Improvement of fluvastatin bioavailability by loading on nanostructured lipid carriers

Abstract

The aim of this study is to prepare fluvastatin nanostructured lipid carriers (FLV-NLCs) in order to find an innovative way to alleviate FLV-associated disadvantages. The limitations include poor solubility and extensive first-pass metabolism, resulting in low (30%) bioavailability and short elimination half-life (1–3 hours). FLV-NLCs were prepared by hot emulsification–ultrasonication method. Ten runs were created by three-level factorial design (32) to optimize FLV-NLCs formulation process. In this study, two factors, four responses, and three-level factorial design were endorsed. The studied variables were lipid:oil ratio (X₁) and sonication time (X₂). However, the responses parameter determined the particle size (Y₁, nm), entrapment efficiency percent (EE%, Y₂), particles zeta potential (Y₃), and 80% of the drug release after 24 hours (X₄). Furthermore, stability and in vivo pharmacokinetics were studied in rats. The optimized consisted formula had an average particle size of 165 nm with 75.32% entrapment efficiency and 85.32% of drug released after 24 hours, demonstrating a sustaining drug release over 24 hours. An in vivo pharmacokinetic study revealed enhanced bioavailability by >2.64-fold, and the mean residence time was longer than that of FLV. We concluded that NLCs could be promising carriers for sustained/prolonged FLV release with enhanced oral bioavailability.

Keywords:

• factorial design
• nano-vesicles
• hyperlipidemia
• statins

Acknowledgments

This work was supported by the Deanship of Scientific Research (DSR), King Abdulaziz University, Jeddah, under grant number (166/942/D1435). The authors, therefore, gratefully acknowledge the DSR technical and financial support.

Disclosure

The authors report no conflicts of interest in this work.