Results 111 to 120 of about 1,503 (160)

The impact of peritoneal dialysis on oxypurinol and urate elimination in people with gout

open access: yesNephrology
AbstractGout affects 15%–30% of individuals with advanced kidney disease. Allopurinol which is rapidly and extensively metabolised to an active metabolite, oxypurinol, is the most commonly prescribed urate‐lowering therapy. Oxypurinol is almost entirely eliminated by the kidneys (>95%) and has an elimination half‐life of 18–30 h in those with normal
Suetonia Palmer   +2 more
exaly   +4 more sources

The pharmacokinetics of oxypurinol in people with gout [PDF]

open access: yesBritish Journal of Clinical Pharmacology, 2012
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT• Response to allopurinol in patients with gout is often suboptimal due to large variability in pharmacokinetics.• The sources of the variability in oxypurinol pharmacokinetics have not been systematically identified and quantified.• A therapeutic target 15–23 mg l−1for oxypurinol concentrations has recently been
Sophie Stocker   +2 more
exaly   +7 more sources

Allopurinol and oxypurinol are hydroxyl radical scavengers [PDF]

open access: yesFEBS Letters, 1987
Allopurinol is a scavenger of the highly reactive hydroxyl radical (k 2 approx. 109 M−1s−1). One product of attack of hydroxyl radical upon allopurinol is oxypurinol, which is a major metabolite of allopurinol. Oxypurinol is a better hydroxyl radical scavenger than is allopurinol (k 2 approx.
Barry Halliwell   +2 more
exaly   +3 more sources

Effect of Oxypurinol on Renal Reperfusion Injury in the Rat

open access: yesRenal Failure, 1993
Oxygen-based free radicals produced by the enzyme xanthine oxidase may be involved in postischemic reperfusion injury. To determine whether oxypurinol, a xanthine oxidase inhibitor and the major metabolite of allopurinol, attenuates renal ischemic reperfusion injury, and, if so, to determine its most effective dose, oxypurinol 2.5, 5, 10 or 20 mg/kg BW
William F Finn, W F Finn
exaly   +3 more sources
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Oxypurinol attenuates ischemia-induced hippocampal damage in the gerbil

Brain Research Bulletin, 1989
Oxypurinol, an inhibitor of the enzyme xanthine oxidase, reduced ischemic hippocampal damage and the associated hypermotility in Mongolian gerbils. Cerebral ischemia was induced in unanesthetized gerbils by a bilateral 5-min occlusion of the carotid arteries.
J W Phillis, J W Phillis
exaly   +3 more sources

An allopurinol adherence tool using plasma oxypurinol concentrations

British Journal of Clinical Pharmacology, 2022
AbstractAimsThis study aimed to develop and evaluate an allopurinol adherence tool based on steady‐state oxypurinol plasma concentrations, allopurinol's active metabolite.MethodsPlasma oxypurinol concentrations were simulated stochastically from an oxypurinol pharmacokinetic model for allopurinol doses of 100‐800 mg daily, accounting for differences in
Natalia Smith‐Diaz   +6 more
openaire   +2 more sources

The population pharmacokinetics of allopurinol and oxypurinol in patients with gout

European Journal of Clinical Pharmacology, 2013
The aims of this study were to develop a population pharmacokinetic model for allopurinol and oxypurinol and to explore the influence of patient characteristics on allopurinol and oxypurinol pharmacokinetics.Data from 92 patients with gout and 12 healthy volunteers were available for analysis.
Daniel F B Wright   +2 more
exaly   +3 more sources

Clinical Pharmacokinetics and Pharmacodynamics of Allopurinol and Oxypurinol

Clinical Pharmacokinetics, 2007
Allopurinol is the drug most widely used to lower the blood concentrations of urate and, therefore, to decrease the number of repeated attacks of gout. Allopurinol is rapidly and extensively metabolised to oxypurinol (oxipurinol), and the hypouricaemic efficacy of allopurinol is due very largely to this metabolite.
Richard O, Day   +5 more
openaire   +2 more sources

Oxypurinol Protects Normothermic Ischemic Hearts

Journal of Cardiac Surgery, 1990
Rabbit hearts were mounted on a Langendorff apparatus and after measurement of baseline hemodynamic function exposed to 30 minutes normothermic arrest. Hearts were reperfused at 37 degrees C with buffer solution containing oxypurinol in different concentration: group II (0.01 mM), group III (0.1 mM), group IV (1 mM). Group I did not receive active drug
J, Bergsland   +4 more
openaire   +2 more sources

Allopurinol and oxypurinol in human breast milk

The Clinical Investigator, 1993
To pregnant or breast feeding women drugs should be given with caution. We report the case of a 5-week-old breast-fed infant whose mother was taking 300mg allopurinol/day for 4 weeks. Allopurinol and oxypurinol were detected by HPLC in maternal plasma and breast milk with a method first described here.
I, Kamilli, U, Gresser
openaire   +2 more sources

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