首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >A phase conversion headspace technique for the determination of anti-anaerobic activity of drug candidate based on the metabolic acidity change in culture medium
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A phase conversion headspace technique for the determination of anti-anaerobic activity of drug candidate based on the metabolic acidity change in culture medium

机译:基于培养基代谢酸度变化的药物候选抗厌氧活性的相位转换网状空间技术

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Screening for anti-anaerobic drug candidates is still challenging although the anaerobic bacteria are important sources for human infections, because the method for anti-anaerobic activity testing is not readily available with low-cost and -expertise. We report a novel method for the determination of the anti-anaerobic activity of drug candidates by automated headspace-gas chromatography (HS-GC). Anaerobic bacteria were inoculated in an anaerobic atmosphere or rapidly using sterile syringe in an air-tight manner, and incubated with and without drugs for 48 h. The metabolic acidities of the cultured media were used as an indicator of cell activities and measured as end-products in place by HS-GC after being completely converted to CO2 with sodium bicarbonate. The present method is precise (relative standard deviation is below 5%) and validated by excellent agreements with a reference method on the determinations of the inhibition rates (root-mean-square error = 10%, n = 48) and half maximal inhibitory concentrations (R-2 = 0.996, n = 8) of both pure drug compounds and plant extracts. Advantageously, the present method is sensitive in response to cell activity, safe with regard to cross contamination, and suitable for routine screening of diversified drug candidates for anti-anaerobic activity. (C) 2020 Elsevier B.V. All rights reserved.
机译:抗厌氧药物候选者的筛查仍然挑战,尽管厌氧细菌是人类感染的重要来源,因为抗厌氧活性测试的方法不容易获得低成本和绝佳的。我们通过自动通顶气相色谱(HS-GC)报告了一种新的方法来测定药物候选物的抗厌氧活性。厌氧细菌在厌氧气氛中接种,或以空气密封的方式使用无菌注射器,并与48小时一起孵育和没有药物。培养介质的代谢酸性用作细胞活性的指示剂,并在用碳酸氢钠完全转化为CO 2后,通过HS-GC作为最终产物测量。本方法精确(相对标准偏差低于5%)并通过优异的符合抑制率的测定(根平均误差= 10%,n = 48)和半最大抑制浓度的参考方法验证(R-2 = 0.996,n = 8)两种纯药物化合物和植物提取物。有利地,本方法响应于细胞活性敏感,在交叉污染方面是安全的,并且适用于常规筛选用于抗厌氧活性的多样化药物候选物。 (c)2020 Elsevier B.v.保留所有权利。

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