An excellent delivery system for improving the oral bioavailability of natural vitamin e in rats

AAPS PharmSciTech

Volumn 13, Issue 3, 2012, Pages 961-966

  Gong, Yinhua ^a   Wu, Yunkai ^b   Zheng, Chunli ^a   Fan, Liya ^c   Xiong, Fei ^d   Zhu, Jiabi ^a  

^a CHINA PHARMACEUTICAL UNIVERSITY   (China)

^b ANHUI MEDICAL UNIVERSITY   (China)

^c INNER MONGOLIA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^d SOUTHEAST UNIVERSITY   (China)

Author keywords

Key word: Antioxidation; Nanoemulsion; Natural vitamin E; Oral bioavailability

Indexed keywords

ALPHA TOCOPHEROL; ANTIOXIDANT; MALONALDEHYDE; SUPEROXIDE DISMUTASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; AREA UNDER THE CURVE; ARTICLE; CONTROLLED STUDY; DRUG BIOAVAILABILITY; DRUG DELIVERY SYSTEM; DRUG FORMULATION; EMULSION; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; MALE; MAXIMUM PLASMA CONCENTRATION; NANOEMULSION; NONHUMAN; PHYSICOCHEMICAL MODEL; PLASMA CONCENTRATION-TIME CURVE; PRIORITY JOURNAL; RAT; SINGLE DRUG DOSE; TIME TO MAXIMUM PLASMA CONCENTRATION;

ADMINISTRATION, ORAL; ANIMALS; ANTIOXIDANTS; BIOLOGICAL AVAILABILITY; DRUG DELIVERY SYSTEMS; MALE; RATS; RATS, SPRAGUE-DAWLEY; VITAMIN E;

EID: 84866110675     PISSN: None     EISSN: 15309932     Source Type: Journal    
DOI: 10.1208/s12249-012-9819-y     Document Type: Article

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