4.7 Article

Cell viability and drug evaluation biosensing system based on disposable AuNPs/MWCNT nanocomposite modified screen-printed electrode for exocytosis dopamine detection

期刊

TALANTA
卷 254, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.talanta.2022.124118

关键词

Cell viability and drug evaluation biosensing; system; Cytotoxicity evaluation; Drug screening; Dopamine; Screen-printed electrode biosensor

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A simple and low-cost cell viability and drug evaluation biosensing system was constructed using multi-walled carbon nanotubes, gold nanoparticles, and Nafion modified screen-printed electrode (SPE) biosensor for the detection of dopamine released from living cells and the evaluation of cytotoxicity of antineoplastic drugs. The biosensing system showed exceptional selectivity, sensitivity, and stability in complex bio-samples. The obtained IC50 curves by the biosensing system and tetrazolium colorimetric assay provided similar IC50 value but distinctly different dose-effect relationship, demonstrating the potential of the biosensor in cell viability and drug efficacy profiling.
Cell viability, as an important index to evaluate drug effects, usually was measured by tetrazolium colorimetric assay, playing a key role in drug development and drug screening. Tedious operating procedures, unsatisfactory sensitivity and abominable environments perplex researchers to acquire more detailed in vivo-relevant biological information. Herein, a simple and low-cost cell viability and drug evaluation biosensing system-based on mul-tiwalled carbon nanotubes, gold nanoparticles and Nafion modified screen-printed electrode (SPE) biosensor was constructed for detection of dopamine (DA) released from living cells to evaluate cytotoxicity of antineoplastic drugs such as cisplatin and resveratrol. The biosensing system was demonstrated to display exceptional selec-tivity, excellent flexibility and good stability toward DA measurement in complex bio-samples. Additionally, the satisfactory recoveries of DA in real samples revealed the reliability and accuracy of the biosensing system in practical application. The IC50 curves respectively obtained by the biosensing system and tetrazolium colori-metric assay provided similar IC50 value but distinctly different dose-effect relationship, which confirmed the enormous potential of the biosensor in cell viability and described drug efficacy profiles in cell function. In short, the cell viability and drug evaluation system using SPE biosensor paves a new way in drug screening and pharmaceutical application to measure bioactive molecule such as DA.

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