Amphiphilic Polysaccharides as
Inert Surface Coatings
Stella Bauer,1,2 Maria Pilar Arpa Sancet,1,2 John Finlay,3 Maureen
Callow,3 James Callow,3 Nick Aldred,4 Anthony
Clare4 and A.Rosenhahn1,2
1 Institute
of Functional Interfaces, IFG, Karlsruhe Institute of Technology, Germany
2 Applied
Physical Chemistry, Ruprecht-Karls-University Heidelberg, Germany
3
School of Biosciences, University of Birmingham, United Kingdom
4
School of Marine Science and Technology, Newcastle University, United Kingdom
Biofouling, the
unwanted adhesion of macromolecules and growth of organisms on manmade surfaces
is an economical and ecological challenge for modern surface research.1 The potential of polysaccharides for
fouling-resistant coatings lies in their chemical structure: due to the
presence of hydroxyl-groups, they are highly hydropihilic and able to form
water-storing hydrogels. Their resistance against bacteria and mammalian cells
was e.g. demonstrated by Morra and Cassinelli.2 Cao et.
al.3 applied these materials to the marine environment and
showed that different acidic polysaccharides have a high anti-fouling potential
in terms of protein resistance, but loose this promising property in the marine
environment. This collapse is caused by a complexation of bivalent cations like
Ca2+.4 In this study, the free carboxyl-groups of two
polysaccharides, hyaluronic acid (HA) and chondroitin sulfate (CS)
were postmodified with the hydrophobic amine 2,2,2-trifluoroethylamine (TFEA).
With this strategy, different intentions could be realized: a blocking of free
carboxyl groups to prevent complexation of ions and a preservation of the
resistance in marine environment, a shifting of the contact angle towards the
minimum in the Baier curve to maximize inert properties5 and the introduction of amphiphilic properties due to
the hydrophobic fluoro-groups.6 Subsequently, the coatings were tested towards their
protein resistance and different fouling relevant species to evaluate their
resistance properties.
(1) Rosenhahn, A.; Schilp, S.; Kreuzer, H. J.; Grunze,
M. Physical Chemistry Chemical Physics
2010, 12, 4275.
(2) Morra,
M.; Cassineli, C. J. Biomater.
Sci.-Polym. Ed. 1999, 10, 1107.
(3) Cao,
X. Y.; Pettit, M. E.; … Rosenhahn, A. Biomacromolecules
2009, 10, 907.
(4) Grant,
G. T.;… Thom, D. FEBS Letters 1973, 32, 195.
(5) Vogler,
E. A. Adv. Colloid Interface Sci. 1998, 74, 69.
(6) Krishnan, S.; Wang, N.;
Ober, C. K.; … Fischer, D. A. Biomacromolecules 2006, 7, 1449.