Asian Journal of Pharmaceutical Sciences · 2016 · 40 citations · 32 references
PharmacyPharmacokineticsPharmacologyBioavailabilityDrug DeliveryOral Drug DeliveryLiposomal FormulationsLiposome-based DeliveryMucosal AbsorptionOral BioavailabilityOral Bioavailability EnhancementOral NanocarriersDissolution EfficiencyDissolution ProcessesEntrapmentIntestinal Absorption EnhancementIntestinal BioavailabilityIntestinal DissolutionOral Drug BioavailabilityPhysicochemical Properties
of ITZ-Lip-NaDC was also decreased. Our results indicated that ITZ-Lip-NaDC liposome was facilitated to improve dissolution efficiency, augment transmembrane absorption, and then enhance the oral bioavailability of ITZ, successfully.
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