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普罗替林血药浓度的药代动力学方面

Pharmacokinetic aspects of protriptyline plasma levels.

作者信息

Moody J P, Whyte S F, MacDonald A J, Naylor G J

出版信息

Eur J Clin Pharmacol. 1977;11(1):51-6. doi: 10.1007/BF00561788.

Abstract

Plasma levels of protriptyline have been determined in 30 patients undergoing antidepressant therapy. After 3 1/2 weeks treatment at dosage levels of 40 mg/day, protriptyline plasma levels ranged from 430 to 1430 nmol/l. During this period only two-thirds of the subjects had definitely achieved asymptotic concentrations. Single dose studies in 5 volunteers suggest that the volume of distribution of protriptyline shows little intersubject variation. The half life of the drug, however, may vary appreciably from subject to subject, ranging from 54 to 198 h. The effects of two sedatives on mean protriptyline plasma levels have been determined. Mean plasma levels for nitrazepam recipients are indistinguishable from those for patients receiving no night sedation. The mean plasma levels for a group of patients receiving sodium amylobarbitone were significantly reduced. The problems of choice and early adjustment of dosages in order to achieve satisfactory plasma levels is discussed. For practical purposes it is suggested that early values may be of predictive significance in allowing early dosage adjustments to be made.

摘要

已对30名接受抗抑郁治疗的患者测定了普罗替林的血浆水平。在以40毫克/天的剂量水平治疗3.5周后,普罗替林血浆水平在430至1430纳摩尔/升之间。在此期间,只有三分之二的受试者达到了稳定浓度。对5名志愿者进行的单剂量研究表明,普罗替林的分布容积个体间差异不大。然而,该药物的半衰期个体间可能有明显差异,范围为54至198小时。已测定了两种镇静剂对普罗替林平均血浆水平的影响。接受硝西泮的患者的平均血浆水平与未接受夜间镇静的患者的平均血浆水平无明显差异。一组接受戊巴比妥钠的患者的平均血浆水平显著降低。讨论了为达到满意的血浆水平而进行剂量选择和早期调整的问题。出于实际目的,建议早期值在允许进行早期剂量调整方面可能具有预测意义。

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