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片剂中的巴比妥缓冲液作为补体结合试验(CFT)的溶剂

[Barbital buffer in tablets as a solvent for complement fixation test (CFT)].

作者信息

Królak M, Janicki S, Starostka K, Błaszczyk B

出版信息

Pol Arch Weter. 1982;23(2):111-22.

PMID:7167394
Abstract

The purpose of this paper was to develop a tableting technology of barbital buffer as a standard diluent easy in use for complement fixation test (CFT). As starting point, barbital (veronal) buffer after Alton et al. [1] was assumed. Among 4 solubilizers polyvinyl pyrrolidone (PVP 10 000) was chosen, which provided a good solubility of the barbital in distilled water at 20 degrees C and it affected favourably the complement activity (C'). PVP 10 000 added to the components of barbital buffer at an amount of 0.275 per 10 tablets, in the form of solution for granulation, provided the required physical properties of the tablets. As compared with the barbital buffer after Alton et al. [1], the tablets produced affected favourably C' activity, decreased the range of spontaneous haemocyte lysis, and they did not effect CFT titers of two anti-Brucella abortus standard sera as well as 77 sera of cattle infected with brucellosis under natural conditions. The described physical and biological properties of the barbital buffer tablets with PVP addition indicate their usability as diluent for CFT. A standard diluent used in the form of tablets in all Poland's laboratories should provide a better reproducibility of CFT results in diagnostic examinations towards brucellosis as well as other infectious diseases in men and animals.

摘要

本文的目的是开发一种巴比妥缓冲剂压片技术,该缓冲剂作为标准稀释剂,便于用于补体结合试验(CFT)。作为起点,采用了奥尔顿等人[1]之后的巴比妥(佛罗那)缓冲剂。在4种增溶剂中,选择了聚乙烯吡咯烷酮(PVP 10000),它能使巴比妥在20℃的蒸馏水中具有良好的溶解性,且对补体活性(C')有有利影响。以制粒溶液的形式,按每10片0.275的量将PVP 10000添加到巴比妥缓冲剂的成分中,可使片剂具有所需的物理性质。与奥尔顿等人[1]之后的巴比妥缓冲剂相比,所制得的片剂对C'活性有有利影响,降低了自发血细胞溶解的范围,并且对两种抗流产布鲁氏菌标准血清以及77份自然感染布鲁氏菌病的牛血清的CFT效价没有影响。所描述的添加PVP的巴比妥缓冲剂片剂的物理和生物学性质表明其可作为CFT的稀释剂使用。在波兰所有实验室以片剂形式使用的标准稀释剂应能在对布鲁氏菌病以及人和动物的其他传染病的诊断检查中,使CFT结果具有更好的可重复性。

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