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作 者:赵晶晶[1] 方真华[1] 黄若昆[1] 肖凯[1] 李静[1] 谢鸣[1] 勘武生[1]
出 处:《生物医学工程学杂志》2014年第4期811-815,共5页Journal of Biomedical Engineering
基 金:武汉市临床医学科研项目资助(WX14A05)
摘 要:载骨形态发生蛋白-2(BMP-2)活性多肽P24的聚三甲基碳酸酯-(聚氧乙烯)-聚三甲基碳酸酯(PTMC11-F127-PTMC11)注射型可降解凝胶诱导大鼠体内异位成骨,测定P24体外释放曲线。将P24与不同质量浓度的PTMC11-F127-PTMC11水凝胶复合,采用二喹啉甲酸(BCA)法测定,绘制P24释放曲线。将复合P24凝胶植于大鼠骶棘肌,行组织学切片HE染色检测其异位成骨能力。PTMC11-F127-PTMC11浓度大于20%的复合凝胶其P24经突释期后可维持缓释1个月左右,满足缓释材料要求。组织学显示第6周切片可见骨小梁。载BMP-2活性多肽P24PTMC11-F127-PTMC11凝胶在体内能有效发挥其诱导成骨活性,有望成为生长因子合适载体。We investigated the development of an injectable, biodegradable hydrogel composite of poly(trimethylene carbonate)-F127-poly(trimethylene carbonate)(PTMC11-F127-PTMC11 )loaded with bone morphogenetic protein-2 (BMP-2) derived peptide P24 for ectopic bone formation in vivo and evaluated its release kinetics in vitro. Then we evaluated P24 peptide release kinetics from different concentration of PTMC11-F127-PTMC11 hydrogel in vitro using bicinchoninic acid (BCA)assay. P24/PTMC11-F127-PTMC11 hydrogel was implanted into each rat's erector muscle of spine and ectopic bone formation of the implanted gel in vivo was detected by hematoxylin and eosin stain (HE). PTMC11-F127-PTMC11 hydrogel with concentration more than 20 percent showed sustained slow release for one month after the initial burst release. Bone trabeculae surround the P24/PTMCH-F127-PTMC11 hydrogel was shown at the end of six weeks by hematoxylin and eosin stain. These results indicated that encapsulated bone morphogenetic protein (BMP-2) derived peptide P24 remained viable in vivo, thus suggesting the potential of PTMC11-F127-PT- MC11 composite hydrogels as part of a novel strategy for localized delivery of bioactive molecules.
分 类 号:R318.08[医药卫生—生物医学工程]
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