Colistin Crosslinked Gemcitabine Micelles to Eliminate Tumor Drug Resistance Caused by Intratumoral Microorganisms.
Qian QiuDi LuGengqi LiuXingyue YangJiexin LiHe RenJingang LiuBoyang SunYumiao ZhangPublished in: Bioconjugate chemistry (2022)
In the tumor microenvironment, there exist microorganisms that metabolize anticancer drugs, leading to chemotherapy failure. To solve this problem, herein, we develop antibiotic and anticancer drug co-delivery micelles, termed colistin crosslinked gemcitabine micelle (CCGM). A self-immolative linker enables colistin and gemcitabine to be released on demand without affecting their antibacterial and anticancer effects. Once CCGM is delivered to the tumor microenvironment, intracellular glutathione triggers the release of colistin and gemcitabine, inhibiting the growth of microbes in the tumor, thus eliminating the microbe-induced drug resistance of tumor.
Keyphrases
- escherichia coli
- acinetobacter baumannii
- pseudomonas aeruginosa
- klebsiella pneumoniae
- locally advanced
- multidrug resistant
- gram negative
- drug resistant
- drug delivery
- hyaluronic acid
- rectal cancer
- cancer therapy
- drug induced
- cystic fibrosis
- emergency department
- signaling pathway
- radiation therapy
- drug release
- high glucose
- diabetic rats
- endothelial cells
- oxidative stress