Algul Derya, Gokce Alper, Onal Ayberk, Servet Erkan, Dogan Ekici Asiye Isın, Yener Fatma Gulgun
a Faculty of Pharmacy, Department of Pharmaceutical Technology , Yeditepe University , Istanbul , Turkey.
b Department of Ortopedic Prothestic and Orthotics , Nisantasi University , Istanbul , Turkey.
J Biomater Sci Polym Ed. 2016;27(5):431-40. doi: 10.1080/09205063.2016.1140501. Epub 2016 Feb 9.
Biomimetic three-layered monolithic scaffold (TLS) intended for the treatment of osteocondral defects was prepared by using alginate, chitosan and β-tricalcium phosphate (β-TCP) to study drug release behavior of the alternative drug delivery system and to investigate the therapeutic efficacy of the scaffold. Dexamethasone sodium phosphate (Dex) as a model drug was incorporated into the scaffold by solvent sorption method and in vitro release studies were conducted. In addition, the scaffold was implanted into the defects formed in the trochlea of Sprague-Dawley rats to assess the healing potential of the TLS on the osteochondral defect against reference Maioregen® comparatively. The release studies showed that after an initial burst at 3rd h, dexamethasone is released slowly during a 72-h period. In vivo studies indicated that the TLS has good tissue biocompatibility and biodegradation rate and showed better results during osteochondral healing process compared to the reference. All results demonstrated that the alginate-chitosan/β-TCP scaffold could be evaluated as a good candidate for osteochondral tissue applications.
通过使用藻酸盐、壳聚糖和β-磷酸三钙(β-TCP)制备了用于治疗骨软骨缺损的仿生三层整体支架(TLS),以研究替代药物递送系统的药物释放行为,并研究该支架的治疗效果。通过溶剂吸附法将磷酸地塞米松钠(Dex)作为模型药物掺入支架中,并进行体外释放研究。此外,将该支架植入Sprague-Dawley大鼠滑车形成的缺损中,以比较评估TLS对骨软骨缺损的愈合潜力与参考产品Maioregen®。释放研究表明,在第3小时出现初始突释后,地塞米松在72小时内缓慢释放。体内研究表明,TLS具有良好的组织生物相容性和生物降解率,与参考产品相比,在骨软骨愈合过程中显示出更好的结果。所有结果表明,藻酸盐-壳聚糖/β-TCP支架可被评估为骨软骨组织应用的良好候选材料。