In situ cross-linkable hyaluronic acid hydrogels using copper free click chemistry for cartilage tissue engineering. Issue 1 (3rd November 2017)

• Record Type: Journal Article
• Authors: Han, Sang-Soo; Yoon, Hong Yeol; Yhee, Ji Young; Cho, Myeong Ok; Shim, Hye-Eun; Jeong, Ji-Eun; Lee, Dong-Eun; Kim, Kwangmeyung; Guim, Hwanuk; Lee, John Hwan; Huh, Kang Moo; Kang, Sun-Woong
• Is Part Of: Polymer chemistry. Volume 9:Issue 1(2018)
• Page Start: 20
• Page End: 27
• Publication Date: 2017-11-03
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c7py01654a
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : We develop a biocompatible and in situ HA hydrogel via a bioorthogonal click reaction for cartilage tissue engineering. Abstract : We report a biocompatible and in situ cross-linkable hydrogel derived from hyaluronic acid via a bioorthogonal reaction and confirm the clinical potential of our hydrogel through in vivo cartilage regeneration. Gelation is attributed to copper-free click reactions between an azide and dibenzyl cyclooctyne. HA-PEG4-DBCO was synthesized and cross-linked via 4-arm PEG azide. The effects of the ratio of HA-PEG4-DBCO to 4-arm PEG azide on the gelation time, microstructure, surface morphology, equilibrium swelling, and compressive modulus were examined. The potential of a hydrogel as an injectable scaffold was demonstrated by the encapsulation of chondrocytes within the hydrogel matrix in vitro and in vivo . The results demonstrated that the hydrogel supported cell survival, and the cells regenerated cartilaginous tissue. In addition, these characteristics provide potential opportunities for the use of injectable hydrogels in tissue engineering applications.