4.6 Article

Comparison of Cytotoxicity Evaluation of Anticancer Drugs between Real-Time Cell Analysis and CCK-8 Method

Journal

ACS OMEGA
Volume 4, Issue 7, Pages 12036-12042

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.9b01142

Keywords

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Funding

  1. National Natural Science Foundation of China [U1703118]
  2. Natural Science Foundation of Jiangsu Province [BK20181364]
  3. Scientific Research Foundation of Jiangsu Health and Health Committee [H2018087]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  5. Jiangsu Shuangchuang Program, Open project of the National Laboratory of Biomacromolecules [2017kf05]
  6. Southeast university [2018DN0004]
  7. Nanjing Medical University [2018DN0004]
  8. Jiangsu Specially-Appointed Professor project, China

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Critical cytotoxicity evaluation of pharmaceuticals is necessary for the clinical practice of chemotherapy. To quantitatively evaluate cell viability, currently there are two main types of sensitive methods including real-time cell analysis (RTCA) and CCK-8 assay, in which RTCA records electrochemical signal changes around an incubated cell, whereas CCK-8 is based on the colorimetric method. Despite the different detection principles adopted for the cytotoxicity assessment, the comparison of the two methods in terms of the application scope is lacking. In this study, comparison studies were conducted between the RTCA and CCK-8 assays using anticancer drugs including doxorubicin hydrochloride, curcumin, irinotecan (CPT-11), taxol, and oxaliplatin, which are classified into two groups of drug molecules in the absence and presence of additives. The cytotoxicity evaluation of these drugs on cancer cells revealed that the physicochemical properties of drug formulations such as optical and electrochemical properties are closely linked with the readout of cytotoxic methods. The experimental results suggested that the preselection of cytotoxic assay is critical for the quantitative measurement of cytotoxicity of anticancer drugs, which is of clinical importance for their therapeutic usage.

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