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Intratracheal Administration of Dry Powder Formulation in Mice
Published on: July 25, 2020
Novel sustained release microspheres for pulmonary drug delivery
Robert O Cook1, Rupi K Pannu, Ian W Kellaway
1Department of Pharmaceutics, University of London School of Pharmacy, 29/39 Brunswick Square, London, WC1N 1AX, UK. rcook@mappharma.com
Abstract:
A novel process for generating sustained release (SR) particles for pulmonary drug delivery is described. High purity nanoparticles of a hydrophilic, ionised drug are entrapped within hydrophobic microspheres using a spray-drying approach. Sustained release of the model drug, terbutaline sulphate (TS), from the microspheres was found to be proportional to drug loading and phospholipid content. Microspheres with a 33% drug loading exhibited sustained release of 32.7% over 180 min in phosphate buffer. Release was not significantly different in simulated lung fluids. No significant burst release was observed which suggested that nanoparticles were coated effectively during spray-drying. The absence of nanoparticles at the microsphere surface was confirmed with confocal microscopy. The sustained release microspheres were formulated as a carrier-free dry powder for inhalation, and exhibited a favourable Fine Particle Fraction (FPF) of 46.5+/-1.8% and Mass Median Aerodynamic Diameter (MMAD) of 3.93+/-0.12 microm.
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