Nanostructured Systems for the Organelle-specific Delivery of Anticancer Drugs

被引:12
|
作者
Joanitti, Graziella Anselmo [1 ,2 ]
Ganassin, Rayane [2 ]
Rodrigues, Mosar Correa [2 ]
Figueiro Longo, Joao Paulo [2 ]
Jiang, Cheng-Shi [3 ]
Gu, Jinsong [3 ]
Leal Pinto, Sandra Milena [2 ]
Menezes Almeida dos Santos, Maria de Fatima [2 ]
de Azevedo, Ricardo Bentes [2 ]
Muehlmann, Luis Alexandre [1 ,2 ]
机构
[1] Univ Brasilia, Fac Ceilandia, BR-72220900 Brasilia, DF, Brazil
[2] Univ Brasilia, Inst Biol Sci, Dept Genet & Morphol, BR-70910900 Brasilia, DF, Brazil
[3] Univ Jinan, Sch Biol Sci & Technol, Jinan 250022, Shandong, Peoples R China
关键词
Anticancer therapy; chemotherapy; nanostructured drug delivery systems; nanotechnology; subcellular delivery; LYSOSOMAL MEMBRANE PERMEABILIZATION; NUCLEAR-LOCALIZATION SIGNAL; PHOTODYNAMIC THERAPY; CANCER-CELLS; IN-VITRO; POLYAMIDOAMINE DENDRIMER; TARGETING MITOCHONDRIA; CALRETICULIN EXPOSURE; ENDOPLASMIC-RETICULUM; PLASMA-MEMBRANE;
D O I
10.2174/1389557516666161013104554
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Nanotechnology has provided powerful tools to improve the chemotherapy of cancer. Different nanostructures have been developed which deliver the anticancer drugs more selectively to tumor than to healthy tissues. The result has generally been the increase in efficacy and safety of classical anticancer drugs. In recent years, several studies have focused not only on the delivery of anticancer drugs to tumors, but also on delivering the drugs to specific organelles of cancer cells. Endoplasmic reticulum, Golgi apparatus, lysosomes, mitochondria, and nucleus have been the targets of different nanostructured drug delivery systems developed with the goal of circumventing drugresistance, increasing drug efficacy, and so on. So far, the results described in the literature show that this strategy may be used to improve chemotherapy outcomes. In this review a discussion is presented on the strategies described in the literature to deliver anticancer drugs to specific organelles of cancer cells by using nanostructures.
引用
收藏
页码:224 / 236
页数:13
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