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Graphene oxide scaffold accelerates cellular proliferative response and alveolar bone healing of tooth extraction socket

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/61975

Title: Graphene oxide scaffold accelerates cellular proliferative response and alveolar bone healing of tooth extraction socket
Authors: Nishida, Erika Browse this author
Miyaji, Hirofumi Browse this author →KAKEN DB
Kato, Akihito Browse this author →KAKEN DB
Takita, Hiroko Browse this author →KAKEN DB
Iwanaga, Toshihiko Browse this author →KAKEN DB
Momose, Takehito Browse this author
Ogawa, Kosuke Browse this author
Murakami, Shusuke Browse this author
Sugaya, Tsutomu Browse this author →KAKEN DB
Kawanami, Masamitsu Browse this author →KAKEN DB
Keywords: biocompatibility
biomaterial
bone tissue engineering
cell ingrowth
collagen sponge
macrophage
nanocarbon
Issue Date: 24-May-2016
Publisher: Dove Medical Press
Journal Title: International Journal of Nanomedicine
Volume: 11
Start Page: 2265
End Page: 2277
Publisher DOI: 10.2147/IJN.S104778
Abstract: Graphene oxide (GO) consisting of a carbon monolayer has been widely investigated for tissue engineering platforms because of its unique properties. For this study, we fabricated a GO-applied scaffold and assessed the cellular and tissue behaviors in the scaffold. A preclinical test was conducted to ascertain whether the GO scaffold promoted bone induction in dog tooth extraction sockets. For this study, GO scaffolds were prepared by coating the surface of a collagen sponge scaffold with 0.1 and 1 μg/mL GO dispersion. Scaffolds were characterized using scanning electron microscopy (SEM), physical testing, cell seeding, and rat subcutaneous implant testing. Then a GO scaffold was implanted into a dog tooth extraction socket. Histological observations were made at 2 weeks postsurgery. SEM observations show that GO attached to the surface of collagen scaffold struts. The GO scaffold exhibited an interconnected structure resembling that of control subjects. GO application improved the physical strength, enzyme resistance, and adsorption of calcium and proteins. Cytocompatibility tests showed that GO application significantly increased osteoblastic MC3T3-E1 cell proliferation. In addition, an assessment of rat subcutaneous tissue response revealed that implantation of 1 μg/mL GO scaffold stimulated cellular ingrowth behavior, suggesting that the GO scaffold exhibited good biocompatibility. The tissue ingrowth area and DNA contents of 1 μg/mL GO scaffold were, respectively, approximately 2.5-fold and 1.4-fold greater than those of the control. Particularly, the infiltration of ED2-positive (M2) macrophages and blood vessels were prominent in the GO scaffold. Dog bone-formation tests showed that 1 μg/mL GO scaffold implantation enhanced bone formation. New bone formation following GO scaffold implantation was enhanced fivefold compared to that in control subjects. These results suggest that GO was biocompatible and had high bone-formation capability for the scaffold. The GO scaffold is expected to be beneficial for bone tissue engineering therapy.
Rights: http://creativecommons.org/licenses/by-nc/3.0/
Type: article
URI: http://hdl.handle.net/2115/61975
Appears in Collections:歯学院・歯学研究院 (Graduate School of Dental Medicine / Faculty of Dental Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 宮治 裕史

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