Drug Development and Industrial Pharmacy · 2000 · 99 citations · 14 references
Pharmaceutical ScienceExtracellular MicrovesiclesPharmacotherapyVitro ReleaseNiosome VesiclesNanomedicineMedicinal ChemistryAnti-cancer AgentCytarabine HydrochlorideDrug Delivery SystemRadiation OncologyCell-based Drug DeliveryBiochemistryPharmacologyRelease MechanismLipid PreparationDrug TargetingPolymer-drug ConjugateNatural SciencesLipid Hydration MethodProlonged Release ProfileMedicinePharmacokineticsDrug DiscoveryNonionic Surfactant Vesicles
Niosome vesicles of cytarabine hydrochloride were prepared by a lipid hydration method that excluded dicetylphosphate. The sizes of the vesicles obtained ranged from 600 to 1000 nm, with the objective of producing more blood levels in vivo. The study of the release of drug from niosomes exhibited a prolonged release profile as studied over a period of 16 hr. The drug entrapment efficiency was about 80% with Tween 80, Span 60 and Tween 20; for Span 80, it was 67.5%. The physical stability profile of vesicular suspension was good as studied over a period of 4 weeks.
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M. N. Azmin, Alastair J. Florence, Rose-Marie Handjani-Vila et al. · Journal of Pharmacy and Pharmacology · 1985 · 319 citations
Pharmacotherapy, Experimental Pharmacology, Non-ionic Surfactant Vesicle +16