Cell Resistant Peptidomimetic Poly (2-ethyl-2-oxazoline) Coatings Developed by Low Pressure Inductively Excited Pulsed Plasma Polymerization for Biomedical Purpose

被引:21
作者
Bhatt, Sudhir [1 ,2 ]
Pulpytel, Jerome [1 ,2 ]
Mirshahi, Massoud [3 ]
Arefi-Khonsari, Farzaneh [1 ,2 ]
机构
[1] Sorbonne Univ, Univ Paris 06, UMR8235, LISE, Paris, France
[2] CNRS, UMR8235, LISE, Paris, France
[3] Fac Med Paris VI, Ctr Rech Cordeliers, UMRS 872, Paris, France
关键词
alternative of PEG; biomedical applications; cell resistance coatings; nano thick peptidomimetic coatings; plasma polymerization; poly (2-ethyl-2oxazoline); THIN-FILMS; ADSORPTION; PROTEINS; COPOLYMERIZATION; ADHESION; GLYCOL);
D O I
10.1002/ppap.201400169
中图分类号
O59 [应用物理学];
学科分类号
摘要
In the present work, for the first time, nano-thick peptidomimetic coatings were developed using a LP inductively excited pulsed plasma polymerization of 2-ethyl-2-oxazoline (ppEtOz) to control the cell-surface interactions for biological applications. The different ppEtOz coated surfaces were investigated by FTIR-ATR, XPS, Ellipsometric, and WCA analysis. Using Gaussian deconvolution method for IR spectra, we compared the modifications obtained in the chemical compositions for ppEtOz coated samples obtained under different plasma parameters. It was found that the amide I/amide II ratios decreased as the effective plasma power increased, which in turn decreased the surface hydrophilicity for ppEtOz coatings. Cell repellent properties of the ppEtOz coatings deposited at P-eff=1W and 2.5W were achieved.
引用
收藏
页码:519 / 532
页数:14
相关论文
共 39 条
[1]   Poly(2-oxazolines) in biological and biomedical application contexts [J].
Adams, Nico ;
Schubert, Ulrich S. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (15) :1504-1520
[2]  
Anderson J.M., 2000, Infections Associated with Indwelling Medical Devices, V3rd, P89, DOI DOI 10.1128/9781555818067.CH5
[3]  
Andrea R. S., 2005, J AM CHEM SOC, V127, P7972
[4]  
Arslanoglu J., 2003, WAAC Newsletter, V25, P12
[5]   Infrared spectroscopy of proteins [J].
Barth, Andreas .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2007, 1767 (09) :1073-1101
[6]   Chemisorbed poly(propylene sulphide)-based copolymers resist biomolecular interactions [J].
Bearinger, JP ;
Terrettaz, S ;
Michel, R ;
Tirelli, N ;
Vogel, H ;
Textor, M ;
Hubbell, JA .
NATURE MATERIALS, 2003, 2 (04) :259-264
[7]   Nano thick poly(ε-caprolactone)-poly(ethylene glycol) coatings developed by catalyst-free plasma assisted copolymerization process for biomedical applications [J].
Bhatt, Sudhir ;
Pulpytel, Jerome ;
Mirshahi, Massoud ;
Arefi-Khonsari, Farzaneh .
RSC ADVANCES, 2012, 2 (24) :9114-9123
[8]   Catalyst-Free Plasma-Assisted Copolymerization of Poly(ε-caprolactone)-poly(ethylene glycol) for Biomedical Applications [J].
Bhatt, Sudhir ;
Pulpytel, Jerome ;
Mirshahi, Massoud ;
Arefi-Khonsari, Farzaneh .
ACS MACRO LETTERS, 2012, 1 (06) :764-767
[9]   Nanostructure Protein Repellant Amphiphilic Copolymer Coatings with Optimized Surface Energy by Inductively Excited Low Pressure Plasma [J].
Bhatt, Sudhir ;
Pulpytel, Jerome ;
Ceccone, Giacomo ;
Lisboa, Patricia ;
Rossi, Francois ;
Kumar, Virendra ;
Arefi-Khonsari, Farzaneh .
LANGMUIR, 2011, 27 (23) :14570-14580
[10]   Effect of bioactive glass crystallization on the conformation and bioactivity of adsorbed proteins [J].
Buchanan, Laura A. ;
EI-Ghannam, Ahmed .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2010, 93A (02) :537-546