Wang Jonathan, Masehi-Lano Jacqueline J, Chung Eun Ji
Department of Biomedical Engineering, University of Southern California, Los Angeles, CA 90089, USA.
Biomater Sci. 2017 Jul 25;5(8):1450-1459. doi: 10.1039/c7bm00271h.
The kidney is one of the body's main filtration organs, and hence, opportunity exists for designing nanomedicine that can naturally accumulate in the kidneys for renal diseases. In addition to traditional physiochemical properties for kidney accumulation, such as size and charge, synthesized nanoparticles can be conjugated with targeting ligands which further home the nanocarriers to cell types of interest. In this review, we highlight key studies that have shown success in utilizing peptide- or antibody-based ligands in nanoparticles to target the glomerulus, podocytes, or renal tubule cells in the kidney. In addition, other ligand candidates which have shown renal affinity, but have not yet been integrated into a nanoparticle are also presented. These studies can provide insight into the design of novel clinical solutions for improved detection, prevention, and treatment of renal diseases using nanomedicine efforts.
肾脏是人体主要的过滤器官之一,因此,存在设计可自然在肾脏中蓄积以用于治疗肾脏疾病的纳米药物的机会。除了用于肾脏蓄积的传统物理化学性质,如尺寸和电荷外,合成的纳米颗粒还可以与靶向配体缀合,这进一步使纳米载体归巢至感兴趣的细胞类型。在本综述中,我们重点介绍了一些关键研究,这些研究成功地利用基于肽或抗体的配体修饰纳米颗粒,以靶向肾脏中的肾小球、足细胞或肾小管细胞。此外,还介绍了其他已显示出肾脏亲和力但尚未整合到纳米颗粒中的配体候选物。这些研究可为利用纳米医学手段设计新型临床解决方案提供思路,以改进肾脏疾病的检测、预防和治疗。