University of Texas at Austin, College of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery, 2409 West University Avenue, Austin, TX 78712, United States.
University of Texas at Austin, College of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery, 2409 West University Avenue, Austin, TX 78712, United States; LaMontagne Center for Infectious Disease, The University of Texas at Austin, United States.
Int J Pharm. 2018 Aug 25;547(1-2):489-498. doi: 10.1016/j.ijpharm.2018.05.036. Epub 2018 May 17.
Delivery of drugs to the lungs via dry powder inhaler (DPI) is a promising approach for the treatment of both local pulmonary conditions and systemic diseases. Though DPIs are widely used for the pulmonary deposition of potent bronchodilators, anticholinergics, and corticosteroids, there is growing interest in the utilization of this delivery system for the administration of high drug doses to the lungs, as made evident by recent regulatory approvals for anti-microbial, anti-viral and osmotic agents. However, the formulation of high dose DPIs carries several challenges from both a physiological and physicochemical standpoint. This review describes the various formulation techniques utilized to overcome the barriers associated with the pulmonary delivery of high dose powders.
通过干粉吸入器(DPI)将药物递送到肺部是治疗局部肺部疾病和全身疾病的一种很有前途的方法。尽管 DPI 广泛用于肺部沉积强效支气管扩张剂、抗胆碱能药和皮质类固醇,但人们越来越感兴趣地利用这种递药系统将高剂量药物递送到肺部,最近对抗微生物、抗病毒和渗透剂的监管批准就证明了这一点。然而,高剂量 DPI 的配方在生理和物理化学方面都存在一些挑战。本文综述了各种制剂技术,用于克服与高剂量粉末肺部递药相关的障碍。
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