Surface modification of poly(l -lactic acid) with biomolecules to promote endothelialization
Author(s) -
Yun Xia,
Freddy Boey,
Subbu S. Venkatraman
Publication year - 2010
Publication title -
biointerphases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 45
eISSN - 1934-8630
pISSN - 1559-4106
DOI - 10.1116/1.3467508
Subject(s) - surface modification , biomolecule , contact angle , gelatin , adhesion , chitosan , chemistry , wetting , acrylic acid , cell adhesion , polymer chemistry , swelling , lactic acid , chemical engineering , biophysics , materials science , polymer , biochemistry , organic chemistry , copolymer , composite material , biology , bacteria , engineering , genetics
Rapid endothelialization is important for biodegradable blood-contacting devices not only to prevent thrombosis but also to prevent degradation debris from entering the bloodstream and causing further complications. Here the authors report a three-step surface modification method, by which biomolecules, such as gelatin and chitosan, are covalently immobilized on the surface of plasma-treated poly(L-lactic acid) (PLLA) via -COOH groups introduced by acrylic acid grafting polymerization. Surface characterization techniques, including x-ray photoelectron spectroscopy, contact angle measurement, and colorimetric methods for surface density of functional groups, proved the feasibility and stability of this surface modification method. Surface wettability was increased by biomolecules immobilization. The -COOH surface density was measured to be 4.17±0.15 μmol/cm(2), the and amount of gelatin immobilized was 4.8 μg/cm(2). Human umbilical vein endothelial cell was used during in vitro study at seeding density of 10(4) cells/cm(2). PLLA-gAA-gelatin surface was found to enhance cell adhesion, spreading, focal adhesion formation, and proliferation significantly. Chitosan-modified PLLA shows marginally improvement in cell adhesion and proliferation. Endothelialization was achieved within 7 days on both modified PLLA surfaces. In conclusion, this work demonstrates the feasibility of the surface modification method, and its ability to promote complete endothelialization for cardiovascular applications.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom