Pharmacokinetics, tissue distribution and relative bioavailability of geniposide-solid lipid nanoparticles following oral administration

Journal of Microencapsulation

Volumn 31, Issue 4, 2014, Pages 382-389

  Wang, Fugang ^a   Cao, Juan ^a   Hao, Jifu ^a   Liu, Ke ^a  

^a TAISHAN MEDICAL UNIVERSITY   (China)

Author keywords

Bioavailability; Geniposide; Geniposide SLNs; Pharmacokinetics; Tissue distribution

Indexed keywords

GENIPOSIDE; SOLID LIPID NANOPARTICLE; DRUG CARRIER; IRIDOID; LIPID; NANOPARTICLE;

ANIMAL TISSUE; AREA UNDER THE CURVE; ARTICLE; BRAIN; DRUG BIOAVAILABILITY; DRUG CLEARANCE; DRUG DELIVERY SYSTEM; DRUG DISTRIBUTION; DRUG HALF LIFE; HEART; KIDNEY; LIVER; LUNG; MAXIMUM PLASMA CONCENTRATION; NONHUMAN; RAT; SPLEEN; TIME TO MAXIMUM PLASMA CONCENTRATION; TISSUE DISTRIBUTION; ANIMAL; ANTIBODY SPECIFICITY; BIOAVAILABILITY; CHEMISTRY; DRUG EFFECTS; ORAL DRUG ADMINISTRATION; SPRAGUE DAWLEY RAT;

ADMINISTRATION, ORAL; ANIMALS; BIOLOGICAL AVAILABILITY; DRUG CARRIERS; IRIDOIDS; LIPIDS; NANOPARTICLES; ORGAN SPECIFICITY; RATS; RATS, SPRAGUE-DAWLEY;

EID: 84901349228     PISSN: 02652048     EISSN: 14645246     Source Type: Journal    
DOI: 10.3109/02652048.2013.863396     Document Type: Article

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