Poly[tri(ethylene glycol) ethyl ether methacrylate]-Coated Surfaces for Controlled Fibroblasts Culturing

被引:49
作者
Dworak, Andrzej [1 ]
Utrata-Wesolek, Alicja [1 ]
Szweda, Dawid [1 ]
Kowalczuk, Agnieszka [1 ]
Trzebicka, Barbara [1 ]
AnioL, Jacek [2 ]
Sieron, Aleksander L. [2 ]
Klama-Baryla, Agnieszka [3 ]
Kawecki, Marek [3 ]
机构
[1] Polish Acad Sci, Ctr Polymer & Carbon Mat, PL-41819 Zabrze, Poland
[2] Med Univ Silesia, Dept Gen Mol Biol & Genet, PL-40752 Katowice, Poland
[3] Ctr Burn Treatment, PL-41100 Siemianowice Slaskie, Poland
关键词
poly[tri(ethylene glycol) monoethyl ether methacrylate; thermosensitive surfaces; surface-initiated atom transfer radical polymerization; fibroblasts culture; surface modification; cell sheet engineering; TRANSFER RADICAL POLYMERIZATION; CONTROLLED CELL-ADHESION; THERMORESPONSIVE POLYMER; INITIATED POLYMERIZATION; BRUSHES; TEMPERATURE; CHAIN; DETACHMENT; SILICON; SILANIZATION;
D O I
10.1021/am3031882
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Well-defined thermosensitive poly[tri(ethylene glycol) monoethyl ether methacrylate] (P(TEGMA-EE)) brushes were synthesized on a solid substrate by the surface-initiated atom transfer radical polymerization of TEGMA-EE. The polymerization reaction was initiated by 2-bromo-2-methylpropionate groups immobilized on the surface of the wafers. The changes in the surface composition, morphology, philicity, and thickness that occurred at each step of wafer functionalization confirmed that all surface modification procedures were successful. Both the successful modification of the surface and bonding of the P(TEGMA-EE) layer were confirmed by X-ray photoelectron spectroscopy (XPS) measurements. The thickness of the obtained P(TEGMA-EE) layers increased with increasing polymerization time. The increase of environmental temperature above the cloud point temperature of P(TEGMA-EE) caused the changes of surface philicity. A simultaneous decrease in the polymer layer thickness confirmed the thermosensitive properties of these P(TEGMA-EE) layers. The thermosensitive polymer surfaces obtained were evaluated for the growth and harvesting of human fibroblasts (basic skin cells). At 37 degrees C, seeded cells adhered to and spread well onto the P(TEGMA-EE)-coated surfaces. A confluent cell sheet was formed within 24 h of cell culture. Lowering the temperature to an optimal value of 17.5 degrees C (below the cloud point temperature of the polymer, T-CP, in cell culture medium) led to the separation of the fibroblast sheet from the polymer layer. These promising results indicate that the surfaces produced may successfully be used as substrate for engineering of skin tissue, especially for delivering cell sheets in the treatment of burns and slow-healing wounds.
引用
收藏
页码:2197 / 2207
页数:11
相关论文
共 59 条
[31]   Point by point comparison of two thermosensitive polymers exhibiting a similar LCST:: Is the age of poly(NIPAM) over? [J].
Lutz, Jean-Francois ;
Akdemir, Oezguer ;
Hoth, Ann .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (40) :13046-13047
[32]   Combining ATRP and "click" chemistry:: a promising platform toward functional biocompatible polymers and polymer bioconjugates [J].
Lutz, Jean-Francois ;
Boerner, Hans G. ;
Weichenhan, Katja .
MACROMOLECULES, 2006, 39 (19) :6376-6383
[33]   Preparation of ideal PEG analogues with a tunable thermosensitivity by controlled radical copolymerization of 2-(2-methoxyethoxy)ethyl methacrylate and oligo(ethylene glycol) methacrylate [J].
Lutz, JF ;
Hoth, A .
MACROMOLECULES, 2006, 39 (02) :893-896
[34]   Protein-resistant polymer coatings on silicon oxide by surface-initiated atom transfer radical polymerization [J].
Ma, HW ;
Li, DJ ;
Sheng, X ;
Zhao, B ;
Chilkoti, A .
LANGMUIR, 2006, 22 (08) :3751-3756
[35]   Preparation of thermoresponsive polymer brush surfaces and their interaction with cells [J].
Mizutani, Aya ;
Kikuchi, Akihiko ;
Yamato, Masayuki ;
Kanazawa, Hideko ;
Okano, Teruo .
BIOMATERIALS, 2008, 29 (13) :2073-2081
[36]   Poly(N-isopropylacrylamide) Thin Films Densely Grafted onto Gold Surface: Preparation, Characterization, and Dynamic AFM Study of Temperature-Induced Chain Conformational Changes [J].
Montagne, Franck ;
Polesel-Maris, Jerome ;
Pugin, Raphael ;
Heinzelmann, Harry .
LANGMUIR, 2009, 25 (02) :983-991
[37]   Permanent, non-leaching antibacterial surfaces - 2: How high density cationic surfaces kill bacterial cells [J].
Murata, Hironobu ;
Koepsel, Richard R. ;
Matyjaszewski, Krzysztof ;
Russell, Alan J. .
BIOMATERIALS, 2007, 28 (32) :4870-4879
[38]   Temperature-responsive intelligent interfaces for biomolecular separation and cell sheet engineering [J].
Nagase, Kenichi ;
Kobayashi, Jun ;
Okano, Teruo .
JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2009, 6 :S293-S309
[39]   Thermo-responsive poly(NiPAAm-co-DEGMA) substrates for gentle harvest of human corneal endothelial cell sheets [J].
Nitschke, Mirko ;
Gramm, Stefan ;
Goetze, Thomas ;
Valtink, Monika ;
Drichel, Juliane ;
Voit, Brigitte ;
Engelmann, Katrin ;
Werner, Carsten .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2007, 80A (04) :1003-1010
[40]   Surface-initiated controlled polymerization as a convenient method for designing functional polymer brushes: From self-assembled monolayers to patterned surfaces [J].
Olivier, Aurore ;
Meyer, Franck ;
Raquez, Jean-Marie ;
Damman, Pascal ;
Dubois, Philippe .
PROGRESS IN POLYMER SCIENCE, 2012, 37 (01) :157-181