A novel low-friction surface for biomedical applications: modification of poly(dimethylsiloxane) (PDMS) with polyethylene glycol(PEG)-DOPA-lysine.

A novel low-friction surface for biomedical applications: modification of poly(dimethylsiloxane) (PDMS) with polyethylene glycol(PEG)-DOPA-lysine.
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DOI:
10.1002/jbm.a.32141
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发表时间:
2009-09-01
影响因子:
4.9
通讯作者:
Spencer, Nicholas D.
Spencer, Nicholas D.
中科院分区:
工程技术3区
文献类型:
--
作者:
Chawla, Kanika;Lee, Seunghwan;Lee, Bruce P.;Dalsin, Jeffrey L.;Messersmith, Phillip B.;Spencer, Nicholas D.

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Aqueous biocompatible tribosystems are desirable for a variety of tissue-contacting medical devices. L-3,4-dihydroxyphenylalanine (DOPA) and lysine (K) peptide mimics of mussel adhesive proteins strongly interact with surfaces and may be useful for surface attachment of lubricating polymers in tribosystems. Here, we describe a significant improvement in lubrication properties of poly(dimethylsiloxane) (PDMS) surfaces when modified with PEG-DOPA-K. Surfaces were characterized by optical and atomic force microscopy, contact angle, PM-IRRAS, and X-ray photoelectron spectroscopy. Such surfaces, tested over the course of 200 rotations (~8m in length), maintained an extremely low friction coefficient (μ) (0.03±0.00) compared to bare PDMS (0.98±0.02). These results indicate the potential applications of PEG-DOPA-K for the modification of device surfaces. Extremely low μ values were maintained over relatively long length scales and a range of sliding speeds without the need for substrate pre-activation and in the absence of excess polymer in aqueous solution. These results were only obtained when DOPA was bound to lysine (modification with PEG-DOPA did not have an effect on μ) suggesting the critical role of lysine in obtaining a lowered friction coefficient.
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