Advances with Lipid-Based Nanosystems for siRNA Delivery to Breast Cancers

被引:27
作者
Subhan, Md Abdus [1 ,2 ]
Filipczak, Nina [3 ]
Torchilin, Vladimir P. [3 ,4 ]
机构
[1] ShahJalal Univ Sci & Technol, Dept Chem, Sylhet 3114, Bangladesh
[2] Univ Rochester, Med Ctr, Sch Med & Dent, Div Nephrol, 601 Elmwood Ave,Box 675, Rochester, NY 14642 USA
[3] Northeastern Univ, Ctr Pharmaceut Biotechnol & Nanomed, Dept Pharmaceut Sci, Boston, MA 02115 USA
[4] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
关键词
lipid NPs; breast cancer; siRNA delivery; gene silencing; personalized therapy; CALCIUM-PHOSPHATE NANOPARTICLES; POLYMER HYBRID NANOPARTICLES; IN-VIVO; CO-DELIVERY; CATIONIC LIPOSOME; RNA INTERFERENCE; THERAPEUTIC DELIVERY; GENE; PACLITAXEL; CELL;
D O I
10.3390/ph16070970
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Breast cancer is the most frequently diagnosed cancer among women. Breast cancer is also the key reason for worldwide cancer-related deaths among women. The application of small interfering RNA (siRNA)-based drugs to combat breast cancer requires effective gene silencing in tumor cells. To overcome the challenges of drug delivery to tumors, various nanosystems for siRNA delivery, including lipid-based nanoparticles that protect siRNA from degradation for delivery to cancer cells have been developed. These nanosystems have shown great potential for efficient and targeted siRNA delivery to breast cancer cells. Lipid-based nanosystems remain promising as siRNA drug delivery carriers for effective and safe cancer therapy including breast cancer. Lipid nanoparticles (LNPs) encapsulating siRNA enable efficient and specific silencing of oncogenes in breast tumors. This review discusses a variety of lipid-based nanosystems including cationic lipids, sterols, phospholipids, PEG-lipid conjugates, ionizable liposomes, exosomes for effective siRNA drug delivery to breast tumors, and the clinical translation of lipid-based siRNA nanosystems for solid tumors.
引用
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页数:22
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