Fabrication and Characterization of Photo-Crosslinked Poly(L-glutamic acid) Hydrogels

被引:0
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作者
Wang B. [1 ]
Li G. [1 ]
Zong H. [1 ]
Yan S. [1 ]
Yin J. [1 ]
机构
[1] Department of Polymer Materials, School of Materials Science and Engineering, Shanghai University, Shanghai
关键词
Biocompatibility; Photo-crosslinking hydrogel; Poly (L-glutamic acid); Polyethylene glycol acrylate;
D O I
10.16865/j.cnki.1000-7555.2020.0010
中图分类号
学科分类号
摘要
The poly(L-glutamic acid) (PLGA) graft polymer PLGA-g-APEG with a side-linked polyethylene glycol acrylate (APEG) was used as precursor, and the hydrogel was prepared by UV-crosslinking. Then the effects of grafting ratio of APEG and mass concentration of the precursor on the mechanical properties of photocrosslinked hydrogels were studied. When the grafting ratio of APEG reaches 44.7% and the mass fraction of PLGA-g-APEG reaches 15%, the mechanical properties of hydrogel achieve the best. The storage modulus is 16238.2 Pa, and the compressive failure stress is 0.16 MPa. At the same time, the hydrogel was subjected to several cycles of compression test. The results show that the cyclic compression curves are almost completely coincident, the hydrogel has excellent resilience performance. Finally, the results of MTT and the dead/live experiments show that the PLGA-g-APEG precursor and its photocrosslinked hydrogel have good biocompatibility, the hydrogel has potential application in the fields of regenerative medicine. © 2020, Editorial Board of Polymer Materials Science & Engineering. All right reserved.
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页码:126 / 133
页数:7
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共 13 条
  • [1] Lutolf M.P., Hubbell J.A., Synthetic biomaterials as instructive extracellular microenvironments for morphogenesis in tissue engineering, Nat Biotechno.l., 23, pp. 47-55, (2005)
  • [2] Wei Z., Yang J.H., Chen Y.M., Et al., Self-healing gels based on constitutional dynamic chemistry and their potential applications, Chem. Soc. Rev., 43, pp. 8114-8131, (2014)
  • [3] Li Y., Rodrigues J., Tomas H., Injectable and biodegradablehydrogels: gelation, biodegradation and biomedical applications, Chem. Soc. Rev., 41, pp. 2193-2221, (2012)
  • [4] Yang J., Yeom J., Hahn S.K., Et al., In situ-forming injectable hydrogels for regenerative medicine, Prog. Polym. Sci., 39, pp. 1973-1986, (2014)
  • [5] Khademhosseini A., Langer R., Microengineered hydrogels fortissue engineering, Biomaterials, 28, pp. 5087-5092, (2007)
  • [6] Ifkovits J.L., Burdick J.A., Review: Photopolymerizable anddegradable biomaterials for tissue engineering applications, Tissue Eng., 13, pp. 2369-2385, (2007)
  • [7] Bryant S.J., Nuttelman C.R., Anseth K.S., Cytocompatibility of UV and visible light photoinitiating systems on cultured NIH/3T3 fibroblasts in vitro, J. Biomater. Sci., Polym. Ed., 11, pp. 439-457, (2012)
  • [8] Fedorovich N.E., Oudshoorn M.H., Alblas J., Et al., The effect of photopolymerization on stem cells embedded in hydrogels, Biomaterials, 30, pp. 344-353, (2009)
  • [9] Zhang K., He S., Yin J., Et al., Regeneration of hyaline-like cartilage and subchondral bone simultaneously by poly(L-glutamic acid) based osteochondral scaffolds with induced autologous adipose derived stem cells, J. Mater. Chem., B, 4, pp. 2628-2645, (2016)
  • [10] Zhang K., Li G., Yin J., Et al., In-situ birth of MSCs multicellular spheroids in poly(L-glutamic acid)chitosan scaffold for hyaline-like cartilage regeneration, Biomaterials, 71, pp. 24-34, (2015)