4.7 Article

Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering

Journal

INTERNATIONAL JOURNAL OF NANOMEDICINE
Volume 14, Issue -, Pages 8891-8903

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S210329

Keywords

three-dimensional scaffold; flurbiprofen; freeze-drying; amidation; skin tissue engineering

Funding

  1. National Natural Science Foundation [81671920, 81871753, 81772341]
  2. National Key Research and Development Program of China [2018YFC 1106200, 2018YFC1106202]
  3. Collaborative Innovation Transformation Project of Shanghai Jiao Tong University School of Medicine [TM201736]
  4. Project of Shenkang Hospital Development Center of Shanghai [16CR3108B]
  5. Technology Support Project of Science and Technology Commission of Shanghai Municipality of China [18441902800]

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Aim: In this study, we attempted to regulate the preparation of Alg-CS-Flu three-dimensional scaffolds via a facile freeze-drying method combined with amidation. Materials and methods: Three-dimensional porous flurbiprofen-grafted alginate (Alg)-chitosan (CS) scaffolds were successfully prepared by a facile freeze-drying method combined with amidation for skin tissue engineering applications. Alg-CS composite was first used to load flurbiprofen (Flu), which is a kind of anti-inflammatory non-steroidal molecule. The Flu-loaded Alg/CS composite solution, through freeze-drying and 1-ethyl-3(3-(dimethylamino)propyl) carbodiimide/N-hydroxysuccinimide crosslinking to form an Alg-CS-Flu scaffold, exhibited a uniform and porous morphology that was characterized using scanning electron microscopy. The Alg-CS-Flu as-prepared scaffold was also characterized using Fourier-transform infrared spectroscopy, water contact angle, thermal properties, and stress-strain testing. Results: The results reveal that Flu was successfully grafted onto the surfaces of the Alg-CS-Flu scaffold, which showed good hydrophilicity and appropriate mechanical properties. Furthermore, cell viability, cell morphology from cells cultured in vitro, and hematoxylineosin staining after the graft was subcutaneously embedded in mice for 7 d demonstrated that the Alg-CS-Flu scaffold had no unfavorable effects on the adhesion and proliferation of fibroblasts, as well as a good anti-inflammatory property. Conclusion: The developed Alg-CS-Flu scaffold is proposed as a promising material or skin tissue engineering application.

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