Prince Peter J, Matsuda Katherine C, Retter Mw, Scott G
Pharmacokinetics and Drug Metabolism (PKDM), Amgen Inc., 1201 Amgen Court West, Seattle, Washington, USA.
Bioanalysis. 2010 Aug;2(8):1449-60. doi: 10.4155/bio.10.97.
Quantitating levels of therapeutic proteins in serum or plasma is critical for determining exposure levels and establishing pharmacokinetic parameters. Traditionally, whole blood is not used, mostly due to its inability to be frozen and potential issues with assay interference. To investigate the ability to reproducibly quantitate therapeutic antibodies present in dried blood spots (DBS) compared with a typical serum sample-based method, we used ELISA and electrochemiluminescence immunoassays to measure therapeutic drug levels present in DBS samples.
Measurements of antibody therapeutics in DBS were reproducible, yielding methods that are precise, accurate and met expected sensitivity requirements compared with plasma-based methods.
DBS are a viable alternative to the use of conventional serum or plasma samples for quantitative therapeutic antibody measures.
定量测定血清或血浆中治疗性蛋白质的水平对于确定暴露水平和建立药代动力学参数至关重要。传统上,不使用全血,主要是因为其无法冷冻以及存在检测干扰的潜在问题。为了研究与基于典型血清样本的方法相比,在干血斑(DBS)中可重复定量治疗性抗体的能力,我们使用酶联免疫吸附测定(ELISA)和电化学发光免疫测定法来测量DBS样本中存在的治疗药物水平。
DBS中抗体治疗药物的测量具有可重复性,与基于血浆的方法相比,所产生的方法精确、准确且符合预期的灵敏度要求。
对于定量治疗性抗体测量,DBS是使用传统血清或血浆样本的可行替代方法。