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  3. An in vitro study of fibrin sealant as a carrier system for recombinant human bone morphogenetic protein (rhBMP)–9 for bone tissue engineering
 

An in vitro study of fibrin sealant as a carrier system for recombinant human bone morphogenetic protein (rhBMP)–9 for bone tissue engineering

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BORIS DOI
10.7892/boris.95121
Date of Publication
January 2017
Publication Type
Article
Division/Institute

Departement Klinische...

Universitätsklinik fü...

Contributor
Kobayashi, Masako
Departement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
Mottini, Matthias
Departement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
Kobayashi, Eizaburo
Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
Departement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
Zhang, Yufeng
Schaller, Benoît
Departement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
Miron, Richard John
Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
Subject(s)

600 - Technology::610...

Series
Journal of cranio-maxillo-facial surgery
ISSN or ISBN (if monograph)
1010-5182
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.jcms.2016.10.008
PubMed ID
27840120
Uncontrolled Keywords

BMP9

Bone morphogenetic pr...

Bone regeneration

Fibrin glue

Fibrin sealant

Osteogenesis

Description
In the craniofacial bone field, fibrin sealants are used as coagulant and adhesive tools to stabilize grafts during surgery. Despite this, their exact role in osteogenesis is poorly characterized. In the present study, we aimed to characterize the osteogenic potential of TISSEEL fibrin sealant and used its technology to incorporate growth factors within its matrix. We focused on recombinant human bone morphogenetic protein (rhBMP)-9, which has previously been characterized as one of the strongest osteogenetic inducers in the BMP family. TISSEEL displayed an excellent ability to retain rhBMP9, which was gradually released over a 10-day period. Although TISSEEL decreased bone stromal ST2 cell attachment at 8 h, it displayed normal cell proliferation at 1, 3, and 5 days when compared to tissue culture plastic. Interestingly, TISSEEL had little influence on osteoblast differentiation; however its combination with rhBMP9 significantly increased ALP activity at 7 days, Alizarin Red staining at 14 days, and mRNA levels of osteoblast differentiation markers ALP, bone sialoprotein, and osteocalcin. In summary, although fibrin sealants were shown to have little influence on osteogenesis, their combination with bone-inducing growth factors such as rhBMP9 may serve as an attractive carrier/scaffold for future bone regenerative strategies. Future animal studies are now necessary.
Copyright © 2016 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.

KEYWORDS:
BMP9; Bone morphogenetic proteins; Bone regeneration; Fibrin glue; Fibrin sealant; Osteogenesis
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/192907
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1-s2.0-S1010518216302438-main.pdftextAdobe PDF979.81 KBpublisherpublished restricted
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