Formation of ciprofloxacin nanocrystals within liposomes by spray drying for controlled release via inhalation.

Abstract

The present study was conducted to harness spray drying technology as a novel method of producing Ciprofloxacin nanocrystals inside liposomes (CNL) for inhalation delivery. Liposomal ciprofloxacin dispersions were spray dried with sucrose as a lyoprotectant in different mass ratios (0.5:1, 1:1 and 2:1 sucrose to lipids), along with 2%w/w magnesium stearate and 5%w/w isoleucine as aerosolization enhancers. Spray drying conditions were: inlet air temperature 50°C, outlet air temperature 33-35°C, atomizer rate 742L/h and aspirator 35m3/h. After spray drying, the formation of ciprofloxacin nanocrystals inside the liposomes was confirmed by cryo- transmission electron microscopy. The physiochemical characteristics of the spray dried powder (particle size, morphology, crystallinity, moisture content, drug encapsulation efficiency (EE), in vitro aerosolization performance and drug release) were determined. The EE of the liposomes was found to vary between 44 and 87% w/w as the sucrose content was increased from 25 to 57% w/w. The powders contained partially crystalline particles with a volume median diameter of ~1µm. The powders had low water content (~2% wt.) and were stable at high relative humidity. Aerosol delivery using the Osmohaler® inhaler at a flow rate of 100L/min produced an aerosol fine particle fraction (% wt. <5µm) of 58-64%. The formulation with the highest sucrose content (2:1w/w sucrose to lipid) demonstrated extended ciprofloxacin release from liposomes (80% released within 7h) in comparison to the original liquid formulation (80% released within 2h). In conclusion, a stable and inhalable CNL powder with controlled drug release was successfully prepared by spray drying.