Industry Healthcare, bioMérieux SA, Craponne, 69290, France.
Industry Healthcare, bioMérieux Germany GmbH, Nürtingen, 72622, Germany.
Biotechniques. 2021 May;70(5):290-300. doi: 10.2144/btn-2020-0165. Epub 2021 May 6.
Testing of parenteral pharmaceuticals and medical devices for pyrogens (fever-inducing substances) is critical to patient safety. The original rabbit pyrogen test has largely been replaced by different bacterial endotoxin tests based on amebocyte lysate (LAL), sourced from the blood equivalent of horseshoe crabs after comparative studies to the rabbit pyrogen test. Since 2004 a bacterial endotoxin test based on recombinant factor C (rFC), the endotoxin sensor protein inside of LAL, has been used as an animal-free alternative to LAL. Likewise, numerous studies compared LAL and rFC. Here we describe the history of pyrogen and bacterial endotoxin testing and summarize the evidence presented by those studies. We demonstrate that rFC and LAL are equivalent and comparable.
用于检测注射用药物和医疗器械中热原(致热物质)的测试对于患者安全至关重要。最初的兔热原试验已在很大程度上被不同的基于鲎试剂(来源于马蹄蟹的血液等价物)的细菌内毒素试验所取代,这些试验是在与兔热原试验进行对比研究后建立的。自 2004 年以来,一种基于重组因子 C(rFC)的细菌内毒素试验已被用作替代鲎试剂的无动物试验方法,rFC 是鲎试剂内部的内毒素传感器蛋白。同样,也有许多研究比较了鲎试剂和 rFC。本文描述了热原和细菌内毒素检测的历史,并总结了这些研究提出的证据。我们证明 rFC 和鲎试剂是等效且可比较的。