Ding Li, Wang Jieliang, Cai Shihao, Smyth Hugh, Cui Zhengrong
Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA.
Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA.
Int J Pharm. 2021 Jul 15;604:120768. doi: 10.1016/j.ijpharm.2021.120768. Epub 2021 Jun 3.
Certain pulmonary diseases, such as cystic fibrosis (CF), non-CF bronchiectasis, chronic obstructive pulmonary disease, and ventilator-associated pneumonia, are usually accompanied by respiratory tract infections due to the physiological alteration of the lung immunological defenses. Recurrent infections may lead to chronic infection through the formation of biofilms. Chronic biofilm-based infections are challenging to treat using antimicrobial agents. Therefore, effective ways to eradicate biofilms and thus relieve respiratory tract infection require the development of efficacious agents for biofilm destruction, the design of delivery carriers with biofilm-targeting and/or penetrating abilities for these agents, and the direct delivery of them into the lung. This review provides an in-depth description of biofilm-based infections caused by pulmonary diseases and focuses on current existing agents that are administered by inhalation into the lung to treat biofilm, which include i) inhalable antimicrobial agents and their combinations, ii) non-antimicrobial adjuvants such as matrix-targeting enzymes, mannitol, glutathione, cyclosporin A, and iii) liposomal formulations of anti-biofilm agents. Finally, novel agents that have shown promise against pulmonary biofilms as well as traditional and new devices for pulmonary delivery of anti-biofilm agents into the lung are also discussed.
某些肺部疾病,如囊性纤维化(CF)、非CF支气管扩张症、慢性阻塞性肺疾病和呼吸机相关性肺炎,由于肺部免疫防御的生理改变,通常伴有呼吸道感染。反复感染可能通过生物膜的形成导致慢性感染。基于生物膜的慢性感染使用抗菌药物治疗具有挑战性。因此,根除生物膜从而缓解呼吸道感染的有效方法需要开发有效的生物膜破坏剂,设计具有生物膜靶向和/或穿透能力的这些药物的递送载体,并将它们直接递送至肺部。本综述深入描述了由肺部疾病引起的基于生物膜的感染,并重点关注目前通过吸入肺部给药以治疗生物膜的现有药物,其中包括:i)可吸入抗菌药物及其组合;ii)非抗菌佐剂,如基质靶向酶、甘露醇、谷胱甘肽、环孢素A;iii)抗生物膜药物的脂质体制剂。最后,还讨论了对肺部生物膜显示出前景的新型药物以及将抗生物膜药物肺部递送的传统和新型装置。