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用于测试氯喹对疟原虫β-血红素形成抑制活性的实验条件。

Experimental conditions for testing the inhibitory activity of chloroquine on the formation of beta-hematin.

作者信息

Baelmans R, Deharo E, Muñoz V, Sauvain M, Ginsburg H

机构信息

Instituto Boliviano de Biologia de Altura (IBBA), Casilla 717, La Paz, Bolivia.

出版信息

Exp Parasitol. 2000 Dec;96(4):243-8. doi: 10.1006/expr.2000.4558.

Abstract

Some antimalarial drugs act by inhibiting the process of ferriprotoporphyrin IX polymerization which protects the parasite against the noxious effect of this product of host cell hemoglobin digestion. As the quest for new drugs with a similar mode of action continues, high-throughput screening methods are needed. We demonstrate herein that such a recently described screening technique (Basilico et al., J. Antimicrob. Chemother. 42, 55-60, 1998) is considerably disturbed by certain ions. Thus, at the assay's pH 2.6, the phosphate ions are responsible for the inhibitory activity of chloroquine phosphate, rather than chloroquine itself. Using a combination of solubility tests and Fourier transform infrared spectrometry we also show that two alternative methods using higher pH's are also prone to salt effects and demonstrate that these can be minimized by extensive washing of the product with DMSO.

摘要

一些抗疟药物通过抑制铁原卟啉IX聚合过程发挥作用,该过程可保护寄生虫免受宿主细胞血红蛋白消化产物的有害影响。随着对具有类似作用方式的新药的探索仍在继续,需要高通量筛选方法。我们在此证明,这样一种最近描述的筛选技术(巴西利科等人,《抗菌化疗杂志》42,55 - 60,1998)受到某些离子的显著干扰。因此,在测定pH值为2.6时,磷酸根离子是磷酸氯喹抑制活性的原因,而非氯喹本身。通过溶解度测试和傅里叶变换红外光谱法相结合,我们还表明使用较高pH值的两种替代方法也容易受到盐效应的影响,并证明通过用二甲基亚砜对产物进行充分洗涤可将这些影响降至最低。

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