Bone regeneration in osteoporosis by delivery BMP-2 and PRGF from tetronic-alginate composite thermogel

被引:45
作者
Segredo-Morales, Elisabet [1 ]
Garcia-Garcia, Patricia [1 ]
Reyes, Ricardo [2 ,3 ]
Perez-Herrero, Edgar [1 ,3 ]
Delgado, Araceli [1 ,3 ]
Evora, Carmen [1 ,3 ]
机构
[1] Univ La Laguna, Dept Chem Engn & Pharmaceut Technol, San Cristobal la Laguna 38200, Spain
[2] Univ La Laguna, Dept Biochem Microbiol Cell Biol & Genet, San Cristobal la Laguna 38200, Spain
[3] Univ La Laguna, Ctr Biomed Res Canary Isl CIBICAN, Inst Biomed Technol ITB, San Cristobal la Laguna 38200, Spain
关键词
Hydrogel; Tetronic-alginate; Sustained release; BMP-estradiol; Osteoporosis; GROWTH-FACTORS; PLASMA RICH; DRUG-DELIVERY; OSTEOGENIC DIFFERENTIATION; MORPHOGENETIC PROTEIN-2; RHEOLOGICAL PROPERTIES; CONTROLLED-RELEASE; ESTROGEN-RECEPTOR; STEM-CELLS; ER-BETA;
D O I
10.1016/j.ijpharm.2018.03.034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
As the life expectancy of the world population increases, osteoporotic (OP) fracture risk increase. Therefore in the present study a novel injectable thermo-responsive hydrogel loaded with microspheres of 17 beta-estradiol, microspheres of bone morphogenetic protein-2 (BMP-2) and plasma rich in growth factors (PRGF) was applied locally to regenerate a calvaria critical bone defect in OP female rats. Three systems were characterized: Tetronic((R)) 1307 (T-1307) reinforced with alginate (T-A), T-A with PRGF and T-A-PRGF with microspheres. The addition of the microspheres increased the viscosity but the temperature for the maximum viscosity did not change (22-24 degrees C). The drugs were released during 6 weeks in one fast phase (three days) followed by a long slow phase. In vivo evaluation was made in non-OP and OP rats treated with T-A, T-A with microspheres of 17 beta estradiol (T-A-beta E prepared with PRGF (T-A-PRGF-beta E), T-A-beta E with microspheres of BMP-2 (T-A-beta E-BMP-2) and the combination of the three (T-A-PRGF-beta E-BMP). After 12 weeks, histological and histomorphometric analyzes showed a synergic effect due to the addition of BMP-2 to the T-A-beta E formulation. The PRGF did not increased the bone repair. The new bone filling the OP defect was less mineralized than in the non-OP groups.
引用
收藏
页码:160 / 168
页数:9
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