Study of LAL and Recombinant Cascade Reagents Methods for Bacterial Endotoxin Testing in Pharmaceutical Products.

Q3 Medicine
Dr Prasad Thota, Piyush Kumar, Dr Anil Kumar Teotia, Anshika Kaushik, Roshni Rajpali, Dr Manoj Pandey, Dr Meenakshi Dahiya, Dr V Kalaiselwan
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引用次数: 0

Abstract

The bacterial endotoxin method uses amoebocyte lysate reagents from the horseshoe crab (Limulus polyphemus or Tachypleus tridentatus) to detect and quantify bacterial endotoxin in injectable medications and medical devices. Two types of recombinant reagents have been introduced by various manufacturers, and the equivalency of these results to natural Limulus Amoebocyte Lysate (LAL) reagents has been recently assessed by the United States, European, and Japanese Pharmacopoeia. Recombinant reagents and amoebocyte lysate reagents appear to be highly comparable, according to several investigations.Limulus Amoebocyte Lysate assays are currently the gold standard. LAL is used in vitro for the precise detection of endotoxins and is based on the endotoxin-activated Factor C-mediated clotting cascade. In our quality control laboratory, we tested several categories of drug samples using different compendial methods for detection of bacterial endotoxin method that provides reliable and consistent results. Since 2024, a bacterial endotoxin test based on recombinant cascade reagent (rCR), the endotoxin sensor recombinant factor C, factor B, and pro-clotting enzyme inside of LAL, has been used as an animal-free alternative to LAL. The non-animal derived reagents rCR, which uses cloned genes from the genome of the Limulus polyphemus horseshoe crab to detect and measure bacterial endotoxins.In addition to providing ethical and environmental benefits over traditional LAL assays, rCR eliminates interfering Horseshoe Crab blood components, allowing for extremely specific endotoxin detection. For rCR test performance in routine setting, a comparative study was conducted of compendial bacterial endotoxin testing by LAL with alternates animal-free reagents rCR and summarize the evidence presented by using analysis of different categories of pharmaceutical products. According to the compendial endotoxin testing requirements, all results were acceptable. When the rCR assay was applied rather of the LAL test, no interference was seen in certain samples. In this study, that rCR and LAL are equivalent and comparable.

LAL和重组级联试剂法检测药品细菌内毒素的研究。
细菌内毒素法使用马蹄蟹(鲎)的变形虫细胞裂解试剂检测和定量注射药物和医疗器械中的细菌内毒素。不同的制造商已经推出了两种类型的重组试剂,最近美国、欧洲和日本药典评估了这些结果与天然鲎试剂(LAL)的等效性。根据几项调查,重组试剂和阿米巴细胞裂解试剂似乎具有高度可比性。鲎试剂是目前的金标准。LAL在体外用于内毒素的精确检测,是基于内毒素活化因子c介导的凝血级联。在质控实验室,我们采用不同的药典方法对几类药品样品进行了细菌内毒素检测,结果可靠一致。自2024年以来,基于重组级联试剂(rCR)、内毒素传感器重组因子C、因子B和LAL内部的促凝酶的细菌内毒素检测已被用作LAL的无动物替代方法。非动物源性试剂rCR,利用鲎基因组克隆基因检测细菌内毒素。与传统的LAL测定法相比,rCR除了具有伦理和环境方面的优势外,还消除了马蹄蟹血液成分的干扰,从而实现了极具特异性的内毒素检测。针对常规环境下rCR检测的性能,对LAL法与替代无动物试剂rCR法进行药典细菌内毒素检测的比较研究,并通过对不同类别药品的分析总结证据。根据药典内毒素检查要求,所有结果均可接受。当应用rCR试验而不是LAL试验时,在某些样品中没有看到干扰。在本研究中,rCR和LAL是等价的,具有可比性。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
34
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