Fiel Stanley B
Morristown Medical Center/Atlantic Health System, 100 Madison Avenue, Morristown, NJ 07960, USA.
Expert Rev Respir Med. 2014 Jun;8(3):305-14. doi: 10.1586/17476348.2014.896205.
Inhaled antibiotic therapy, targeting Pseudomonas aeruginosa, is a fundamental component of cystic fibrosis (CF) management. Tobramycin inhalation solution (TIS) was approved in the United States (US) in 1998. Subsequent research efforts focused on developing products with a reduced treatment time burden. Aztreonam for inhalation solution (AZLI), administered via a more efficient nebulizer than TIS, was approved in the US in 2010. Dry powder for inhalation (DPI) formulations provide alternatives to nebulized therapy: tobramycin powder for inhalation (also known as TIP™) was approved in the US in 2013, and colistimethate sodium DPI received European approval in 2012. Other aerosolized antibiotics and regimens combining inhaled antibiotics are in development. Inhaled antibiotic rotation (e.g., TIS alternating with AZLI) is an important concept being actively tested in CF.
针对铜绿假单胞菌的吸入性抗生素疗法是囊性纤维化(CF)治疗的基本组成部分。妥布霉素吸入溶液(TIS)于1998年在美国获批。随后的研究工作集中在开发治疗时间负担较轻的产品上。吸入用氨曲南溶液(AZLI)通过比TIS更高效的雾化器给药,于2010年在美国获批。吸入用干粉(DPI)制剂为雾化治疗提供了替代方案:吸入用妥布霉素粉末(也称为TIP™)于2013年在美国获批,多粘菌素甲磺酸钠DPI于2012年获得欧洲批准。其他雾化抗生素以及联合吸入性抗生素的治疗方案正在研发中。吸入性抗生素轮换(例如,TIS与AZLI交替使用)是一个正在CF中积极测试的重要概念。