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Development of Nevirapine Loaded Novel Surfactant Free Polymeric Emulsion and Investigations for Its Suitability as Drug Delivery Vehicle

机译:奈韦拉平负载型新型无表面活性剂的聚合物乳液的开发及其作为载药载体的研究

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The main aim of this study was to prepare the surfactant free polymeric emulsion by using chitosan (CHI), a ubiquitous biopolymer for the delivery of Nevirapine (NVP). The developed system was characterized in terms of stability and payload efficiency The entrapment efficiency (EE) of NVP was 92.57±2.52% when the emulsion was prepared with optimized 2 wt% CHI solution with globule size of 1.013±1.07 m. The release of NVP formulation with high CHI concentration (2 wt%) was fairly sustained: 50.23±1.05% in 24 h. The zeta potential of optimized 2 wt% CHI formulation was found to be +74.6 mV which is helpful to develop high-energy barrier which causes repulsion of adjacent droplets, resulting in the formation of stabilized emulsions. The fluorescence microscopy data revealed that the emulsion formed is O/W. It was shown that it is possible to have stable emulsions of oil in the aqueous solution by adding only CHI without any additional surfactant. This result implies that a stable emulsion can be developed devoid of surfactants and can be used as sustained delivery vehicle for hydrophobic drugs avoiding surfactant induced toxicity in bio-system.
机译:这项研究的主要目的是通过使用壳聚糖(CHI)(一种用于递送奈韦拉平(NVP)的普遍存在的生物聚合物)制备不含表面活性剂的聚合物乳液。所开发的系统具有稳定性和有效负载效率的特点。当用优化的2 wt%CHI溶液(球尺寸为1.013±1.07 m)制备乳液时,NVP的包封率(EE)为92.57±2.52%。高CHI浓度(2 wt%)的NVP制剂的释放相当持续:24小时内为50.23±1.05%。发现优化的2 wt%CHI配方的zeta电位为+74.6 mV,这有助于形成高能垒,该势垒导致相邻液滴的排斥,从而形成稳定的乳液。荧光显微镜数据表明形成的乳液为O / W。已经表明,通过仅添加CHI而不添加任何其他表面活性剂,可以在水溶液中具有稳定的油乳液。该结果表明可以开发出不含表面活性剂的稳定乳液,并且可以用作疏水性药物的持续输送载体,从而避免了表面活性剂在生物系统中引起的毒性。

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