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我们是否有令人满意的细胞活力检测方法?对目前市售检测方法的综述。

Do We have a Satisfactory Cell Viability Assay? Review of the Currently Commercially-Available Assays.

机构信息

VP Translational Medicine, Biomarkers & Diagnostics, Celldex Therapeutics, 53 Frontage Road, Suite 220, Hampton, NJ 08827-4032, United States.

出版信息

Curr Drug Discov Technol. 2020;17(1):2-22. doi: 10.2174/1570163815666180925095433.

Abstract

Cell-based assays are an important part of the drug discovery process and clinical research. One of the main hurdles is to design sufficiently robust assays with adequate signal to noise parameters while maintaining the inherent physiology of the cells and not interfering with the pharmacology of target being investigated. A plethora of assays that assess cell viability (or cell heath in general) are commercially available and can be classified under different categories according to their concepts and principle of reactions. The assays are valuable tools, however, suffer from a large number of limitations. Some of these limitations can be procedural or operational, but others can be critical as those related to a poor concept or the lack of proof of concept of an assay, e.g. those relying on differential permeability of dyes in-and-out of viable versus compromised cell membranes. While the assays can differentiate between dead and live cells, most, if not all, of them can just assess the relative performance of cells rather than providing a clear distinction between healthy and dying cells. The possible impact of relatively high molecular weight dyes, used in most of the assay, on cell viability has not been addressed. More innovative assays are needed, and until better alternatives are developed, setup of current cell-based studies and data interpretation should be made with the limitations in mind. Negative and positive control should be considered whenever feasible. Also, researchers should use more than one orthogonal method for better assessment of cell health.

摘要

基于细胞的测定法是药物发现过程和临床研究的重要组成部分。主要障碍之一是设计足够稳健的测定法,具有足够的信号噪声参数,同时保持细胞的固有生理学特性,并且不干扰正在研究的靶标的药理学。有大量评估细胞活力(或一般细胞健康)的测定法可在商业上获得,并且可以根据其概念和反应原理进行不同的分类。这些测定法是有价值的工具,但存在许多局限性。其中一些局限性可能是程序性或操作性的,但其他局限性可能是关键性的,例如那些与测定法的概念较差或缺乏概念验证相关的局限性,例如那些依赖于染料在活细胞和受损细胞膜内外的渗透率差异的测定法。虽然这些测定法可以区分死活细胞,但大多数(如果不是全部)测定法只能评估细胞的相对性能,而不能清楚地区分健康细胞和垂死细胞。在大多数测定法中使用的相对高分子量染料对细胞活力的可能影响尚未得到解决。需要更具创新性的测定法,并且在更好的替代品开发出来之前,应考虑当前基于细胞的研究的设置和数据解释的局限性。只要可行,就应考虑阴性和阳性对照。此外,研究人员应使用多种正交方法来更好地评估细胞健康状况。

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