Difference in absorption of the two structurally similar flavonoid glycosides, hyperoside and isoquercitrin, in rats

European Journal of Pharmaceutics and Biopharmaceutics

Volumn 59, Issue 3, 2005, Pages 549-555

  Chang, Qi ^a,c   Zuo, Zhong ^a   Chow, Moses S S ^a   Ho, Walter K K ^b  

^a and Hong Kong Branch of CAS Center for Excellence in Animal Evolution and Genetics   (Hong Kong)

^b CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^c INSTITUTE OF MEDICINAL PLANT DEVELOPMENT   (China)

Author keywords

Absorption; Flavonoids; Hyperoside; Isoquercitrin

Indexed keywords

DRUG METABOLITE; FLAVONOID GLYCOSIDE; HYPERIN; HYPERIN AGLYCONE; ISOQUERCITRIN; ISOQUERCITRIN AGLYCONE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BLOOD SAMPLING; CONTROLLED STUDY; DRUG ABSORPTION; DRUG BLOOD LEVEL; DRUG CONJUGATION; DRUG DETERMINATION; DRUG GLUCURONIDATION; DRUG HYDROLYSIS; DRUG STABILITY; DRUG STRUCTURE; GASTROINTESTINAL TRACT; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; IN VITRO STUDY; JUGULAR VEIN; MALE; NONHUMAN; RAT; STRUCTURE ANALYSIS; VENOUS BLOOD;

EID: 14844317357     PISSN: 09396411     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejpb.2004.10.004     Document Type: Article

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