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用于检测细胞毒性和预测急性毒性的微电子细胞传感器检测法。

Microelectronic cell sensor assay for detection of cytotoxicity and prediction of acute toxicity.

作者信息

Xing James Z, Zhu Lijun, Gabos Stephan, Xie Li

机构信息

Department of Laboratory Medicine and Pathology, 261 HMRC, University of Alberta, Edmonton, Alta., Canada T6G 2S2.

出版信息

Toxicol In Vitro. 2006 Sep;20(6):995-1004. doi: 10.1016/j.tiv.2005.12.008. Epub 2006 Feb 14.

Abstract

This study reports in-house assessment of a real-time cell electronic sensing (RT-CES) system used as a test platform for both cytotoxicity assay and predicting acute toxicity. For cytotoxicity determination, the RT-CES assay displayed equal sensitivity and coefficients of variation values with good correlation to NRU assay. The IC50 values and the LD50 values for the cytotoxicity reference materials were compared in the context of the proposed prediction model for acute rodent toxicity. The results obtained from RT-CES assay fitted within the acceptance limits of the prediction model and showed that the RT-CES cytotoxicity assay met the qualification guidelines in NIH Publication #01-4500 to accurately predict acute toxicity. In addition to cell viability, the RT-CES assay provided dynamic information that can be used to identify maximum toxicity and reversibility of the toxic effects which are difficult to achieve by the endpoint assays and, therefore, the RT-CES assay is more accurate for assessment of cytotoxicity. The features of the RT-CES assay, such as labeling free, automatic detection, and easy operation, give this assay potential to replace BALB/c 3T3 NRU assay and be used as routine setting for drug monitoring in the toxicological laboratory.

摘要

本研究报告了对一种实时细胞电子传感(RT-CES)系统的内部评估,该系统用作细胞毒性测定和预测急性毒性的测试平台。对于细胞毒性测定,RT-CES测定显示出与中性红摄取(NRU)测定相当的灵敏度和变异系数值,且具有良好的相关性。在拟议的急性啮齿动物毒性预测模型的背景下,比较了细胞毒性参考物质的半数抑制浓度(IC50)值和半数致死剂量(LD50)值。RT-CES测定获得的结果符合预测模型的接受限度,表明RT-CES细胞毒性测定符合美国国立卫生研究院(NIH)第01-4500号出版物中准确预测急性毒性的鉴定指南。除了细胞活力外,RT-CES测定还提供了动态信息,可用于识别最大毒性和毒性作用的可逆性,而这些是终点测定难以实现的,因此,RT-CES测定在评估细胞毒性方面更准确。RT-CES测定的特点,如无需标记、自动检测和操作简便,使其有潜力取代BALB/c 3T3 NRU测定,并用作毒理学实验室药物监测的常规方法。

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