Document Type

Article

Publication Date

10-6-2015

Keywords

RhBMP-2, Osteogenesis, Collagen–hydroxyapatite, Controlled release, Bone tissue regeneration, Rat calvarial defect model

Funder/Sponsor

Science Foundation Ireland under Grant SFI 12/TIDA/B2383. E.Q. & F.J.O’B acknowledge the European Research Council for the funding (239685-CollRegen-ERC-2009-STG). E.T. acknowledges the Health Research Board of Ireland (HRA_POR/2011/27).

Comments

This article is also available at http://www.journals.elsevier.com/journal-of-controlled-release/

Abstract

The clinical utilization of recombinant human bone morphogenetic protein 2 (rhBMP-2) delivery systems for bone regeneration has been associated with very severe side effects, which are due to the non-controlled and non-targeted delivery of the growth factor from its collagen sponge carrier post-implantation which necessitates supraphysiological doses. However, rhBMP-2 presents outstanding regenerative properties and thus there is an unmet need for a biocompatible, fully resorbable delivery system for the controlled, targeted release of this protein. With this in mind, the purpose of this work was to design and develop a delivery system to release low rhBMP-2 doses from a collagen-hydroxyapatite (CHA) scaffold which had previously been optimized for bone regeneration and recently demonstrated significant healing in vivo. In order to enhance the potential for clinical translation by minimizing the design complexity and thus upscaling and regulatory hurdles of the device, a microparticle and chemical functionalization-free approach was chosen to fulfill this aim. RhBMP-2 was combined with a CHA scaffold using a lyophilization fabrication process to produce a highly porous CHA scaffold supporting the controlled release of the protein over the course of 21days while maintaining in vitro bioactivity as demonstrated by enhanced alkaline phosphatase activity and calcium production by preosteoblasts cultured on the scaffold. When implanted in vivo, these materials demonstrated increased levels of healing of critical-sized rat calvarial defects 8weeks post-implantation compared to an empty defect and unloaded CHA scaffold, without eliciting bone anomalies or adjacent bone resorption. These results demonstrate that it is possible to achieve bone regeneration using 30 times less rhBMP-2 than INFUSE®, the current clinical gold standard; thus, this work represents the first step of the development of a rhBMP-2 eluting material with immense clinical potential.

Disciplines

Anatomy

Citation

Quinlan E, Thompson EM, Matsiko A, O'Brien FJ, López-Noriega A. Long-term controlled delivery of rhBMP-2 from collagen-hydroxyapatite scaffolds for superior bone tissue regeneration. Journal of Controlled Release. 2015;207:112-9.

PubMed ID

25817394

DOI Link

10.1016/j.jconrel.2015.03.028

Creative Commons License


This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 4.0 License.

Included in

Anatomy Commons

Share

COinS