Biological chemotaxis-guided self-thermophoretic nanoplatform augments colorectal cancer therapy through autonomous mucus penetration

被引:52
作者
Wang, Zhi-Hao [1 ,2 ,3 ,4 ]
Chu, Mengyu [1 ,2 ,3 ]
Yin, Na [1 ,2 ,3 ]
Huang, Wanting [1 ,2 ,3 ]
Liu, Wei [1 ,2 ,3 ,4 ]
Zhang, Zhenzhong [1 ,2 ,3 ,4 ]
Liu, Junjie [1 ,2 ,3 ,4 ]
Shi, Jinjin [1 ,2 ,3 ,4 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
[2] Henan Key Lab Targeting Therapy & Diag Crit Dis, Zhengzhou 450001, Peoples R China
[3] Minist Educ, Key Lab Adv Drug Preparat Technol, Zhengzhou 450001, Peoples R China
[4] State Key Lab Esophageal Canc Prevent & Treatment, Zhengzhou 450001, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
DRUG-DELIVERY; NANOPARTICLES; BARRIER; CELLS;
D O I
10.1126/sciadv.abn3917
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oral drug delivery systems have great potential to treat colorectal cancer (CRC). However, the drug delivery efficiency is restricted by limited CRC-related intestine positioning and dense mucus barrier. Here, we present a biological chemotaxis-guided self-thermophoretic nanoplatform that facilitates precise intestinal positioning and autonomous mucus penetration. The nanoplatform introduces asymmetric platinum-sprayed mesoporous silica to achieve autonomous movement in intestinal mucus. Furthermore, inspired by the intense interaction between pathogenic microbes and CRC, the nanoplatform is camouflaged by Staphylococcus aureus membrane to precisely anchor in CRC-related intestine. Owing to 4.3-fold higher biological chemotactic anchoring of CRC-related intestine and 14.6-fold higher autonomous mucus penetration performance, the nanoplatform vastly improves the oral bioavailability of cisplatin, leading to a tumor inhibition rate of 99.1% on orthotopic CRC-bearing mice. Together, the exquisitely designed nanoplatform to overcome multiple physiological barriers provides a new horizon for the development of oral drug delivery systems.
引用
收藏
页数:17
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