Nanoclay-Modified Hyaluronic Acid Microspheres for Bone Induction by Sustained rhBMP-2 Delivery

Microspheres (MSs) are ideal candidates as biological scaffolds loading with growth factors or cells for bone tissue engineering to repair irregular alveolar bone defects by minimally invasive injection. However, the high initial burst release of growth factor and low cell attachment limit the application of microspheres. The modification of microspheres often needs expensive experiments facility or complex chemical reactions, which is difficult to achieve and may bring other problems. In this study, a sol-grade nanoclay, laponite XLS is used to modify the surface of MSs to enhance its affinity to either positively or negatively charged proteins and cells without changing the interior structure of the MSs. Recombinant human bone morphogenetic protein-2 (rhBMP-2) is used as a representation of growth factor to check the osteoinduction ability of laponite XLS-modified MSs. By modification, the protein sustained release, cell loading, and osteoinduction ability of MSs are improved. Modified by 1% laponite XLS, the MSs can not only promote osteogenic differentiation of MC3T3-E1 cells by themselves, but also enhance the effect of the rhBMP-2 below the effective dose. Collectively, the study provides an easy and viable method to modify the biological behavior of microspheres for bone tissue regeneration. This study explores an easy and sound way to modify the biological behavior of microspheres for bone tissue regeneration. Nanoclay can successfully sediment on the surface of microspheres, binding with either positively or negatively charged proteins. These properties facilitate cell proliferation and minimize the use of BMP-2.image

Automated summary

This study explores an easy and sound way to modify the biological behavior of microspheres for bone tissue regeneration. Nanoclay can successfully sediment on the surface of microspheres, binding with either positively or negatively charged proteins. These properties facilitate cell proliferation and minimize the use of BMP-2.