姜黄素
淀粉
纳米颗粒
傅里叶变换红外光谱
化学
粒径
乙酰化
化学工程
生物相容性
控制释放
氢键
食品科学
核化学
有机化学
材料科学
纳米技术
分子
生物化学
物理化学
工程类
基因
作者
Leonardo Acevedo-Guevara,Leonardo Nieto-Suaza,Leidy T. Sánchez,Magda I. Pinzón,Cristian C. Villa
标识
DOI:10.1016/j.ijbiomac.2018.01.063
摘要
In recent years, starch nanoparticles have been of great interest for drug delivery due to their relatively easy synthesis, biocompatibility, and vast amount of botanical sources. Native and acetylated starch obtained from green bananas were used for synthesis of curcumin-loaded starch nanoparticles. Mean particle size, encapsulation efficiency, and curcumin release in simulated gastric and intestinal fluids were studied. Both nanosystems showed sizes lower than 250 nm and encapsulation efficiency above 80%, with acetylated banana starch nanoparticles having the capacity to encapsulate more curcumin molecules. Both FTIR and XRD analyses showed that starch acetylation allows stronger hydrogen bond interaction between curcumin and the starch matrix, thus, higher encapsulation efficiency. Finally, curcumin release studies showed that acetylated banana starch nanoparticles allowed more controlled release, probably due to their stronger hydrogen bond interaction with curcumin.
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