Suppr超能文献

雷氯必利缓释胶囊在精神科患者中的耐受性和药代动力学开放性研究:一项加拿大研究。

An open study of tolerability and pharmacokinetics of raclopride extended release capsules in psychiatric patients: a Canadian study.

作者信息

Gendron A, Sirois G, Nair N P, Bloom D, Movin-Osswald G, Uppfeldt G

机构信息

Faculté de pharmacie, Université de Montréal, Québec, Canada.

出版信息

J Psychiatry Neurosci. 1995 Jul;20(4):287-96.

Abstract

The tolerability and pharmacokinetics of raclopride extended release (ER) capsules have been evaluated after a single oral dose and at steady state, with 3 different daily doses in 4 male patients requiring neuroleptic treatment. In this 3-week open study, the drug was administered to patients in increasing bid doses of 8 mg, 12 mg and 16 mg, respectively, for each 1-week treatment period, following a 1-week placebo washout. With this limited number of patients, assessments of clinical chemistry, hematology, cardiovascular variables and adverse symptoms suggest that raclopride is safe and well-tolerated in the group studied. The administration of repeated doses of raclopride showed linear pharmacokinetics based on parameter values which are either constant (effective elimination half-life, total plasma clearance, and dose-normalized area under the plasma concentration-time curve) or varying proportionally (trough plasma concentration, peak plasma concentration, average plasma concentration and the area under the plasma concentration-time curve for a dosage interval at steady state) with the doses. The linear 1-compartment open model with zero-order absorption was the most appropriate pharmacokinetic model describing the raclopride plasma concentration profile after a single 8 mg dose of raclopride ER capsules. The ER formulation reduced the fluctuation between peak and trough plasma drug concentrations which has been reported before with instant release dosage forms. In this study, the increase of plasma prolactin concentrations above the normal limit was transient and returned to normal levels. Although the plasma prolactin concentration tended to increase with the drug dose, no direct relationship between raclopride dose and prolactin plasma concentrations was found. The correlation of plasma prolactin response with the plasma raclopride concentration showed a low level of hysteresis.

摘要

在4名需要使用抗精神病药物治疗的男性患者中,单次口服雷氯必利缓释(ER)胶囊后及稳态时,以3种不同日剂量对其耐受性和药代动力学进行了评估。在这项为期3周的开放性研究中,经过1周的安慰剂洗脱期后,在每个为期1周的治疗期内,分别以递增的每日两次剂量8 mg、12 mg和16 mg给患者用药。由于患者数量有限,临床化学、血液学、心血管变量和不良症状的评估表明,在所研究的组中雷氯必利是安全且耐受性良好的。基于恒定(有效消除半衰期、总血浆清除率和血浆浓度-时间曲线下剂量标准化面积)或成比例变化(谷血浆浓度、峰血浆浓度、平均血浆浓度以及稳态时一个给药间隔的血浆浓度-时间曲线下面积)的参数值,重复给药雷氯必利显示出线性药代动力学。具有零级吸收的线性单室开放模型是描述单次口服8 mg雷氯必利ER胶囊后雷氯必利血浆浓度曲线的最合适药代动力学模型。ER制剂减少了之前速释剂型所报道的峰谷血浆药物浓度之间的波动。在本研究中,血浆催乳素浓度升高至正常上限以上是短暂的,并恢复到正常水平。虽然血浆催乳素浓度倾向于随药物剂量增加,但未发现雷氯必利剂量与催乳素血浆浓度之间存在直接关系。血浆催乳素反应与血浆雷氯必利浓度的相关性显示出低水平的滞后现象。

相似文献

本文引用的文献

5
A rating scale for extrapyramidal side effects.锥体外系副作用评定量表。
Acta Psychiatr Scand Suppl. 1970;212:11-9. doi: 10.1111/j.1600-0447.1970.tb02066.x.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验