4.6 Review

Simvastatin Embedded into Poly(Lactic-Co-Glycolic Acid)-Based Scaffolds in Promoting Preclinical Bone Regeneration: A Systematic Review

Journal

APPLIED SCIENCES-BASEL
Volume 12, Issue 22, Pages -

Publisher

MDPI
DOI: 10.3390/app122211623

Keywords

drug delivery systems; simvastatin; bone regeneration; polylactic acid-polyglycolic acid copolymer; systematic review

Funding

  1. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior-Brasil (CAPES-Coordination for the Improvement of Higher Education Personnel), Brazil
  2. University Clinic of Dentistry of the Medical University of Vienna

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This systematic review evaluates the doses of simvastatin used in preclinical studies and their impact on bone regeneration. The results suggest that lower doses of simvastatin can consistently promote bone formation, but there is no significant correlation between the relative bone gain and the doses of simvastatin. However, the interpretation of these findings should consider factors such as scaffold heterogeneity, defect anatomy, observation period, and evaluation method.
Simvastatin embedded into poly(lactic-co-glycolic acid) (PLGA)-based scaffolds can stimulate bone regeneration in preclinical models. However, the ideal pharmacological dose has not been evaluated. This systematic review reports on the simvastatin doses used in preclinical studies and evaluates the regeneration of critical-sized bone defects. References were selected in a two-phase process. Electronic databases (Embase, LILACS, LIVIVO, PubMed, SCOPUS, and Web of Science) and grey literature databases (Google Scholar, Open Grey, and ProQuest) were searched until September 2022. The risk of bias was considered to be low based on the SYRCLE tool. We identified four studies in rat, two in parietal and two in calvaria bone, one in mouse parietal bone, and one in rabbit femur bone. Simvastatin, ranging from 8 to 100 mu g, significantly increased bone formation in five studies, as compared to the scaffold alone based on mu-computed tomography, histomorphometric, and radiography analysis. The median increase in bone formation caused by simvastatin was 2.1-fold compared to the PLGA-based scaffold alone. There was, however, no significant correlation between the relative bone gain and the doses of simvastatin (p = 0.37). The data suggest that relatively lower doses of simvastatin can consistently promote preclinical bone regeneration. However, the interpretation of these data must consider the heterogenicity of the PLGA-scaffolds, the defect anatomy, the observation period, and the evaluation method.

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