Literature DB >> 12720355

Scanning electrochemical microscopy-based drug sensitivity test for a cell culture integrated in silicon microstructures.

Yu-Suke Torisawa1, Takatoshi Kaya, Yuki Takii, Daisuke Oyamatsu, Matsuhiko Nishizawa, Tomokazu Matsue.   

Abstract

The respiratory activity of collagen-embedded living cells was imaged by scanning electrochemical microscopy (SECM) with the objective to study anticancer drug sensitivity. Two kinds of cancer cells, the human erythroleukemia cell line (K562) and its adriamycin-resistant subline (K562/ADM), were immobilized at the array of microholes micromachined on a silicon wafer for comparative characterization of their sensitivity to the anticancer drug, ADM. The results obtained by the SECM method showed correspondence to a conventional colorimetric assay (SDI assay). Furthermore, since the SECM assay is based on the noninvasive measurement of the respiration activity, continuous monitoring of a dose response was possible.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12720355     DOI: 10.1021/ac026317u

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  3 in total

1.  A multiwell electrochemical biosensor for real-time monitoring of the behavioural changes of cells in vitro.

Authors:  Daman J Adlam; David E Woolley
Journal:  Sensors (Basel)       Date:  2010-04-13       Impact factor: 3.576

Review 2.  Modern micro and nanoparticle-based imaging techniques.

Authors:  Marketa Ryvolova; Jana Chomoucka; Jana Drbohlavova; Pavel Kopel; Petr Babula; David Hynek; Vojtech Adam; Tomas Eckschlager; Jaromir Hubalek; Marie Stiborova; Jozef Kaiser; Rene Kizek
Journal:  Sensors (Basel)       Date:  2012-11-02       Impact factor: 3.576

Review 3.  Nanostructured surfaces for analysis of anticancer drug and cell diagnosis based on electrochemical and SERS tools.

Authors:  Waleed A El-Said; Jinho Yoon; Jeong-Woo Choi
Journal:  Nano Converg       Date:  2018-04-24
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.