Kularatne Sumith A, Low Philip S
Department of Chemistry and Purdue Cancer Center, Purdue University, West Lafayette, IN, USA.
Methods Mol Biol. 2010;624:249-65. doi: 10.1007/978-1-60761-609-2_17.
Nanoparticulate medicines offer the advantage of allowing delivery of large quantities of unmodified drug within the same particle. Nanoparticle uptake by cancer cells can, however, be compromised due to the large size and hydrophilicity of the particle. To circumvent cell penetration problems and simultaneously improve tumor specificity, nanoparticulate medicines have been linked to targeting ligands that bind to malignant cell surfaces and enter cells by receptor-mediated endocytosis. In this chapter, we summarize multiple methods for delivering nanoparticles into cancer cells by folate receptor-mediated endocytosis, devoting special emphasis to folate-targeted liposomes. Folate receptor-mediated endocytosis has emerged as an attractive strategy for nanoparticle delivery due to both overexpression of the folate receptor on cancer cells and the rapid internalization of the receptor by receptor-mediated endocytosis.
纳米颗粒药物具有在同一颗粒内递送大量未修饰药物的优势。然而,由于颗粒尺寸较大且具有亲水性,癌细胞对纳米颗粒的摄取可能会受到影响。为了规避细胞穿透问题并同时提高肿瘤特异性,纳米颗粒药物已与靶向配体相连,这些配体可与恶性细胞表面结合并通过受体介导的内吞作用进入细胞。在本章中,我们总结了通过叶酸受体介导的内吞作用将纳米颗粒递送至癌细胞的多种方法,特别着重于叶酸靶向脂质体。由于叶酸受体在癌细胞上的过度表达以及该受体通过受体介导的内吞作用实现快速内化,叶酸受体介导的内吞作用已成为纳米颗粒递送的一种有吸引力的策略。