Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, Ohio, USA.
Affinity Therapeutics, Cleveland, Ohio, USA.
J Biomed Mater Res A. 2024 Aug;112(8):1305-1316. doi: 10.1002/jbm.a.37680. Epub 2024 Feb 21.
Pulmonary infections complicate chronic lung diseases requiring attention to both the pathophysiology and complexity associated with infection management. Patients with cystic fibrosis (CF) struggle with continuous bouts of pulmonary infections, contributing to lung destruction and eventual mortality. Additionally, CF patients struggle with airways that are highly viscous, with accumulated mucus creating optimal environments for bacteria colonization. The unique physiology and altered airway environment provide an ideal niche for bacteria to change their phenotype often becoming resistant to current treatments. Colonization with multiple pathogens at the same time further complicate treatment algorithms, requiring drug combinations that can challenge CF patient tolerance to treatment. The goal of this research initiative was to explore the utilization of a microparticle antibiotic delivery system, which could provide localized and sustained antibiotic dosing. The outcome of this work demonstrates the feasibility of providing efficient localized delivery of antibiotics to manage infection using both preclinical in vitro and in vivo CF infection models. The studies outlined in this manuscript demonstrate the proof-of-concept and unique capacity of polymerized cyclodextrin microparticles to provide site-directed management of pulmonary infections.
肺部感染使慢性肺病复杂化,需要注意与感染管理相关的病理生理学和复杂性。囊性纤维化(CF)患者肺部不断感染,导致肺部破坏和最终死亡。此外,CF 患者的气道非常粘稠,积聚的粘液为细菌定植创造了最佳环境。独特的生理学和改变的气道环境为细菌改变其表型提供了理想的小生境,使它们经常对现有治疗产生耐药性。同时感染多种病原体进一步使治疗算法复杂化,需要使用可能挑战 CF 患者对治疗耐受性的药物组合。本研究计划的目的是探索使用微粒抗生素递送系统的可能性,该系统可以提供局部和持续的抗生素给药。这项工作的结果表明,使用临床前体外和体内 CF 感染模型,通过高效局部递送抗生素来管理感染是可行的。本手稿中概述的研究证明了聚合环糊精微粒提供肺部感染靶向管理的概念验证和独特能力。