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Formulation, characterization and in vitro release study of 5-fluorouracil loaded chitosan nanoparticles

机译:5-氟尿嘧啶载壳聚糖纳米粒子的制剂,表征和体外释放研究

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The main objective of this study was to evaluate the most suitable conditions to prepare 5-fluorouracil (5-FU) loaded chitosan nanoparticles (CSNPs). loaded CSNPs were prepared employing the ionic gelation tech- nique using three different molecular weights of CS with the polyanion sodium tripolyphosphate (STPP) as cross-linking agent. The preparation was based on the ionic interaction of positively charged CS and negatively charged STPP. The entrapment efficiency (EE%) of CSNPs was in the range of 3.86-21.82% EE% exhibited a clear increase with increasing CS concentration. The averge partides size was in the nanosize range and monodisperse in nature whereas transmission electron microscope micrographs showed that the prepared nanopartides have a spherical shape. Fourier transform infrared (FTIR), X- ray differaction (XRD) and differential scanning calorimetry (DSC) confirmed successful incorporation of 5-FU in prepared CSNPs. In vitro release of 5-FU from selected formulations exhibited sustained release from the nanopartides where slower release was observed when higher molecular weight CS was used. The study of drug release kinetics revealed that the release of 5-FU from CSNPs followed a diffusion controlled pattern. (C) 2020 Elsevier B.V. All rights reserved.
机译:主要目的本研究的是评估最适合的条件,以制备5-氟尿嘧啶(5-FU)壳聚糖纳米颗粒(CSNP报文)。制备负载CSNP报文采用使用CS的三种不同的分子量与聚阴离子的三聚磷酸钠(STPP)作为交联剂的离子凝胶化tech- NIQUE。编制是基于带负电荷的STPP带正电的CS的离子相互作用和。 CSNP报文的包封率(EE%)在该范围的3.86-21.82%EE%表现出与增加CS浓度明显增加。所述averge partides大小是在纳米尺寸范围和在自然界中单分散而透射电子显微镜显微照片表明,制得纳米颗粒具有球形形状。傅立叶变换红外(FTIR),X-射线differaction(XRD)和差示扫描量热法(DSC)确认了制得的CSNP报文5-FU的成功掺入。在选自配制剂5-FU体外释放显示出从使用较高分子量CS当其中观察到较慢的释放的纳米颗粒持续释放。药物释放动力学的研究显示,从CSNP报文5-FU的释放遵循扩散控制图案。 (c)2020 Elsevier B.v.保留所有权利。

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