نتایج جستجو برای: pharmacokinetic

تعداد نتایج: 25201  

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2014
Khaled Abduljalil Theresa Cain Helen Humphries Amin Rostami-Hodjegan

Prediction accuracy of pharmacokinetic parameters is often assessed using prediction fold error, i.e., being within 2-, 3-, or n-fold of observed values. However, published studies disagree on which fold error represents an accurate prediction. In addition, "observed data" from only one clinical study are often used as the gold standard for in vitro to in vivo extrapolation (IVIVE) studies, des...

منوچهری, دکترسعید, ابوطالب, دکتراحسان ,

Abstract Introduction: Bioequivalence studies are the most important way of evaluating the quality and efficacy of pharmaceutical formulations. In a bioequivalence study, the rate and extent of drug absorption into the general circulation is measured and the pharmacokinetic parameters should be calculated and statistically evaluated for the reference and test products. Pharmacokinetic paramete...

A Aboofazeli A Shafaati

The pharmacokinetic parameters of domestic and imported ranitidine hydrochloride tablets (Ranitidine, formulated and manufactured by Kharazmi Pharmaceuticals, Iran, and Zantac ? manufactured by Glaxo, UK) were measured in 14 healthy subjects following oral administration of a single 300-mg dose of each brand and compared for bioequivalence evaluation. The pharmaceutical equivalency of both fo...

A Aboofazeli A Shafaati

The pharmacokinetic parameters of domestic and imported ranitidine hydrochloride tablets (Ranitidine, formulated and manufactured by Kharazmi Pharmaceuticals, Iran, and Zantac ? manufactured by Glaxo, UK) were measured in 14 healthy subjects following oral administration of a single 300-mg dose of each brand and compared for bioequivalence evaluation. The pharmaceutical equivalency of both fo...

Journal: :iranian journal of basic medical sciences 0
katayoun derakhshandeh nano drug delivery research center, kermanshah university of medical sciences, kermanshah, iran department of pharmaceutics, school of pharmacy, hamadan university of medical sciences, hamadan, iran moin karimi department of pharmaceutics, school of pharmacy, hamadan university of medical sciences, hamadan, iran abbas hemati azandaryani department of pharmaceutics, school of pharmacy, hamadan university of medical sciences, hamadan, iran gholamreza bahrami department of pharmacology and toxicology, school of pharmacy, kermanshah university of medical sciences, kermanshah kiumras ghanbari department of pharmacology and toxicology, school of pharmacy, kermanshah university of medical sciences, kermanshah

objective(s): the purpose of the current study was to assess the feasibility of microspheres from biocompatible polymer for oral bioavailability (ba) enhancement of potent sulfonamide- type loop diuretic- furosemide - which used in the treatment of congestive heart failure, caused edema, cirrhosis, renal disease and as an adjunct in acute pulmonary edema. the comparatively poor and inconstant b...

Journal: :iranian journal of pharmaceutical sciences 0
hossein danafar school of pharmacy zanjan university mehrdad hamidi school of pharmacy zanjan university

a rapid and sensitive liquid chromatography–tandem mass spectrometry (lc-ms) method for the estimation of enalapril and enalaprilat in human plasma. detection of analytes was achieved by tandem mass spectrometry with electrospray ionization (esi) interface in positive ion mode was operated under the multiple-reaction monitoring mode. sample pretreatment involved in a one-step protein precipitat...

Journal: :iranian journal of pharmaceutical sciences 0
shiva moghtadaee biopharmaceutics and pharmacokinetics division, department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences,tehran, iran yalda hossein-zade ardakani biopharmaceutics and pharmacokinetics division, department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences,tehran, iran hoda lavasani biopharmaceutics and pharmacokinetics division, department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences,tehran, iran mohammadreza rouini biopharmaceutics and pharmacokinetics division, department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences,tehran, iran

imatinib is an orally administered tyrosine kinase inhibitor which inhibits the bcr-abl protein-tyrosine kinase with high selectivity. imatinib is rapidly absorbed from the gut, after oral intake and has an almost absolute bioavailability of 98%. the metabolism of imatinib is mediated by the cytochrome p450 (cyp) isoenzymes in the liver and gut wall. cgp74588 is a major active metabolite of ima...

Journal: :iranian journal of pharmaceutical sciences 0
sayed abolfazl mostafavi faculty of pharmacy and pharmaceutical sciences, isfahan university of medical sciences kianoosh dormiani farabi pharmaceutical company, isfahan, iran yahya khazaie farabi pharmaceutical company, isfahan, iran abbas azmian farabi pharmaceutical company, isfahan, iran mohammad reza zargarzadeh farabi pharmaceutical company, isfahan, iran

the pharmacokinetic properties of amoxicillin and clavulanic acid when used alone or in combination may be different and show interaction between these two agents that might decrease the absolute bioavailability of clavulanic acid. in an open, randomized, replicated latin square under fasting condition, pharmacokinetics of new formulations of amoxicillin/clavulanic acid were compared with a ref...

2017
Oluwaseun Egbelowo Charis Harley Byron Jacobs

We extend the nonstandard finite difference method of solution to the study of pharmacokinetic-pharmacodynamic models. Pharmacokinetic (PK) models are commonly used to predict drug concentrations that drive controlled intravenous (I.V.) transfers (or infusion and oral transfers) while pharmacokinetic and pharmacodynamic (PD) interaction models are used to provide predictions of drug concentrati...

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