埃洛石
材料科学
药物输送
化学工程
傅里叶变换红外光谱
扫描电子显微镜
透射电子显微镜
控制释放
聚合物
核化学
纳米技术
复合材料
化学
工程类
作者
Feng Liu,Libin Bai,Hailei Zhang,Hongzan Song,Liandong Hu,Yonggang Wu,Xinwu Ba
标识
DOI:10.1021/acsami.7b10867
摘要
A novel chemical hydrogel was facilely achieved by coupling 1,4-phenylenebisdiboronic acid modified halloysite nanotubes (HNTs-BO) with compressible starch. The modified halloysite nanotubes (HNTs) and prepared hydrogel were characterized by solid-state nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscope (TEM). The linkage of B-C in the hydrogel can be degraded into B-OH and C-OH units in the presence of H2O2 and result in the degradation of the chemical hydrogel. Pentoxifylline was loaded into the lumen of the HNTs-BO, and then gave the pentoxifylline-loaded hydrogel. The drug release profile shows that it was no more than 7% dissolved when using phosphate buffer solution (PBS) as the release medium. Notably, a complete release (near 90%) can be achieved with the addition of H2O2 ([H2O2] = 1 × 10-4 M), suggesting a high H2O2 responsiveness of the as-formed hydrogel. The drug release results also show that the "initial burst release" can be effectively suppressed by loading pentoxifylline inside the lumen of the HNTs rather than embedding the drug in the hydrogel network. The drug-loaded hydrogel with H2O2-responsive release behavior may open up a broader application in the field of biomedicine.
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