首页> 美国卫生研究院文献>Pharmaceutics >Brief Effect of a Small Hydrophobic Drug (Cinnarizine) on the Physicochemical Characterisation of Niosomes Produced by Thin-Film Hydration and Microfluidic Methods
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Brief Effect of a Small Hydrophobic Drug (Cinnarizine) on the Physicochemical Characterisation of Niosomes Produced by Thin-Film Hydration and Microfluidic Methods

机译:小型疏水性药物(肉桂碱)对薄膜水化和微流化法制备的脂质体的理化特性的简要影响

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摘要

Novel niosomal formulations containing cinnarizine were developed to enhance its drug characteristics. In this work, niosomes (non-ionic surfactant vesicles) were prepared by conventional thin-film hydration (TFH) and microfluidic (MF) methods with sorbitan monostearate (Span® 60), cholesterol, and co-surfactants (Cremophor® ELP, Cremophor® RH40 and Solutol® HS15) as key excipients. The aim was to study the effect of cinnarizine on the characteristics of different niosomal formulations manufactured by using different methods. For effective targeted oral drug delivery, the efficacy of niosomes for therapeutic applications is correlated to their physiochemical properties. Niosome vesicles prepared were characterised using dynamic light scattering technique and the morphology of niosomes dispersion was characterised using optical microscopy. Dialysis was carried out to purify niosome suspensions to determine drug loading and drug release studies was performed to study the potential use of niosomal systems for cinnarizine.
机译:开发了包含肉桂那嗪的新型肽制剂以增强其药物特性。在这项工作中,通过常规的薄膜水合作用(TFH)和微流体(MF)方法,用脱水山梨醇单硬脂酸酯(Span ® 60),胆固醇和共-油制备了脂质体(非离子表面活性剂囊泡)。表面活性剂(Cremophor ® ELP,Cremophor ® RH40和Solutol ® HS15)作为关键赋形剂。目的是研究肉桂利嗪对使用不同方法制备的不同碘代制剂的特性的影响。为了有效地靶向口服药物递送,将脂质体用于治疗应用的功效与其生理化学性质相关。使用动态光散射技术表征制备的脂质体囊泡,并利用光学显微镜表征脂质体分散体的形态。进行透析以纯化脂质体悬浮液,以确定载药量,并进行了药物释放研究,以研究尼古斯丁系统对肉桂利嗪的潜在用途。

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