Investigation of cannabidiol gastro retentive tablets based on regional absorption of cannabinoids in rats

被引:15
|
作者
Izgelov, Dvora [1 ]
Freidman, Michael [1 ]
Hoffman, Amnon [1 ]
机构
[1] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, Inst Drug Res, POB 12065, IL-91120 Jerusalem, Israel
关键词
Cannabinoids; Gastro retentive dosage forms; Controlled release; Regional absorption; Bioavailability; GASTROINTESTINAL-TRACT; DRUG-DELIVERY; DOSAGE FORMS; PHARMACOKINETICS; METFORMIN; SYSTEMS;
D O I
10.1016/j.ejpb.2020.05.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The cannabis plant has been widely researched for many therapeutic indications and found to be effective in many chronic conditions such as epilepsy, neuropathic or chronic pain and more. However, biased opinion against compounds of the plant, regulatory as well as compounding challenges have led to very few approved cannabinoid medicinal products. Those formulations which are approved are dosed several times a day, creating an unmet need for controlled release (CR) formulations of cannabinoids. Conventional CR formulations rely on prolonged absorption of the drug, including absorption from the colon. The purpose of this work is to investigate regional absorption of major cannabinoids THC and CBD from the colon and develop a suitable CR formulation. As hypothesized by researchers, THC and CBD have poor absorption from the colon compared to small intestine, suggesting that these compounds have a narrow absorption window. The suggested CR formulation examined in-vitro was a floating gastro retentive tablet based on egg albumin matrix, gas generating agents and surfactants. In-vivo investigation of CBD containing formulation in the freely moving rat model proved a prolonged absorption phase with a substantial increase in bioavailability compared to CBD solution. The findings of this paper answer a crucial question regarding potential application of CR dosage forms for cannabinoids and shed light on the regional intestinal absorption of these compounds. Ultimately, these results cement the way for future development of cannabinoid gastro retentive dosage forms.
引用
收藏
页码:229 / 235
页数:7
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