1. Simvastatin loaded chitosan guided bone regeneration membranes stimulate bone healing
- Author
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James M Christian, Joel D. Bumgardner, Najib Ghadri, Sidney H. Stein, Vishnu Priya Murali, Jessica A. Jennings, Richard A. Smith, and Fernanda D. Guerra
- Subjects
0301 basic medicine ,Simvastatin ,medicine.medical_specialty ,Bone Regeneration ,Biocompatibility ,Bone healing ,Chitosan ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Osteogenesis ,In vivo ,Internal medicine ,medicine ,Animals ,Bone regeneration ,Membranes, Artificial ,030206 dentistry ,Rats ,Resorption ,030104 developmental biology ,Membrane ,Endocrinology ,chemistry ,Periodontics ,medicine.drug - Abstract
Background and objective Electrospun chitosan membranes (ESCM) modified with short-chain fatty acids have the ability to control the release of simvastatin (SMV), an anti-cholesterol drug with osteogenic potential, for guided bone regeneration (GBR) applications. This study evaluated in vivo osteogenic effects of rapid short release of SMV (4 weeks) vs long sustained release (8 weeks) from acetic anhydride (AA)-and hexanoic anhydride (HA)-modified ESCMs, respectively. Methods AA ESCMs loaded with 10 or 50 µg SMV and HA ESCMs loaded with 50 µg SMV were evaluated for biocompatibility and bone formation at 4 and 8 weeks, in 5 mm critical size rat calvarial defects, using histological evaluation and micro-CT analysis. Results No severe inflammatory response was noticed around the ESCMs. Less hydrophobic AA membranes showed signs of resorption by week 4 and were almost completely resorbed by week 8 whereas the more hydrophobic HA membranes resorbed slowly, remaining intact over 8 weeks. In micro-CT analysis, 10 µg SMV-loaded AA membranes did not show significant bone formation as compared to non-loaded AA membranes at either evaluation time points. 50 µg SMV-loaded AA membranes stimulated significantly more bone formation than non-loaded AA membranes by week 4 (%bone = 31.0 ± 5.9% (AA50) vs 18.5 ± 13.7% (AA0)) but showed no difference at week 8. HA membranes with 50 µg SMV showed significantly more bone formation as compared to corresponding non-loaded membranes by week 8 (%bone = 61.7 ± 8.9% (HA50) vs 33.9 ± 29.7% (HA0)), though such an effect was not significant at week 4. Conclusion These results indicate that modified ESCMs may be used to control the release of SMV and promote bone healing in GBR applications.
- Published
- 2021
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