光热治疗
细菌
癌症研究
材料科学
跨细胞
质粒
肿瘤坏死因子α
体内
化学
生物
纳米技术
DNA
免疫学
生物化学
细胞
内吞作用
生物技术
遗传学
作者
Jin‐Xuan Fan,Zi-Hao Li,Xinhua Liu,Di‐Wei Zheng,Ying Chen,Xian‐Zheng Zhang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2018-03-20
卷期号:18 (4): 2373-2380
被引量:216
标识
DOI:10.1021/acs.nanolett.7b05323
摘要
Oral drug administration is widely adopted for diverse drugs and is convenient to use due to the capability of reaching different parts of the body via the bloodstream. However, it is generally not feasible for biomacromolecular antitumor drugs such as protein and nucleic acids due to the limited absorption through gastrointestinal tract (GIT) and the poor tumor targeting. Here, we report a noninvasive thermally sensitive programmable therapetic system using bacteria E. coli MG1655 as an vehicle for tumor treatments via oral administration. Thermally sensitive programmable bacteria (TPB) are transformed with plasmids expressing therapeutic protein TNF-α and then decorated with biomineralized gold nanoparticles (AuNPs) to obtain TPB@Au. AuNPs and TNF-α plasmids efficaciously protected by TPB in the gut can be transported into internal microcirculation via transcytosis of microfold cells (M cells). After that, the bacteria-based antitumor vehicles accumulate at tumor sites due to the anaerobic bacterial feature of homing to tumor microenvironments. In vitro and in vivo experiments verify the successful delivery of AuNPs and TNF-α plasmids by TPB. Importantly, under remote activation the expression of TNF-α in tumor sites can be procisely controlled by the heat generated from photothermal AuNPs to exert therapeutic actions. The biological security evaluation demonstrates that this strategy would not disturb the balance of intestinal flora.
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