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Surface modification of poly(ethylene‐co‐vinyl alcohol) (EVA). Part I. Introduction of carboxyl groups and immobilization of collagen

Identifieur interne : 008D85 ( Main/Exploration ); précédent : 008D84; suivant : 008D86

Surface modification of poly(ethylene‐co‐vinyl alcohol) (EVA). Part I. Introduction of carboxyl groups and immobilization of collagen

Auteurs : Kazuaki Matsumura [Japon] ; Suong-Hyu Hyon [Japon] ; Naoki Nakajima [Japon] ; Chunyan Peng [Japon] ; Sadami Tsutsumi [Japon]

Source :

RBID : ISTEX:376B50C7C8A67D35FFAADBCB6D2D393B7A73C62F

Descripteurs français

English descriptors

Abstract

To enhance the surface biocompatibility of poly(ethylene‐co‐vinyl alcohol) (EVA) and high‐density polyethylene (HDPE), carboxyl groups were introduced by ozone exposure. Type I collagen was immobilized onto the surface through polyion complexing. The carboxyl groups on the EVA were characterized by electron spectroscopy for chemical analysis and neutralization. The amounts of the carboxylic group and collagen increased with increases in time and temperature of exposure. Water‐soluble fragments were produced by ozone exposure to EVA, and they acted as collagen crosslinkers. The differences in charge distribution of carboxyl groups affected the amount of collagen immobilization. Graft polymerization of acrylic acid was also carried out onto EVA and HDPE surfaces. The amount of collagen immobilized by graft polymerization was much higher than that by ozone exposure despite the introduction of almost the same amounts of carboxylic groups. It was suggested that the negative charge distribution influences the amount of collagen immobilized onto films. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res, 50, 512–517, 2000.

Url:
DOI: 10.1002/(SICI)1097-4636(20000615)50:4<512::AID-JBM6>3.0.CO;2-G


Affiliations:


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Le document en format XML

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<term>Cell culture</term>
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<div type="abstract" xml:lang="en">To enhance the surface biocompatibility of poly(ethylene‐co‐vinyl alcohol) (EVA) and high‐density polyethylene (HDPE), carboxyl groups were introduced by ozone exposure. Type I collagen was immobilized onto the surface through polyion complexing. The carboxyl groups on the EVA were characterized by electron spectroscopy for chemical analysis and neutralization. The amounts of the carboxylic group and collagen increased with increases in time and temperature of exposure. Water‐soluble fragments were produced by ozone exposure to EVA, and they acted as collagen crosslinkers. The differences in charge distribution of carboxyl groups affected the amount of collagen immobilization. Graft polymerization of acrylic acid was also carried out onto EVA and HDPE surfaces. The amount of collagen immobilized by graft polymerization was much higher than that by ozone exposure despite the introduction of almost the same amounts of carboxylic groups. It was suggested that the negative charge distribution influences the amount of collagen immobilized onto films. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res, 50, 512–517, 2000.</div>
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