Comparative pharmacology and abuse potential of oral dexamphetamine and lisdexamfetamine-A literature review.

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Human Psychopharmacology: Clinical and Experimental Pub Date : 2024-07-18 DOI:10.1002/hup.2910
Wolfgang Kämmerer
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引用次数: 0

Abstract

Objective: To compare the pharmacology and abuse potential of oral dexamphetamine and lisdexamfetamine (LDX).

Methods: A search of Medline and Embase was conducted to identify relevant articles for this literature review.

Results: Dexamphetamine and LDX, a prodrug of dexamphetamine, are indicated for the treatment of attention-deficit/hyperactivity disorder. It has been suggested that LDX may have a reduced potential for oral abuse compared to immediate-release dexamphetamine. As a prodrug, LDX has the same pharmacodynamic properties as dexamphetamine. A study in healthy adults showed that the pharmacokinetic profile of dexamphetamine following oral administration of LDX is essentially identical to that of an equimolar dose of dexamphetamine administered 1 h later. In addition, dexamphetamine produced subjective drug liking effects comparable to those produced by LDX. LDX showed linear dose proportional pharmacokinetics up to a dose of 250 mg, indicating a lack of overdose protection at supratherapeutic doses. Furthermore, the exposure to dexamphetamine released from LDX may be prolonged by the consumption of alkalizing agents.

Conclusions: The available evidence from pharmacodynamic, pharmacokinetic and abuse liability studies suggests a comparable potential for oral abuse of dexamphetamine and LDX.

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口服右旋苯丙胺和利眠宁的比较药理学和滥用潜力--文献综述。
目的比较口服右旋苯丙胺和利眠宁(LDX)的药理学和滥用潜力:方法:对 Medline 和 Embase 进行检索,为本文献综述确定相关文章:右旋苯丙胺和右旋苯丙胺原药 LDX 适用于治疗注意力缺陷/多动症。有观点认为,与速释右旋苯丙胺相比,LDX 的口服滥用可能性较低。作为一种原药,LDX 具有与右旋苯丙胺相同的药效学特性。一项针对健康成年人的研究表明,口服 LDX 后的右旋苯丙胺药代动力学特征与 1 小时后服用等摩尔剂量的右旋苯丙胺基本相同。此外,右旋苯丙胺产生的主观药物喜欢效应与LDX产生的效应相当。在 250 毫克剂量以下,LDX 显示出线性剂量比例药代动力学,表明在超治疗剂量时缺乏过量保护。此外,服用碱性药物可能会延长从 LDX 中释放的右苯丙胺的暴露时间:来自药效学、药代动力学和滥用责任研究的现有证据表明,右旋苯丙胺和LDX口服滥用的可能性相当。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal: -All aspects of clinical psychopharmacology- Efficacy and safety studies of novel and standard psychotropic drugs- Studies of the adverse effects of psychotropic drugs- Effects of psychotropic drugs on normal physiological processes- Geriatric and paediatric psychopharmacology- Ethical and psychosocial aspects of drug use and misuse- Psychopharmacological aspects of sleep and chronobiology- Neuroimaging and psychoactive drugs- Phytopharmacology and psychoactive substances- Drug treatment of neurological disorders- Mechanisms of action of psychotropic drugs- Ethnopsychopharmacology- Pharmacogenetic aspects of mental illness and drug response- Psychometrics: psychopharmacological methods and experimental design
期刊最新文献
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