Chitosan-coated hydroxyapatite and drug-loaded polytrimethylene carbonate/polylactic acid scaffold for enhancing bone regeneration. (1st February 2021)

• Record Type: Journal Article
• Authors: He, Jian; Hu, Xulin; Cao, Jianfei; Zhang, Yu; Xiao, Jianping; Peng, liJun; Chen, Dongliang; Xiong, Chengdong; Zhang, Lifang
• Is Part Of: Carbohydrate polymers. Volume 253(2021)
• Publication Date: 2021-02-01
• Subjects: Chitosan coating -- Oleic acid-hydroxyapatite -- Microsphere scaffold -- Polylactic acid -- Osteogenic differentiation; Polysaccharides -- Periodicals; Polysaccharides -- Periodicals; Polysaccharides -- Périodiques; Electronic journals; 547.78
• DOI: 10.1016/j.carbpol.2020.117198
• Languages: English
• ISSNs: 0144-8617

Abstract

Graphical abstract: Highlights: We have developed a novel CS-PTMC/PLLA/OA-HA/VH scaffolds. The scaffold can provide drug release and excellent biocompatibility. Enhance the mechanical properties and hydrophilicity of the composite scaffold. The scaffold can provide good surface properties and controlled biodegradability. The scaffold with a CS-coated is conducive to cell adhesion and enrichment. 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.