Orthopedic Research Center, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Department of Physiology, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Int J Mol Sci. 2018 Dec 18;19(12):4099. doi: 10.3390/ijms19124099.
The fragile nature of porous bioceramic substitutes cannot match the toughness of bone, which limits the use of these materials in clinical load-bearing applications. Statins can enhance bone healing, but it could show rhabdomyolysis/inflammatory response after overdosing. In this study, the drug-containing bone grafts were developed from poly(lactic acid-co-glycolic acid)-polyethylene glycol (PLGA-PEG) nanoparticles encapsulating simvastatin (SIM) (SIM-PP NPs) loaded within an appropriately mechanical bioceramic scaffold (BC). The combination bone graft provides dual functions of osteoconduction and osteoinduction. The mechanical properties of the bioceramic are enhanced mainly based on the admixture of a combustible reverse-negative thermoresponsive hydrogel (poly(-isopropylacrylamide base). We showed that SIM-PP NPs can increase the activity of alkaline phosphatase and osteogenic differentiation of bone marrow stem cells. To verify the bone-healing efficacy of this drug-containing bone grafts, a nonunion radial endochondral ossification bone defect rabbit model ( = 3/group) and a nonunion calvarial intramembranous defect Sprague Dawley (SD) rat model ( = 5/group) were used. The results indicated that SIM-PP NPs combined with BC can improve the healing of nonunion bone defects of the radial bone and calvarial bone. Therefore, the BC containing SIM-PP NPs may be appropriate for clinical use as a synthetic alternative to autologous bone grafting that can overcome the problem of determining the clinical dosage of simvastatin drugs to promote bone healing.
多孔生物陶瓷替代品的脆弱性质无法与骨骼的韧性相匹配,这限制了这些材料在临床承重应用中的使用。他汀类药物可以促进骨愈合,但过量使用可能会导致横纹肌溶解/炎症反应。在本研究中,载药骨移植物由聚(乳酸-共-乙醇酸)-聚乙二醇(PLGA-PEG)纳米粒子包载辛伐他汀(SIM)(SIM-PP NPs)制备而成,负载于机械性能合适的生物陶瓷支架(BC)内。组合骨移植物提供了骨传导和骨诱导的双重功能。生物陶瓷的机械性能主要通过添加可燃负逆温响应水凝胶(聚(异丙基丙烯酰胺基)增强。我们表明,SIM-PP NPs 可以增加碱性磷酸酶的活性和骨髓干细胞的成骨分化。为了验证载药骨移植物的骨愈合功效,建立了非愈合桡骨末端软骨骨缺损兔模型(每组 n = 3)和非愈合颅骨膜内缺损 SD 大鼠模型(每组 n = 5)。结果表明,SIM-PP NPs 与 BC 联合使用可以改善桡骨和颅骨非愈合骨缺损的愈合。因此,载 SIM-PP NPs 的 BC 可能适合临床应用,作为自体骨移植的合成替代物,可以克服确定促进骨愈合的辛伐他汀药物临床剂量的问题。