Thermosensitive Injectable Gradient Hydrogel‐Induced Bidirectional Differentiation of BMSCs

Abstract

Osteochondral defects threaten the quality of life of patients to a great extent. To simulate gradient changes in osteochondral tissue, a gradient-mixing injection device consisting of a controller and injection pumps is design. Bioactive glass (BG) and gellan gum (GG) are used to prepare thermosensitive injectable gradient hydrogels (B 0.5 G, B 1 G) with an upper critical solution temperature (UCST) range of 37.7-40.2 °C using this device for the first time. The mechanical properties of gradient hydrogels are significantly better than those of pure GG hydrogels. The gradients in the composition, structure, and morphology of gradient hydrogels are confirmed via physicochemical characterization. Cytocompatibility tests show that hydrogels, especially B 0.5 G gradient hydrogels, promote the proliferation of bone marrow mesenchymal stem cells (BMSCs). Most importantly, qRT-PCR shows that the different components in B 0.5 G gradient hydrogels simultaneously induce the osteogenic and chondrogenic differentiation of BMSCs. Experimental injection in porcine osteochondral defects indicates that the B 0.5 G gradient hydrogel seamlessly fills irregular osteochondral defects in a less invasive manner by controlling the temperature to avoid cellular and tissue damage arising from crosslinkers or other conditions. These results show that thermosensitive injectable B 0.5 G gradient hydrogels have the potential for less invasive integrated osteochondral repair.

Gums as Macromolecular Crowding Agents in Human Skin Fibroblast Cultures

“…Furter, the cytocompatibility of CR has been well-established in the literature [58,93] and has even been used effectively in clinical settings [94,95]. Similarly, all assessed gums are used extensively in the biomaterials field with an equal well-documented cytocompatibility (e.g., GA [96][97][98][99], GG [100][101][102][103][104], GK [105][106][107], GX [108][109][110]) with a diverse range of cell populations.…”