期刊
ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 49, 页码 42639-42652出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b15845
关键词
shear-thinning hydrogels; PGF-18; chitin PLGA; bone regeneration; craniofacial bone regeneration; calcium sulfate
资金
- Nanomission, Department of Science and Technology (DST), Government of India, under the Thematic Projects on Frontiers of Nano Science and Technology (TPF-Nano) program
- DST, India
- Japan Society for the Promotion of Science (JSPS), Japan [DST/INT/JSPS/P-160/2013]
- Council of Scientific and Industrial Research (CSIR) [09/963 (0038) 2K17-EMR-I]
- Council of Scientific and Industrial Research [9/963(0034)2K13-EMR-I]
- Grants-in-Aid for Scientific Research [16K15746] Funding Source: KAKEN
For craniofacial bone regeneration, shear-thinning injectable hydrogels are favored over conventional scaffolds because of their improved defect margin adaptability, easier handling, and ability to be injected manually into deeper tissues. The most accepted method, after autografting, is the use of recombinant human bone morphogenetic protein-2 (BMP-2); however, complications such as interindividual variations, edema, and poor cost-efficiency in supraphysiological doses have been reported. The endogenous synthesis of BMP-2 is desirable, and a molecule which induces this is fibroblast growth factor-18 (FGF-18) because it can upregulate the BMP-2 expression by supressing noggin. We developed a chitin poly(lactide-co-glycolide) (PLGA) composite hydrogel by regeneration chemistry and then incorporated CaSO4 and FGF-18 for this purpose. Rheologically, a 7-fold increase in the elastic modulus was observed in the CaSO4-incorporated chitin PLGA hydrogels as compared to the chitin PLGA hydrogel. Shear-thinning Herschel Bulkley fluid nature was observed for both hydrogels. Chitin PLGA/CaSO4 gel showed sustained release of FGF-18. In vitro osteogenic differentiation showed an enhanced alkaline phosphatase (ALP) expression in the FGF-18-containing chitin PLGA/CaSO4 gel when compared to cells alone. Further, it was confirmed by studying the expression of osteogenic genes [RTJNX2, ALP, BMP-2, osteocalcin (OCN), and osteopontin (OPN)], immunofluorescence staining of BMP-2, OCN, and OPN, and alizarin red S staining. Incorporation of FGF-18 in the hydrogel increased the endothelial cell migration. Further, the regeneration potential of the prepared hydrogels was tested in vivo, and longitudinal live animal mu-CT was performed. FGF-18-loaded chitin PLGA/CaSO4 showed early and almost complete bone healing in comparison with chitin PLGA/CaSO4, chitin PLGA/FGF-18, chitin PLGA, and sham control systems, as confirmed by hematoxylin and eosin and osteoid tetrachrome stainings.: This shows that the CaSO4 and FGF-18-incorporated hydrogel is a potential candidate for craniofacial bone defect regeneration.
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