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Polymer Pen Lithography with Lipids for Large-Area Gradient Patterns.
Kumar, Ravi; Urtizberea, Ainhoa; Ghosh, Souvik; Bog, Uwe; Rainer, Quinn; Lenhert, Steven; Fuchs, Harald; Hirtz, Michael.
Afiliación
  • Kumar R; Institute of Nanotechnology (INT) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT) , 76131 Karlsruhe, Germany.
  • Urtizberea A; Physical Institute and Center for Nanotechnology (CeNTech), University of Münster , 48149 Münster, Germany.
  • Ghosh S; Institute of Nanotechnology (INT) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT) , 76131 Karlsruhe, Germany.
  • Bog U; Institute of Nanotechnology (INT) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT) , 76131 Karlsruhe, Germany.
  • Rainer Q; Sardar Vallabhbhai National Institute of Technology (SVNIT) , Surat, Gujarat 395007, India.
  • Lenhert S; Institute of Nanotechnology (INT) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT) , 76131 Karlsruhe, Germany.
  • Fuchs H; Florida State Univ , Dept Biol Sci and Integrat NanoSci Inst, Tallahassee, Florida 32306 United States.
  • Hirtz M; Florida State Univ , Dept Biol Sci and Integrat NanoSci Inst, Tallahassee, Florida 32306 United States.
Langmuir ; 33(35): 8739-8748, 2017 09 05.
Article en En | MEDLINE | ID: mdl-28650173
ABSTRACT
Gradient patterns comprising bioactive compounds over comparably (in regard to a cell size) large areas are key for many applications in the biomedical sector, in particular, for cell screening assays, guidance, and migration experiments. Polymer pen lithography (PPL) as an inherent highly parallel and large area technique has a great potential to serve in the fabrication of such patterns. We present strategies for the printing of functional phospholipid patterns via PPL that provide tunable feature size and feature density gradients over surface areas of several square millimeters. By controlling the printing parameters, two transfer modes can be achieved. Each of these modes leads to different feature morphologies. By increasing the force applied to the elastomeric pens, which increases the tip-surface contact area and boosts the ink delivery rate, a switch between a dip-pen nanolithography (DPN) and a microcontact printing (µCP) transfer mode can be induced. A careful inking procedure ensuring a homogeneous and not-too-high ink-load on the PPL stamp ensures a membrane-spreading dominated transfer mode, which, used in combination with smooth and hydrophilic substrates, generates features with constant height, independently of the applied force of the pens. Ultimately, this allows us to obtain a gradient of feature sizes over a mm2 substrate, all having the same height on the order of that of a biological cellular membrane. These strategies allow the construction of membrane structures by direct transfer of the lipid mixture to the substrate, without requiring previous substrate functionalization, in contrast to other molecular inks, where structure is directly determined by the printing process itself. The patterns are demonstrated to be viable for subsequent protein binding, therefore adding to a flexible feature library when gradients of protein presentation are desired.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Polímeros Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Polímeros Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article País de afiliación: Alemania