Many technological advances are currently being developed for nano- and micro- fabrication, offering the ability to create and control patterns of soft materials with sub micrometric precision. In this work we report the deposition of cells on organic semiconductor ultra-thin films. This is a first step towards the development of active bio/non bio systems for electrical transduction that could be integrated directly in vitro. Thin films of pentacene molecules, whose thickness was systematically varied between 1 and 50 nm, were grown by high vacuum sublimation. Human astrocytoma cells and NE-4C neural stem cells were grown and maintained in culture in standard condition (37oC, 95% humidity, 5%CO2) in medium supplemented. Small molecules (PL, laminine, APTES, dodecylamine, PEG etc.) were patterned onto the surface by template-assisted deposition in order to spatially modulate the cell adhesion on the surface. Released pre-patterned multilayers were exposed to cell culture medium incubated at 37oC for 70h. Viability of cells in time was measured as a function of roughness and the characteristic morphology of ultra thin organic film, as well as the features of the patterned molecules. Optical fluorescence microscope coupled to atomic force microscope was used to monitor the presence, density and shape of deposited cells. Acknowledgements This work is supported by Project EU-NMP-STRP 032652 BIODOT.
Growth of neural cells on ultra thin organic semiconductors
E Bystrenova;C Dionigi;F Biscarini
2007
Abstract
Many technological advances are currently being developed for nano- and micro- fabrication, offering the ability to create and control patterns of soft materials with sub micrometric precision. In this work we report the deposition of cells on organic semiconductor ultra-thin films. This is a first step towards the development of active bio/non bio systems for electrical transduction that could be integrated directly in vitro. Thin films of pentacene molecules, whose thickness was systematically varied between 1 and 50 nm, were grown by high vacuum sublimation. Human astrocytoma cells and NE-4C neural stem cells were grown and maintained in culture in standard condition (37oC, 95% humidity, 5%CO2) in medium supplemented. Small molecules (PL, laminine, APTES, dodecylamine, PEG etc.) were patterned onto the surface by template-assisted deposition in order to spatially modulate the cell adhesion on the surface. Released pre-patterned multilayers were exposed to cell culture medium incubated at 37oC for 70h. Viability of cells in time was measured as a function of roughness and the characteristic morphology of ultra thin organic film, as well as the features of the patterned molecules. Optical fluorescence microscope coupled to atomic force microscope was used to monitor the presence, density and shape of deposited cells. Acknowledgements This work is supported by Project EU-NMP-STRP 032652 BIODOT.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.