以电纺丝蛋白纤维为模板的pH响应性介孔SiO2纳米管的制备及药物释放

Preparation and drug release of pH-responsive mesoporous SiO2 nanotubes by electrospun silk fibroin nanofibers as templates

  • 摘要: 以资源丰富的家蚕丝为原料,氯化钙/甲酸为溶解体系,利用静电纺丝法制得丝素蛋白(SF)纳米纤维;以SF纤维为模板在其表面涂覆SiO2,经煅烧后获得了介孔SiO2纳米管(MSNTs);在MSNTs管壁上接枝醛基(-CHO),利用醛基与盐酸阿霉素(DOXHCl)氨基之间的动态共价键制得了pH响应性药物释放体系。通过SEM、TEM、TG、比表面积(BET)分析、FTIR及紫外-可见吸收(UV-Vis)光谱对MSNTs的微观结构、功能化及载药体系的pH响应性进行了表征。结果表明:当SF浓度在15wt%~17wt%时,可获得圆柱状且直径在(113±27)~(134±32)nm范围内可调的SF纤维模板;通过调整涂覆液中十六烷基三甲基溴化铵(CTAB)的浓度来调节MSNTs管壁的厚度,当CTAB用量从1.25 mg/mL增加到3.75 mg/mL时,MSNTs管壁厚度从30~39 nm增加到63~65 nm,对应的比表面积从154 m2/g下降到98 m2/g,介孔平均孔径从12.5 nm下降到10.0 nm;醛基修饰的MSNTs载DOXHCl(MSNT-CHO-DOX)体系,在pH值分别为7.4、6.5和5.5的磷酸氢二钾-磷酸二氢钾(PB)缓冲溶液中进行释放,100 h时释药率分别达到23%、35%和75%,实现了MSNT-CHO-DOX载药体系的pH响应性释放。

     

    Abstract: The silk fibroin (SF) nanofibers were prepared by electrospinning with rich domestic silk as raw material and calcium chloride/formic acid as dissolve system. The mesoporous SiO2 nanotubes (MSNTs) were obtained with calcining after coating SiO2 on SF nanofibers templates. Utilizing dynamic covalent bond between aldehyde group (-CHO), which grafting on the wall of MSNTs, and amino group in doxorubicin hydrochloride (DOXHCl), pH-sensitive drug release system was prepared. The microstructure, functionalization of MSNTs and pH-responsive performance of drug loading system were characterized by SEM, TEM, TG, specific surface area (BET) analysis, FTIR and ultraviolet and visible (UV-Vis) spectroscopy. The results show that when SF concentration is 15wt%-17wt%, cylindrical SF fiber templates can be obtained with adjustable diameters ranging from (113±27) nm to (134±32) nm. The wall thickness of MSNTs can be regulated by adjusting the concentration of cetyl trimethyl ammonium bromide (CTAB) in the coating solution. When the concentration of CTAB increases from 1.25 mg/mL to 3.75 mg/mL, the wall thickness of MSNTs increases from 30-39 nm to 63-65 nm, the corresponding specific surface area decreasing from 154 m2/g to 98 m2/g, and the average mesoporous diameter decreasing from 12.5 nm to 10.0 nm. The drug release rate of the MSNTs modified by aldehyde loading with DOXHCl (MSNT-CHO-DOX) reach 23%, 35% and 75% respectively at 100 h when the release is carried out in dipotassium hydrogen phosphate-potassium phosphate monobasic (PB) buffer solution with pH values of 7.4, 6.5 and 5.5, respectively, achieving pH-responsive release of MSNT-CHO-DOX system.

     

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