Harrison L I, Smallridge R C, Lasseter K C, Goldlust M B, Shamblen E C, Gam V W, Chang S F, Kvam D C
Am Rev Respir Dis. 1986 Aug;134(2):254-7. doi: 10.1164/arrd.1986.134.2.254.
The inhalation of atropine sulfate was investigated in a randomized, 4-period, rising-dose study. Atropine sulfate 2, 4, and 6 mg by inhalation, and atropine free base 1.67 mg (equivalent to 2.0 mg atropine sulfate) by intramuscular (IM) injection were given to 8 healthy, nonsmoking subjects. Serum atropine sulfate concentrations were monitored during an 8-h period by radioimmunoassay. Mean serum concentrations and area under the serum concentration-versus-time curves (AUC) increased as the inhaled dose increased. Peak concentrations (mean +/- SD) were 11.5 +/- 3.4, 16.4 +/- 6.2, and 18.0 +/- 3.1 ng/ml for the 2, 4, and 6 mg doses, and 11.7 +/- 2.5 ng/ml for the IM dose. The time to peak concentration for each dose was similar (mean, 0.8 to 1.9 h). The AUC ratio of the 2-mg inhaled and IM doses was 1.11 +/- 0.41. The observed bronchodilating, anticholinergic, and other pharmacologic effects were seen after all dose concentrations and were typical of atropine. This study showed that inhalation is an efficient way to administer atropine sulfate for systemic use.
在一项随机、4期、递增剂量研究中对硫酸阿托品吸入进行了调查。将2毫克、4毫克和6毫克硫酸阿托品通过吸入给予8名健康、不吸烟的受试者,并将1.67毫克(相当于2.0毫克硫酸阿托品)阿托品游离碱通过肌肉注射给予这些受试者。在8小时期间通过放射免疫分析法监测血清硫酸阿托品浓度。随着吸入剂量增加,平均血清浓度和血清浓度-时间曲线下面积(AUC)增加。2毫克、4毫克和6毫克剂量的峰值浓度(平均值±标准差)分别为11.5±3.4、16.4±6.2和18.0±3.1纳克/毫升,肌肉注射剂量的峰值浓度为11.7±2.5纳克/毫升。各剂量达到峰值浓度的时间相似(平均值,0.8至1.9小时)。2毫克吸入剂量与肌肉注射剂量的AUC比值为1.11±0.41。在所有剂量浓度后均观察到支气管舒张、抗胆碱能及其他药理作用,且均为阿托品的典型作用。该研究表明,吸入是全身应用硫酸阿托品的一种有效给药方式。