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Templated Mineralization of Synthetic Hydrogels for Bone-Like Composite Materials: Role of Matrix Hydrophobicity

Year: 2010

Journal: Biomacromolecules, 2010, 11 (8), pp 2060–2068, 20111221

Authors: Ameya Phadke, † Chao Zhang, † YongSung Hwang, ‡ Kenneth Vecchio, § and Shyni Varghese ,†

Organizations: Department of Biongineering, MC 0412, University of California—San Diego, 9500 Gilman Drive, La Jolla, California 92093-0412, Materials Science and Engineering Program, University of California—San Diego, 9500 Gilman Drive, La Jolla, California 92093-0418, and Department of NanoEngineering, MC 0448, University of California—San Diego, La Jolla, California 92092-0448

Bone-mimetic mineral-polymer composite materials have several applications ranging from artificial bone grafts to scaffolds for bone tissue engineering; templated mineralization is an effective approach to fabricate such composites. In this study, we synthesized bone-like composites using synthetic hydrogels having pendant side chains terminating with carboxyl groups as a template for mineralization. The role of matrix hydrophobicity on mineralization was examined using poly(ethylene glycol) hydrogels modified with varying lengths of anionic pendant side chains (CH2═CHCONH(CH2)nCOOH, where n = 1, 3, 5, and 7). The ability of these hydrogels to undergo templated mineralization was found to be strongly dependent upon the length of the pendant side chain as is evident from the extent of calcification and morphology of the minerals. Moreover, mineralized phases formed on the hydrogels were confirmed to resemble apatite-like structures. In addition to demonstrating the importance of material hydrophobicity as a design parameter for the development of bone-like synthetic materials, our study also provides a potential explanation for the in vitro differences between the apatite-nucleating capacity of aspartate-rich osteopontin and glutamate-rich bone sialoprotein.