Comparative pharmacokinetic interactions of Quercetin and Rutin in rats after oral administration of European patented formulation containing Hipphophae rhamnoides and Co-administration of Quercetin and Rutin
ANIMAL EXPERIMENT;
AREA UNDER THE CURVE;
ARTICLE;
CONTROLLED STUDY;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG CLEARANCE;
DRUG STRUCTURE;
ELIMINATION HALF-LIFE;
ELIMINATION RATE CONSTANT;
HIPPHOPHAE RHAMNOIDES;
IN VIVO STUDY;
LIMIT OF QUANTITATION;
LIQUID CHROMATOGRAPHY;
MALE;
MASS SPECTROMETRY;
MAXIMUM PLASMA CONCENTRATION;
MEAN RESIDENCE TIME;
MEASUREMENT ACCURACY;
MEASUREMENT PRECISION;
NONHUMAN;
PLANT;
RAT;
SINGLE DRUG DOSE;
TIME TO MAXIMUM PLASMA CONCENTRATION;
VALIDATION STUDY;
ANIMAL;
BIOAVAILABILITY;
COMPARATIVE STUDY;
DRUG INTERACTION;
HIPPOPHAE;
MEDICINAL CHEMISTRY;
METABOLISM;
ORAL DRUG ADMINISTRATION;
PHYSIOLOGY;
PROCEDURES;
WISTAR RAT;
Pharmacodynamic interaction studies of Gingiko biloba with cilostazol and clopidogrel in healthy human subjects
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Drug-herb interaction among commonly used conventional medicines: A compendium for health care professionals
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Quantitative determiniation of isorhamnetin, quercetin and kaempferol in rat plasma by liquid chromatography with electron spray ionization tandem mass spectrometry and its application to the pharmacokinetic study of isorhamnetin
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Plant polyphenols exhibit lipoprotein-bond antioxidant activity using an in vitro oxidation model for heart disease
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Identificaiton of rutin deglycosylated metabolites produced by human intestinal bacteria using UPLC-Q TOF/MS
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Yang J et al (2012) Identificaiton of rutin deglycosylated metabolites produced by human intestinal bacteria using UPLC-Q TOF/MS. J Chromatogr B 898(1):95-100