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用于代谢活性初步筛选的24孔板分光光度法测定

24-well plate spectrophotometric assay for preliminary screening of metabolic activity.

作者信息

Yang Yuansheng, Balcarcel R Robert

机构信息

Department of Chemical Engineering, Vanderbilt University, Nashville, TN 37235-1604, USA.

出版信息

Assay Drug Dev Technol. 2003 Jun;1(3):461-8. doi: 10.1089/154065803322163777.

Abstract

A 90-min assay using 24-well plates was developed for screening overall metabolic effects of toxic chemicals by measuring extracellular acidification rate of mammalian cells. During the 90-min test, the pH of each well of a 24-well plate is monitored by measuring the absorbance of phenol red using a spectrophotometric plate reader. The acidification rate is then calculated from the change in pH divided by the time interval and cell density, which is also estimated non-invasively by spectroscopy. The assay was verified by testing the effects of five well-characterized chemical toxins on fibroblast cell cultures. As expected, the responses of the fibroblasts were dependent on the dose and type of toxin. They also corresponded with the established mechanisms of the toxins and with measured lactate production rates. The set-up is simple, inexpensive, and amenable to being automated. The method is easy to perform and rapid. Uses include screening compounds for gross metabolic effects in mammalian cell lines, determining preliminary metabolic dose-response curves for guiding further research, and designing and optimizing media for in vitro systems utilizing cell cultures.

摘要

开发了一种使用24孔板的90分钟检测方法,通过测量哺乳动物细胞的细胞外酸化率来筛选有毒化学物质的整体代谢效应。在90分钟的测试过程中,使用分光光度酶标仪测量酚红的吸光度,以此监测24孔板中每个孔的pH值。然后根据pH值的变化除以时间间隔和细胞密度来计算酸化率,细胞密度也通过光谱法进行无创估计。通过测试五种特征明确的化学毒素对成纤维细胞培养物的影响来验证该检测方法。正如预期的那样,成纤维细胞的反应取决于毒素的剂量和类型。它们还与已确定的毒素作用机制以及测得的乳酸产生率相符。该设置简单、成本低且适合自动化。该方法易于操作且快速。其用途包括筛选化合物对哺乳动物细胞系的总体代谢效应、确定初步的代谢剂量反应曲线以指导进一步研究,以及为利用细胞培养的体外系统设计和优化培养基。

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