School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, United States; Research Institute for Bioscience and Biotechnology (RIBB), Nakkhu, Lalitpur 44600, Nepal.
School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, United States.
Biotechnol Adv. 2020 Sep-Oct;42:107339. doi: 10.1016/j.biotechadv.2019.01.006. Epub 2019 Jan 11.
Clinical translation of nanoparticle drug (nanodrug) delivery systems for cancer therapy is primarily hindered by short half-life of nanodrugs in blood circulation and their poor ability of tumor targeting and penetration in vivo. Circulatory cells have garnered much attention in cancer therapy as drug delivery vehicles due to their biocompatibility, high mobility, biodegradability, tissue targeting capability, high drug loading capacity, ability to cross biological barriers and inherent ability to remain in blood circulation long enough to accumulate within the tumors. Here, we review the progress and potential of circulatory cells as nanodrug delivery vehicles, especially for cancer therapy.
临床中,纳米药物(纳米药物)输送系统在癌症治疗方面的应用主要受到纳米药物在血液循环中半衰期短和体内肿瘤靶向和穿透能力差的限制。循环细胞由于其生物相容性、高迁移性、生物降解性、组织靶向能力、高载药能力、穿越生物屏障的能力以及在血液循环中足够长时间停留以在肿瘤内积累的固有能力,已引起人们对癌症治疗作为药物输送载体的极大关注。在此,我们综述了循环细胞作为纳米药物载体,特别是用于癌症治疗的进展和潜力。