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Macromol Biosci. 2019 Nov;19(11):e1900226. doi: 10.1002/mabi.201900226. Epub 2019 Sep 24.

Investigation of Sustained BMP Delivery in the Prevention of Medication-Related Osteonecrosis of the Jaw (MRONJ) in a Rat Model.

Author information

1
Institute of Health and Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove, Queensland, 4059, Australia.
2
Royal Brisbane and Women's Hospital, Butterfield Street, Herston, Queensland, 4006, Australia.
3
School of Chemistry, Physics and Mechanical Engineering, Queensland University of Technology, 2 George Street, Brisbane, Queensland, 4001, Australia.
4
Leibniz Institute of Polymer Research Dresden e.V., Max Bergmann Center for Biomaterials, Hohe Straße 6, 01069, Dresden, Saxony, Germany.
5
Gold Coast University Hospital, 1 Hospital Boulevard, Southport, Queensland, 4215, Australia.
6
Center for Regenerative Therapies Dresden, Technische Universität Dresden, Fetscherstraße 105, 01307, Dresden, Saxony, Germany.

Abstract

Medication-related osteonecrosis of the jaw (MRONJ) poses an ongoing challenge for clinicians and researchers. Currently, there is a lack of preventative measures available for at-risk patients undergoing tooth extractions, especially those with prior bisphosphonate treatment due to osteoporosis or bone metastasis diagnoses. Here, these issues are addressed using a preventative tissue engineering strategy against MRONJ development. This study evaluates the efficacy of a poly(ethylene glycol)-heparin hydrogel as a tool for the delivery of arginylglycylaspartic acid (RGD) and recombinant human bone morphogenic protein-2 (rhBMP-2). Three groups of skeletally mature rats each receive two doses of intravenous zoledronic acid prior to surgery and undergo extraction of the right first mandibular molar with gingival closure. Experimental groups either have the sockets left empty, filled with hydrogel minus rhBMP-2, or filled with hydrogel plus rhBMP-2. Eight weeks postoperatively specimens are analyzed using radiological, histological, and scanning electron microscopy (SEM) techniques. µCT analysis shows increased bone formation with hydrogel/rhBMP-2 delivery compared to the empty socket. Hydrogel-treated groups display increased presence of osteocytes and increased osteoclastic action compared to the empty sockets. These results represent the first step toward improved delivery of rhBMP-2 and a potential MRONJ preventative for patients undergoing bisphosphonate treatment.

KEYWORDS:

bisphosphonatesm; bone morphogenetic; bone regeneration; hydrogel; medication-related osteonecrosis of the jaw

PMID:
31549786
DOI:
10.1002/mabi.201900226

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