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在与抗胆碱能药物同时治疗期间奋乃静及其主要代谢物的血浆水平。

Plasma levels of perphenazine and its major metabolites during simultaneous treatment with anticholinergic drugs.

作者信息

Hansen L B, Elley J, Christensen T R, Larsen N E, Naestoft J, Hvidberg E F

出版信息

Br J Clin Pharmacol. 1979 Jan;7(1):75-80. doi: 10.1111/j.1365-2125.1979.tb00900.x.

Abstract
  1. A gas chromatographic method was applied to study plasma levels of perphenazine (PPZ) and its major metabolites in man before and during simultaneous antiparkinson treatment. Twenty-six psychotic patients received various forms of PPZ administration as well as antiparkinson drugs. 2. Biperidine (5 mg) was administered intravenously to each of five patients, who 5 days earlier had had a single dose of PPZ-enanthate i.m. No significant alterations in plasma concentrations of PPZ were observed. 3. In fourteen patients receiving oral PPZ treatment the plasma levels of PPZ and its metabolites did not deviate significantly from controls after addition of biperidine or orphenadine given for 3 weeks in fixed oral doses. 4. The ratio between PPZ plasma concentration measured 4 and 7 h after the morning dose was not affected by concomitant antiparkinson therapy. 5. It is concluded that no clinically relevant pharmacokinetic interaction takes place between PPZ and two generally used antiparkinson drugs during steady-state conditions in psychotic patients.
摘要
  1. 采用气相色谱法研究了在帕金森病同步治疗前及治疗期间人体中奋乃静(PPZ)及其主要代谢产物的血浆水平。26例精神病患者接受了各种形式的PPZ给药以及抗帕金森病药物治疗。2. 对5例患者静脉注射了5mg比哌立登,这5例患者在5天前曾肌肉注射过单剂量的庚酸奋乃静。未观察到PPZ血浆浓度有明显变化。3. 在14例接受口服PPZ治疗的患者中,给予固定口服剂量的比哌立登或邻甲苯海明3周后,PPZ及其代谢产物的血浆水平与对照组相比无明显差异。4. 早晨服药后4小时和7小时测得的PPZ血浆浓度之比不受同步抗帕金森病治疗的影响。5. 得出的结论是,在精神病患者的稳态条件下,PPZ与两种常用的抗帕金森病药物之间未发生临床上相关的药代动力学相互作用。

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