Simvastatin-Incorporated Drug Delivery Systems for Bone Regeneration
Source abstract
Abstract
Local drug delivery systems composed of biomaterials and osteogenic substances provide promising strategies for the reconstruction of large bone defects. In recent years, simvastatin has been studied extensively for its pleiotropic effects other than lowering of cholesterol, including its ability to induce osteogenesis and angiogenesis. Accordingly, several studies of simvastatin incorporated drug delivery systems have been performed to demonstrate the feasibility of such systems in enhancing bone regeneration. Therefore, this review explores the molecular mechanisms by which simvastatin affects bone metabolism and angiogenesis. The simvastatin concentrations that promote osteogenic differentiation are analyzed. Furthermore, we summarize and discuss a variety of simvastatin-loaded drug delivery systems that use different loading methods and materials. Finally, current shortcomings of and future development directions for simvastatin-loaded drug delivery systems are summarized. This review provides various advanced design strategies for simvastatin-incorporated drug delivery systems that can enhance bone regeneration.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polymer Surface Interaction Studies · Bone Tissue Engineering Materials · Orthopaedic implants and arthroplasty
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Orthopedics, The Second Hospital of Jilin University, Changchun 130041, P.R. China
Department of Pain, The Second Hospital of Jilin University, Changchun 130041, P.R. China
Department of Orthopedics, Weihai Guanghua Hospital, Weihai 264200, P.R. China
Funding
Ministry of Science and Technology of the People's Republic of China · People's Government of Jilin Province · Department of Science and Technology of Jilin Province · National Natural Science Foundation of China · Jilin Department of Health
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