ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 0 مورد
نسخه الکترونیک
medimedia.ir

Pharmacokinetic properties of selected barbiturates

Pharmacokinetic properties of selected barbiturates
Drug Vd pKa Protein binding Half-life (parent drug, unless noted)*
Long-acting (>6 hours)
Phenobarbital 0.6 L/kg 7.3 48% 70 to 140 hours
Primidone 0.6 to 0.75 L/kg 12.3 <20%

Parent drug: 5 to 16 hours

Active metabolites:
  • Phenylethylmalonamide (PEMA): 16 to 50 hours
  • Phenobarbital: 70 to 140 hours
Intermediate-acting (2 to 6 hours)
Amobarbital 1 L/kg 7.84 40 to 60% 16 to 40 hours
Butalbital 0.8 L/kg 7.48 45% 35 to 88 hours
Short-acting (<2 hours)
Methohexital 1.1 L/kg 7.73 73% 1.6 to 3.9 hours
Pentobarbital 1 L/kg 8.1 45 to 70% 15 to 50 hours
Thiopental 4.4 L/kg 7.55 80% 9 to 11 hours
Overdose can saturate metabolic pathways and protein binding, thus prolonging duration of effect beyond predicted and increasing the fraction of unbound (ie, free and pharmacologically active) agent.

* The duration of clinical effect does not always correspond to the elimination half-life, but rather to rate of redistribution from the central nervous system. Highly lipid soluble and highly protein bound barbiturates (eg, thiopental, methohexital) redistribute quickly and have a short duration of effect despite long terminal elimination half-lives. Less lipid-soluble drugs with lower protein binding (eg, phenobarbital) have longer durations of effect.

¶ Butalbital is available in multi-ingredient preparations (ie, co-formulated with acetaminophen, aspirin, caffeine, and/or codeine).
References:
  1. Lexicomp. https://online.lexi.com/ (Accessed on December 4, 2023).
  2. PubChem. https://pubchem.ncbi.nlm.nih.gov/ (Accessed on December 4, 2023).
  3. The Human Metabolome Database. https://hmdb.ca/metabolites/ (Accessed on December 4, 2023).
Graphic 143593 Version 1.0

آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟