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赖右苯丙胺二甲磺酸盐:前药递送、苯丙胺暴露及疗效持续时间。

Lisdexamfetamine Dimesylate: Prodrug Delivery, Amphetamine Exposure and Duration of Efficacy.

作者信息

Ermer James C, Pennick Michael, Frick Glen

机构信息

Shire, Wayne, PA, USA.

Shire, Basingstoke, UK.

出版信息

Clin Drug Investig. 2016 May;36(5):341-56. doi: 10.1007/s40261-015-0354-y.

Abstract

Lisdexamfetamine dimesylate (LDX) is a long-acting d-amphetamine prodrug used to treat attention-deficit/hyperactivity disorder (ADHD) in children, adolescents and adults. LDX is hydrolysed in the blood to yield d-amphetamine, and the pharmacokinetic profile of d-amphetamine following oral administration of LDX has a lower maximum plasma concentration (Cmax), extended time to Cmax (Tmax) and lower inter- and intra-individual variability in exposure compared with the pharmacokinetic profile of an equivalent dose of immediate-release (IR) d-amphetamine. The therapeutic action of LDX extends to at least 13 h post-dose in children and 14 h post-dose in adults, longer than that reported for any other long-acting formulation. Drug-liking scores for LDX are lower than for an equivalent dose of IR d-amphetamine, which may result from the reduced euphorigenic potential associated with its pharmacokinetic profile. These pharmacokinetic and pharmacodynamic characteristics of LDX may be beneficial in the management of symptoms in children, adolescents and adults with ADHD.

摘要

赖右苯丙胺二甲磺酸盐(LDX)是一种长效右旋苯丙胺前体药物,用于治疗儿童、青少年和成人的注意力缺陷多动障碍(ADHD)。LDX在血液中水解生成右旋苯丙胺,与等效剂量的速释(IR)右旋苯丙胺的药代动力学特征相比,口服LDX后右旋苯丙胺的药代动力学特征具有较低的最大血浆浓度(Cmax)、延长的达峰时间(Tmax)以及较低的个体间和个体内暴露变异性。LDX的治疗作用在儿童给药后至少持续13小时,在成人给药后持续1小时,比任何其他长效制剂报道的时间都长。LDX的药物喜好评分低于等效剂量的IR右旋苯丙胺,这可能是由于与其药代动力学特征相关的致欣快潜力降低所致。LDX的这些药代动力学和药效学特征可能有助于管理患有ADHD的儿童、青少年和成人的症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca2c/4823324/c115e8fd5218/40261_2015_354_Fig1_HTML.jpg

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