نتایج جستجو برای: diclofenac residues

تعداد نتایج: 91305  

Journal: :Molecules 2017
Gergely Zachár Naved I K Deshmukh Andrea Petróczi Andrea D Székely Iltaf Shah James Barker Declan P Naughton

In vitro studies show that diclofenac inhibits enzymatic steroid glucuronidation. This study was designed to investigate the influence of diclofenac on the excretion of stanozolol and 3'-hydroxystanozolol via analyses in hair, blood and urine in vivo in a rat study. Brown Norway rats were administered with stanozolol (weeks 1-3) and diclofenac (weeks 1-6). Weekly assessment of steroid levels in...

2011
Christer B. Aakeröy Angela B. Grommet John Desper

In the pharmaceutical industry, co-crystals are becoming increasingly valuable as crystalline solids that can offer altered/improved physical properties of an active pharmaceutical ingredient (API) without changing its chemical identity or biological activity. In order to identify new solid forms of diclofenac-an analgesic with extremely poor aqueous solubility for which few co-crystal structur...

Journal: :JPMA. The Journal of the Pakistan Medical Association 1998
I A Jokhio K A Siddiqui T Waraich M Abbas A Ali

A comparative, multi-centre study, was conducted during June to December, 1996 to evaluate the efficacy and tolerance of Ketoprofen 100 mg Enteric Coated (EC) tablet and 100 mg intra-muscular injection; with that of Diclofenac Sodium 50 mg tablet and 75 mg intra-muscular injection in acute rheumatic and traumatic disorders. Total of 180 patients (90 per drug), were studied, 82 men and 98 women,...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2009
Jurjen S Lagas Cornelia M M van der Kruijssen Koen van de Wetering Jos H Beijnen Alfred H Schinkel

Diclofenac is an important analgesic and anti-inflammatory drug, widely used for treatment of postoperative pain, rheumatoid arthritis, and chronic pain associated with cancer. Consequently, diclofenac is often used in combination regimens and undesirable drug-drug interactions may occur. Because many drug-drug interactions may occur at the level of drug transporting proteins, we studied intera...

Journal: :The Journal of General Physiology 2005
Ya-Chin Yang Chung-Chin Kuo

The Na+ channel is the primary target of anticonvulsants carbamazepine, phenytoin, and lamotrigine. These drugs modify Na+ channel gating as they have much higher binding affinity to the inactivated state than to the resting state of the channel. It has been proposed that these drugs bind to the Na+ channel pore with a common diphenyl structural motif. Diclofenac is a widely prescribed anti-inf...

2016
Sandra Jerkovic Gulin Anca Chiriac

Allergic contact dermatitis is an immune-mediated antigen-specific skin reaction to an allergenic chemical that corresponds to a delayed-type hypersensitivity response (type IV reaction). Allergic contact dermatitis should be suspected when skin lesions are localized to the site of previous applications of the culprit drug. Lesions appear after re-exposure in susceptible persons, with delayed o...

Journal: :مجله بین المللی علوم آزمایشگاهی 0
mohammad hossein dashti-r mohammad davud qane farzane shefaie mohammadreza nazemian yazdu seyyed majid bagheri

backgrounds and aims: cinnamomum zeylanicum is a medicinal herb used in iranian traditional medicine as an analgesic spice, which its analgesic effect has been experimentally confirmed. thus, this study was conducted to compare the antinociceptive effect of cinnamon essential oil (ceo) with those of morphine and diclofenac in mice. materials and methods: 80 male albino mice were selected and ra...

Journal: :the iranian journal of pharmaceutical research 0
esmaeil akbari department of physiology and pharmacology, school of medicine, mazandaran university of medical sciences, sari, iran. ebrahim mirzaei school of pharmacy, mazandaran university of medical sciences, sari, iran. naghi shahabi majd department of physiology and pharmacology, school of medicine, mazandaran university of medical sciences, sari, iran.

this study investigates the effectiveness of the antinociceptive effects of diclofenac, an nsaid, on the nociceptive behavior of morphine-treated rats on formalin test.rats were treated with morphine-containing drinking water for twenty one days, which induced morphine dependence. the antinociceptive effects of 8, 16, and 32 mg/kg doses of diclofenac were then evaluated and compared with distil...

Journal: :Acta biochimica Polonica 2015
Monika Nowrotek Aleksandra Ziembińska-Buczyńska Korneliusz Miksch

Pharmaceutical substances and their residues are increasingly present in the environment. Therefore, attempts at their removal are made by using different processes. Increasingly important among these processes are those modeled on natural phenomena which occur in wetland ecosystems, called technical scale constructed wetlands. Microbial degradation is an important process in these constructed ...

Journal: :British medical journal 1984
M Broggini E Corbetta E Grossi C Borghi

We studied 30 consecutive outpatients (14 men and 16 women; mean (SD) age 46 (11-8) years) with gallstone disease, confirmed by ultrasonography or radiography or at operation, who complained of biliary colic. Patients were randomly treated under double blind conditions with either 75 mg diclofenac sodium given intramuscularly or placebo and were followed up for 24 hours. All patients had given ...

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