茚达特罗
喇嘛
噻托溴铵
福莫特罗
药理学
医学
吸入器
支气管扩张剂
慢性阻塞性肺病
富马酸福莫特罗
沙美特罗
B2受体
毒蕈碱拮抗剂
支气管扩张
支气管扩张药
哮喘
麻醉
毒蕈碱乙酰胆碱受体
内科学
吸入
受体
布地奈德
肺
缓激肽
肺功能
作者
Paolo Montuschi,Giovanni Ciabattoni
摘要
Inhaled bronchodilators, including long-acting muscarinic receptor antagonists (LAMA) and long-acting β2-adrenoreceptor agonists (LABA), are the mainstay of pharmacological treatment of stable chronic obstructive pulmonary disease (COPD). Among approved LAMA, tiotropium bromide, glycopyrronium bromide, and umeclidinium bromide are administered once daily, whereas aclidinium bromide is administered every 12 h. New LAMA are under development for COPD. Among the approved LABA, indacaterol has a 24 h duration of action, whereas salmeterol and formoterol require twice-daily administration. New once-daily LABA, including vilanterol, olodaterol, milveterol, carmoterol, and abediterol, are in development. LAMA/LABA fixed dose combinations (FDCs) provide the convenience of two bronchodilators with different mechanism of action in a single inhaler. Indacaterol/glycopyrronium, umeclidinium/vilanterol, and olodaterol/tiotropium FDCs have been approved or are under approval and are likely to become a standard pharmacological strategy for COPD. Inhaled dual-pharmacology compounds, combining muscarinic antagonism and β2-agonism (MABA) in a single molecule, potentially provide additive or synergistic bronchodilation over either inhaled antimuscarinic or β2-agonist monotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI