水凝胶纳米颗粒给药系统的制备与评价

R. Kaur, Vishal K. Gupta, S. Ch, P. ra, ey
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引用次数: 2

摘要

水凝胶纳米颗粒(NPs)可用于结肠给药,以甲氨蝶呤(MTX)为模型药物。采用pH敏感的聚丙烯酰胺接枝胶(PAAm-g-Gg)制备了负载MTX的水凝胶NPs。采用自由基聚合法制备了PAAm-g-Gg。以PAAm-g-Gg为原料,采用纳米乳化交联法制备了MTX负载水凝胶NPs。FT-IR和DSC研究表明,水凝胶NPs中MTX未发生化学变化。制备的水凝胶NPs的平均直径为238±0.57 nm ~ 1064±0.99 nm。包封率为39.11% ~ 48.84%。在pH为1.2和7.4的条件下,研究了聚丙烯酰胺接枝胶凝胶NPs对甲氨蝶呤的体外释放性。结果显示,F6在pH值为7.4的胃内无明显释药量,12 h后释药率为97.28%。根据结果,配方F6被认为是最佳配方,并进一步进行了稳定性研究和表面形貌表征。SEM照片显示水凝胶NPs呈球形,稳定性研究数据表明药物含量没有明显变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and Evaluation of Hydrogel Nanoparticles as Drug Delivery System
Hydrogel nanoparticles (NPs) can be used for colon drug delivery, utilizing Methotrexate (MTX) as a model drug. MTX loaded hydrogel NPs were prepared using Poly-acrylamide-grafted- gum ghatti (PAAm-g-Gg), which is pH sensitive. PAAm-g-Gg was synthesized by free radical polymerization. MTX loaded hydrogel NPs was prepared from PAAm-g-Gg by using nanoemulsification polymer crosslinking method. FT-IR and DSC studies of the prepared NPs indicated no chemical change of MTX in the hydrogel NPs. The prepared hydrogel NPs showed mean diameters in the range of 238 ± 0.57 nm to 1064 ± 0.99 nm. The encapsulation efficiency of the drug was found to be 39.11% to 48.84%. The suitability of the polyacrylamide grafted gum ghatti hydrogel NPs for the release of Methotrexate was studied by in vitro release at pH 1.2 and 7.4. It was observed that, there was no significant amount of drug release in gastric pH and 97.28% of drug release at pH 7.4 for formulation F6 at the end of 12 hrs. Based on result formulation F6 was considered as the best formulation and further evaluated for stability studies and characterized for surface morphology using SEM. SEM photographs have shown that the hydrogel NPs are spherical in shape and the stability study data indicated no significant change in the drug content.
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