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首页> 外文期刊>Materials science & engineering >Stability facilitation of nanoparticles prepared by ultrasound assisted solvent-antisolvent method: Effect of neem gum, acrylamide grafted neem gum and carboxymethylated neem gum over size, morphology and drug release
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Stability facilitation of nanoparticles prepared by ultrasound assisted solvent-antisolvent method: Effect of neem gum, acrylamide grafted neem gum and carboxymethylated neem gum over size, morphology and drug release

机译:超声辅助溶剂-抗溶剂法制备的纳米颗粒的稳定性促进:印em胶,丙烯酰胺接枝印em胶和羧甲基化印em胶的尺寸,形态和药物释放的影响

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In present research, etoricoxib nanoparticles were prepared using newly developed ultrasonication assisted solvent-antisolvent method. Neem gum (NGP) and their semisynthetic derivatives NGP-g-Am (acrylamide graft copolymer of neem gum) and CMNGP (carboxymethylated neem gum) were used to provide stability to drug nanoprecipitates. In this research response surface methodology based on 32factorial design was utilized to evaluate the effect of two independent variables (concentration of drug and polymer) over size and entrapment efficiency of nanoparticles (dependent variables). When compared with pure drug nanocrystals, polymer stabilized molecular composite nanoparticles were of smaller size and spherical shape. CMNGP stabilized composite nanoparticles shown smaller size hence better performance in terms of solubility and dissolution rate as compared to NGP and NGP-g-Am. As shown by zeta seizer analysis for the same concentration of drug and stabilizer, size of nanoparticles were found in the range of NGP-g-Am > NGP > CMNGP and reverse case was observed for dissolution rate. Contact angle determination easily predict better hydrophilicity of CMNGP than NGP followed by NGP-g-Am. DSC thermogram predict the amorphous nature of CMNGP than NGP and NGP-g-Am. SEM revealed spherical shaped and non-aggregation of nanoparticles. Prepared nanosuspension show no aggregation and Ostwald repining after 45 days when ultrasonicated for 5 s. t90%of optimized formulations of NGP (N9), NGP-g-Am (A8) and CMNGP (C1) was found to be 249.46 min, 296.63 min and 223.39 min and followed 1° order, Higuchi and 1° order kinetics of drug, respectively. Similarity factor analysis predict that release pattern of drug from three different polymer stabilized nanoparticles are significantly differ to each other. Particle size of nanoparticles was studied in presence of solvent and findings showed no change in size after 45 days.
机译:在目前的研究中,使用新开发的超声辅助溶剂-抗溶剂方法制备了依托考昔纳米颗粒。印em胶(NGP)及其半合成衍生物NGP-g-Am(印em胶的丙烯酰胺接枝共聚物)和CMNGP(羧甲基化印em胶)用于为药物纳米沉淀提供稳定性。在这项研究中,基于32因子设计的响应面方法用于评估两个独立变量(药物和聚合物的浓度)对纳米粒子的尺寸和包封效率(因变量)的影响。当与纯药物纳米晶体相比时,聚合物稳定的分子复合纳米颗粒具有较小的尺寸和球形。与NGP和NGP-g-Am相比,CMNGP稳定的复合纳米粒子显示出较小的尺寸,因此在溶解度和溶出度方面具有更好的性能。如在相同浓度的药物和稳定剂的zeta检定仪分析中所显示的,发现纳米颗粒的大小在NGP-g-Am> NGP> CMNGP的范围内,并且观察到相反的溶出速率。确定接触角比NGP其次是NGP-g-Am更容易预测CMNGP的亲水性。 DSC热分析图预测CMNGP的非晶态性质要比NGP和NGP-g-Am大。 SEM显示球形和纳米颗粒的非聚集。制备的纳米悬浮液在超声处理5 s后的45 d天未显示聚集和奥斯特瓦尔德固溶。发现NGP(N9),NGP-g-Am(A8)和CMNGP(C1)的优化配方的t90%为249.46 min,296.63 min和223.39 min,并且遵循1°阶,Higuchi和1°阶的药物动力学, 分别。相似因素分析预测,从三种不同的聚合物稳定的纳米颗粒释放药物的方式会显着不同。在溶剂存在下研究了纳米粒子的粒径,发现在45天后粒径没有变化。

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