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首页> 外文期刊>Ultrasonics sonochemistry >Ultrasonically tailored, chemically engineered and 'QbD' enabled fabrication of agomelatine nanoemulsion; optimization, characterization, ex-vivo permeation and stability study
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Ultrasonically tailored, chemically engineered and 'QbD' enabled fabrication of agomelatine nanoemulsion; optimization, characterization, ex-vivo permeation and stability study

机译:超声定制,化学工程化和“QBD”的制备聚焦纳米乳液; 优化,表征,前体内渗透和稳定性研究

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The objective of present study was to develop a nanoemulsion formulation of agomelatine (BCS class II drug) for the solubility enhancement. Capmul MCM, Tween 80 and PEG-400 were selected as oil, surfactant and co-surfactant respectively. The high energy ultrasonication method was used for the preparation of nanoemulsion. Three-factor three-level central composite design was employed to get the best formulation. The independent variables selected for the optimization were % oil, %S-mix and sonication time (second). Based on the constraints applied to independent and dependent variables, the optimized formulation was selected with 2% oil, 10% Smix and 45 s sonication time. The experimental values for dependent variables such as hydrodynamic diameter (nm), % transmittance and % CDR were found to be 73.72 +/- 2.53 nm, 98.2 +/- 0.42%, 84.71 +/- 4.05% respectively. TEM and AFM - assisted morphological characterization of optimized Ago-NE was done and it was found with a spherical shape. The PDI, Zeta potential and the refractive index of optimized Ago-NE were found to be 0.137 +/- 0.016, -7.40 +/- 0.12 mV and 1.423 +/- 0.045 respectively. The viscosity, pH and drug content of optimized Ago-NE were found as 25.12 +/- 0.67 cP, 6.4 +/- 0.17 and 97.83 +/- 1.03% respectively. The ex-vivo permeation profile of optimized Ago-NE and agomelatine suspension through goat nasal mucosa were compared till 12 h and % cumulative drug permeated was found to be 90% and 40% respectively. The higher drug permeation profile of optimized Ago-NE confirmed that the solubility of agomelatine has been improved.
机译:目前研究的目的是开发用于溶解性增强的阿莫米兰(BCS II类药物)的纳米乳液制剂。选择Capmul MCM,吐温80和PEG-400分别为油,表面活性剂和共表面活性剂。高能量超声处理方法用于制备纳米乳液。采用三因素三级中央复合设计来获得最佳配方。选择优化的独立变量为%油,%S-MIX和超声处理时间(第二)。基于应用于独立和依赖性变量的约束,用2%的油,10%SMIX和45次超声时间选择优化的制剂。发现诸如流体动力直径(NM),%透射率和%CDR的依赖变量的实验值为73.72 +/- 2.53nm,98.2 +/- 0.42%,84.71 +/- 4.05%。 TEM和AFM - 辅助形态学表征优化以前 - NE已经完成,并以球形形状发现。发现PDI,Zeta潜力和优化前的折射率-NE的折射率分别为0.137 +/- 0.016,-7.40 +/- 0.12 mV和1.423 +/- 0.045。优化以前-NE的粘度,pH和药物含量分别被发现为25.12 +/- 0.67cp,6.4 +/- 0.17和97.83 +/- 1.03%。通过山羊鼻粘膜优化前Agay-Ne和Agomelatine悬浮液的前体内渗透曲线悬浮液,直至12小时,渗透累积药物渗透量分别为90%和40%。优化以前的较高药物渗透谱证实,胍兰的溶解度得到改善。

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