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Ink-jet printing of proteins and functional nanoparticles for automated functionalization of surfaces

 
: Knaupp, Markus; Grzesiak, Andrzej; Weber, Achim; Hirth, Thomas; Tovar, Günter E.M.; Borchers, Kirsten

BioStar 2008 - Science in Exchange. Meeting Abstracts : 3rd Congress on Regenerative Biology and Medicine, 3rd Congress of the German Society for Stem Cell Research, October 9-11, 2008, Stuttgart, Germany
New Rochelle/NY: Liebert, 2009 (Tissue engineering. Part A 15.2009, Nr.3)
ISSN: 1937-3341
S.723
Congress on Regenerative Biology and Medicine <3, 2008, Stuttgart>
German Society for Stem Cell Research (Congress) <3, 2008, Stuttgart>
Englisch
Abstract
Fraunhofer IGB ()
Fraunhofer IPA ()
Inkjet; Nanobeschichtung; Protein; Oberflächeneigenschaft; Druckverfahren; Farbstrahldruck; inkjet printing; Protein-Stabilisierung

Abstract
Ink-jet printing is a relatively straightforward fabrication process. The targeted material deposition avoids material spill-over and is therefore very much applicable for processing of high-cost materials such as biological substances. Our objective is to identify biocompatible fluids that meet the needs for a stable piezo ink-jet printing process. We will present results concerning substrateactivation, ink-preparation, and the maintenance of biological functions during the ink-jet process. Recently, ink-jet printing technology has been used to fabricate electronic, medical, optical and polymeric devices [1, 2, 3, 4]. In contrast to classical coating techniques as spin-coating, dip-coating or spray-coating printing allows for patterned material deposition. Many formats of 2-D drawings can be rasterized into X- and Y-coordinates and directly be converted into multi-material patterns via the printing process. The physico-chemical properties of inks determine their jettability: surface tension and viscosity are two primary chemical properties that determine printing success. The optimum viscosities for jettable fluids in piezo drop-on-demand printheads are 5 mPa s to 12 mPa s, surface tension has to be in the range of 24 mN/m to 33 mN/m. However, most biological materials are water-based and exhibit very low viscosities (0.1 mPa s to 1 mPa s) and very high surface tension values (58 mN/m to 60 mN/m). In order to enable economical biofunctional substrate-coating and to integrate substrate-functionalization in a process capable of being fully automated we develop ink formulations containing biomolecules or (bio-)functional components.

: http://publica.fraunhofer.de/dokumente/N-93027.html