A pure molecular drug hydrogel for post-surgical cancer treatment

被引:36
|
作者
Qian, Qiuhui [1 ,3 ]
Wang, Dali [1 ]
Shi, Leilei [1 ]
Zhang, Zhihao [1 ]
Qian, Jiwen [1 ]
Shen, Jian [2 ]
Yu, Chunyang [1 ]
Zhu, Xinyuan [1 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Sch Chem & Chem Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Nanjing Normal Univ, Coll Chem & Mat Sci, Jiangsu Key Lab Biomed Mat, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Nanjing 210046, Peoples R China
[3] Suzhou Univ Sci & Technol, Sch Environm Sci & Engn, Natl & Local Joint Engn Lab Municipal Sewage Reso, Suzhou 215009, Peoples R China
基金
中国国家自然科学基金;
关键词
Raltitrexed; Self-delivery hydrogels; Tumor recurrence; Drug delivery; Supramolecular chemistry; THERAPY; RECURRENCE; SCAFFOLDS;
D O I
10.1016/j.biomaterials.2020.120403
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Local drug delivery systems, especially hydrogels, show superior strengths in postoperative recurrence prevention. Despite great advances, clinical translation of the hydrogels has been largely restricted as these drug delivery systems generally require chemical modification or additional carrier molecules to form hydrogels, which results in side effects correlative with local inflammation and systemic toxicity. Here, we developed a pure molecular anticancer drug hydrogel that reduced post-surgical tumor recurrence. The macroscopic pure molecular hydrogel was generated via ultrasonication of anticancer drug raltitrexed in aqueous solution, which was facile and environmentally friendly without involving chemical synthesis. Molecular dynamics simulations confirmed that raltitrexed self-assembled into a nanofibrous hydrogel through hydrogen bond and pi-pi interaction. Delivered as a hydrogel, raltitrexed could effectively decrease tumor recurrence rate and promote the inhibition of tumor growth in vivo. This raltitrexed self-delivery hydrogel has the potential to serve as a powerful auxiliary implement for preventing postoperative local tumor recurrence.
引用
收藏
页数:10
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