| Literature DB >> 33278972 |
Jian He1, Xulin Hu1, Jianfei Cao2, Yu Zhang1, Jianping Xiao3, liJun Peng4, Dongliang Chen1, Chengdong Xiong1, Lifang Zhang5.
Abstract
Biocompatible polymers and drug-delivery scaffolds have driven development in bone regeneration. In this study, we fabricated a chitosan (CS)-coated polytrimethylene carbonate (PTMC)/polylactic acid (PLLA)/oleic acid-modified hydroxyapatite (OA-HA)/vancomycin hydrochloride (VH) microsphere scaffold for drug release with excellent biocompatibility. The incorporation of PLLA, OA-HA, and VH into PTMC microspheres not only slowed the biodegradability of the scaffold but also enhanced its mechanical properties and surface properties. Moreover, the CS coating stimulated extensive adhesion of osteoblasts before OA-HA incorporation, which facilitated the controlled release of OA-HA. The scaffolds were characterized via scanning electron microscopy, in vitro comprehensive performance testing, cell culturing, and microcomputer tomography scanning. The results indicated that the surface of the composite microsphere scaffold was suitable for osteoblast adhesion. Additionally, the release of OA-HA stimulated osteogenic proliferation. Our findings suggest that the CS-PTMC/PLLA/OA-HA/VH microsphere scaffold is promising for bone tissue engineering applications.Entities:
Keywords: Chitosan coating; Microsphere scaffold; Oleic acid-hydroxyapatite; Osteogenic differentiation; Polylactic acid
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Year: 2020 PMID: 33278972 DOI: 10.1016/j.carbpol.2020.117198
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381