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首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >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:通过超声辅助溶剂 - 抗溶剂法制备的纳米颗粒的稳定性促进方法:Neem Gum,丙烯酰胺接枝Neem Gum和羧甲基含有尺寸,形态和药物释放的影响

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摘要

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 3(2) factorial 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 5s. t(90%) 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 degrees order, Higuchi and 1 degrees 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,使用新开发的超声波辅助溶剂 - 抗溶剂方法制备肠道毒氧纳米粒子。使用Neem Gum(NGP)及其半合成衍生物NGP-G-AM(丙烯酰胺接枝共聚物(Neem Gum)和CMngp(羧甲基化的Neem Gum),为药物纳米沉淀物提供稳定性。在该研究中,利用基于3(2)个因子设计的表面方法来评估纳米颗粒(依赖变量)的两个独立变量(药物和聚合物浓度)的效果。与纯药物纳米晶体相比,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稳定的复合纳米颗粒所示的尺寸较小,因此在溶解度和溶解速率方面的性能更好。如Zeta Seizer分析所示,同样浓度的药物和稳定剂,纳米颗粒的尺寸在NGP-G-AM&GT的范围内被发现。 ngp&观察到CMNGP和反向壳体以溶出速率。接触角测定容易预测CMNGP的更好的亲水性而不是NGP,然后是NGP-G-AM。 DSC热分析图预测CMNGP的无定形性,而不是NGP和NGP-G-AM。 SEM揭示了纳米颗粒的球形和非聚集。准备好的纳米悬臣在超声波5秒后显示出45天后的聚集和Ostwald释放。发现NGP(N9)的优化配方T(90%),NGP-G-AM(A8)和CMNGP(C1)为249.46分钟,296.63分钟和223.39分钟,然后遵循1度阶,HIGUCHI和1度顺序药物的动力学分别。相似性因子分析预测来自三种不同聚合物稳定纳米颗粒的药物的释放模式彼此显着不同。在溶剂存在下研究纳米颗粒的粒径,结果显示在45天后没有尺寸的变化。

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