Spatiotemporal delivery of bone morphogenetic protein enhances functional repair of segmental bone defects

• Published in: Bone (New York, N.Y.) N.Y.), 2011-09, Vol.49 (3), p.485-492
• Main Authors: Kolambkar, Yash M, Boerckel, Joel D, Dupont, Kenneth M, Bajin, Mehmet, Huebsch, Nathaniel, Mooney, David J, Hutmacher, Dietmar W, Guldberg, Robert E
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Biomechanical Phenomena; Bone Morphogenetic Protein 2 - pharmacology; Bone Morphogenetic Proteins - pharmacology; Bone Regeneration - drug effects; Drug Carriers - chemistry; Drug Delivery Systems; Female; Femur - anatomy & histology; Femur - diagnostic imaging; Femur - pathology; Femur - physiology; Fundamental and applied biological sciences. Psychology; Humans; Nanofibers; Orthopedics; Osteogenesis - drug effects; Rats; Rats, Sprague-Dawley; Recombinant Proteins - pharmacology; Stress, Mechanical; Transforming Growth Factor beta - pharmacology; Vertebrates: anatomy and physiology, studies on body, several organs or systems; X-Ray Microtomography
• ISSN: 8756-3282; 1873-2763; 1873-2763
• DOI: 10.1016/j.bone.2011.05.010

Abstract Osteogenic growth factors that promote endogenous repair mechanisms hold considerable potential for repairing challenging bone defects. The local delivery of one such growth factor, bone morphogenetic protein (BMP), has been successfully translated to clinical practice for spinal fusion and bone fractures. However, improvements are needed in the spatial and temporal control of BMP delivery to avoid the currently used supraphysiologic doses and the concomitant adverse effects. We have recently introduced a hybrid protein delivery system comprised of two parts: a perforated nanofibrous mesh that spatially confines the defect region and a functionalized alginate hydrogel that provides temporal growth factor release kinetics. Using this unique spatiotemporal delivery system, we previously demonstrated BMP-mediated functional restoration of challenging 8 mm femoral defects in a rat model. In this study, we compared the efficacy of the hybrid system in repairing segmental bone defects to that of the current clinical standard, collagen sponge, at the same dose of recombinant human BMP-2. In addition, we investigated the specific role of the nanofibrous mesh tube on bone regeneration. Our results indicate that the hybrid delivery system significantly increased bone regeneration and improved biomechanical function compared to collagen sponge delivery. Furthermore, we observed that presence of the nanofiber mesh tube was essential to promote maximal mineralized matrix synthesis, prevent extra-anatomical mineralization, and guide an integrated pattern of bone formation. Together, these results suggest that spatiotemporal strategies for osteogenic protein delivery may enhance clinical outcomes by improving localized protein retention.