一种在体外客观筛选大量抗卡氏肺囊虫化合物的放射学方法。

The Journal of protozoology Pub Date : 1991-11-01
J C Comley, R J Mullin, L A Wolfe, M H Hanlon, R Ferone
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引用次数: 0

摘要

本文报道了一种相对简单的方法,用于准确定量体外培养的卡氏肺囊虫叶酸中[3H]对氨基苯甲酸(pABA)的掺入,并随后开发了一种高灵敏度和可重复性的96孔微滴板药物筛选系统。在优化的条件下,[3H]pABA的掺入被用作卡氏假单胞菌体外活力的选择性指标,并对潜在药物的抑制作用进行了量化。抗肺孢子虫药物喷他脒、磺胺甲恶唑、566C80和吡曲欣的中位抑制浓度分别为7.3、0.1、1.4和约100微米。结果表明,该96孔板卡氏疟原虫[3H] paba结合系统适合作为检测抗肺囊虫活性化合物的快速高通量体外一级筛选系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A radiometric method for objectively screening large numbers of compounds against Pneumocystis carinii in vitro.

A relatively simple method is reported for accurately quantitating the incorporation of [3H]para aminobenzoic acid (pABA) into the folates of Pneumocystis carinii cultured in vitro, and the subsequent development of a highly sensitive and reproducible 96-well microtitre plate drug screening system. Incorporation of [3H]pABA under optimized conditions has been utilized as a selective indicator of the in vitro viability of P. carinii against which the inhibitory effects of potential drugs were quantified. The anti-Pneumocystis agents pentamidine, sulfamethoxazole, 566C80 and piritrexim gave median inhibitory concentration values of 7.3, 0.1, 1.4 and approximately 100 microM, respectively in this assay. The results suggest that this 96-well plate P. carinii [3H]pABA-incorporation system is suitable as a rapid high throughput primary in vitro screen for detecting compounds with anti-Pneumocystis activity.

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