Bioanalytical Development, Alexion Pharmaceuticals Inc., 100 College Ave, New Haven, Connecticut, USA.
AAPS J. 2018 Oct 2;20(6):106. doi: 10.1208/s12248-018-0266-x.
Complement protein C5a is recognized as an important component of the alternative complement pathway. Its role is prominent enough to garner interest not only as a biomarker, but also as a potential therapeutic target. Bioanalytical challenges have been posed in proper quantitation of free C5a due to interference from its precursor, C5. Additionally, free therapeutic target quantitation can be difficult due to effects of sample dilution and prolonged sample incubation when therapeutic is used as capture reagent. Gyrolab technology enables quantitation of free target analyte with minimal sample dilution and rapid sample incubations, thus enabling in vitro results that are more representative of in vivo pharmacodynamics. When coupled with strategic sample pretreatment, Gyrolab offers an opportunity to quantitate free C5a in human plasma with an assay that vastly diminishes C5 interference. A Gyrolab assay for the quantitation of free C5a in human plasma was developed and validated. Validation results confirmed that proper sample pretreatment and use of the Gyrolab platform yield accurate and reliable results. Due to the advantages that it provides, Gyrolab has become our default technology of choice for quantitation of free target.
补体蛋白 C5a 被认为是替代补体途径的重要组成部分。它的作用非常突出,不仅引起了人们对其作为生物标志物的兴趣,也引起了人们对其作为潜在治疗靶点的兴趣。由于其前体 C5 的干扰,正确定量游离 C5a 带来了生物分析方面的挑战。此外,由于治疗剂用作捕获试剂时样品稀释和长时间孵育的影响,游离治疗目标的定量也可能很困难。Gyrolab 技术可实现最小化样品稀释和快速样品孵育条件下的游离靶标分析物定量,从而使体外结果更能代表体内药效动力学。当与策略性样品预处理相结合时,Gyrolab 提供了一种机会,可以用一种大大减少 C5 干扰的测定法来定量人血浆中的游离 C5a。开发并验证了用于定量人血浆中游离 C5a 的 Gyrolab 测定法。验证结果证实,适当的样品预处理和 Gyrolab 平台的使用可产生准确可靠的结果。由于它提供的优势,Gyrolab 已成为我们用于定量游离靶标的首选技术。