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首页> 外文期刊>International Journal of Nanomedicine >Brain Targeting of Duloxetine HCL via Intranasal Delivery of Loaded Cubosomal Gel: In vitro Characterization, ex vivo Permeation, and in vivo Biodistribution Studies
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Brain Targeting of Duloxetine HCL via Intranasal Delivery of Loaded Cubosomal Gel: In vitro Characterization, ex vivo Permeation, and in vivo Biodistribution Studies

机译:脑靶向甲氧乙胺HCl通过鼻内递送加载的缔约置凝胶:体外表征,离体渗透,体内生物分布研究

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Purpose:Duloxetine (DLX) is dual serotonin and norepinephrine reuptake inhibitor suffering from limited bioavailability (≈ 40%) due to extensive hepatic metabolism. This work aims to formulate and evaluate DLX intranasal thermoreversible cubosomal gels to enhance its bioavailability and ensure efficient brain targeting.Materials and Methods:Cubo-gels were prepared by 3 3 central composite design with three independent factors, lipid ratio (glycerol monooleate: glycerol tripalmitate), Pluronic F127%, and Pluronic F68%. The prepared formulations were evaluated for their particle size (PS), gelling temperature (GT), entrapment efficiency (EE%), and in vitro release. The cubo-gel with the highest desirability (0.88) was chosen as the optimized formulation. DLX cubo-gel was evaluated using differential scanning calorimetry, Fourier-transform infrared spectroscopy, X-ray powder diffraction, and transmission electron microscopy. Cytotoxicity study, ex vivo permeation study and in vivo bio-distribution study were conducted to evaluate the safety and efficacy of brain targeting.Results:The optimum cubo-gel was composed of 3.76 lipid ratio, 20% w/v PF127, and 5% w/v PF68. It had PS of 265.13 ± 9.85 nm, GT of 32 ± 0.05°C, EE% of 98.13 ± 0.50%, and showed controlled release behavior where 33% DLX was released within 6 hrs. The plain in situ cubo-gel had a significantly higher IC 50 compared to DLX solution and DLX-loaded in situ cubo-gel. The ex vivo permeation study showed 1.27 enhancement in the drug permeation from DLX in situ cubo-gel. According to the in vivo bio-distribution study in plasma and brain, the intranasal DLX in situ cubo-gel showed a 1.96 fold improvement in brain bioavailability compared to the intranasal solution. Its BTE% and DTP% were 137.77 and 10.5, respectively, indicating efficient brain targeting after intranasal administration.Conclusion:Accordingly, intranasal DLX in situ cubo-gel can be considered as an innovative nano-carrier delivery system for bioavailability enhancement and efficient brain targeting of DLX to maximize its effect.? 2020 Elsenosy et al.
机译:目的:Duloxetine(DLX)是由于广泛的肝脏代谢引起的患有有限的生物利用度(≈40%)的双血清素和去甲肾上腺素再摄取抑制剂。该工作旨在配制和评估DLX鼻内热可逆型立方体凝胶,以提高其生物利用度,并确保高效的脑靶向。通过3 3个中央复合设计,三个独立因子,脂质比(甘油单烯烃:甘油三通时为甘油三丙酸酯制备浴凝胶),Pluronic F127%,Pluronic F68%。评价制备的制剂,用于粒度(PS),胶凝温度(GT),夹带效率(EE%)和体外释放。选择具有最高令人恢复性(0.88)的杯状凝胶作为优化的制剂。使用差示扫描量热法,傅里叶变换红外光谱,X射线粉末衍射和透射电子显微镜评估DLX级凝胶。进行细胞毒性研究,进行前体内渗透研究和体内生物分布研究,以评估脑靶向的安全性和功效。结果:最佳的浴凝胶由3.76脂质比,20%w / v pf127和5%组成。 w / v pf68。它具有265.13±9.85nm,gt为32±0.05℃,ee%的98.13±0.50%,并显示出33%dlx在6小时内释放33%的释放行为。与DLX溶液和DLX装载的原位浴凝胶相比,平原的IC 50具有显着更高的IC 50。前体内渗透研究表明,在原位浴凝胶中的DLX药物渗透中增强了1.27。根据血浆和大脑的体内生物分布研究,与鼻内溶液相比,鼻内DLX患有原位级凝胶的提高1.96倍的脑生物利用性。其BTE%和DTP%分别为137.77和10.5,分别表明鼻内施用后的有效脑靶向。结论:因此,原位级凝胶的鼻内DLX可以被认为是一种用于生物利用度增强和高效脑靶向的创新纳米载体输送系统DLX最大化其效果。 2020 Elsenosy等。

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