In vitro release and In vivo biocompatibility studies of biomimetic multilayered alginate-chitosan/β-TCP scaffold for osteochondral tissue

被引:29
作者
Algul, Derya [1 ]
Gokce, Alper [2 ]
Onal, Ayberk [3 ]
Servet, Erkan [4 ]
Ekici, Asiye Isin Dogan [5 ]
Yener, Fatma Gulgun [6 ]
机构
[1] Yeditepe Univ, Dept Pharmaceut Technol, Fac Pharm, Istanbul, Turkey
[2] Nisantasi Univ, Dept Ortoped Prothest & Orthot, Istanbul, Turkey
[3] Agri Govt Hosp, Dept Orthoped & Traumatol, Agri, Turkey
[4] Medicalpark Gaziantep Hosp, Dept Orthoped & Traumatol, Gaziantep, Turkey
[5] Yeditepe Univ, Sch Med, Dept Pathol, Istanbul, Turkey
[6] Istanbul Univ, Dept Pharmaceut Technol, Fac Pharm, Istanbul, Turkey
关键词
scaffold; chitosan; osteochondral defect; Release; alginate; COMPOSITE; DEXAMETHASONE; DELIVERY;
D O I
10.1080/09205063.2016.1140501
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biomimetic three-layered monolithic scaffold (TLS) intended for the treatment of osteocondral defects was prepared by using alginate, chitosan and beta-tricalcium phosphate (beta-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 (R) comparatively. The release studies showed that after an initial burst at 3rdh, 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/beta-TCP scaffold could be evaluated as a good candidate for osteochondral tissue applications.
引用
收藏
页码:431 / 440
页数:10
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