Bone critical defect repair with poloxamine-cyclodextrin supramolecular gels

被引:27
作者
del Rosario, C. [1 ]
Rodriguez-Evora, M. [1 ]
Reyes, R. [1 ,2 ]
Simoes, S. [3 ]
Concheiro, A. [4 ]
Evora, C. [1 ,2 ]
Alvarez-Lorenzo, C. [4 ]
Delgado, A. [1 ,2 ]
机构
[1] Univ La Laguna, Dept Chem Engn & Pharmaceut Technol, San Cristobal la Laguna 38200, Spain
[2] Univ La Laguna, Inst Biomed Technol ITB, San Cristobal la Laguna 38200, Spain
[3] Univ Coimbra, Ctr Neurosci & Cell Biol, P-3004517 Coimbra, Portugal
[4] Univ Santiago de Compostela, Fac Farm, Dept Farm & Tecnol Farmaceut, Santiago De Compostela 15782, Spain
关键词
Simvastatin; BMP-2; Poloxamine; alpha-Cyclodextrin; Gels; Bone regeneration; Syringeability; Critical bone defect; CRITICAL SIZE DEFECTS; MORPHOGENETIC PROTEIN-2; CONTROLLED-RELEASE; LOCAL APPLICATION; IN-VITRO; SIMVASTATIN; BMP-2; REGENERATION; DELIVERY; SYSTEM;
D O I
10.1016/j.ijpharm.2015.09.003
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The aim of this study was to evaluate the osteoinductive capacity of a poloxamine (Tetronic (R) 908, T) and alpha-cyclodextrin (alpha CD) supramolecular gel (T-CD) as scaffold in a critical size defect in rat calvaria. The T-CD gel was evaluated solely and after being loaded with simvastatin (SV) and bone morphogenetic protein (BMP-2) separately and in combinations in order to reduce the doses of the active substances. Three doses of SV (7.5, 75, 750 mu g) and two doses of BMP-2 (3 and 6 mu g) were tested. The histology and histomorphometrical analysis showed improved bone repair with T-CD compared to T, probably due to better release control of both SV and BMP-2. In addition, as T-CD eroded more slowly than poloxamine alone, it remained longer in the defect site. Although synergism was not obtained with BMP-2 and SV, according to the observed regeneration of the defect, the dose of BMP-2 and SV can be reduced to 3 mu g and 7.5 mu g, respectively. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:463 / 473
页数:11
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