نتایج جستجو برای: pharmacokinetic parameters

تعداد نتایج: 599351  

Journal: :Antimicrobial agents and chemotherapy 1993
P Bourget H Fernandez V Quinquis C Delouis

The purpose of the present work was to study the pharmacokinetics and the protein binding (free fraction of the drug) of ceftriaxone (CTX) during pregnancy. Nine pregnant women (ages, 20 to 34 years) whose gestational ages ranged from 28 4/7 to 40 5/7 weeks were included. The diagnosis of infection was established in all cases; i.e., four women had chorioamnionitis and five women had pyelonephr...

Journal: :British journal of anaesthesia 1980
P Duvaldestin J Saada D Henzel G Saumon

Serum concentrations of fazadinium were measured in eight patients with cirrhosis and eight patients with total biliary obstruction who underwent abdominal surgery. A biexponential decay of the concentration was observed after a single i.v. injection of fazadinium. A two-compartment open model was used in the pharmacokinetic analysis of the data. The pharmacokinetic parameters were compared wit...

Journal: :Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements 2007
Iman Y Zaghloul Mahasen A Radwan Zinat H Aly

Cadmium has been associated with a number of adverse health effects but the impact of those effects on the pharmacokinetics of different drugs has not been investigated. Therefore, the pharmacokinetics of theophylline and ciprofloxacin were studied in cadmium-exposed and control rats (72 rats) following i.p. (6.5mg/kg) and p.o. (10mg/kg) administration, respectively. The third-generation offspr...

Journal: :Antimicrobial agents and chemotherapy 2011
Anna Annerberg Khin Maung Lwin Niklas Lindegardh Sakchai Khrutsawadchai Elizabeth Ashley Nicholas P J Day Pratap Singhasivanon Joel Tarning Nicholas J White François Nosten

Dihydroartemisinin-piperaquine is a new, highly effective, and well-tolerated combination treatment for uncomplicated falciparum malaria. The lipophilic characteristic of piperaquine suggests that administration together with fat will increase the oral bioavailability of the drug, and this has been reported for healthy volunteers. This pharmacokinetic study monitored 30 adult patients with unco...

Journal: :Polish journal of pharmacology 2002
Daria Orszulak-Michalak Jacek Owczarek Anna K Wiktorowska-Owczarek

The majority of antiarrhythmic drugs have very narrow therapeutic range, and they may cause some side effects at doses used for curing cardiac arrhythmias. These drugs may enter different interactions. Procainamide also may interact with other drugs. Also some other drugs may change pharmacokinetics of procainamide, for example the iv anesthetics influence on pharmacokinetic parameters of proca...

2017
Tianou Zhang Jing Shao Yike Gao Chi Chen Dan Yao Yi Fang Chu Jodee Johnson Chounghun Kang Dongwook Yeo Li Li Ji

Background Avenanthramides (AVA) are a group of diphenolic acids found only in oats that have anti-inflammatory and antioxidant effects. Absorption of AVAs in humans after oral consumption of natural oat flour is unknown. Objective To examine the appearance of AVAs in plasma after oral ingestion of oat cookies and estimate key pharmacokinetic parameters. Methods Male and female nonobese par...

Journal: :Antimicrobial agents and chemotherapy 1996
A Deslandes F Camus C Lacroix C Carbon R Farinotti

We compared the effects of nifedipine and diltiazem on the uptake of cefpodoxime proxetil (CP). The study was aimed at establishing the impact of increased mesenteric blood flow due to calcium channel blockers on passive transport. Twelve volunteers were given CP (200 mg) orally in a crossover design. The absorption, disposition, and elimination parameters of cefpodoxime were compared among the...

Journal: :Journal of animal science 2006
P J Ferre V Laroute J P Braun J Cazaux P L Toutain H P Lefebvre

Evaluation of skeletal muscle tolerance during development of new drug formulations for i.m. use is most often based on terminal methods performed in the target species after slaughtering. The objective of this study was to evaluate the effect of muscle damage on the pharmacokinetic parameters of the drug delivered into the muscle using an alternative, noninvasive method. Phenylbutazone (PBZ) w...

Journal: :Acta poloniae pharmaceutica 2010
Dorota Krasucka Cezary Jacek Kowalski

Pharmacokinetic studies are used to discover the fate of drug in the body. Knowledge of the route of removal, metabolic paths and the degree of efficiency are vital informations for the right dosage, which protects the body against potential drug toxicity (1ñ5). Amoxicillin (AMX) is a semisynthetic penicillin (2, 5, 6ñ8) belonging to aminopenicillin group with a wide range of bactericidal activ...

Journal: :Anesthesiology 1999
T D Egan S Kuramkote G Gong J Zhang S W McJames P L Bailey

BACKGROUND It is common clinical practice to administer reduced doses of opioid to patients suffering from hemorrhagic shock to minimize adverse hemodynamic consequences and to prevent prolonged opioid effect However, the scientific foundation supporting this practice is not well established. The aim of this study was to test the hypothesis that hemorrhagic shock alters both the distribution an...

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