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一种通用沙丁胺醇定量气雾剂的评估:气雾剂预充的重要性。

Evaluation of a generic albuterol metered-dose inhaler: importance of priming the MDI.

作者信息

Blake K V, Harman E, Hendeles L

机构信息

College of Pharmacy, Division of Pediatric Pulmonary Disease, University of Florida, Gainesville.

出版信息

Ann Allergy. 1992 Feb;68(2):169-74.

PMID:1739192
Abstract

Since the patent on albuterol metered-dose inhalers (MDI) expired in 1989, several manufacturers have developed generic products. In order to determine whether one generic albuterol MDI is equivalent to a reference product (Ventolin MDI), we compared the relative efficacy of two puffs (180 micrograms) of each inhaler in 17 intermittent or mild chronic adult asthmatics (FEV1 48% to 77% predicted) in a randomized, single-blind, crossover manner. The test dose was the first two puffs out of each canister. Pulmonary function was measured before each test dose and at frequent intervals over eight hours. Baseline FEV1 values on both study days were within 20%. The mean +/- SD peak effect was 80.5 +/- 15.5% of maximum achievable improvement in FEV1 after the generic compared with 92.2 +/- 8.8% after Ventolin (P = .006). The area under the curve (AUC) for this same measurement during the first four hours was 242 +/- 75%.hr-1 after the generic compared with 297 +/- 40%.hr-1 after Ventolin, a mean difference of 19% (P = .002). The study was then repeated with the MDI primed prior to the test dose (ie, two puffs were first discharged into a waste basket) in subjects willing to return for re-study (n = 11). There was no significant difference in AUC in the second study: 215 +/- 77%.hr-1 after generic and 228 +/- 82%.hr-1 after Ventolin (P = .65); however, there was only a 35% chance of detecting a 20% difference in AUC with this sample size. These data indicate that, without priming, an MDI may deliver less drug, and thereby less therapeutic effect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

自沙丁胺醇定量吸入器(MDI)的专利在1989年到期后,几家制造商已开发出通用产品。为了确定一种通用沙丁胺醇MDI是否等同于一种参比产品(万托林MDI),我们以随机、单盲、交叉的方式比较了17名间歇性或轻度慢性成年哮喘患者(预计第一秒用力呼气量[FEV1]为48%至77%)使用每种吸入器两喷(180微克)后的相对疗效。测试剂量为每个药罐的前两喷。在每次测试剂量前以及随后8小时内频繁测量肺功能。两个研究日的基线FEV1值相差在20%以内。通用产品使用后FEV1的平均±标准差峰值效应为最大可达到改善的80.5±15.5%,而使用万托林后为92.2±8.8%(P = 0.006)。通用产品使用后前4小时该测量值的曲线下面积(AUC)为242±75%·小时-1,万托林使用后为297±40%·小时-1,平均差异为19%(P = 0.002)。然后,在愿意返回重新研究的受试者(n = 11)中,在测试剂量前对MDI进行预充(即先向废纸篓喷出两喷)后重复该研究。在第二项研究中AUC无显著差异:通用产品使用后为215±77%·小时-1,万托林使用后为228±82%·小时-1(P = 0.65);然而,以此样本量检测到AUC有20%差异的可能性仅为35%。这些数据表明,如果不进行预充,MDI可能递送较少的药物,从而产生较小的治疗效果。(摘要截短为250字)

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