Oligonucleotide and Parylene Surface Coating of Polystyrene and ePTFE for Improved Endothelial Cell Attachment and Hemocompatibility
Author(s) -
Martina Schleicher,
Jan Hansmann,
Bentsian Elkin,
Petra J. Kluger,
Simone Liebscher,
Agnes J. Huber,
Olaf Fritze,
Christine Schille,
Michaela Müller,
Katja SchenkeLayland,
Martina Seifert,
Heike Walles,
Hans-Peter Wendel,
Ulrich A. Stock
Publication year - 2012
Publication title -
international journal of biomaterials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.576
H-Index - 28
eISSN - 1687-8795
pISSN - 1687-8787
DOI - 10.1155/2012/397813
Subject(s) - oligonucleotide , thrombogenicity , materials science , in vivo , biomedical engineering , endothelial progenitor cell , protein adsorption , coating , chemistry , endothelial stem cell , dna , nanotechnology , in vitro , composite material , polymer , biochemistry , immunology , medicine , biology , platelet , microbiology and biotechnology
In vivo self-endothelialization by endothelial cell adhesion on cardiovascular implants is highly desirable. DNA-oligonucleotides are an intriguing coating material with nonimmunogenic characteristics and the feasibility of easy and rapid chemical fabrication. The objective of this study was the creation of cell adhesive DNA-oligonucleotide coatings on vascular implant surfaces. DNA-oligonucleotides immobilized by adsorption on parylene (poly(monoaminomethyl-para-xylene)) coated polystyrene and ePTFE were resistant to high shear stress (9.5 N/m 2 ) and human blood serum for up to 96 h. Adhesion of murine endothelial progenitor cells, HUVECs and endothelial cells from human adult saphenous veins as well as viability over a period of 14 days of HUVECs on oligonucleotide coated samples under dynamic culture conditions was significantly enhanced ( P < 0.05). Oligonucleotide-coated surfaces revealed low thrombogenicity and excellent hemocompatibility after incubation with human blood. These properties suggest the suitability of immobilization of DNA-oligonucleotides for biofunctionalization of blood vessel substitutes for improved in vivo endothelialization.
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