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DOI 10.1080/21691401.2018.1458033

Медицинская библиотека · Artificial cells, nanomedicine, and biotechnology · 2018

Phelligridin D-loaded oral nanotube titanium implant enhances osseointegration and prevents osteolysis in rat mandible.

Kim Ji-Eun, Takanche Jyoti Shrestha, Kim Jeong-Seok, Lee Min-Ho, Jeon Jae-Gyu, Park Il-Song, Yi Ho-Keun

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Аннотация

Poor bone quality and osteolysis are the major causes of implant failure in dentistry. Here, this study tested the effect of phelligridin D-loaded nanotubes titanium (Ti) for bone formation around the dental implants. The purpose of this study was to enhance osseointegration of phelligridin D-loaded implant into the bone for bone formation and prevention of osteolysis. Cell viability, crystal violet staining, Western blot, alizarin red S staining, alkaline phosphatase activity, tartrate-resistant acid phosphatase staining, micro-computed tromography (μ-CT), hematoxylin and eosin (H&E) and immunohistochemical staining were used in vitro and in vivo to test the biocompatibility of phelligridin D. Phelligridin D enhanced osteoblast differentiation and mineralization by increasing bone morphogenic protein-2/7 (BMP-2/7), Osterix, Runx-2, osteoprotegerin (OPG), alkaline phosphatase and inhibited osteoclast differentiation by decreasing receptor activator of nuclear factor kappa-B ligand (RANKL) in MC-3T3 E1 cells. Further, phelligridin D promoted bone regeneration around nanotube Ti implant surface by increasing the levels of BMP-2/7 and OPG in a rat model. Phelligridin D also inhibited osteolysis by suppressing the expression of RANKL. These findings strongly suggest that phelligridin D is a new compound representing a potential therapeutic candidate for implant failure caused by osteolysis and poor bone quality of teeth.

Для цитирования: Kim Ji-Eun, Takanche Jyoti Shrestha, Kim Jeong-Seok, Lee Min-Ho, Jeon Jae-Gyu, Park Il-Song, Yi Ho-Keun. Phelligridin D-loaded oral nanotube titanium implant enhances osseointegration and prevents osteolysis in rat mandible.. Artificial cells, nanomedicine, and biotechnology. 2018. DOI: 10.1080/21691401.2018.1458033.

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