Fabrication of 3-D gelatin-patterned glass substrates with layer-by-layer and lift-off (LbL-LO) technology

The assembly of multilayer films of gelatin onto glass substrates using layer-by-layer and lift-off (LbL-LO) technology to modify the surface topography and chemistry properties of in vitro cell culture scaffolds is described. The ability to generate such nanoscale systems containing cell-adhesive m...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:IEEE transactions on nanotechnology 2004-03, Vol.3 (1), p.115-123
Hauptverfasser: Mengyan Li, Kondabatni, K.K., Tianhong Cui, McShane, M.J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The assembly of multilayer films of gelatin onto glass substrates using layer-by-layer and lift-off (LbL-LO) technology to modify the surface topography and chemistry properties of in vitro cell culture scaffolds is described. The ability to generate such nanoscale systems containing cell-adhesive materials on optically transparent substrates with microscale lateral dimensions, nanoscale vertical dimensions, molecular vertical precision, and flexibility in material selection has important implications for tissue engineering, drug discovery, and basic research in cell biology. Toward this goal, a systematic study on the electrostatic adsorption properties of fluorescein 5-isothiocyanate-gelatin B (FITC-gelatin) was completed. In addition, the integration of protein nanoassembly with microlithographic feature definition was used to pattern three-dimensional FITC-gelatin nanofilms on planar glass substrates. The experimental results indicate that FITC-gelatin is negatively charged at pH 9 and can be alternately assembled with a positively charged polyion, poly(diallyldimethylammonium chloride) (PDDA), to form multilayer films on solid templates with thickness of 5-10 nm per bilayer. Furthermore, images of protein/polymer nanocomposites indicate that LbL-LO is an efficient way to realize the designed substrates. These findings will benefit future research on cell culture and tissue engineering that require methods of generating protein patterns to fabricate novel in vitro cell culture systems.
ISSN:1536-125X
1941-0085
DOI:10.1109/TNANO.2003.820818