Brain Targeted Intranasal Zaleplon Solid Dispersion in Hydrophilic Carrier System; 23 Full Factorial Design and In-vivo Determination of GABA Neurotransmitter.

Brain Targeted Intranasal Zaleplon Solid Dispersion in Hydrophilic Carrier System; 23 Full Factorial Design and In-vivo Determination of GABA Neurotransmitter.

Drug Dev Ind Pharm. 2017 Dec 13;:1-25

Authors: Abd-Elrasheed E, Nageeb El-Helaly S, El-Ashmoony MM, Salah S

Abstract
Intranasal Zaleplon solid dispersion was formulated to enhance the solubility, bioavailability and deliver an effective therapy. Zaleplon belongs to Class II drugs, and undergoes extensive first-pass metabolism after oral absorption exhibiting 30% bioavailability. A 23full factorial design was chosen for the investigation of solid dispersion formulations. The effects of different variables include drug to carrier ratio (1:1 and 1:2), carrier type (polyethylene glycol 4000 and poloxamer 407), and preparation method (solvent evaporation and freeze drying) on different dissolution parameters were studied. The dependent variables determined from the in-vitro characterization and their constraints were set as follows: minimum mean dissolution time, maximum dissolution efficiency and maximum percentage release. Numerical optimization was performed according to the constraints set based on the utilization of desirability functions. Differential Scanning Calorimetry, Infrared Spectroscopy, X-ray Diffraction and Scanning Electron Microscopy were performed. Ex-vivo estimation of nasal cytotoxicity and assessment of the gamma aminobutyric acid level in plasma and brain one hour after nasal SD administration in rabbits compared to the oral market product were conducted. The selected ZP-SD, with a desirability 0.9, composed of poloxamer 407 at drug to carrier ratio 1:2 successfully enhanced the bioavailability showing 44% increase in GABA concentration than the marketed tablets.

PMID: 29235903 [PubMed - as supplied by publisher]

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