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CANNABIDIOL DIFFUSION ACROSS HUMAN TRACHEO-BRONCHIAL TISSUE (EPIAIRWAY™) AND INTRANASAL ABSORPTION IN RATS.

Agu1, R., Valiveti1, S., Paudel1, K., and Klausner2, M., Hayden2, P. University of Kentucky College of Pharmacy, Lexington, KY; 2MatTek Corporation, Ashland, MA.
Abstract

Some cannabinoids are potentially useful in cancer symptom management to alleviate pain and control chemotherapy-induced nausea and vomiting. The drugs have also been shown to possess anticonvulsant, antianxiety/antipsychotic, and immuno-modulatory effects. The non-psychoactive cannabinoid, cannabidiol (CBD), is a clinical candidate for management of medical conditions where emesis and pain are prevalent. Considering the rapid onset of drug action following nasal administration, which sometimes superimposes intravenous (IV) doses, the nasal route appears to be a suitable route for systemic administration of cannabinoids. Therefore, a preclinical evaluation of CBD nasal permeation and the mechanism of its diffusion across the mucosa were completed.

Keywords

Cannabidiol, Cannabinoid, Drug delivery studies, EpiAirway, HEPES buffer, Intranasal (IN), Intravenous (IV), MTT, MTT ET-50 tissue viability assay, MTT assay, Mucocillary clearance, Mucosal tolerance, Mucous dilution, Mucous protection, Nasal absorption, Nasal mucosa, Permeability, Permeability coefficient, Permeation, Perripheral cannabinoid receptors, Pharmacokinetic, Rat nasal epithelium, Toxicity studies, Tracheal/Bronchial epithelial cells

Materials Tested

Cannabidiol

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