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氯硝西泮经鼻内和颊部给药后的吸收情况。

Absorption of clonazepam after intranasal and buccal administration.

作者信息

Schols-Hendriks M W, Lohman J J, Janknegt R, Korten J J, Merkus F W, Hooymans P M

机构信息

Department of Clinical Pharmacy and Toxicology, Maasland Hospital, Sittard, The Netherlands.

出版信息

Br J Clin Pharmacol. 1995 Apr;39(4):449-51. doi: 10.1111/j.1365-2125.1995.tb04476.x.

Abstract

Serum concentrations of clonazepam after intranasal, buccal and intravenous administration were compared in a cross-over study in seven healthy male volunteers. Each subject received a 1.0 mg dose of clonazepam intranasally and buccally and 0.5 mg intravenously. A Cmax of 6.3 +/- 1.0 ng ml-1 (mean; +/- s.d.) was measured 17.5 min (median) (range 15-20 min) after intranasal administration. A second peak (4.6 +/- 1.3 ng ml-1) caused by oral absorption was seen after 1.7 h (range 0.7-3.0 h). After buccal administration a Cmax of 6.0 +/- 3.0 ng ml-1 was measured after 50 min (range 30-90 min) with a second peak of 6.5 +/- 2.5 ng ml-1 after 3.0 h (range 2.0-4.0 h). Two minutes after i.v. injection of 0.5 mg clonazepam the serum concentration was 27 +/- 18 ng ml-1. It is concluded that intranasal clonazepam is an alternative to buccal administration. However, the Cmax of clonazepam after intranasal administration is not high enough to recommend the intranasal route as an alternative to intravenous injection.

摘要

在一项针对7名健康男性志愿者的交叉研究中,比较了氯硝西泮经鼻内、口腔和静脉给药后的血清浓度。每位受试者经鼻内和口腔分别接受1.0毫克氯硝西泮剂量,静脉注射接受0.5毫克剂量。经鼻内给药后17.5分钟(中位数)(范围15 - 20分钟)测得最大血药浓度(Cmax)为6.3±1.0纳克/毫升(平均值;±标准差)。口服吸收导致的第二个峰值(4.6±1.3纳克/毫升)在1.7小时后出现(范围0.7 - 3.0小时)。口腔给药后,50分钟(范围30 - 90分钟)测得Cmax为6.0±3.0纳克/毫升,3.0小时后(范围2.0 - 4.0小时)出现第二个峰值6.5±2.5纳克/毫升。静脉注射0.5毫克氯硝西泮两分钟后,血清浓度为27±18纳克/毫升。结论是经鼻内氯硝西泮可作为口腔给药的替代方式。然而,经鼻内给药后氯硝西泮的Cmax不够高,不足以推荐经鼻内途径作为静脉注射的替代方式。

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