Interfacial properties and protein resistance of nano-scale polysaccharide coatings

被引:31
作者
Griesser, HJ [1 ]
Hartley, PG [1 ]
McArthur, SL [1 ]
McLean, KM [1 ]
Meagher, L [1 ]
Thissen, H [1 ]
机构
[1] CSIRO Mol Sci, Clayton, Vic 3169, Australia
关键词
D O I
10.1088/0964-1726/11/5/305
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
For many applications, it is essential to be able to control the interface between devices and the biological environment by nanoscale control of the composition of the surface chemistry and the surface topography. Application of molecular thickness coatings of biologically active macromolecules provides predictable interfacial control over interactions with biological media. The covalent surface immobilization of polysaccharides, proteins and synthetic oligopeptides can be achieved via nanometres thick, interfacial bonding layers deposited by gas plasma methods, and the multi-step coating schemes are verified by XPS analyses. Interactions between biomolecular coatings and biological fluids are studied by MALDI mass spectrometry and ELISA assays. Using a colloid-modified AFM tip, quantitative measurement of interfacial forces is achieved. Comparison with theoretical predictions allows elucidation of the key interfacial forces that operate between surfaces and approaching bio-macromolecules. In this way, it is possible to unravel the fundamental information required for the guided design and optimization of biologically active nanoscale coatings that confer predictable properties to synthetic carriers used for the fabrication of bio-diagnostics and biomedical devices. By studying the relationships between interfacial forces and the adsorption of proteins, we have established the key properties that make specific polysaccharide coatings resistant to the adsorption of proteins, which is applicable to biomaterial, biosensor and biochip research.
引用
收藏
页码:652 / 661
页数:10
相关论文
共 20 条
[1]  
BRYERS JD, 1994, COLLOID SURFACE B, V2, P9, DOI 10.1016/0927-7765(94)80013-8
[2]  
CHATELIER R, 1994, Patent No. 9406485
[3]   THEORY OF CONTACT ANGLES AND THE FREE-ENERGY OF FORMATION OF IONIZABLE SURFACES - APPLICATION TO HEPTYLAMINE RADIOFREQUENCY PLASMA-DEPOSITED FILMS [J].
CHATELIER, RC ;
DRUMMOND, CJ ;
CHAN, DYC ;
VASIC, ZR ;
GENGENBACH, TR ;
GRIESSER, HJ .
LANGMUIR, 1995, 11 (10) :4122-4128
[4]  
CHATELIER RC, 1993, Patent No. 9302420
[5]   MICROBIAL BIOFILMS [J].
COSTERTON, JW ;
LEWANDOWSKI, Z ;
CALDWELL, DE ;
KORBER, DR ;
LAPPINSCOTT, HM .
ANNUAL REVIEW OF MICROBIOLOGY, 1995, 49 :711-745
[6]   MOLECULAR-WEIGHT DEPENDENCY OF THE ACQUIRED ANTICOMPLEMENTARY AND ANTICOAGULANT ACTIVITIES OF SPECIFICALLY SUBSTITUTED DEXTRANS [J].
CREPON, B ;
MAILLET, F ;
KAZATCHKINE, MD ;
JOZEFONVICZ, J .
BIOMATERIALS, 1987, 8 (04) :248-253
[7]   DIRECT MEASUREMENT OF COLLOIDAL FORCES USING AN ATOMIC FORCE MICROSCOPE [J].
DUCKER, WA ;
SENDEN, TJ ;
PASHLEY, RM .
NATURE, 1991, 353 (6341) :239-241
[8]  
Fleer G., 1993, Polymers at interfaces
[9]   SMALL-SCALE REACTOR FOR PLASMA PROCESSING OF MOVING SUBSTRATE WEB [J].
GRIESSER, HJ .
VACUUM, 1989, 39 (05) :485-488
[10]   Surface masking technique for the determination of plasma polymer film thickness by AFM [J].
Hartley, Patrick G. ;
Thissen, Helmut ;
Vaithianathan, Tharshan ;
Griesser, Hans J. .
Plasmas and Polymers, 2000, 5 (01) :47-60