海藻酸钠
共轭体系
钠
化学
离子键合
乳腺癌
化学工程
材料科学
聚合物
癌症
离子
有机化学
医学
内科学
工程类
作者
Raviraj Pansuriya,Tapas Patel,Kuldeep Singh,Azza Al Ghamdi,Naresh Kasoju,Arvind Kumar,Suresh Kumar Kailasa,Naved I. Malek
标识
DOI:10.1016/j.ijbiomac.2024.134112
摘要
Designing stimuli-responsive drug delivery vehicles with higher drug loading capacity, sustained and targeted release of anti-cancer drugs and able to mitigate the shortcomings of traditional systems is need of hour. Herein, we designed stimuli-responsive, self-healable, and adhesive hydrogel through synergetic interaction between [Cho][Gly] (Choline-Glycine) and sodium alginate (SA). The hydrogel was formed as a result of non-covalent interaction between the components of the mixture forming the fibre kind morphology; confirmed through FTIR/computational analysis and SEM/AFM images. The hydrogel exhibited excellent mechanical strength, self-healing ability, adhesive character and most importantly; adjustable injectability. In vitro biocompatibility of the hydrogel was tested on HaCaT and MCF-7 cells, showing >92 % cell viability after 48 h. The hemolysis ratio (<4 %) of the hydrogel confirmed the blood compatibility of the hydrogel. When tested for drug-loading capacity, the hydrogel show 1500 times drug loading for the 5-fluorouracil (5-FU) against the SA based hydrogel. In vitro release data indicated that 5-FU have more preference towards the cancerous cell condition, i.e. acidic pH (>85 %), whereas the drug-loaded hydrogel successfully killed the MCF-7 and HeLa cell with a
科研通智能强力驱动
Strongly Powered by AbleSci AI