Surface modification and property analysis of biomedical polymers used for tissue engineering

被引:528
作者
Ma, Zuwei
Mao, Zhengwei
Gao, Changyou [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, Hangzhou 310027, Peoples R China
[2] Minist Educ, Key Lab Macromol Synthesis & Funct, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
biomaterials; surface modification; biocompatibility; tissue engineering; cells;
D O I
10.1016/j.colsurfb.2007.06.019
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
The response of host organism in macroscopic, cellular and protein levels to biomaterials is, in most cases, closely associated with the materials' surface properties. In tissue engineering, regenerative medicine and many other biomedical fields, surface engineering of the bio-inert synthetic polymers is often required to introduce bioactive species that can promote cell adhesion, proliferation, viability and enhanced ECM-secretion functions. Up to present, a large number of surface engineering techniques for improving biocompatibility have been well established, the work of which generally contains three main steps: (1) surface modification of the polymeric materials; (2) chemical and physical characterizations; and (3) biocompatibility assessment through cell culture. This review focuses on the principles and practices of surface engineering of biomedical polymers with regards to particular aspects depending on the authors' research background and opinions. The review starts with an introduction of principles in designing polymeric biomaterial surfaces, followed by introduction of surface modification techniques to improve hydrophilicity, to introduce reactive functional groups and to immobilize functional protein molecules. The chemical and physical characterizations of the modified biomaterials are then discussed with emphasis on several important issues such as surface functional group density, functional layer thickness, protein surface density and bioactivity. Three most commonly used surface composition characterization techniques, i.e. ATR-FTIR, XPS, SIMS, are compared in terms of their penetration depth. Ellipsometry, CD, EPR, SPR and QCM's principles and applications in analyzing surface proteins are introduced. Finally discussed are frequently applied methods and their principles to evaluate biocompatibility of biomaterials via cell culture. In this section, current techniques and their developments to measure cell adhesion, proliferation, morphology, viability, migration and gene expression are reviewed. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:137 / 157
页数:21
相关论文
共 185 条
[1]
Bulk and surface modification of silicone rubber for biomedical applications [J].
Abbasi, F ;
Mirzadeh, H ;
Katbab, AA .
POLYMER INTERNATIONAL, 2002, 51 (10) :882-888
[2]
Atomic force microscopy visualization of poly(urethane urea) microphase rearrangements under aqueous environment [J].
Agnihotri, A ;
Garrett, JT ;
Runt, J ;
Siedlecki, CA .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2006, 17 (1-2) :227-238
[3]
MOLECULAR AND CELLULAR PROPERTIES OF PECAM-1 (ENDOCAM/CD31) - A NOVEL VASCULAR CELL CELL-ADHESION MOLECULE [J].
ALBELDA, SM ;
MULLER, WA ;
BUCK, CA ;
NEWMAN, PJ .
JOURNAL OF CELL BIOLOGY, 1991, 114 (05) :1059-1068
[4]
Osteoblast adhesion on biomaterials [J].
Anselme, K .
BIOMATERIALS, 2000, 21 (07) :667-681
[5]
Arwin H, 2001, PHYS STATUS SOLIDI A, V188, P1331, DOI 10.1002/1521-396X(200112)188:4<1331::AID-PSSA1331>3.0.CO
[6]
2-1
[7]
Ellipsometry on thin organic layers of biological interest: characterization and applications [J].
Arwin, H .
THIN SOLID FILMS, 2000, 377 :48-56
[8]
Endothelial cells in culture: A model for studying vascular functions [J].
Bachetti, T ;
Morbidelli, L .
PHARMACOLOGICAL RESEARCH, 2000, 42 (01) :9-19
[9]
Confocal laser scanning microscopy examination of cell distribution in macroporous microcarriers [J].
Bancel, S ;
Hu, WS .
BIOTECHNOLOGY PROGRESS, 1996, 12 (03) :398-402
[10]
Acrylic acid grafting and collagen immobilization on poly(ethylene terephthalate) surfaces for adherence and growth of human bladder smooth muscle cells [J].
Bisson, I ;
Kosinski, M ;
Ruault, S ;
Gupta, B ;
Hilborn, J ;
Wurm, F ;
Frey, P .
BIOMATERIALS, 2002, 23 (15) :3149-3158