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Marine Adhesive Containing Nanocomposite Hydrogel with Enhanced Materials and Bioadhesive Properties

Published online by Cambridge University Press:  19 June 2013

Yuan Liu
Affiliation:
Department of Biomedical Engineering, Michigan Technological University, Houghton, MI 49931, U. S. A.
Hao Zhan
Affiliation:
Department of Biomedical Engineering, Michigan Technological University, Houghton, MI 49931, U. S. A.
Sarah Skelton
Affiliation:
Department of Biomedical Engineering, Michigan Technological University, Houghton, MI 49931, U. S. A.
Bruce P. Lee*
Affiliation:
Department of Biomedical Engineering, Michigan Technological University, Houghton, MI 49931, U. S. A.
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Abstract

4-arm poly(ethylene glycol) end-capped with mimics of adhesive moiety found in mussel adhesive protein, dopamine, was combined with a biocompatible nano-silicate, Laponite, in creating a nanocomposite hydrogel with improved materials and adhesive properties. Dopamine’s ability to form both irreversible covalent (cohesive and interfacial) and reversible physical (with Laponite) crosslinks was exploited in creating an injectable tissue adhesive. Incorporation of Laponite did not interfere with the curing of the adhesive. In some instances, increasing Laponite content reduced gelation time as dopamine-Laponite bond reduced the required number of covalent bonds needed for network formation. Incorporation of Laponite also increased compressive materials properties (e.g., max strength, energy to failure, etc.) of the nanocomposite without compromising its compliance as strain at failure was also increased. From lap shear adhesion test using wetted pericardium as the substrate, incorporating Laponite increased work of adhesion by 5 fold over that of control. Strong, physical bonds formed between dopamine and Laponite increased bulk materials properties, which contributed to the enhanced adhesive properties.

Type
Articles
Copyright
Copyright © Materials Research Society 2013 

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References

REFERENCES

Hidalgo, M., Castillo, M. J., Eymar, J. L. and Hidalgo, A., Hernia 9, 242 (2005).CrossRefGoogle Scholar
Stark, E., Oestreich, K., Wendl, K., Rumstadt, B. and Hagmüller, E., Surg. Endosc. 13, 878 (1999).CrossRefGoogle Scholar
Ikada, Y., In Wound Closure Biomaterials and Devices, edited by Chu, C. C., Von Fraunhofer, J. A. and Greisler, H. P., (CRC press, 1997) pp. 317.Google Scholar
Lee, B. P., Messersmith, P. B., Israelachvili, J. N., and Waite, J. H., Annu. Rev. Mater. Res. 41, 99 (2011).CrossRefGoogle Scholar
Lee, H., Scherer, N. F. and Messersmith, P. B., Proc. Natl. Acad. Sci. 103, 12999 (2006).CrossRefGoogle Scholar
Burke, S. A., Ritter-Jones, M., Lee, B. P., Messersmith, P. B., Biomed. Mater. 2, 203 (2007).CrossRefGoogle Scholar
Ratner, B. D. and Bryant, S. J., Annu. Rev. Biomed. Eng. 6, 41 (2004).CrossRefGoogle Scholar
Haraguchi, K. and Takehisa, T., Adv. Mater. 14, 1120 (2002).3.0.CO;2-9>CrossRefGoogle Scholar
Skelton, S., Bostwick, M., O'Connor, K., Konst, S., Casey, S. and Lee, B. P., Soft Matter 9, 3825 (2013).CrossRefGoogle Scholar
Dalsin, J. L., Lee, B. P., Vollenweider, L., Silvary, S., Murphy, J. L., Xu, F., Spitz, A. and Lyman, A., U.S. Patent No. 8,119,742 (21 February 2012).Google Scholar
Lee, B. P., Dalsin, J. L. and Messersmith, P. B., Biomacromol. 3, 1038 (2002).CrossRefGoogle Scholar
Murphy, J. L., Vollenweider, L., Xu, F. and Lee, B. P., Biomacromol. 11, 2976 (2010).CrossRefGoogle Scholar
Brodie, M., Vollenweider, L., Murphy, J. L., Xu, F., Lyman, A., Lew, W. D. and Lee, B. P., Biomed. Mater. 6, 015014 (2011).CrossRefGoogle Scholar