Thin polymer layers formed by polyelectrolyte multilayer techniques on biological surfaces

Citation
Dl. Elbert et al., Thin polymer layers formed by polyelectrolyte multilayer techniques on biological surfaces, LANGMUIR, 15(16), 1999, pp. 5355-5362
Citations number
33
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LANGMUIR
ISSN journal
07437463 → ACNP
Volume
15
Issue
16
Year of publication
1999
Pages
5355 - 5362
Database
ISI
SICI code
0743-7463(19990803)15:16<5355:TPLFBP>2.0.ZU;2-9
Abstract
Thin polymer films were formed on models of tissue surfaces using polyelect rolyte multilayer techniques, to evaluate the feasibility of using such tec hniques to build barrier materials onto the surfaces of tissues to improve postsurgical healing, or on the surfaces of tissue-engineered implants. By incubating heterogeneous surfaces with a polycation, followed by a polyanio n, layers of polyelectrolyte were deposited onto the surfaces, as confirmed by ellipsometry and water contact angle measurement. Particularly favorabl e properties were found using the polyelectrolytes polylysine and alginate, which are capable of forming complex gels at physiologic pH; whereas other s have demonstrated linear growth in film thickness, with this system, expo nential growth was observed under certain conditions, which may be very use ful in the coating of heterogeneous surfaces. Surfaces that were treated wi th multilayer techniques included gelatin, fibroblast extracellular matrix, and fibrillar type I collagen. All surfaces tested were highly heterogeneo us and highly adhesive to cells before treatment. The formed thin polymer l ayers were found to be relatively bioinert, and the thicknesses of the asse mbles were found to be correlated with bioinertness, such that interactions of cells with the underlying proteinaceous surface could be prevented. The thickness of the polymer layers could be changed by increasing the number of bilayers adsorbed and also by changing the treatment and washing conditi ons so as to enhance the formation of complex gels.