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Characterization of surface‐modified polyalkanoate films for biomedical applications
Author(s) -
Garrido Leoncio,
Jiménez Ignacio,
Ellis Gary,
Cano Pilar,
GarcíaMartínez Jesús M.,
López Laura,
de la Peña Enrique
Publication year - 2010
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.32920
Subject(s) - contact angle , hacat , argon , materials science , attenuated total reflection , biomaterial , oxygen , absorption (acoustics) , chemical engineering , infrared spectroscopy , surface modification , casting , plasma , spectroscopy , nitrogen , polymer chemistry , analytical chemistry (journal) , chemistry , nanotechnology , composite material , organic chemistry , biochemistry , physics , quantum mechanics , engineering , in vitro
Abstract Poly(3‐hydroxybutyrate‐ co ‐3‐hydroxyvalerate) (PHBHV) films prepared by solvent casting were treated with oxygen, argon, and nitrogen radiofrequency‐generated plasmas. The analysis by attenuated total reflectance infrared spectroscopy and X‐ray absorption near edge spectroscopy of modified surfaces showed an increase of hydroxyl and unsaturated groups, compared with unmodified surfaces. Water contact angles decreased after a short time of exposure (<30 s) for all types of plasma. At long exposure times (>30 s), the water contact angles appeared to be independent of treatment time for nitrogen and argon plasmas, whereas they continuously decreased for films treated with oxygen. HaCaT cultures on nontreated and treated PHBHV films showed that short plasma exposures of 10–20 s improve cell attachment to a greater extent than long exposure times habitually used in polymer surface plasma treatment. The film surface topology did not influence cell attachment. These results illustrate the importance of a detailed characterization of the surface physicochemistry in plasma‐modified substrates designed as part of a strategy to optimize specific cell–biomaterial interactions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011