Schüttler J, Stoeckel H, Wilms M, Schwilden H, Lauven P M
Anaesthesist. 1980 Dec;29(12):662-6.
An intravenous infusion scheme was established in five healthy volunteers on the basis of pharmacokinetic analysis as described by J.G. Wagner. Concentrations of etomidate in plasma were measured by gas chromatography after solvent extraction. The monitoring of EEG background activity was used for the correlation to the pharmacodynamic effect. The minimal plasma level producing an hypnotic effect was about 0.3 microgram/ml) etomidate. An infusion model was developed for a therapeutic plasma concentration of 0.5 microgram/ml etomidate. An initial fast constant-rate infusion (8 mg/min) was followed by an infusion with 0.8 mg/min for the entire duration of the application. The measured plasma levels coincided fairly well with the predicted steady state plasma levels and were accompanied by a distinct hypnotic effect in all volunteers.
根据J.G. 瓦格纳所述的药代动力学分析,为五名健康志愿者制定了静脉输注方案。溶剂萃取后,采用气相色谱法测定血浆中依托咪酯的浓度。通过监测脑电图背景活动来关联药效学效应。产生催眠作用的最低血浆水平约为0.3微克/毫升依托咪酯。建立了一个输注模型,以达到0.5微克/毫升依托咪酯的治疗血浆浓度。初始快速恒速输注(8毫克/分钟),随后在整个用药期间以0.8毫克/分钟的速度输注。测得的血浆水平与预测的稳态血浆水平相当吻合,并且所有志愿者均出现了明显的催眠作用。