2014 · 16 citations · 8 references
PharmacyPharmaceuticsPharmacologyDrug DeliveryPharmaceutical FormulationTransdermal Drug DeliveryNanomaterials For Drug DeliveryNanoparticle DesignTransdermal FormulationsEntrapmentLarge Unilamellar VesiclesLipid VesiclesPhospholipid-based Formulations
This research study was in aim to formulate and evaluation of ethosomes containing piroxicam by using phospholipid (1-3%), ethanol (20-40%), propylene glycol (10%) and distilled water by cold method. Prepared ethosomal vesicles evaluated for vesicular size, shape, entrapment efficiency; in vitro skin diffusion, skin irritation and stability studies were carried out. Scanning electron microscopy and size analyser results showed that ethosomes were in spherical, unilamellar, nanometric size. The formulation EF5 showed highest entrapment efficiency of 73.59%. Then, optimized formulation of ethosomal vesicles was further formulated to gel by using carbopol. EFG2 was found to have shown excellent invitro drug release comparing gel containing free piroxicam drug. The kinetic study was found to be fit in first order model and observed no remarkable symptoms on skin from skin irritation study.
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Analysis of Fickian and non-Fickian drug release from polymers.
Nicholas A. Peppas · PubMed · 1985 · 2.1K citations
Carriers for skin delivery of trihexyphenidyl HCl: ethosomes vs. liposomes
Nava Dayan, Elka Touítou · Biomaterials · 2000 · 421 citations
Pharmacy, Dermatology, Pharmaceutics +14