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Sustained release liposome for pulmonary drug delivery

机译:肺药递送的持续释放脂质体

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Purpose: The objective of this study was to establish drug loaded liposome with sustained release property for pulmonary application. Methods: The drug for lung disease therapy (drug A) loaded liposome was prepared by ammonium ion gradient method. Physicochemical characteristics such as particle size and drug encapsulation efficiency were evaluated. The drug release profiles of the different formulation of liposomes were analyzed by dialysis method. Results: Loading of drug A into liposome of around 60% entrapment efficiency was achieved by an ammonium ion gradient method. Entrapment efficiency could be controlled by changing the lipid properties and incubation temperature on processing. The release profile of drug A from liposome prepared by this method exhibited the sustained release. The drug release pattern depended on the phase transition temperature of lipid and ammonium salt using preparation process of liposome. Surface modification with hydrophilic polymer prolonged the drugs releasing from liposome. Conclusion: These results indicate that drug A loaded liposome prepared by ammonium ion gradient method have a high potential for pulmonary delivery with sustained release property.
机译:目的:目的本研究是建立载药脂质体与肺应用缓释性。方法:对于肺部疾病的治疗(药物A)加载的脂质体的药物由铵离子梯度法来制备。物理化学特性如粒度和药物包封效率进行了评价。脂质体的不同制剂的药物释放曲线,通过透析法进行分析。结果:药物A装载到60%左右包封率的脂质体是由一个铵离子梯度法来实现的。包封率可以通过改变上加工脂质特性和温育温度来控制。从用这种方法制备的脂质体药物A的释放曲线表现出持续释放。药物释放模式依赖于使用脂质体的制备方法,脂质和铵盐的相转变温度。与亲水性聚合物表面修饰延长了药物从脂质体释放。结论:这些结果表明,药物A装入脂质体通过铵离子梯度法制备具有用于与缓释性经肺递送的高潜力。

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