Jann M W, Saklad S R, Ereshefsky L, Richards A L, Harrington C A, Davis C M
Psychopharmacology (Berl). 1986;90(4):468-70. doi: 10.1007/BF00174062.
Plasma concentrations of haloperidol and its reduced metabolite (reduced haloperidol) were investigated in cigarette smokers (N = 23) and nonsmokers (N = 27). Steady-state plasma concentrations were obtained 12 h post bedtime dose. Haloperidol and reduced haloperidol concentrations were determined by RIA. Reduced haloperidol was separated by selective succinylation and liquid chromatography. Patients were clinically assessed with the Clinical Global Impression Scale (CGIS). Smokers had significantly lower haloperidol and reduced haloperidol plasma concentrations than nonsmokers (P less than 0.01, P less than 0.05). Clearance of haloperidol was significantly greater in smokers compared to nonsmokers (P = 0.0052). CGIS assessments did not show significant differences between smokers and nonsmokers. Plasma concentrations should be carefully monitored when patients either start or stop smoking.
对吸烟患者(N = 23)和非吸烟患者(N = 27)的血浆中氟哌啶醇及其还原代谢物(还原氟哌啶醇)浓度进行了研究。在睡前给药12小时后获得稳态血浆浓度。通过放射免疫分析法测定氟哌啶醇和还原氟哌啶醇浓度。还原氟哌啶醇通过选择性琥珀酰化和液相色谱法分离。采用临床总体印象量表(CGIS)对患者进行临床评估。吸烟者的氟哌啶醇和还原氟哌啶醇血浆浓度显著低于非吸烟者(P < 0.01,P < 0.05)。与非吸烟者相比,吸烟者中氟哌啶醇的清除率显著更高(P = 0.0052)。CGIS评估显示吸烟者和非吸烟者之间无显著差异。当患者开始或停止吸烟时,应仔细监测血浆浓度。