Lens epithelial cell response to atmospheric pressure plasma modified poly(methylmethacrylate) surfaces

被引:20
作者
D'Sa, Raechelle A. [1 ]
Burke, George A. [1 ]
Meenan, Brian J. [1 ]
机构
[1] Univ Ulster, Sch Engn, NIBEC, Newtownabbey BT37 0QB, Antrim, North Ireland
关键词
DIELECTRIC BARRIER DISCHARGE; TYROSINE PHOSPHORYLATION; POLY(ETHYLENE GLYCOL); OPERATING PARAMETERS; POLYMER SURFACE; IN-VITRO; ADHESION; INTEGRIN; OXIDATION; IMMOBILIZATION;
D O I
10.1007/s10856-010-4030-8
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Selective control of cellular response to polymeric biomaterials is an important consideration for many ocular implant applications. In particular, there is often a need to have one surface of an ophthalmic implant capable of promoting cell attachment while the other needs to be resistant to this effect. In this study, an atmospheric pressure dielectric barrier discharge (DBD) has been used to modify the surface region of poly(methyl methacrylate) (PMMA), a well established ocular biomaterial, with the aim of promoting a controlled response to human lens epithelial cells (LEC) cultured thereon. The DBD plasma discharge environment has also been employed to chemically graft a layer of poly(ethylene glycol) methyl ether methacrylate (PEGMA) onto the PMMA and the response to LEC likewise determined. Two different molecular weights of PEGMA, namely 1000 and 2000 MW were used in these experiments. The LEC response to DBD treated polystyrene (PS) samples has also been examined as a positive control and to help to further elucidate the nature of the modified surfaces. The LEC adhered and proliferated readily on the DBD treated PMMA and PS surfaces when compared to the pristine polymer samples which showed little or no cell response. The PMMA and PS surfaces that had been DBD grafted with the PEGMA(1000) layer were found to have some adhered cells. However, on closer inspection, these cells were clearly on the verge of detaching. In the case of the PEGMA(2000) grafted surfaces no cells were observed indicating that the higher molecular weight PEGMA has been able to attain a surface conformation that is capable of resisting cell attachment in vitro.
引用
收藏
页码:1703 / 1712
页数:10
相关论文
共 46 条
  • [1] ANDRADE J D, 1991, Journal of Biomaterials Science Polymer Edition, V2, P161
  • [2] Mechanism for transition from initial to stable cell-cell adhesion: Kinetic analysis of E-cadherin-mediated adhesion using a quantitative adhesion assay
    Angres, B
    Barth, A
    Nelson, WJ
    [J]. JOURNAL OF CELL BIOLOGY, 1996, 134 (02) : 549 - 557
  • [3] The surface oxidation of selected polymers using an atmospheric pressure air dielectric barrier discharge. Part II
    Borcia, G
    Anderson, CA
    Brown, NMD
    [J]. APPLIED SURFACE SCIENCE, 2004, 225 (1-4) : 186 - 197
  • [4] Borcia G, 2004, APPL SURF SCI, V221, P203, DOI 10.1016/S0169-4332(03)00879-1
  • [5] Protein repellant silicone surfaces by covalent immobilization of poly(ethylene oxide)
    Chen, H
    Zhang, Z
    Chen, Y
    Brook, MA
    Sheardown, H
    [J]. BIOMATERIALS, 2005, 26 (15) : 2391 - 2399
  • [6] Plasma-surface modification of biomaterials
    Chu, PK
    Chen, JY
    Wang, LP
    Huang, N
    [J]. MATERIALS SCIENCE & ENGINEERING R-REPORTS, 2002, 36 (5-6) : 143 - 206
  • [7] Surface oxidation of a Melinex 800 PET polymer material modified by an atmospheric dielectric barrier discharge studied using X-ray photoelectron spectroscopy and contact angle measurement
    Cui, Nai-Yi
    Upadhyay, Deepesh J.
    Anderson, Colin A.
    Meenan, Brian J.
    Brown, Norman M. D.
    [J]. APPLIED SURFACE SCIENCE, 2007, 253 (08) : 3865 - 3871
  • [8] Chemical Grafting of Poly(ethylene glycol) Methyl Ether Methacrylate onto Polymer Surfaces by Atmospheric Pressure Plasma Processing
    D'Sa, Raechelle A.
    Meenan, Brian J.
    [J]. LANGMUIR, 2010, 26 (03) : 1894 - 1903
  • [9] Doan Kim T, 2002, Curr Opin Ophthalmol, V13, P24, DOI 10.1097/00055735-200202000-00006
  • [10] Surface treatments of polymers for biocompatibility
    Elbert, DL
    Hubbell, JA
    [J]. ANNUAL REVIEW OF MATERIALS SCIENCE, 1996, 26 : 365 - 394