Literature DB >> 1907841

Ponalrestat does not cause a protein binding interaction with warfarin in diabetic patients.

R F Moulds1, R O Fullinfaw, R W Bury, W E Plehwe, N Jacka, K M McGrath, F I Martin.   

Abstract

Ponalrestat (Statil, ICI; Prodiax, Merck Sharp and Dohme) is an aldose reductase inhibitor which is highly protein bound. Ponalrestat markedly displaced warfarin from its protein binding in vitro at a concentration of 500 micrograms ml-1, but not at a concentration of 50 or 100 micrograms ml-1. Twelve diabetic patients (six males), age range 38-65 years, in receipt of chronic stable warfarin therapy, were given ponalrestat (600 mg daily) for 2 weeks in an open trial. A matching placebo tablet was administered for 1 week before and after the active treatment period. Patients were seen ten times (four times during the ponalrestat phase), and during the ponalrestat phase, plasma samples were also taken before and at 3 h after the daily dose of ponalrestat. At none of the visits was there any significant change in prothrombin ratio (INR), plasma total or unbound warfarin concentrations, or percentage protein binding of warfarin. No clinical complications of combination treatment were detected. The maximum ponalrestat concentration observed in the patients was approximately 100 micrograms ml-1. We conclude that no significant interaction between these drugs occurs at the doses of ponalrestat studied.

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Year:  1991        PMID: 1907841      PMCID: PMC1368588          DOI: 10.1111/j.1365-2125.1991.tb05601.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  10 in total

1.  [Diabetes mellitus and its degenerative complications: a prospective study of 4,400 patients observed between 1947 and 1973 (2nd part) (author's transl)].

Authors:  J Pirart
Journal:  Diabete Metab       Date:  1977-09

2.  Pharmacokinetic consequences of drug displacement from blood and tissue proteins.

Authors:  J J MacKichan
Journal:  Clin Pharmacokinet       Date:  1984-01       Impact factor: 6.447

3.  Prevention of defects of axonal transport and nerve conduction velocity by oral administration of myo-inositol or an aldose reductase inhibitor in streptozotocin-diabetic rats.

Authors:  J H Mayer; D R Tomlinson
Journal:  Diabetologia       Date:  1983-11       Impact factor: 10.122

4.  Plasma protein binding of warfarin: methodological considerations.

Authors:  D Mungall; Y Y Wong; R L Talbert; M H Crawford; J Marshall; D W Hawkins; T M Ludden
Journal:  J Pharm Sci       Date:  1984-07       Impact factor: 3.534

5.  [Diabetes mellitus and its degenerative complications: a prospective study of 4,400 patients observed between 1947 and 1973 (3rd and last part) (author's transl)].

Authors:  J Pirart
Journal:  Diabete Metab       Date:  1977-12

6.  Determination of warfarin in human plasma by high performance liquid chromatography and photodiode array detector.

Authors:  P M Ueland; G Kvalheim; P E Lønning; S Kvinnsland
Journal:  Ther Drug Monit       Date:  1985       Impact factor: 3.681

Review 7.  Clinical pharmacokinetics of oral anticoagulants.

Authors:  J G Kelly; K O'Malley
Journal:  Clin Pharmacokinet       Date:  1979 Jan-Feb       Impact factor: 6.447

8.  Properties of ICI 128,436, a novel aldose reductase inhibitor, and its effects on diabetic complications in the rat.

Authors:  D Stribling; D J Mirrlees; H E Harrison; D C Earl
Journal:  Metabolism       Date:  1985-04       Impact factor: 8.694

9.  Reduced glomerular sodium/potassium adenosine triphosphatase activity in acute streptozocin diabetes and its prevention by oral sorbinil.

Authors:  M P Cohen; A Dasmahapatra; E Shapiro
Journal:  Diabetes       Date:  1985-11       Impact factor: 9.461

10.  Human diabetic endoneurial sorbitol, fructose, and myo-inositol related to sural nerve morphometry.

Authors:  P J Dyck; W R Sherman; L M Hallcher; F J Service; P C O'Brien; L A Grina; P J Palumbo; C J Swanson
Journal:  Ann Neurol       Date:  1980-12       Impact factor: 10.422

  10 in total
  2 in total

Review 1.  Clinically significant drug interactions with the oral anticoagulants.

Authors:  M D Freedman; A G Olatidoye
Journal:  Drug Saf       Date:  1994-05       Impact factor: 5.606

Review 2.  Physiological and Pathological Roles of Aldose Reductase.

Authors:  Mahavir Singh; Aniruddh Kapoor; Aruni Bhatnagar
Journal:  Metabolites       Date:  2021-09-27
  2 in total

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