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The Hypotonic Environmental Changes Affect Liposomal Formulations for Nose-to-Brain Targeted Drug Delivery
Authors:Iren Yeeling Wu  Trygg Einar Nikolaisen  Nataša Škalko-Basnet  Massimiliano Pio di Cagno
Affiliation:1. Drug Transport and Delivery Research Group, Department of Pharmacy, University of Tromsø–The Arctic University of Norway, Universitetsvegen 57, 9037 Tromsø, Norway;2. Department of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, Sem Sælands vei 3, 0371 Oslo, Norway
Abstract:Systemic administration of drugs is ineffective in the treatment of central nervous system disorders because of the blood-brain barrier. Nasal administration has been suggested as an alternative administration route as drugs absorbed in the olfactory epithelium bypass the blood-brain barrier and reach the brain within minutes. However, the nasal mucosa properties (e.g., tonicity, pH) are not constant because of physiological and environmental factors, and this might limit the therapeutic outcome of nanocarrier-based formulations. To shine light on the impact of environmental ionic strength on nanocarrier-based formulations, we have studied how liposomal formulations respond to the change of tonicity of the external environment. Large unilamellar vesicles loaded with 6 different drugs were exposed to different hypotonic environments, creating an osmotic gradient within the inner core and external environment of the liposomes up to 650 mOsm/kg. Both size and polydispersity of liposomes were significantly affected by tonicity changes. Moreover, the release kinetics of hydrophilic and lipophilic drugs were largely enhanced by hypotonic environments. These results clearly demonstrate that the environmental ionic strength has an impact on liposomal formulation stability and drug release kinetics and it should be considered when liposomal formulations for nose-to-brain targeted drug delivery are designed.
Keywords:liposomes  osmotic pressure  particle size  passive diffusion  controlled release  membrane resistance  drug transport  drug delivery system  CNS  central nervous system  EE  entrapment efficiency  LUVs  large unilamellar vesicles  PBS  phosphate buffered saline  PI  polydispersity index  resistance to drug transport through regenerated cellulose barrier  resistance to drug transport through liposomal bilayer  total resistance to drug transport  SD  standard deviation  SPC  soy-phosphatidylcholine  ZP  ζ-potential  ΔmOsm/kg  tonicity difference between the inner core and external environment of liposomes
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