Zhao Jiangqi, Lu Canhui, He Xu, Zhang Xiaofang, Zhang Wei, Zhang Ximu
State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute at Sichuan University , No. 24 South Section 1, Yihuan Road, Chengdu 610065, China.
ACS Appl Mater Interfaces. 2015 Feb 4;7(4):2607-15. doi: 10.1021/am507601m. Epub 2015 Jan 20.
Aerogels from polyethylenimine-grafted cellulose nanofibrils (CNFs-PEI) were developed for the first time as a novel drug delivery system. The morphology and structure of the CNFs before and after chemical modification were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Water-soluble sodium salicylate (NaSA) was used as a model drug for the investigation of drug loading and release performance. The CNFs-PEI aerogels exhibited a high drug loading capability (287.39 mg/g), and the drug adsorption process could be well described by Langmuir isotherm and pseudo-second-order kinetics models. Drug release experiments demonstrated a sustained and controlled release behavior of the aerogels highly dependent on pH and temperature. This process followed quite well the pseudo-second-order release kinetics. Owing to the unique pH- and temperature-responsiveness together with their excellent biodegradability and biocompatibility, the CNFs-PEI aerogels were very promising as a new generation of controlled drug delivery carriers, offering simple and safe alternatives to the conventional systems from synthetic polymers.
首次开发了由聚乙烯亚胺接枝纤维素纳米原纤维(CNFs-PEI)制成的气凝胶作为一种新型药物递送系统。通过扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)对化学改性前后CNFs的形态和结构进行了表征。使用水溶性水杨酸钠(NaSA)作为模型药物来研究药物负载和释放性能。CNFs-PEI气凝胶表现出高药物负载能力(287.39 mg/g),药物吸附过程可以用Langmuir等温线和伪二级动力学模型很好地描述。药物释放实验表明气凝胶具有高度依赖于pH和温度的持续控释行为。该过程很好地遵循伪二级释放动力学。由于其独特的pH和温度响应性以及优异的生物降解性和生物相容性,CNFs-PEI气凝胶作为新一代控释药物载体非常有前景,为传统合成聚合物系统提供了简单安全的替代方案。