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新型基于环糊精的共聚物:制备、表征及释放行为。

Novel -cyclodextrin based copolymers: fabrication, characterization and release behavior.

作者信息

Han Xiao, Zhu Pinpin, Zhang Guoquan

机构信息

College of Equipment Management and Supportability, Engineering University of People's Armed Police, Xi'an, Shaanxi, China.

College of Food Science and Engineering, Northwest A&F University, Yangling, Shaanxi, China.

出版信息

J Biomater Sci Polym Ed. 2022 Jan;33(1):77-92. doi: 10.1080/09205063.2021.1980358. Epub 2021 Oct 3.

Abstract

A novel cyclodextrin-contained copolymer poly(AAc--SA-AC--allyl-β-CD) was synthesized based on the method of redox radical polymerization. Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance (H NMR) spectra were used to study the structure of the obtained copolymer. The molecular weight of the copolymer was studied by gel permeation chromatography (GPC). The polymeric nanoparticles (NPs) were fabricated by a solvent evaporation method. The morphology and particle size distribution of the cargo-free NPs were investigated with transmission electron microscope (TEM), atomic force microscope (AFM), and laser particle analyzer, respectively. Curcumin (Cur) was selected as a model drug and encapsulated into the above NPs. The distribution of Cur in the drug-loaded NPs was analyzed by the method of differential scanning calorimetry (DSC) and X-ray diffraction (XRD). Moreover, the release profiles of Cur from Cur-loaded NPs were studied in pH 6.8 and 7.4 buffers. The results of FTIR and H NMR spectra confirmed the successful synthesis of poly(AAc--SA-AC--allyl-β-CD). GPC curve proved that the molecular weight of the copolymer was more than 60 kDa. TEM and AFM images illustrated that the cargo-free NPs were in spherical shape with a diameter about 40 nm. XRD patterns and DSC curves indicated that most of Cur distributed in the Cur-loaded NPs with amorphous state. Importantly, the medicated NPs showed sustained release characteristics toward Cur.

摘要

基于氧化还原自由基聚合法合成了一种新型的含环糊精共聚物聚(丙烯酸 - 淀粉 - 丙烯酸 - 烯丙基 - β - 环糊精)。采用傅里叶变换红外光谱(FTIR)和质子核磁共振(H NMR)光谱研究所得共聚物的结构。通过凝胶渗透色谱(GPC)研究共聚物的分子量。采用溶剂蒸发法制备聚合物纳米颗粒(NPs)。分别用透射电子显微镜(TEM)、原子力显微镜(AFM)和激光粒度分析仪研究了无载药NPs的形态和粒径分布。选择姜黄素(Cur)作为模型药物并将其包封到上述NPs中。通过差示扫描量热法(DSC)和X射线衍射(XRD)方法分析了Cur在载药NPs中的分布。此外,研究了载Cur的NPs在pH 6.8和7.4缓冲液中Cur的释放曲线。FTIR和H NMR光谱结果证实了聚(丙烯酸 - 淀粉 - 丙烯酸 - 烯丙基 - β - 环糊精)的成功合成。GPC曲线证明共聚物的分子量大于60 kDa。TEM和AFM图像表明无载药NPs呈球形,直径约为40 nm。XRD图谱和DSC曲线表明大部分Cur以无定形状态分布在载Cur的NPs中。重要的是,含药NPs对Cur表现出缓释特性。

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