槲皮素
壳聚糖
纳米颗粒
化学
药物输送
毒品携带者
体内
控制释放
核化学
纳米技术
化学工程
材料科学
有机化学
生物技术
抗氧化剂
工程类
生物
作者
Piyasi Mukhopadhyay,Subhajit Maity,Sudipto Mandal,Abhay Sankar Chakraborti,Akhilesh Prajapati,Patit Paban Kundu
标识
DOI:10.1016/j.carbpol.2017.10.098
摘要
The study aims for development of an efficient polymeric carrier for evaluating pharmaceutical potentialities in modulating the drug profile of quercetin (QUE) in anti-diabetic research. Alginate and succinyl chitosan are focused in this investigation for encapsulating quercetin into core-shell nanoparticles through ionic cross linking. The FT-IR, XRD, NMR, SEM, TEM, drug entrapment and loading efficiency are commenced to examine the efficacy of the prepared nanoparticles in successful quercetin delivery. Obtained results showed the minimum particle size of ∼91.58nm and ∼95% quercetin encapsulation efficiently of the particles with significant pH sensitivity. Kinetics of drug release suggested self-sustained QUE release following the non-fickian trend. A pronounced hypoglycaemic effect and efficient maintenance of glucose homeostasis was evident in diabetic rat after peroral delivery of these quercetin nanoparticles in comparison to free oral quercetin. This suggests the fabrication of an efficient carrier of oral quercetin for diabetes treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI