Department of Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China.
Chem Asian J. 2018 Nov 16;13(22):3333-3340. doi: 10.1002/asia.201800149. Epub 2018 Mar 30.
The application of nanotechnology in the treatment of tumors has boomed owing to the vigorous development in cancer nanomedicine. Despite the great success achieved in this field, nanomedicine has not realized its full potential owing to a delivery barrier, the mononuclear phagocytic system (MPS), which cuts off more than 95 % of the administrated nanoparticles. This results in an extremely low drug-delivery efficacy to the tumor and leads to poor therapeutic outcomes. Moreover, the injection of excess nanoparticles also raises toxicity concerns induced by the accumulation of nanomaterials in organs, such as the liver and spleen. Therefore, a reduction in the uptake of nanomedicines by the MPS is vital to enhance the cancer therapeutic effect and decrease side effects. In this critical review, we will summarize the new strategies to reduce nanoparticle uptake by the MPS based on current knowledge of the bio-nano interaction. Further directions will also be highlighted for the development of cancer nanomedicine with a lower off-target rate and better therapeutic outcomes.
由于癌症纳米医学的蓬勃发展,纳米技术在肿瘤治疗中的应用得到了迅猛发展。尽管在该领域取得了巨大的成功,但由于存在一个输送障碍——单核吞噬细胞系统(MPS),纳米医学尚未发挥其全部潜力,该系统阻断了超过 95%的给予的纳米颗粒。这导致了药物向肿瘤的递送效率极低,从而导致治疗效果不佳。此外,过量的纳米粒子注射也会引起人们对纳米材料在肝脏和脾脏等器官中积累所引起的毒性的关注。因此,减少 MPS 对纳米药物的摄取对于提高癌症治疗效果和降低副作用至关重要。在这篇重要的综述中,我们将根据目前对生物-纳米相互作用的认识,总结减少 MPS 摄取纳米颗粒的新策略。此外,还将突出强调具有更低脱靶率和更好治疗效果的癌症纳米医学的发展方向。