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首页> 外文期刊>International Journal of Pharmaceutics >Proliposome powders prepared using a slurry method for the generation of beclometasone dipropionate liposomes
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Proliposome powders prepared using a slurry method for the generation of beclometasone dipropionate liposomes

机译:使用浆液方法制备的前脂质体粉末用于生成倍氯米松二丙酸酯脂质体

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摘要

A novel "slurry method" was described for the preparation of proliposome powders using soya phosphatidylcholine (SPC) with cholesterol (1:1) and for incorporation of beclometasone dipropionate (BDP) at 2 mole% of the total lipid phase. Proliposomes made with a range of lipid to sucrose carrier ratios were studied in terms of surface morphology using scanning electron microscopy (SEM) and thermal properties using differential scanning calorimetry (DSC). Following hydration of proliposomes, the resultant vesicles were compared to liposomes made using the traditional proliposome method, in terms of vesicle size and drug entrapment efficiency. SEM showed that sucrose was uniformly coated with lipid regardless of lipid to carrier ratio. Liposomes generated using the slurry proliposome method tended to have smaller median size than those generated with the conventional proliposome method, being in the range of 4.72-5.20 mu m and 5.89-7.72 mu m respectively. Following centrifugation of liposomes using deuterium oxide (D2O) as dispersion medium, vesicles entrapping BDP were separated as a floating creamy layer, whilst the free drug was sedimented as crystals. Drug entrapment was dependent on formulation composition and preparation method. When 1:15 w/w lipid to carrier was used, liposomes generated using the slurry method had an entrapment efficiency of 47.05% compared to 18.67% for those generated using the conventional proliposome method. By contrast, liposomes made by the thin-film hydration method had an entrapment efficiency of 25.66%. DSC studies using 50 mole% BDP demonstrated that the drug was amorphous in the proliposome formulation and tended to crystallize on hydration, resulting in low drug entrapment. In conclusion, a novel approach to the preparation of proliposomes using a slurry method has been introduced, offering higher entrapment for BDP than liposomes made using the conventional proliposome method and those prepared by thin-film hydration technique. (C) 2015 Elsevier B.V. All rights reserved.
机译:描述了一种新颖的“浆料方法”,其用于使用大豆磷脂酰胆碱(SPC)和胆固醇(1:1)来制备脂质体粉末,并以总脂质相的2摩尔%掺入倍氯米松二丙酸酯(BDP)。研究了使用一定范围的脂质与蔗糖载体比率制备的脂质体,使用扫描电子显微镜(SEM)的表面形态和使用差示扫描量热法(DSC)的热性质。在脂质体水合后,就囊泡大小和药物包封效率而言,将所得的囊泡与使用传统脂质体方法制备的脂质体进行比较。 SEM显示,无论脂质与载体的比例如何,蔗糖均被脂质均匀地包被。用浆体脂质体方法产生的脂质体的中值尺寸倾向于小于用常规脂质体方法产生的脂质体,分别在4.72-5.20μm和5.89-7.72μm的范围内。使用氧化氘(D2O)作为分散介质离心脂质体后,将包裹BDP的囊泡分离为漂浮的乳脂层,而游离的药物则沉淀为晶体。药物截留取决于制剂的组成和制备方法。当使用脂质与载体的重量比为1:15 w / w时,使用淤浆法生成的脂质体的包封率为47.05%,而使用常规脂质体原方法生成的脂质体的包封率为18.67%。相比之下,通过薄膜水化法制得的脂质体的包封率为25.66%。使用50摩尔%BDP的DSC研究表明,该药物在脂质体制剂中为无定形,在水化后易于结晶,导致药物截留率低。总之,已经介绍了一种使用浆液法制备脂质体的新方法,与使用常规脂质体方法和薄膜水化技术制备的脂质体相比,BDP的包埋率更高。 (C)2015 Elsevier B.V.保留所有权利。

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