Event Abstract

Graphene oxide-bone morphogenic protein2 complex coating by electrophoretic deposition

  • 1 Institute of Tissue Regeneration Engineering, Nanobiomedical Science, Korea

Introduction: Surface modification of metallic implants through a coating method using bioactive and degradable compositions is very useful to improve the osteogenic properties of implants. Furthermore, drug deliverable coating can induce more effective tissue regeneration. Electrophoretic deposition (EPD) is one of the most effective coating methods available, due to its simplicity, uniformity, the short process time and low-temperature process to use in biomedical applications[1]. This study was aimed to produce graphene oxide (GO)-bone morphogenic protein2 (BMP2) complex coatings on Ti for osteogenic surface with sustained drug release. GO has been reported it has high capacity as a delivery carrier for biomolecules as well as supportive material for osteogenic improvement of stem cells[2]. The BMP2 incorporation is considered to enhance the osteo-conductivity. Therefore, it is expected that the GO-BMP2 coating is contributed to improve tissue-compatibility of metallic implants.

Materials and Methods: The GO-BMP2 were deposited on Ti substrate (10 mm ´ 10 mm) through the EPD process. In order to prepare deposit materials, the BMP2 (100 ㎍/ml) was combined with GO (50 ㎍/ml) 10 % ethanol. The coating layers were observed by scanning electron microscopy (SEM, Hitachi S-3000H). The cellular behavior of the composite coating was investigated using mesenchymal stem cells (MSCs), and the result was compared with bare Ti as a control. The BMP2 release was monitored up to 20 days.

Results and Discussion: Figs. 1 show the picture of GO-BMP2 coated Ti plates and the morphology of the composite coating surface generated through the EPD process, respectively.

Fig. 1. Picture (A) and  SEM images of the surface morphology of the EPD composite coating layer. The GO-BMP2 complex was strongly deposited on the Ti surface. We could obtaine uniform coating [ Fig 1(A)]. However, in detailed view through the SEM, the deposition of GO-BMP2 complex (black arrows) induced the surface morphology change slightly, compared to bare Ti surface.

Fig. 2. Cumulative BMP2 released in PBS.

BMP2 release profiles for 20 days are presented in fig 2. The composite coatings revealed continuous and long-term release patterns of BMP2, and the amount of BMP2 released from the coatings were approximately 65%.

Fig 3. Differentiation levels of MSCs on samples after culturing for 10 days.

The ALP activity was assessed to evaluate the effect of composite coating on the osteogenic properties of metallic implants. The ALP activity of the GO-BMP2 composite coating was improved compared with the bare Ti.

Conclusion: The GO-BMP2 composite coatings were successfully produced via electrophoretic deposition (EPD) technique. The composite coatings showed a thin and uniform surface morphology. The composite coatings continuously released BMP2 for 20 days. The biological property of coatings, particularly ALP activity, was improved compared with that of the bare Ti.

References:
[1] Chen F et al. Mater Sci Eng 2007;27:325-332
[2] Tapas R et al. ACS Nano 2011;5(6):4670-4678

Keywords: Bone Regeneration, Implant, biofunctionalization, bioactive interface

Conference: 10th World Biomaterials Congress, Montréal, Canada, 17 May - 22 May, 2016.

Presentation Type: Poster

Topic: Surface and interfacial characterization

Citation: Lee E and Kim H (2016). Graphene oxide-bone morphogenic protein2 complex coating by electrophoretic deposition. Front. Bioeng. Biotechnol. Conference Abstract: 10th World Biomaterials Congress. doi: 10.3389/conf.FBIOE.2016.01.03032

Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters.

The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated.

Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed.

For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions.

Received: 28 Mar 2016; Published Online: 30 Mar 2016.