biologics. This UHPLC-MS/MS method illustrates that digestion of large molecules directly off blood spot cards allows quantitation of these molecules. In addition, DBS technologies are amenable to immunoassay analysis. The immunoassay was 20-fold more sensitive than the UHPLC-MS/MS method, however the UHPLC-MS/MS assay had a much broader dynamic range.
干血斑(DBS)采样最近在生物分析领域受到关注,用于小分子定量分析。由于制药行业对生物制药的投资持续增加,因此对DBS技术进行了研究,以确定免疫分析和/或液相色谱-串联质谱(LC-MS/MS)技术是否适用于定量分析大于70 kDa的大型蛋白质治疗药物。
利用DBS技术成功验证了针对该蛋白质治疗药物的方法。采用免疫分析或直接从DBS卡上进行酶消化,随后进行超高效液相色谱-串联质谱(UHPLC-MS/MS)分离和检测,对大鼠血液中的DBS方法进行了该治疗性蛋白质的验证。两种验证均按照国际认可标准定义的现行可接受方法进行。卡片选择对两种DBS方法都至关重要。
DBS技术的优势能够成功应用于生物制品的定量评估。这种UHPLC-MS/MS方法表明,直接从血斑卡上消化大分子可实现这些分子的定量分析。此外,DBS技术适用于免疫分析。免疫分析的灵敏度比UHPLC-MS/MS方法高20倍,然而UHPLC-MS/MS分析具有更宽的动态范围。