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A Spray Freeze Dried Powder for Liposomal Inhaled Aerosol DrugDelivery

机译:喷雾冷冻干燥粉末用于脂质体吸入气雾剂给药

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In this paper, a novel powder formulation for inhaledaerosol drug delivery of liposomes has been preparedusing spray-freeze drying. Aerosol dispersion propertiesof this formulation were assessed using a new passiveinhaler (patent pending), in which the powder wasentrained at a flow rate of 60 l/min. Excellent fine particlefraction (FPF) of more than 80% was achieved for thisformulation with a model drug (ciprofloxacin). Dispersionof powder in various aqueous media gave drugencapsulation efficiencies as follows: 50% in water,93.5% in isotonic saline, 80% in bovine mucin, 75% inporcine mucus and 73% in fivefold diluted ex vivo humancystic fibrosis patient sputum.
机译:在本文中,使用喷雾冷冻干燥制备了用于吸入气雾剂脂质体的新型粉末制剂。使用新型被动吸入器(正在申请专利)评估该制剂的气溶胶分散性能,其中以60升/分钟的流速夹带粉末。使用模型药物(环丙沙星)进行这种配制时,可实现超过80%的优良细颗粒分数(FPF)。粉末在各种水性介质中的分散产生了如下的药物包封效率:在水中50%,在等渗盐水中93.5%,在牛粘蛋白中80%,在猪粘液中75%和在五倍稀释的离体人囊性纤维化患者痰中稀释73%。

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