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pH-responsive magnetic Fe3O4/carboxymethyl chitosan/aminated lignosulfonate nanoparticles with uniform size for targeted drug loading

盐酸阿霉素 纳米颗粒 药物输送 粒径 壳聚糖 磁性纳米粒子 化学 阿霉素 核化学 吸附 朗缪尔吸附模型 纳米技术 化学工程 材料科学 有机化学 物理化学 医学 外科 化疗 工程类
作者
Qian Liu,Zhenrong Tan,Dafeng Zheng,Xueqing Qiu
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:225: 1182-1192 被引量:36
标识
DOI:10.1016/j.ijbiomac.2022.11.179
摘要

In order to improve the effect of anti-tumor drugs, a magnetic delivery system for targeted drug was reported. Firstly, aminated lignosulfonate (ALS) and carboxymethyl chitosan (CMCS) were used to fabricate nano Fe3O4 to obtain pH-responsive magnetic Fe3O 4 /CMCS/ALS nanoparticles. Then the nanoparticles were loaded with doxorubicin hydrochloride (DOX), realizing the targeted delivery and controlled release of anti-tumor drugs. It was found that the amount of crosslinking agent and emulsifier were the key factors affecting the morphology and size of the magnetic nanoparticles. Under optimized conditions, the particle size was about 79.9-169.9 nm, exhibiting excellent pH responsiveness. When the drug-to-material ratio was 11:10, the DOX loading rate and the encapsulation rate of the nanoparticles was 48.68 % and 86.23 %. While the Fe3O4 /CMCS/ALS-DOX particles could release 63.14 %, 56.71 %, and 14.28 % of DOX at pH 4.0, 5.3, and 7.4, respectively. The results showed that the Fe3O4 /CMCS/ALS particles exhibited excellent drug loading and release behavior based on the pH responsiveness, which could be described by Langmuir adsorption model and Fick's law of diffusion respectively. MTT assay and Live/dead staining experiments also showed that the drug-loaded particles had obvious growth inhibition on cancer cells.
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