Enhancement of oral bioavailability of atorvastatin calcium by self-emulsifying drug delivery systems (SEDDS)

Pharmaceutical Development and Technology

Volumn 16, Issue 1, 2011, Pages 65-74

  Kadu, Pawan J ^a   Kushare, Sachin S ^a   Thacker, Dhaval D ^a   Gattani, Surendra G ^a  

^a R C PATEL INSTITUTE OF PHARMACEUTICAL EDUCATION AND RESEARCH   (India)

Author keywords

Atorvastatin calcium; Bioavailability enhancement; Self emulsifying drug delivery system; Triton induced hypercholesterolemic in vivo evaluation

Indexed keywords

ATORVASTATIN; DRUG VEHICLE; LIPID; TYLOXAPOL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; DRUG BIOAVAILABILITY; DRUG DELIVERY SYSTEM; DRUG DISTRIBUTION; DRUG FORMULATION; DRUG SCREENING; DRUG SOLUBILITY; DRUG STABILITY; HYPERCHOLESTEROLEMIA; HYPERLIPIDEMIA; LIPID BLOOD LEVEL; MALE; MICROEMULSION; NONHUMAN; PARTICLE SIZE; PRIORITY JOURNAL; RAT; ZETA POTENTIAL;

ADMINISTRATION, ORAL; ANIMALS; BIOLOGICAL AVAILABILITY; CHEMISTRY, PHARMACEUTICAL; DRUG DELIVERY SYSTEMS; DRUG STABILITY; EMULSIONS; HEPTANOIC ACIDS; HYDROXYMETHYLGLUTARYL-COA REDUCTASE INHIBITORS; LIPIDS; MALE; PARTICLE SIZE; PHASE TRANSITION; PYRROLES; RATS; SOLUBILITY; SURFACE PROPERTIES; VISCOSITY;

EID: 78651110531     PISSN: 10837450     EISSN: 10979867     Source Type: Journal    
DOI: 10.3109/10837450903499333     Document Type: Article

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