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氯米帕明每日一次口服给药期间血浆药物水平的时间进程。

Time course of plasma drug levels during once-daily oral administration of clomipramine.

作者信息

Burch J E, Shaw D M, Michalakeas A, Karajgi B, Roberts S G, Raddats M A

出版信息

Psychopharmacology (Berl). 1982;77(4):344-7. doi: 10.1007/BF00432768.

Abstract

Fourteen depressed in-patients were treated with 150 mg clomipramine (CLO) daily, given as one oral dose. Using a gas-chromatographic method, concentrations of CLO and desmethyl clomipramine (DMCLO) were determined in plasma samples taken at frequent intervals during 24 h. The plasma level of each compound 12 h after the dose correlated well with the average value in the same patient, calculated over the whole 24-h period. Levels at other times gave poorer correlations, and at 24 h it was particularly poor. Plasma DMCLO concentrations were usually maximum 4-6 h after the dose. The ratios of maximum to minimum levels averaged only 1.31 +/- 0.15 SD. Peak CLO levels occurred 3 or 4 h after the dose. Maximum; minimum ratios averaged 2.72 +/- 0.73 SD, contrasting with the much smaller fluctuations of plasma nortriptyline (NT) levels observed in patients given this drug once daily. The difference is not due to a shorter half-life of CLO, but to the absorption and/or distribution behaviour of the two drugs. Although not fully understood, this difference between tertiary and secondary amines appears to hold generally among the tricyclic antidepressants.

摘要

14名住院抑郁症患者每日口服150毫克氯米帕明(CLO)进行治疗。采用气相色谱法,在24小时内定期采集血浆样本,测定其中CLO和去甲氯米帕明(DMCLO)的浓度。给药后12小时各化合物的血浆水平与同一患者在整个24小时期间计算出的平均值相关性良好。其他时间的水平相关性较差,在24小时时尤其差。血浆DMCLO浓度通常在给药后4 - 6小时达到最高。最高水平与最低水平的比值平均仅为1.31±0.15标准差。CLO的峰值水平在给药后3或4小时出现。最高值与最低值的比值平均为2.72±0.73标准差,这与每日服用一次该药物的患者中观察到的血浆去甲替林(NT)水平波动小得多形成对比。这种差异并非由于CLO的半衰期较短,而是由于两种药物的吸收和/或分布行为。尽管尚未完全理解,但叔胺和仲胺之间的这种差异似乎在三环类抗抑郁药中普遍存在。

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