The novel formulation design of self-emulsifying drug delivery systems (SEDDS) type O/W microemulsion III: the permeation mechanism of a poorly water soluble drug entrapped O/W microemulsion in rat isolated intestinal membrane by the Ussing chamber method.

Drug metabolism and pharmacokinetics

Volumn 21, Issue 1, 2006, Pages 45-53

  Araya, Hiroshi ^a   Tomita, Mikio ^a   Hayashi, Masahiro ^a  

^a CHUGAI PHARMACEUTICAL CO LTD   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCYSTEINE; DRUG; IBUPROFEN; MUCIN; NONSTEROID ANTIINFLAMMATORY AGENT; TAUROCHOLIC ACID;

ANIMAL; ARTICLE; CELL MEMBRANE PERMEABILITY; CHEMISTRY; DIFFUSION CHAMBER; DRUG DELIVERY SYSTEM; DRUG DESIGN; DRUG EFFECT; DRUG FORMULATION; EMULSION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; IN VITRO STUDY; INTESTINE; MALE; MASS SPECTROMETRY; MEMBRANE; METABOLISM; MICELLE; PERMEABILITY; RAT; SPRAGUE DAWLEY RAT;

ACETYLCYSTEINE; ANIMALS; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; CELL MEMBRANE PERMEABILITY; CHEMISTRY, PHARMACEUTICAL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DIFFUSION CHAMBERS, CULTURE; DRUG COMPOUNDING; DRUG DELIVERY SYSTEMS; DRUG DESIGN; EMULSIONS; IBUPROFEN; INTESTINES; MALE; MASS SPECTROMETRY; MEMBRANES; MICELLES; MUCINS; PERMEABILITY; PHARMACEUTICAL PREPARATIONS; RATS; RATS, SPRAGUE-DAWLEY; TAUROCHOLIC ACID;

EID: 33645986146     PISSN: 13474367     EISSN: None     Source Type: Journal    
DOI: 10.2133/dmpk.21.45     Document Type: Article

References (0)