Biocompatibility of PDGF-simvastatin double-walled PLGA (PDLLA) microspheres for dentoalveolar regeneration: A preliminary study

被引:21
作者
Chang, Po-Chun [1 ]
Chung, Min-Chun [1 ]
Lei, Chenlu [2 ]
Chong, Li Yen [1 ]
Wang, Chi-Hwa [2 ]
机构
[1] Natl Univ Singapore, Discipline Periodont, Fac Dent, Singapore 119083, Singapore
[2] Natl Univ Singapore, Dept Chem & Biomol Engn, Fac Engn, Singapore 119083, Singapore
基金
英国医学研究理事会;
关键词
biocompatibility; growth factor; electrospinning; microsphere; BONE-FORMATION; IN-VITRO; SUSTAINED-RELEASE; DELIVERY; MATRIX;
D O I
10.1002/jbm.a.34244
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Proper coordination of local signal to harmonize mitogenesis and osteogenic differentiation is one of the prerequisites to optimize dentoalveolar regeneration. In the study, we purpose to fabricate controlled-release microspheres encapsulating platelet-derived growth factor (PDGF) and simvastatin by coaxial electrohydrodynamic atomization. The microspheres demonstrated a distinct core and shell structure encapsulating PDGF and simvastatin respectively, and the encapsulation efficiency was 82.4592.16% in-core and 51.3771.34% in-shell. Sequential release of PDGF and simvastatin was seen in simvastatin-in-core and PDGF-in-shell (SP) design, and simultaneous release was achieved in PDGF-in-core and simvastatin-in-shell (PS) design. All microspheres demonstrated acceptable biocompatibility in vivo, with increased proliferation, reduced apoptosis, and reduced inflammation while PDGF or simvastatin was encapsulated. The PS design significantly reduced apoptosis than control, whereby significant and persistent enhanced proliferation was noted in SP group. The thickness of fibrotic capsules surrounding microspheres significantly reduced in both SP and PS group at day 14. The finding demonstrates that synergism of PDGF and simvastatin favored biocompatibility. Further investigations will aim on confirming the regenerative effect of SP and PS microspheres in a more clinically relevant model. (c) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 100A:29702978, 2012.
引用
收藏
页码:2970 / 2978
页数:9
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