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新型长效抗毒蕈碱支气管扩张剂Ba 679 Br:慢性阻塞性肺疾病的剂量递增初步研究

Ba 679 Br, a new long-acting antimuscarinic bronchodilator: a pilot dose-escalation study in COPD.

作者信息

Maesen F P, Smeets J J, Costongs M A, Wald F D, Cornelissen P J

机构信息

Dept of Respiratory Diseases, De Wever Hospital, Heerlen, The Netherlands.

出版信息

Eur Respir J. 1993 Jul;6(7):1031-6.

PMID:8370429
Abstract

Preclinical studies with Ba 679 Br have demonstrated a significantly longer duration of action than ipratropium bromide. Following inhalation of single doses, no systemic antimuscarinic effects were noted at doses likely to be bronchodilating in man. The objective of the present pilot-study of Ba 679 Br was to establish the dose-range for its bronchodilatory activity in a small number of chronic obstructive pulmonary disease (COPD) patients, before initiating a formal dose- and time-response study. Employing an open cross-over design, the efficacy of Ba 679 Br was tested, following single inhalational administration of five doses of increasing magnitude on separate days in six patients with COPD. A piezoelectric crystal was used, in order to nebulize an aqueous solution into a mist suitable for inhalation. There was a mean increase in forced expiratory volume in one second (FEV1) of 36% 30 min after inhaling ipratropium bromide 40 micrograms. Pulmonary function tests (FEV1, and specific airways conductance (sGaw)) were performed, at regular time intervals up to 24 h after test drug inhalation. The bronchodilatory activity of Ba 679 Br appeared to be dose-related in the dose-range tested (10-160 micrograms). A peak response was reached in 1.5-2 h, and persisted for 10-15 h in the majority of patients with return to baseline FEV1 approximately 19 h after dosing. No changes in physical examination, electrocardiogram (ECG) and laboratory safety tests from predose values were noted, and no serious adverse events were reported by the patients.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

Ba 679 Br的临床前研究表明,其作用持续时间比异丙托溴铵显著更长。单次吸入给药后,在对人体可能具有支气管扩张作用的剂量下,未观察到全身抗毒蕈碱作用。本Ba 679 Br初步研究的目的是,在启动正式的剂量和时间反应研究之前,确定其在少数慢性阻塞性肺疾病(COPD)患者中的支气管扩张活性剂量范围。采用开放交叉设计,在6例COPD患者中,于不同日期单次吸入五剂递增剂量的Ba 679 Br后,测试其疗效。使用压电晶体将水溶液雾化成适合吸入的雾状。吸入40微克异丙托溴铵后30分钟,一秒用力呼气量(FEV1)平均增加36%。在吸入测试药物后长达24小时的定期时间间隔内进行肺功能测试(FEV1和比气道传导率(sGaw))。在测试的剂量范围(10 - 160微克)内,Ba 679 Br的支气管扩张活性似乎与剂量相关。大多数患者在1.5 - 2小时达到峰值反应,并持续10 - 15小时,给药后约19小时FEV1恢复到基线水平。未观察到体格检查、心电图(ECG)和实验室安全测试相对于给药前值有变化,患者也未报告严重不良事件。(摘要截短于250字)

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