PAI Life Sciences, Seattle, Washington 98102; Department of Immunology, University of Washington School of Medicine, Seattle, Washington 98109.
RTI International, Research Triangle Park, North Carolina 27709; Department of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina 27599.
J Pharm Sci. 2019 Oct;108(10):3302-3311. doi: 10.1016/j.xphs.2019.05.024. Epub 2019 May 29.
Tuberculosis (TB) remains the single most serious infectious disease attributable to a single-causative organism. A variety of drugs have been evaluated for pulmonary delivery as dry powders: capreomycin sulfate has shown efficacy and was safely delivered by inhalation at high doses to human volunteers, whereas CPZEN-45 is a new drug that has also been shown to kill resistant TB. The studies here combine these drugs-acting by different mechanisms-as components of single particles by spray-drying, yielding a new combination drug therapy. The spray-dried combination powder was prepared in an aerodynamic particle size range suitable for pulmonary delivery. Physicochemical storage stability was demonstrated for a period of 6 months. The spray-dried combination powders of capreomycin and CPZEN-45 have only moderate affinity for mucin, indicating that delivered drug will not be bound by these mucins in the lung and available for microbicidal effects. The pharmacokinetics of disposition in guinea pigs demonstrated high local concentrations of drug following direct administration to the lungs and subsequent systemic bioavailability. Further studies are required to demonstrate the in vivo efficacy of the combination to confirm the therapeutic potential of this novel combination.
结核病(TB)仍然是由单一病原体引起的最严重的传染病。已经有多种药物被评估用于肺部干粉输送:硫酸卷曲霉素已显示出疗效,并可通过吸入在高剂量下安全地输送给人类志愿者,而 CPZEN-45 是一种新的药物,也已被证明可以杀死耐药结核病。这里的研究将这些通过不同机制发挥作用的药物组合成单个颗粒的喷雾干燥成分,形成一种新的联合药物治疗方法。喷雾干燥的组合粉末在适合肺部输送的空气动力学颗粒尺寸范围内进行制备。在 6 个月的时间里,证明了物理化学储存稳定性。卷曲霉素和 CPZEN-45 的喷雾干燥组合粉末对粘蛋白只有适度的亲和力,这表明输送的药物不会与肺部的这些粘蛋白结合,从而可发挥杀菌作用。豚鼠的药代动力学研究表明,直接向肺部给药后,药物在肺部的局部浓度很高,随后具有全身生物利用度。需要进一步的研究来证明该组合在体内的疗效,以确认这种新型组合的治疗潜力。