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Optimization, preparation and characterization of rutin-quercetin dual drug loaded keratin nanoparticles for biological applications

机译:芦丁-槲皮素双重药物负载角蛋白纳米粒子的生物应用优化,制备和表征

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Objective(s): Response surface methodology (RSM) by central composite design (CCD) was applied to statistically optimize the preparation of Rutin-Quercetin (Ru-Qr) dual drug loaded human hair keratin nanoparticles as well as evaluate the characteristics. Materials and Methods: The effects of three independent parameters, namely, temperature (X1:10-40 C), surfactant (X2: SDS (1), SLS (2), Tween-20 (3)), and organic solvents (X3: acetone (1), methanol (2), chloroform (3)) were investigated to optimize the preparation of dual drug loaded keratin nanoparticles, and to understand the effects of dependent parameters namely, drug releasing capacity, average particle size, total antioxidant power, zeta potential, and polydispersity index of Ru-Qr nanoparticles. Optimization was executed by CCD and RSM using statistical software (Design Expert, version 8.0.7.1, Stat-Ease, Inc., Minneapolis, MN, USA). The optimal Ru-Qr dual drug loaded keratin nanoparticles were obtained at temperature (X1): 40úC, SDS (X2), and acetone (X3). Results: Under this conditions to achieve highest drug releasing capacity of 98.3%, average size of nanoparticles are 125 nm, total antioxidant power 98.68%, zeta potential 28.09 mV, and polydispersity index of 0.54. Although majority of the experimental values were relatively well matched with the predicted values. Conclusion: This optimization study could be useful in pharmaceutical industry, especially for the preparation of new nano-therapeutic formulations encapsulated with drug molecules. This nanotechnology based drug delivery system is to overcome multi drug resistance and site specific action without affecting other organs and tissues. The methodology adopted in this work shall be useful in improvement of quality of human health.
机译:目标:采用中央复合设计(CCD)的响应表面方法(RSM)来统计上优化芦丁-槲皮素(Ru-Qr)双药负载人发角蛋白纳米颗粒的制备,并评估其特性。材料和方法:三个独立参数的作用,即温度(X1:10-40 C),表面活性剂(X2:SDS(1),SLS(2),Tween-20(3))和有机溶剂(X3) :研究了丙酮(1),甲醇(2),氯仿(3)),以优化载有双重药物的角蛋白纳米颗粒的制备,并了解药物释放能力,平均粒径,总抗氧化能力等相关参数的影响,Zeta电位和Ru-Qr纳米粒子的多分散指数。使用统计软件(Design Expert,版本8.0.7.1,Stat-Ease,Inc.,明尼苏达州,明尼苏达州,美国)通过CCD和RSM执行优化。在温度(X1):40°C,SDS(X2)和丙酮(X3)下获得了最佳的Ru-Qr负载双药角蛋白纳米颗粒。结果:在此条件下,药物的最高释放能力为98.3%,纳米颗粒的平均大小为125 nm,总抗氧化剂能力为98.68%,ζ电位为28.09 mV,多分散指数为0.54。尽管大多数实验值与预测值相对较好地匹配。结论:这项优化研究可能对制药业有用,特别是对于制备包裹有药物分子的新型纳米治疗制剂。这种基于纳米技术的药物输送系统将克服多重耐药性和特定部位的作用,而不会影响其他器官和组织。这项工作中采用的方法应有助于改善人类健康质量。

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