Lawson G M, Hurt R D, Dale L C, Offord K P, Croghan I T, Schroeder D R, Jiang N S
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905, USA.
J Clin Pharmacol. 1998 Jun;38(6):502-9. doi: 10.1002/j.1552-4604.1998.tb05787.x.
As part of a clinical trial investigating the level of nicotine replacement with different doses of transdermal therapy for smoking cessation, peak and trough serum nicotine and plasma cotinine concentrations were measured in 70 subjects while they were actively smoking (baseline) and daily for 6 consecutive inpatient days while they were receiving transdermal nicotine. Subjects were randomly assigned to a daily 24-hour patch delivering a transdermal nicotine dose of 0, 11, 22, or 44 mg and stratified by self-reported smoking rate as either light (10-15 cigarettes per day), moderate (16-30 cigarettes per day), or heavy (>30 cigarettes per day). Steady-state concentrations of nicotine and cotinine were attained in 1 and 3 days, respectively, at all doses and were independent of baseline smoking rate. Mean percentage replacement of nicotine was calculated by dividing steady-state peak nicotine or cotinine concentrations by their respective baseline concentrations. Significant underreplacement occurred in subjects receiving the 11 mg/day patch regardless of baseline smoking rate. Underreplacement also occurred in moderate and heavy smokers receiving 22 mg/day and in light smokers at this same dose. Complete replacement occurred only in subjects receiving the 44 mg/day patch. These results have several implications for transdermal nicotine therapy. First, with the higher nicotine and cotinine levels observed with heavier smoking, it is inherent that one size does not fit all, and there is a need to consider more individualization of dosage for nicotine patch therapy. Second, there is substantial underreplacement with the 22 mg/day dose in moderate to heavy smokers and in some light smokers. Third, even with twice the usual dose (i.e., 44 mg/day), there was no accumulation of either nicotine or cotinine. Plasma cotinine levels after achievement of steady state (i.e., after 3 days of patch therapy) can be collected at any time and used to calculate percent replacement using baseline levels.
作为一项临床试验的一部分,该试验旨在研究不同剂量经皮疗法用于戒烟时的尼古丁替代水平,在70名受试者积极吸烟时(基线)以及在接受经皮尼古丁治疗的连续6个住院日期间每日测量其血清尼古丁和血浆可替宁的峰浓度和谷浓度。受试者被随机分配至每日24小时释放0、11、22或44毫克经皮尼古丁剂量的贴片,并按自我报告的吸烟率分层为轻度(每天10 - 15支香烟)、中度(每天16 - 30支香烟)或重度(每天>30支香烟)。在所有剂量下,尼古丁和可替宁的稳态浓度分别在1天和3天达到,且与基线吸烟率无关。尼古丁的平均替代百分比通过将稳态峰尼古丁或可替宁浓度除以其各自的基线浓度来计算。无论基线吸烟率如何,接受11毫克/天贴片的受试者均出现显著的替代不足。接受22毫克/天的中度和重度吸烟者以及该剂量下的轻度吸烟者也出现替代不足。仅接受44毫克/天贴片的受试者实现了完全替代。这些结果对经皮尼古丁治疗有若干启示。首先,随着吸烟量增加观察到更高的尼古丁和可替宁水平,显然一种剂量并不适用于所有人,有必要考虑尼古丁贴片治疗剂量的更多个体化。其次,中度至重度吸烟者以及一些轻度吸烟者使用22毫克/天剂量时存在大量替代不足。第三,即使使用通常剂量的两倍(即44毫克/天),尼古丁或可替宁均未蓄积。达到稳态后(即贴片治疗3天后)的血浆可替宁水平可在任何时间采集,并用于使用基线水平计算替代百分比。