Chen Fa-Ming, Zhao Yi-Min, Sun Hai-Hua, Jin Tao, Wang Qin-Tao, Zhou Wei, Wu Zhi-Fen, Jin Yan
Department of Periodontology and Oral Medicine, School of Stomatology, Fourth Military Medical University, Xi'an 710032, Shaanxi, China.
J Control Release. 2007 Mar 12;118(1):65-77. doi: 10.1016/j.jconrel.2006.11.016. Epub 2006 Nov 24.
Novel thermomechanical hydrogel scaffolds containing our previously prepared microspheres loaded with bone morphogenetic proteins (BMP) were successfully generated by radical crosslinking and low dose gamma-irradiation from combination of two kind of biomaterials: glycidyl methacrylated dextran (Dex-GMA) and gelatin. The structure of those resulting smart hybrid hydrogels was evaluated by mercury intrusion porosimetry (MIP) and scanning electron microscopy (SEM) analyses, and as a function of the degree of Dex-GMA's substitution (DS), the proportion between Dex-GMA and gelatin, and the initial polyethyleneglycol (PEG) concentration used in the preparation of the hydrogels. The swelling and degradation properties and the temperature-sensitive drug release manner were determined by dynamic evaluation methods in vitro, and the gel content was also calculated. MIP analysis showed that by systematically altering the preparation parameters, the overall networks were clearly macroporous with pore sizes ranging from 5.6+/-4.2 to 37.7+/-13.7 microm. As expected, the pore size decreased as DS and initial PEG concentration increased, whereas the opposite was found for the gel content. Moreover, the porosity values ranged from 73.7+/-12.4% up to 89.6+/-6.3%. The SEM results also showed the inter-connective pores as well as microspheres encased into their porous structure of those hydrogels. The swelling and degradation properties of the resultant hydrogels varied according to the DS of Dex-GMA and initial PEG concentration, while the proportion between Dex-GMA and gelatin had no significant influence on those characterizations. By changing the composition ratio of the two precursors, the phase transition temperature (lower critical solution temperature, LSCT) of the hydrogel scaffolds could also be adjusted to be or near the body temperature, so BMP release from microsphere-hydrogel compounds could be accordingly controlled and the release period could be varied from 18 to more than 28 days. These results demonstrated that a novel temperature-sensitive and biodegradable Dex-GMA/gelatin scaffold containing microspheres loaded with BMP could be successfully developed from both dextran- and gelatin-based biomaterials, which could promisingly satisfy the need, desire, and expectation of both self-regulated drug delivery and tissue-engineering applications.
通过自由基交联和低剂量γ辐射,由甲基丙烯酸缩水甘油酯葡聚糖(Dex - GMA)和明胶这两种生物材料成功制备出了新型热机械水凝胶支架,其中含有我们之前制备的负载骨形态发生蛋白(BMP)的微球。通过压汞法(MIP)和扫描电子显微镜(SEM)分析对所得智能杂化水凝胶的结构进行了评估,该结构是Dex - GMA的取代度(DS)、Dex - GMA与明胶的比例以及水凝胶制备中所用初始聚乙二醇(PEG)浓度的函数。通过体外动态评估方法测定了水凝胶的溶胀和降解性能以及温度敏感型药物释放方式,并计算了凝胶含量。MIP分析表明,通过系统地改变制备参数,整体网络具有明显的大孔结构,孔径范围为5.6±4.2至37.7±13.7微米。正如预期的那样,随着DS和初始PEG浓度的增加,孔径减小,而凝胶含量则相反。此外,孔隙率值范围从73.7±12.4%至89.6±6.3%。SEM结果还显示了这些水凝胶的相互连通孔隙以及包裹在其多孔结构中的微球。所得水凝胶的溶胀和降解性能根据Dex - GMA的DS和初始PEG浓度而变化,而Dex - GMA与明胶之间的比例对这些特性没有显著影响。通过改变两种前体的组成比例,水凝胶支架的相变温度(低临界溶液温度,LCST)也可以调节至体温或接近体温,因此微球 - 水凝胶复合物中BMP的释放可以相应地得到控制,释放期可以从18天变化到超过28天。这些结果表明,可以成功地从基于葡聚糖和明胶的生物材料开发出一种新型的含负载BMP微球的温度敏感且可生物降解的Dex - GMA/明胶支架,有望满足自我调节药物递送和组织工程应用的需求、期望和预期。