TY - JOUR
T1 - Spatiotemporal sub-cellular biopatterning using an AFM-assisted electrochemical system
AU - Sekine, Soichiro
AU - Kaji, Hirokazu
AU - Nishizawa, Matsuhiko
N1 - Funding Information:
This study was partially supported by Grants-in-Aid for Scientific Research B (No. 20310070) and for Young Scientists (B) (No. 20710094) from the Ministry of Education, Science, and Culture, Japan.
PY - 2009/9
Y1 - 2009/9
N2 - The integration of electrochemical-based biolithography (ECBL) with an ordinary atomic force microscope (AFM) enables in situ lithography adjacent to a single, cultured cell, consequently allowing the morphological shape of the cell to be manipulated. The tip of a commercially available AFM cantilever was modified to serve as an electrode that could generate the oxidant HBrO for local, controlled etching of a cytophobic material (heparin or albumin) previously layered adjacent to a living cell. A NIH-3T3 fibroblast, initially confined to a patterned area, extended along a bioadhesive surface that had been newly exposed using the ECBL-AFM system.
AB - The integration of electrochemical-based biolithography (ECBL) with an ordinary atomic force microscope (AFM) enables in situ lithography adjacent to a single, cultured cell, consequently allowing the morphological shape of the cell to be manipulated. The tip of a commercially available AFM cantilever was modified to serve as an electrode that could generate the oxidant HBrO for local, controlled etching of a cytophobic material (heparin or albumin) previously layered adjacent to a living cell. A NIH-3T3 fibroblast, initially confined to a patterned area, extended along a bioadhesive surface that had been newly exposed using the ECBL-AFM system.
KW - AFM
KW - Lithography
KW - Single cell
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U2 - 10.1016/j.elecom.2009.07.016
DO - 10.1016/j.elecom.2009.07.016
M3 - Article
AN - SCOPUS:69549116470
SN - 1388-2481
VL - 11
SP - 1781
EP - 1784
JO - Electrochemistry Communications
JF - Electrochemistry Communications
IS - 9
ER -