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Preparation of cationic amphiphilic cellulose copolymers and their self-assembly behavior

机译:阳离子两亲纤维素共聚物的制备及其自组装行为

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Novel amphiphilic cationic cellulose copolymers were prepared by grafting the hydrophobic poly(p-dioxanone)(PDO)chains onto hydrophilic quaternized cellulose derivatives(QC).The grafting ring-opening polymerization was performed in ionic liquids 1-N-butyl-3-methylimidazolium chloride(BmimCl),using the 4-dimethylaminopyridine(DMAP)or 1,8-diazabicyclo(5.4.0)undec-7-ene(DBU)as catalyst.By controlling the molar ratios of p-dioxanone monomer and catalyst to QC,the content ratios of PDO to QC in copolymers were adjusted.The chemical structures and physical properties of copolymers were analyzed by FT-IR,1H-NMR,13C-NMR,X-ray diffraction(XRD),and thermal stability(TGA)techniques.The self-assembly behaviors of QC-g-PDO copolymers was characterized by dynamic light scattering(DLS),transmission electron microscopy(TEM)and fluorescence techniques.It was found that the hydrodynamic radiuses of self-assembled nanomicelles were ranged from 110 nm to 246 nm and the critical micelle concentration(CMC)values were in the range of 0.064-0.253 mg/mL,both of which were decreased with increasing of the grafting ratios of PDO in copolymers.Furthermore,the ζ-potentials of micelles were 39.1-45.4 mV,indicating that the surface charge on the micelles were cationic.Therefore,the prepared nanomicelles were potentially and favorably applied in the fields of drug/gene delivery and bioimaging.
机译:通过将疏水性聚(p-Dioxanone)(PDO)链移植到亲水性型型纤维素衍生物(QC)上来制备新的两亲阳离子纤维素共聚物。在离子液体1-正丁基-3-甲基咪唑鎓中进行接枝开环聚合使用4-二甲基氨基吡啶(DMAP)或1,8-二氮杂双环(5.4.0)UNDC-7-ENE(DBU)作为催化剂的氯化物(Bmimcl)。通过控制对二氧醌单体和催化剂至QC的摩尔比,调节PDO对QC在共聚物中的含量比。通过FT-IR,1H-NMR,13C-NMR,X射线衍射(XRD)和热稳定性(TGA)技术分析共聚物的化学结构和物理性质。QC-G-PDO共聚物的自组装行为以动态光散射(DLS),透射电子显微镜(TEM)和荧光技术为特征。发现,自组装纳米型纳米的流体动力半径为110nm至246nm和临界胶束浓度(CMC)V. alues的范围为0.064-0.253 mg / ml,随着PDO在共聚物中PDO的接枝比率的增加而降低。胶束的△电位为39.1-45.4 mV,表明表面电荷胶束是阳离子。因此,所制备的纳米钙均潜在,有利地应用于药物/基因递送和生物成像的领域。

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