Dynamic nanocomposite microgel assembly with microporosity, injectability, tissue-adhesion and sustained drug release promotes articular cartilage repair and regeneration.
Qi FengDingguo LiQingtao LiShuxian LiHanhao HuangHaofei LiHua DongXiaodong CaoPublished in: Advanced healthcare materials (2021)
Owing to the lack of blood vessels, nerves and lymph in cartilage tissue, articular cartilage defect is difficult to self-repair. Although several cartilage tissue engineering products have been authorized for clinical use, there are still some problems such as large surgical wounds, weak adhesion with the host tissue, limited source of autologous chondrocytes. In this paper, a novel dynamic nanocomposite microgel assembly with excellent microporosity, injectability, tissue-adhesion and sustained kartogenin (KGN) release is reported. Specifically, KGN-loaded cyclodextrin nanoparticles are synthesized through nanoemulsification and incorporated into bone marrow mesenchyml stem cell (BMSCs)-laden microgels via droplet-based microfluidics and photo-crosslinking, which are then bottom-up assembled via dynamic crosslinking between dopamine-modified hyaluronic acid and phenylboronic acid groups on microgel surface. Results reveal that the microgel assembly can avoid the cell endocytosis of nanoparticles, ensure the high BMSC viability during the regular cell culture, cryopreservation and injection process, promote the chondrogenic differentiation of BMSCs. In addition, in vivo animal test proves the newborn cartilages present the typical characteristics of articular cartilage. In a word, this microgel assembly not only offers convenience for clinical use (injectability, tissue adhesion) but also provides good microenvironments for chondrogenesis (controlled drug release, interconnected micropores), indicative of its promising application for articular cartilage repair and regeneration. This article is protected by copyright. All rights reserved.
Keyphrases
- drug release
- stem cells
- bone marrow
- drug delivery
- hyaluronic acid
- tissue engineering
- mesenchymal stem cells
- single cell
- biofilm formation
- cell therapy
- escherichia coli
- high throughput
- cell migration
- ionic liquid
- metabolic syndrome
- reduced graphene oxide
- cancer therapy
- gold nanoparticles
- staphylococcus aureus
- uric acid
- mass spectrometry
- ultrasound guided
- simultaneous determination