Oral bioavailability enhancement of glibenclamide by Self-emulsifying drug delivery systems (SEDDS)

Naha, Anup and Srivastava, Harsha and Kannan, Sivakumar (2019) Oral bioavailability enhancement of glibenclamide by Self-emulsifying drug delivery systems (SEDDS). Latin American Journal of Pharmacy, 38 (7). pp. 1319-1326. ISSN 0326- 2383

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The present work was aimed to improve the oral bioavailability of glibenclamide by developing self-emulsifying drug delivery system (SEDDS). Solubility of glibenclamide was determined in oils, surfactant, and cosurfactant. Pseudoternary phase diagrams were constructed to obtain self-nanoemulsifying region. SEDDS were evaluated for thermodynamic stability, droplet size, in vitro dissolution, in vivo pharmacokinetic, and stability studies. Sunflower oil (3.46 ± 0.32 mg/100 mg), Tween 80 (3.75 ± 0.37 mg/100 mg) and PEG 600 (2.98 ± 0.44 mg/100 mg) were selected as oil, surfactant, and cosurfactant, respectively.Surfactant and cosurfactant mix (Smix) of 3:1, 2:1, and 1:1 showed a larger nanoemulsification region and Ba3 (Smix 3:1) showed minimum emulsion globule size of 122.9 nm with PDI of 0.549 and exhibited highest cumulative drug release (97.6 ± 1.8), as compared to pure glibenclamide (31.2 ± 2.2) and marketed tablet (90.3 ± 2.1). Cmax of Ba3 (10.01 ± 2.14 μg/mL) was significantly higher than pure drug (7.13 ± 1.16 μg/mL) and marketed tablet (9.02 ± 2.23 μg/mL) and AUC of Ba3 (140.39 ± 10.14 μg.h/mL) was found to be significantly higher than pure glibenclamide (100.12 ± 11.45 μg.h/mL), indicating an improvement in the bioavailability of glibenclamide from SEDDS formulation as compared to pure drug.

Item Type: Article
Uncontrolled Keywords: Glibenclamide; nanoemulsion; phase diagram; SEDDS; Smix.
Subjects: Pharmacy > MCOPS Manipal > Pharmaceutics
Depositing User: KMC Library
Date Deposited: 31 Jul 2019 04:35
Last Modified: 31 Jul 2019 04:35
URI: http://eprints.manipal.edu/id/eprint/154219

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