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Effects of Controlled Dual Growth Factor Delivery on Bone Regeneration Following Composite Bone-Muscle Injury

25 Pages Posted: 29 Apr 2020 Publication Status: Accepted

See all articles by Ramesh Subbiah

Ramesh Subbiah

Georgia Institute of Technology - George W. Woodruff School of Mechanical Engineering

Albert Cheng

Georgia Institute of Technology - George W. Woodruff School of Mechanical Engineering

Marissa A. Ruehle

Georgia Institute of Technology - Parker H. Petit Institute for Bioengineering and Bioscience

Marian H. Hettiaratchi

University of Oregon - Knight Campus for Accelerating Scientific Impact

Luiz E. Bertassoni

Oregon Health and Science University - Division of Biomaterials and Biomechanics

Robert E. Guldberg

Georgia Institute of Technology - George W. Woodruff School of Mechanical Engineering

Abstract

The objective of this study was to investigate the controlled release of two growth factors (BMP-2 and VEGF) as a treatment strategy for clinically challenging composite injuries, consisting of a segmental bone defect and volumetric muscle loss. This is the first investigation of dual growth factor delivery in a composite injury model using an injectable smart delivery system consisting of heparin microparticles and alginate gel. The loading efficiency of growth factors into these biomaterials was found to be >90%, revealing a strong affinity of VEGF and BMP-2 to heparin and alginate. The system could achieve simultaneous or sequential release of VEGF and BMP-2 by varying the loading strategy. Single growth factor delivery (VEGF or BMP-2 alone) significantly enhanced vascular growth in vitro. However, no synergistic effect was observed for dual growth factor (BMP-2 + VEGF) delivery in vitro. Effective bone healing was achieved in all treatment groups (BMP-2, simultaneous or sequential delivery of BMP-2 and VEGF) in the composite injury model. The mechanics of the regenerated bone reached a maximum strength of ~52% of intact bone with sequential delivery of VEGF before BMP-2. Overall, simultaneous or sequential co-delivery of low-dose BMP-2 and VEGF failed to fully restore the mechanics of bone in this injury model. Given the severity of the composite injury, VEGF alone may not be sufficient to establish mature and stable blood vessels when compared with previous studies co-delivering BMP-2+VEGF enhanced bone tissue regeneration. Hence, future studies are warranted to develop an alternative treatment strategy focusing on better control over growth factor dose, spatiotemporal delivery, and additional growth factors to regenerate fully functional bone tissue.

Keywords: heparin microparticle, BMP-2, VEGF, composite injury, microvascular fragments, bone regeneration, growth factor delivery

Suggested Citation

Subbiah, Ramesh and Cheng, Albert and Ruehle, Marissa A. and Hettiaratchi, Marian H. and Bertassoni, Luiz E. and Guldberg, Robert E., Effects of Controlled Dual Growth Factor Delivery on Bone Regeneration Following Composite Bone-Muscle Injury. Available at SSRN: https://ssrn.com/abstract=3577289 or http://dx.doi.org/10.2139/ssrn.3577289

Ramesh Subbiah (Contact Author)

Georgia Institute of Technology - George W. Woodruff School of Mechanical Engineering

801 Ferst Drive
Georgia Institute of Technology
Atlanta, GA 30332-0405
United States

Albert Cheng

Georgia Institute of Technology - George W. Woodruff School of Mechanical Engineering

801 Ferst Drive
Georgia Institute of Technology
Atlanta, GA 30332-0405
United States

Marissa A. Ruehle

Georgia Institute of Technology - Parker H. Petit Institute for Bioengineering and Bioscience

Atlanta, GA 30332
United States

Marian H. Hettiaratchi

University of Oregon - Knight Campus for Accelerating Scientific Impact

Eugene, OR
United States

Luiz E. Bertassoni

Oregon Health and Science University - Division of Biomaterials and Biomechanics

Portland, OR
United States

Robert E. Guldberg

Georgia Institute of Technology - George W. Woodruff School of Mechanical Engineering ( email )

801 Ferst Drive
Georgia Institute of Technology
Atlanta, GA 30332-0405
United States

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