Decellularized bone matrix/oleoyl chitosan derived supramolecular injectable hydrogel promotes efficient bone integration

去细胞化 壳聚糖 基质(化学分析) 生物医学工程 超分子化学 材料科学 自愈水凝胶 纳米技术 化学 脚手架 化学工程 医学 高分子化学 复合材料 结晶学 晶体结构 工程类
作者
Sayanti Datta,Arun Prabhu Rameshbabu,Kamakshi Bankoti,Madhurima Roy,Chandrika Gupta,Subhodeep Jana,Amit Kumar Das,Ramkrishna Sen,Santanu Dhara
出处
期刊:Materials Science and Engineering: C [Elsevier BV]
卷期号:119: 111604-111604 被引量:48
标识
DOI:10.1016/j.msec.2020.111604
摘要

Hydrogels derived from decellularized extracellular matrix (ECM) have been widely used as a bioactive matrix for facilitating functional bone tissue regeneration. However, its poor mechanical strength and fast degradation restricts the extensive use for clinical application. Herein, we present a crosslinked decellularized bone ECM (DBM) and fatty acid modified chitosan (oleoyl chitosan, OC) based biohybrid hydrogel (DBM/OC) for delivering human amnion-derived stem cells (HAMSCs) for bone regeneration. DBM/OC hydrogel were benchmarked against collagen-I/OC (Col-I/OC) based hydrogel in terms of their morphological characteristics, rheological analysis, and biological performances. DBM/OC hydrogel with its endogenous growth factors recapitulates the nanofibrillar 3D tissue microenvironment with improved mechanical strength and also exhibited antimicrobial potential along with superior proliferation/differentiation ability. HAMSCs encapsulation potential of DBM/OC hydrogel was established by well spread cytoskeleton morphology post 14 days of cultivation. Further, ex - vivo chick chorioallantoic membrane (CAM) assay revealed excellent neovascularization potential of DBM/OC hydrogel. Subcutaneously implanted DBM/OC hydrogel did not trigger any severe immune response or infection in the host after 21 days. Also, DBM/OC hydrogels and HAMSCs encapsulated DBM/OC hydrogels were implanted at the tibial defect in a rabbit model to assess the bone regeneration ability. Quantitative micro-CT and histomorphological analysis demonstrated that HAMSCs encapsulated DBM/OC hydrogel can support more mature mineralized bone formation at the defect area compared to DBM/OC hydrogel or SHAM. These findings manifested the efficacy of DBM/OC hydrogel as a functional cell-delivery vehicle and osteoinductive template to accelerate bone regeneration. • Self-assembled, nanofibrillar hybrid DBM/OC hydrogel was developed at physiological pH and temperature. • DBM/OC showed improved mechanical strength, reduced degradation as well as excellent antimicrobial potential. • Nanofibrillar biohybrid promoted osteogenic differentiation and demonstrated angiogenic potential in CAM assay. • HAMSCs encapsulated DBM/OC hydrogel stimulated bone tissue regeneration in a critical defect in a rabbit model.
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