Everted gut sac model as a tool in pharmaceutical research: Limitations and applications

Journal of Pharmacy and Pharmacology

Volumn 64, Issue 3, 2012, Pages 326-336

  Alam, Mohd Aftab ^a   Al Jenoobi, Fahad Ibrahim ^a   Al Mohizea, Abdullah M ^a  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

Author keywords

drug interaction; drug transporter; everted sac; P glycoprotein

Indexed keywords

BETA LACTOGLOBULIN; BUTYRIC ACID; CHLORPROMAZINE DERIVATIVE; CREMOPHOR; CURCUMIN; EXCIPIENT; IMIPENEM; METHOCHLORPROMAZINE; MITOMYCIN C; NIMODIPINE; ORNIDAZOLE; POLOXAMER; POLYSORBATE 80; RIFAMPICIN; UNCLASSIFIED DRUG; VALPROIC ACID;

AGE; BIOLOGICAL MODEL; CHRONIC DRUG ADMINISTRATION; CONCENTRATION RESPONSE; DRUG ABSORPTION; DRUG EFFECT; DRUG FORMULATION; DRUG INHIBITION; DRUG MECHANISM; DRUG METABOLISM; DRUG PENETRATION; DRUG POTENTIATION; DRUG RESEARCH; DRUG TRANSPORT; IN VITRO STUDY; INTESTINE ABSORPTION; INTESTINE FUNCTION; NONHUMAN; PH MEASUREMENT; REVIEW; SCREENING TEST; SENSITIVITY ANALYSIS; SEX DIFFERENCE; SPECIES DIFFERENCE; TEMPERATURE SENSITIVITY; TISSUE DISTRIBUTION; TISSUE SPECIFICITY;

ANIMALS; BIOLOGICAL TRANSPORT; BIOMEDICAL RESEARCH; DRUG INTERACTIONS; HUMANS; INTESTINAL ABSORPTION; INTESTINAL MUCOSA; MODELS, BIOLOGICAL;

EID: 84857043007     PISSN: 00223573     EISSN: 20427158     Source Type: Journal    
DOI: 10.1111/j.2042-7158.2011.01391.x     Document Type: Review

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