Key Laboratory of Biomedical Polymers of Ministry of Education and Department of Chemistry , Wuhan University , Wuhan 430072 , People's Republic of China.
The Institute for Advanced Studies , Wuhan University , Wuhan 430072 , People's Republic of China.
Nano Lett. 2018 Apr 11;18(4):2373-2380. doi: 10.1021/acs.nanolett.7b05323. Epub 2018 Mar 22.
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.
口服给药被广泛应用于各种药物,由于其能够通过血液流到达身体的不同部位,因此使用方便。然而,对于蛋白质和核酸等生物大分子抗肿瘤药物,由于通过胃肠道(GIT)吸收有限和肿瘤靶向性差,一般不可行。在这里,我们报告了一种非侵入性的热敏感可编程治疗系统,该系统使用细菌大肠杆菌 MG1655 作为载体,通过口服给药进行肿瘤治疗。热敏可编程细菌(TPB)被表达治疗蛋白 TNF-α的质粒转化,然后用生物矿化金纳米颗粒(AuNPs)修饰,以获得 TPB@Au。AuNPs 和 TNF-α 质粒在肠道中被 TPB 有效保护,可以通过微褶皱细胞(M 细胞)的转胞吞作用被转运到内部微循环中。之后,由于归巢到肿瘤微环境的厌氧菌特性,基于细菌的抗肿瘤载体在肿瘤部位聚集。体外和体内实验验证了 TPB 对 AuNPs 和 TNF-α 质粒的成功递呈。重要的是,在远程激活下,肿瘤部位 TNF-α 的表达可以通过光热 AuNPs 产生的热量精确控制,从而发挥治疗作用。生物安全性评估表明,该策略不会干扰肠道菌群的平衡。