Microcontact printing has emerged as one of the most straightforward methods of surface patterning and has been successfully employed to obtain biologically instructive substrates for a wide range of tissue engineering applications. However, although a consolidated success has been gained in the patterning of smooth surfaces, limited popularity has been achieved in the modification of soft and/or textured substrates.Thus, aim of this study is to transfer protein patterns onto 3D electrospun matrices by a custom-designed microcontact printing setup. The proposed approach has been successfully pursued for precise and gentle transfer of poly-l-lysine patterns from polydimethylsiloxane stamps onto sub-micron-sized poly(?-caprolactone) electrospun fibers without loss of biological activity. In vitro performance of the patterned substrates has been preliminary evaluated in combination with human mesenchymal stem cells. Copyright ? 2014 Curtin University of Technology and John Wiley & Sons, Ltd.
Surface decoration of electrospun scaffolds by microcontact printing
Mozetic P;De Ninno A;Businaro L;Gerardino A;
2014
Abstract
Microcontact printing has emerged as one of the most straightforward methods of surface patterning and has been successfully employed to obtain biologically instructive substrates for a wide range of tissue engineering applications. However, although a consolidated success has been gained in the patterning of smooth surfaces, limited popularity has been achieved in the modification of soft and/or textured substrates.Thus, aim of this study is to transfer protein patterns onto 3D electrospun matrices by a custom-designed microcontact printing setup. The proposed approach has been successfully pursued for precise and gentle transfer of poly-l-lysine patterns from polydimethylsiloxane stamps onto sub-micron-sized poly(?-caprolactone) electrospun fibers without loss of biological activity. In vitro performance of the patterned substrates has been preliminary evaluated in combination with human mesenchymal stem cells. Copyright ? 2014 Curtin University of Technology and John Wiley & Sons, Ltd.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


