School of Chemistry, University of New South Wales, Sydney, NSW 2052, Australia.
Australian Centre for NanoMedicine, University of New South Wales, Sydney, NSW 2052, Australia.
Chem Soc Rev. 2022 Aug 30;51(17):7531-7559. doi: 10.1039/d1cs00707f.
Targeted drug delivery in cancer typically focuses on maximising the endocytosis of drugs into the diseased cells. However, there has been less focus on exploiting the differences in the endocytosis pathways of cancer cells non-cancer cells. An understanding of the endocytosis pathways in both cancer and non-cancer cells allows for the design of nanoparticles to deliver drugs to cancer cells whilst restricting healthy cells from taking up anticancer drugs, thus efficiently killing the cancer cells. Herein we compare the differences in the endocytosis pathways of cancer and healthy cells. Second, we highlight the importance of the physicochemical properties of nanoparticles (size, shape, stiffness, and surface chemistry) on cellular uptake and how they can be adjusted to selectively target the dominated endocytosis pathway of cancer cells over healthy cells and to deliver anticancer drug to the target cells. The review generates new thought in the design of cancer-selective nanoparticles based on the endocytosis pathways.
癌症的靶向药物输送通常侧重于最大限度地增加药物进入病变细胞的内吞作用。然而,人们对利用癌细胞和非癌细胞的内吞途径差异的关注较少。了解癌细胞和非癌细胞的内吞途径可以设计纳米颗粒将药物递送到癌细胞,同时限制健康细胞摄取抗癌药物,从而有效地杀死癌细胞。本文比较了癌细胞和健康细胞的内吞途径的差异。其次,我们强调了纳米颗粒的物理化学性质(大小、形状、硬度和表面化学性质)对细胞摄取的重要性,以及如何调整这些性质以选择性地针对癌细胞而非健康细胞的主导内吞途径,并将抗癌药物递送到靶细胞。该综述基于内吞途径为设计癌症选择性纳米颗粒提供了新的思路。