| Literature DB >> 32387616 |
Po-Chun Chang1, Wei-Chiu Tai2, Hui-Ting Luo1, Chern-Hsiung Lai3, Hsu-Hsiang Lin4, Zhi-Jie Lin4, Ying-Chieh Chang4, Bor-Shiunn Lee5.
Abstract
This study aimed to evaluated the potential of core-shell poly(D,l-lactide-co-glycolide)-chitosan (PLGA-chitosan) nanospheres encapsulating simvastatin (SIM) and doxycycline (DOX) for promoting periodontal and large-sized osseous defects. SIM, and/or DOX were encapsulated in PLGA-chitosan nanospheres using double emulsion technique and were delivered to sites of experimental periodontitis and large-sized mandibular osseous defects of rats for 1-4 weeks. The resultant nanospheres were ~ 200 nm diameter with distinct core-shell structure and released SIM and DOX sustainably for 28 days. DOX and SIM-DOX nanospheres significantly inhibited P. gingivalis and S. sanguinis. In experimental periodontitis sites, SIM-DOX nanospheres significantly down-regulated IL-1b and MMP-8 and significantly reduced bone loss. In mandibular osseous defects, VEGF was up-regulated, and osteogenesis was significantly augmented with SIM nanospheres treatment. In conclusion, core-shell PLGA-chitosan nanospheres released SIM and DOX sustainably. SIM-DOX and SIM nanospheres could be considered to promote the repair of infected periodontal sites and non-infected osseous defects respectively.Entities:
Keywords: Chitosan; Models, animal; Osteogenesis; Periodontitis; Polylactic acid-polyglycolic acid copolymer; Wound healing
Year: 2020 PMID: 32387616 DOI: 10.1016/j.ijbiomac.2020.04.183
Source DB: PubMed Journal: Int J Biol Macromol ISSN: 0141-8130 Impact factor: 6.953