Literature DB >> 16867166

Disposition of valproic acid in self-poisoned adults.

Jolanta Wilimowska1, Ewa Florek, Wojciech Piekoszewski.   

Abstract

Acute intoxication with valproic acid is increasingly being observed in clinical practice. In Poland, such intoxication frequently occurs as a result of mixing different drugs or alcohol. We studied the pharmacokinetics of valproic acid in five intoxicated patients. Apart from valproic acid, barbiturates, chlorprotixene, tricyclic antidepressants, tetrahydrocannabinols and alcohol were detected and measured. The absorption of the drug was rapid and the maximum concentration was observed after the period of 3.5-5.6 hr. The lowering of the valproic acid level in plasma was biphasic, with terminal half-life ranging between 8.8-30.9 hr. The calculated apparent volume of distribution was 0.17-0.72 l/kg and could be affected by varied levels of doses as well as time of drug intake (data from interviews of patients) used for calculation and reduction in plasma protein binding at higher concentration of valproic acid. Frequent multiple drug poisonings oblige toxicological laboratories not only to monitor valproic acid concentration in serum, but also to perform the toxicological screenings.

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Year:  2006        PMID: 16867166     DOI: 10.1111/j.1742-7843.2006.pto_417.x

Source DB:  PubMed          Journal:  Basic Clin Pharmacol Toxicol        ISSN: 1742-7835            Impact factor:   4.080


  2 in total

1.  Valproic acid for the treatment of hemorrhagic shock: a dose-optimization study.

Authors:  John O Hwabejire; Jennifer Lu; Baoling Liu; Yongqing Li; Ihab Halaweish; Hasan B Alam
Journal:  J Surg Res       Date:  2013-10-05       Impact factor: 2.192

2.  Sensitizing primary acute lymphoblastic leukemia to natural killer cell recognition by induction of NKG2D ligands.

Authors:  Laura Jardine; Sophie Hambleton; Venetia Bigley; Sarah Pagan; Xiao-Nong Wang; Matthew Collin
Journal:  Leuk Lymphoma       Date:  2012-09-08
  2 in total

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