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首页> 外文期刊>Journal of liposome research >Nanostructured cubosomes in an in situ nasal gel system: an alternative approach for the controlled delivery of donepezil HCl to brain
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Nanostructured cubosomes in an in situ nasal gel system: an alternative approach for the controlled delivery of donepezil HCl to brain

机译:在原位鼻凝胶系统中的纳米结构型立方体:Deypezil HCl对脑的控制交付的另一种方法

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The purpose of this research was to develop cubosomal mucoadhesive in situ nasal gel to enhance the donepezil HCl delivery to the brain. Glycerol mono-oleate (GMO) and surfactant poloxamer 407 were used to prepare cubosomes. The developed formulations were characterized for particle size (PS), poly dispersity index (PDI), zeta potential (ZP), entrapment efficiency (EE), transmission electron microscopy (TEM), in vitro drug release and in vivo bio-distribution study in blood and brain tissue. Central composite design was used for the optimization purpose and the selected formulation (containing GMO 2?g and poloxamer 1.5%) was prepared in presence of gellan gum and konjac gum as gelling agent and mucoadhesive agent respectively. The optimal cubosomal dispersion and optimal cubosomal mucoadhesive in situ nasal gel were subjected to in vivo bio-distribution studies in rat model. It showed significantly higher transnasal permeation and better distribution to the brain, when compared to the drug solution. Thus, the formulated cubosomal mucoadhesive in situ gel could be considered as a promising carrier for brain targeting of CNS acting drugs through the transnasal route.
机译:本研究的目的是开发原位鼻凝胶的缔约置粘膜粘膜,以增强DOTEPEZIL HCl递送给脑。使用甘油单糖(GMO)和表面活性剂泊洛莫氏407来制备缔约置。开发的制剂的特征在于粒度(PS),聚分层指数(PDI),Zeta电位(ZP),夹带效率(EE),透射电子显微镜(TEM),体外药物释放和体内生物分布研究血液和脑组织。中央复合设计用于优化目的,并将所选制剂(含有GMO 2→G和泊洛克拉姆1.5%)分别作为胶凝剂和粘膜粘附剂在胶林胶和康济猴的存在下制备。原位鼻凝胶的最佳立方体分散和最佳立方体粘膜粘附性在大鼠模型中的体内生物分布研究中进行。与药物溶液相比,它表现出显着更高的跨营渗透和对大脑的分布更好。因此,配制的立方体粘膜粘接性原位凝胶可以被认为是通过跨营养途径对CNS作用药物的脑靶向的有前途的载体。

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