Transethosomes as Breakthrough Tool for Controlled Transdermal Delivery of Dexketoprofen Trometamol: Design, Fabrication, Statistical Optimization, in Vitro, and Ex Vivo Characterization

Soliman, Sara M.; RASHWAN, KAREEM OMAR; Teaima, Mahmoud H.; JASTI, BHASKARA R.; El-Nabarawi, Mohamed A.; Abdel-Haleem, Khaled M

doi:10.22159/ijap.2022v14i6.45726

Cited by 1 publication

(1 citation statement)

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“…The recommended model was chosen and subsequently analysed using ANOVA to discover relevant model terms. The numerical optimization function based on the desirability technique was also employed in the study [36,37].…”

Section: Statistical Optimizationmentioning

confidence: 99%

One Pot Development of Lipid-Based Quercetin Spherical Agglomerates for Bioavailability Enhancement: In Vitro and in Vivo Assessments

2023

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Objective: Quercetin, a wonder flavanoid despite numerous pharmacological actions, has limited clinical applications due to solubility and permeability issues and additionally having shorter biological half-life. The goal of the current work was to design Quercetin lipid-based spherical crystals, to improve its oral bioavailability and sustain its in vivo plasma levels. Methods: An anti-solvent precipitation method was employed to prepare quercetin spherical agglomerates using ethanol and distilled water as good and bad solvents, respectively. As bridging liquid chloroform, dichloromethane, hexane and gelucire 43/01, compritol 888 as lipid carrier were screened. The drug-to-lipid polymer proportion and stirring speed effect were optimized by 3-level, 2-factor, experimental design. Numerical optimization function was employed to identify the optimum level of independent variables. Spectroscopic, micromeritic, surface morphology, size distribution, saturated solubility, in vitro dissolution, in vivo pharmackokinetic and stability studies were performed. Results: Surface morphology studies indicated the agglomeration of quercetin needle-like fragments into a spherical shape, which further showed smooth surfaces due to entrapment of QC in lipid carrier. The spherical agglomerates of quercetin showed a four-fold improvement in aqueous solubility compared to pure drug and showed 92.13% release in 8 h. The optimised formulation showed a 3.69-fold enhancement in relative bioavailability in contrast to the marketed preparation in an in vivo pharmacokinetic analysis in male Wistar rats. Conclusion: The obtained lipid-based spherical crystals of quercetin with enhanced bioavailability could be effectively used for its various potential pharmacological applications. The designed system can also be utilized to deliver other phytochemicals with poor bioavailability due to limited solubility and permeability.

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Section: Statistical Optimizationmentioning

confidence: 99%