Suh SeungBeum, Jo Ami, Traore Mahama A, Zhan Ying, Coutermarsh-Ott Sheryl L, Ringel-Scaia Veronica M, Allen Irving C, Davis Richey M, Behkam Bahareh
Department of Mechanical Engineering Virginia Tech Blacksburg VA 24061 USA.
Department of Chemical Engineering Macromolecules Innovation Institute Virginia Tech Blacksburg VA 24061 USA.
Adv Sci (Weinh). 2018 Dec 5;6(3):1801309. doi: 10.1002/advs.201801309. eCollection 2019 Feb 6.
Cancer drug delivery remains a formidable challenge due to systemic toxicity and inadequate extravascular transport of nanotherapeutics to cells distal from blood vessels. It is hypothesized that, in absence of an external driving force, the serovar Typhimurium could be exploited for autonomous targeted delivery of nanotherapeutics to currently unreachable sites. To test the hypothesis, a nanoscale bacteria-enabled autonomous drug delivery system (NanoBEADS) is developed in which the functional capabilities of the tumor-targeting . Typhimurium VNP20009 are interfaced with poly(lactic-co-glycolic acid) nanoparticles. The impact of nanoparticle conjugation is evaluated on NanoBEADS' invasion of cancer cells and intratumoral transport in 3D tumor spheroids in vitro, and biodistribution in a mammary tumor model in vivo. It is found that intercellular (between cells) self-replication and translocation are the dominant mechanisms of bacteria intratumoral penetration and that nanoparticle conjugation does not impede bacteria's intratumoral transport performance. Through the development of new transport metrics, it is demonstrated that NanoBEADS enhance nanoparticle retention and distribution in solid tumors by up to a remarkable 100-fold without requiring any externally applied driving force or control input. Such autonomous biohybrid systems could unlock a powerful new paradigm in cancer treatment by improving the therapeutic index of chemotherapeutic drugs and minimizing systemic side effects.
由于纳米治疗药物存在全身毒性以及向血管远端细胞的血管外转运不足,癌症药物递送仍然是一项艰巨的挑战。据推测,在没有外部驱动力的情况下,鼠伤寒血清型细菌可用于将纳米治疗药物自主靶向递送至目前无法到达的部位。为了验证这一假设,开发了一种纳米级细菌驱动的自主药物递送系统(NanoBEADS),其中肿瘤靶向鼠伤寒沙门氏菌VNP20009的功能与聚乳酸-乙醇酸纳米颗粒相结合。评估了纳米颗粒偶联对NanoBEADS体外侵袭癌细胞和在三维肿瘤球体中的瘤内转运以及在体内乳腺肿瘤模型中的生物分布的影响。研究发现,细胞间(细胞之间)的自我复制和易位是细菌瘤内渗透的主要机制,并且纳米颗粒偶联不会阻碍细菌的瘤内转运性能。通过开发新的转运指标,证明了NanoBEADS在不需要任何外部施加的驱动力或控制输入的情况下,可将纳米颗粒在实体瘤中的保留和分布提高多达100倍。这种自主生物杂交系统可以通过提高化疗药物的治疗指数并最大限度地减少全身副作用,在癌症治疗中开启一个强大的新范例。