Document Detail


Single-cell bioelectrical impedance platform for monitoring cellular response to drug treatment.
MedLine Citation:
PMID:  21301069     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The response of cells to a chemical or biological agent in terms of their impedance changes in real-time is a useful mechanism that can be utilized for a wide variety of biomedical and environmental applications. The use of a single-cell-based analytical platform could be an effective approach to acquiring more sensitive cell impedance measurements, particularly in applications where only diminutive changes in impedance are expected. Here, we report the development of an on-chip cell impedance biosensor with two types of electrodes that host individual cells and cell populations, respectively, to study its efficacy in detecting cellular response. Human glioblastoma (U87MG) cells were patterned on single- and multi-cell electrodes through ligand-mediated natural cell adhesion. We comparatively investigated how these cancer cells on both types of electrodes respond to an ion channel inhibitor, chlorotoxin (CTX), in terms of their shape alternations and impedance changes to exploit the fine detectability of the single-cell-based system. The detecting electrodes hosting single cells exhibited a significant reduction in the real impedance signal, while electrodes hosting confluent monolayer of cells showed little to no impedance change. When single-cell electrodes were treated with CTX of different doses, a dose-dependent impedance change was observed. This enables us to identify the effective dose needed for this particular treatment. Our study demonstrated that this single-cell impedance system may potentially serve as a useful analytical tool for biomedical applications such as environmental toxin detection and drug evaluation.
Authors:
Fareid Asphahani; Kui Wang; Myo Thein; Omid Veiseh; Sandy Yung; Jian Xu; Miqin Zhang
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Publication Detail:
Type:  Evaluation Studies; Journal Article; Research Support, N.I.H., Extramural     Date:  2011-02-07
Journal Detail:
Title:  Physical biology     Volume:  8     ISSN:  1478-3975     ISO Abbreviation:  Phys Biol     Publication Date:  2011 Feb 
Date Detail:
Created Date:  2011-03-03     Completed Date:  2011-06-08     Revised Date:  2013-06-30    
Medline Journal Info:
Nlm Unique ID:  101197454     Medline TA:  Phys Biol     Country:  England    
Other Details:
Languages:  eng     Pagination:  015006     Citation Subset:  IM    
Affiliation:
Department of Materials Science & Engineering, University of Washington, Seattle, WA 98195, USA.
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MeSH Terms
Descriptor/Qualifier:
Antineoplastic Agents / pharmacology
Biosensing Techniques / instrumentation*
Cell Line, Tumor
Cell Survival / drug effects
Drug Screening Assays, Antitumor / instrumentation*
Electric Impedance*
Electrodes
Equipment Design
Glioblastoma / drug therapy
Humans
Scorpion Venoms / pharmacology
Single-Cell Analysis / instrumentation*
Grant Support
ID/Acronym/Agency:
R01 GM075095-05/GM/NIGMS NIH HHS; R01GM075095/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Antineoplastic Agents; 0/Chlorotoxin; 0/Scorpion Venoms
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