University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160 014, India; UGC-Centre of Excellence in Applications of Nanomaterials, Nanoparticles and Nanocomposites, Panjab University, Chandigarh 160 014, India; Dr S.S. Bhatnagar University Institute of Chemical Engineering & Technology, Panjab University, Chandigarh 160 014, India.
UGC-Centre of Excellence in Applications of Nanomaterials, Nanoparticles and Nanocomposites, Panjab University, Chandigarh 160 014, India.
Drug Discov Today. 2018 May;23(5):960-973. doi: 10.1016/j.drudis.2017.11.003. Epub 2017 Nov 10.
Galactosylated nanocarriers have recently emerged as viable and versatile tools to deliver drugs at an optimal rate specifically to their target tissues or cells, thus maximizing their therapeutic benefits while circumventing off-target effects. The abundance of lectin receptors on cell surfaces makes the galactosylated carriers suitable for the targeted delivery of bioactives. Additionally, tethering of galactose (GAL) to various carriers, including micelles, liposomes, and nanoparticles (NPs), might also be appropriate for drug delivery. Here, we review recent advances in the development of galactosylated nanocarriers for active tumor targeting. We also provide a brief overview of the targeting mechanisms and cell receptor theory involved in the ligand-receptor-mediated delivery of drug carriers.
半乳糖化纳米载体最近作为一种可行且多功能的工具出现,能够以最佳速度将药物递送到特定的靶组织或细胞,从而最大限度地提高治疗效果,同时避免脱靶效应。细胞表面丰富的凝集素受体使半乳糖化载体成为生物活性物质靶向递送的理想选择。此外,将半乳糖(GAL)连接到各种载体上,包括胶束、脂质体和纳米颗粒(NPs),也可能适用于药物递送。在这里,我们综述了用于主动肿瘤靶向的半乳糖化纳米载体的最新进展。我们还简要概述了配体-受体介导的药物载体递送上涉及的靶向机制和细胞受体理论。