透明质酸
自愈水凝胶
化学
骨钙素
骨形态发生蛋白2
体内
酰肼
骨桥蛋白
生物医学工程
骨愈合
体外
生物化学
外科
高分子化学
解剖
有机化学
碱性磷酸酶
内科学
医学
生物技术
生物
酶
作者
Elena Martínez‐Sanz,Dmitri Ossipov,Jöns Hilborn,Sune Larsson,Kenneth B. Jonsson,Oommen P. Varghese
标识
DOI:10.1016/j.jconrel.2011.02.003
摘要
A strategy has been designed to develop hyaluronic acid (HA) hydrogel for in vivo bone augmentation using minimal invasive technique. A mild synthetic procedure was developed to prepare aldehyde modified HA by incorporating an amino-glycerol side chain via amidation reaction and selective oxidation of the pendent group. This modification, upon mixing with hydrazide modified HA formed hydrazone-crosslinked hydrogel within 30 s that was stable at physiological pH. In vitro experiments showed no cytotoxicity of hydrogel with the controlled release of active bone morphogenic protein-2 (BMP-2). In vivo evaluation of this gel as a BMP-2 carrier was performed by injecting gels over the rat calvarium and showed bone formation in 8 weeks in correlation with the amount of BMP-2 loaded (0, 1 and 30 μg) within the gel. Furthermore, hydrogels with 30 μg of BMP-2 induced less bone formation upon subcutaneous injection in comparison with subperiosteal implantation. Histological examination showed newly formed bone with a high expression of osteocalcin, osteopontin and with angiogenic bone marrow when higher BMP-2 concentration was employed. Our result suggests that novel HA hydrogels could be used as a BMP-2 carrier and can promote bone augmentation for potential orthopedic applications.
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