首页> 外文期刊>PDA journal of pharmaceutical science and technology >Quality Control Testing for Tracking Endotoxin-Producing Gram-Negative Bacteria during the Preparation of Polyvalent Snake Antivenom Immunoglobulin.
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Quality Control Testing for Tracking Endotoxin-Producing Gram-Negative Bacteria during the Preparation of Polyvalent Snake Antivenom Immunoglobulin.

机译:在制备多价蛇抗毒免疫球蛋白过程中追踪生产内毒素的革兰氏阴性菌的质量控制测试。

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摘要

Antitoxic sera preparations are the only treatment option for snake bites worldwide. They are prepared by immunizing animals, usually horses, with snake venom and collecting horse plasma, which is then subjected to several purification steps in order to finally prepare the purified immunoglobulins. Components of the bacterial cell wall known as endotoxins can constitute a potential hazardous contamination known as pyrogen in antisera, which can lead to fever and many other adverse reactions to the person subjected to it.In this work, we monitored the environment associated with the different steps of production and purification of snake antivenom prepared from immunized horses. We examined the air quality, surface, and personnel for possible sources of contamination, particularly the presence of Gram-negative bacteria, which is the major source of endotoxin presence. We also monitored all stages of preparation by sterility and endotoxin testing. Our results showed that air contributed to the majority of bacterial isolates. Sterility testing revealed the presence of bacterial contamination in all the intermediate steps, as only the final preparation after filtration was sterile. Endotoxin was present in all tested samples and the final product. Good manufacturing practice procedures are essential in any facility involved in antisera production.
机译:抗毒血清制剂是全世界蛇咬伤的唯一治疗选择。通过用蛇毒免疫动物(通常是马)并收集马血浆来制备它们,然后对它们进行几个纯化步骤,以最终制备纯化的免疫球蛋白。细菌细胞壁的内毒素成分可能会构成潜在的有害污染物,称为抗血清中的热原,它可能导致发烧和对其遭受感染的人产生许多其他不良反应。从被免疫的马制备的蛇抗蛇毒的生产和纯化步骤。我们检查了空气质量,表面和人员可能的污染源,特别是革兰氏阴性细菌的存在,而革兰氏阴性细菌是内毒素存在的主要来源。我们还通过无菌和内毒素测试监测了制备的所有阶段。我们的结果表明,空气促成了大多数细菌分离株。无菌测试表明,在所有中间步骤中都存在细菌污染,因为只有过滤后的最终制剂是无菌的。所有测试样品和最终产品中均存在内毒素。良好的生产规范程序对于涉及抗血清生产的任何工厂都是必不可少的。

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