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RESEARCH PRODUCT
Osseous response on linear and cyclic RGD-peptides immobilized on titanium surfaces in vitro and in vivo
Martin HellerPeer W. KämmererJürgen BriegerAndreas PabstBilal Al-nawasVinay Kumarsubject
Bone growthMaterials sciencebiologyMetals and AlloysBiomedical Engineering030206 dentistry02 engineering and technologyBone healingAdhesion021001 nanoscience & nanotechnologyIn vitroBiomaterials03 medical and health sciences0302 clinical medicineIn vivoCeramics and CompositesFluorescence microscopeOsteocalcinbiology.proteinAlkaline phosphatase0210 nano-technologyBiomedical engineeringdescription
Biomimetic surface modifications of titanium implants using the Arg-Gly-Asp-sequence (RGD) are promising to accelerate bone healing in cases of medical implants. Therefore, we compared the impact of linear and cyclic RGD (l- and c-RGD) covalently coupled onto titanium surfaces on the osseous response in vitro and in vivo. In vitro, osteoblasts' behaviour on different surfaces (unmodified, amino-silanized (APTES), l- and c-RGD) was analysed regarding adhesion (fluorescence microscopy), proliferation (resazurin stain) and differentiation (RT-PCR on alkaline phosphatase (AP) & osteocalcin (OC)). In vivo, osteosynthesis screws (unmodified n=8, l-RGD n=8, c-RGD n=8) were inserted into the proximal tibiae of 12 rabbits and evaluated for bone growth parameters (bone-implant-contact (BIC;%) & vertical bone apposition (VBA;%)) at 3 and 6 weeks. In vitro, c- as well as l-RGD surfaces stimulated osteoblasts' adherence, proliferation and differentiation in a similar manner, with only subtle evidence of superiority of the c-RGD modifications. In vivo, c-RGD-modifications led to a significantly increased VBA after 3 and after 6 weeks. Thus, coating with c-RGD appears to play an important role influencing osteoblasts' behaviour in vitro but especially in vivo. These findings can be applied prospectively to implantable biomaterials with hypothetically improved survival and success rates. This article is protected by copyright. All rights reserved.
year | journal | country | edition | language |
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2017-10-17 | Journal of Biomedical Materials Research Part A |