Cell-Laden Biomimetically Mineralized Shark-Skin-Collagen-Based 3D Printed Hydrogels for the Engineering of Hard Tissues

2020 ◽  
Vol 6 (6) ◽  
pp. 3664-3672 ◽  
Author(s):  
Gabriela S. Diogo ◽  
Catarina F. Marques ◽  
Carmen G. Sotelo ◽  
Ricardo I. Pérez-Martín ◽  
Rogério P. Pirraco ◽  
...  
2013 ◽  
Vol 13 (11) ◽  
pp. 1621-1631 ◽  
Author(s):  
Susana Fernandes-Silva ◽  
Joana Moreira-Silva ◽  
Tiago H. Silva ◽  
Ricardo I. Perez-Martin ◽  
Carmen G. Sotelo ◽  
...  

2019 ◽  
Vol 166 (9) ◽  
pp. B3302-B3308
Author(s):  
Yuji Yasuda ◽  
Kai Zhang ◽  
Osamu Sasaki ◽  
Masaru Tomita ◽  
David Rival ◽  
...  

2021 ◽  
Vol 11 (10) ◽  
pp. 1924-1931
Author(s):  
Meineng Huang ◽  
Sheng Jiang ◽  
Tong Chen ◽  
Xu Han ◽  
Xinyu Yang ◽  
...  

Objective: To evaluate the curative effect of blue shark skin collagen composite gel on oral mucosal ulcer using the rat oral ulcers model stimulated by glacial acetic acid. Methods: Collagen from blue shark skin was isolated and physiochemically characterized by FTIR, SDS-PAGE and scanning electron microscopy (SEM). Seventy standard male rats were divided into seven groups. The surface and the area of the ulcer were observed and calculated daily. After 12 days of administration, rats in the model group and the control group were killed and the ulcer and surrounding tissues were cut to pieces about one mm3 size. The specimens were stained with 10% formalin solution, paraffinembedded sections, HE staining and light microscope were used to observe the histopathological changes in ulcer tissues. Results: The high-dose group had the fastest ulcer healing effects after 12 days of treatment with blue shark skin collagen composite gel. The composite gel was found to significantly accelerate the healing of oral ulcers in a dose-dependent manner. Conclusion: The blue shark skin collagen composite gel in this study may be a good biomedical material candidate for the treatment of oral ulcers in the near future. Potential of other marine fish skin collagen comples on healing oral ulcers should be also considered.


Friction ◽  
2018 ◽  
Vol 7 (6) ◽  
pp. 603-612 ◽  
Author(s):  
Wei Dai ◽  
Masfer Alkahtani ◽  
Philip R. Hemmer ◽  
Hong Liang
Keyword(s):  

LWT ◽  
2014 ◽  
Vol 55 (1) ◽  
pp. 210-217 ◽  
Author(s):  
Shaoyun Wang ◽  
Jun Zhao ◽  
Lin Chen ◽  
Yanfu Zhou ◽  
Jinhong Wu

2017 ◽  
Vol 4 (1) ◽  
Author(s):  
Xian-Rong Shen ◽  
Xiu-Li Chen ◽  
Hai-Xia Xie ◽  
Ying He ◽  
Wei Chen ◽  
...  

Marine Drugs ◽  
2018 ◽  
Vol 16 (10) ◽  
pp. 350 ◽  
Author(s):  
Jeevithan Elango ◽  
Jung Lee ◽  
Shujun Wang ◽  
Yves Henrotin ◽  
José de Val ◽  
...  

Collagen from a marine resource is believed to have more potential activity in bone tissue engineering and their bioactivity depends on biochemical and structural properties. Considering the above concept, pepsin soluble collagen (PSC) and acid soluble collagen (ASC) from blue shark (Prionace glauca) skin were extracted and its biochemical and osteogenic properties were investigated. The hydroxyproline content was higher in PSC than ASC and the purified collagens contained three distinct bands α1, α2, and β dimer. The purity of collagen was confirmed by the RP-HPLC profile and the thermogravimetric data showed a two-step thermal degradation pattern. ASC had a sharp decline in viscosity at 20–30 °C. Scanning electron microscope (SEM) images revealed the fibrillar network structure of collagens. Proliferation rates of the differentiated mouse bone marrow-mesenchymal stem (dMBMS) and differentiated osteoblastic (dMC3T3E1) cells were increased in collagen treated groups rather than the controls and the effect was dose-dependent, which was further supported by higher osteogenic protein and mRNA expression in collagen treated bone cells. Among two collagens, PSC had significantly increased dMBMS cell proliferation and this was materialized through increasing RUNX2 and collagen-I expression in bone cells. Accordingly, the collagens from blue shark skin with excellent biochemical and osteogenic properties could be a suitable biomaterial for therapeutic application.


1995 ◽  
Vol 60 (6) ◽  
pp. 1233-1236 ◽  
Author(s):  
YOSHIHIRO NOMURA ◽  
MASAYA YAMANO ◽  
KUNIO SHIRAI

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