Thermoresponsive Hydrogel-Based Local Delivery of Simvastatin for the Treatment of Periodontitis

Except for routine scaling and root planing, there are few effective nonsurgical therapeutic interventions for periodontitis and associated alveolar bone loss. Simvastatin (SIM), one of the 3-hydroxy-3-methylglutaryl-cosenzyme A reductase inhibitors, which is known for its capacity as a lipid-loweri...

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Published inMolecular pharmaceutics Vol. 18; no. 5; pp. 1992 - 2003
Main Authors Chen, Ningrong, Ren, Rongguo, Wei, Xin, Mukundan, Roshni, Li, Guojuan, Xu, Xiaoke, Zhao, Gang, Zhao, Zhifeng, Lele, Subodh M, Reinhardt, Richard A, Wang, Dong
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 03.05.2021
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Summary:Except for routine scaling and root planing, there are few effective nonsurgical therapeutic interventions for periodontitis and associated alveolar bone loss. Simvastatin (SIM), one of the 3-hydroxy-3-methylglutaryl-cosenzyme A reductase inhibitors, which is known for its capacity as a lipid-lowering medication, has been proven to be an effective anti-inflammatory and bone anabolic agent that has shown promising benefits in mitigating periodontal bone loss. The local delivery of SIM into the periodontal pocket, however, has been challenging due to SIM’s poor water solubility and its lack of osteotropicity. To overcome these issues, we report a novel SIM formulation of a thermoresponsive, osteotropic, injectable hydrogel (PF127) based on pyrophosphorolated pluronic F127 (F127-PPi). After mixing F127-PPi with F127 at a 1:1 ratio, the resulting PF127 was used to dissolve free SIM to generate the SIM-loaded formulation. The thermoresponsive hydrogel’s rheologic behavior, erosion and SIM release kinetics, osteotropic property, and biocompatibility were evaluated in vitro. The therapeutic efficacy of SIM-loaded PF127 hydrogel on periodontal bone preservation and inflammation resolution was validated in a ligature-induced periodontitis rat model. Given that SIM is already an approved medication for hyperlipidemia, the data presented here support the translational potential of the SIM-loaded PF127 hydrogel for better clinical management of periodontitis and associated pathologies.
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N. Chen prepared and characterized all formulations. She also led all in vivo study and drafted the manuscript. R. Ren synthesized F127-PPi. X. Wei, R. Mukundan, G. Li, and Z. Zhao contributed to in vivo efficacy study. S.M. Lele performed all histological analysis with X. Xu’s assistance. G. Zhao contributed to rheology characterization of the hydrogel samples. R.A. Reinhardt contributed to experimental design and data interpretation. D. Wang led the overall experiment design, data interpretation, manuscript review and finalization.
Author Contributions
ISSN:1543-8384
1543-8392
DOI:10.1021/acs.molpharmaceut.0c01196