Efficient intracellular delivery of siRNA with a safe multitargeted lipid-based nanoplatform
- PMID: 23394132
- DOI: 10.2217/nnm.12.174
Efficient intracellular delivery of siRNA with a safe multitargeted lipid-based nanoplatform
Abstract
Aim: The design of novel F3-targeted liposomes with adequate features for systemic administration, to enable efficient intracellular delivery of siRNA toward both cancer and endothelial cells from angiogenic blood vessels.
Materials & methods: Cellular association studies were performed by flow cytometry. Gene silencing was evaluated with eGFP-overexpressing cells, by flow cytometry and real-time reverse-transcription PCR. Safety and immunogenicity was assessed in CD1 mice.
Results: A strong improvement on siRNA internalization by the target cells was achieved, which was correlated with effective downregulation of eGFP. In addition, the F3-targeted liposomes were nonimmunogenic, even in a multiadministration schedule.
Conclusion: Overall, the developed F3-targeted nanocarrier constitutes a valuable tool for the specific and safe systemic delivery of siRNA to solid tumors.
Similar articles
-
Toward a siRNA-containing nanoparticle targeted to breast cancer cells and the tumor microenvironment.Int J Pharm. 2012 Sep 15;434(1-2):9-19. doi: 10.1016/j.ijpharm.2012.05.018. Epub 2012 May 19. Int J Pharm. 2012. PMID: 22617794
-
Impact of anti-PLK1 siRNA-containing F3-targeted liposomes on the viability of both cancer and endothelial cells.Eur J Pharm Biopharm. 2013 Nov;85(3 Pt A):356-64. doi: 10.1016/j.ejpb.2013.04.007. Epub 2013 May 7. Eur J Pharm Biopharm. 2013. PMID: 23659854
-
Mesoporous silicon particles for sustained gene silencing.Methods Mol Biol. 2013;1049:481-93. doi: 10.1007/978-1-62703-547-7_36. Methods Mol Biol. 2013. PMID: 23913239
-
Lipid-based nanoparticles in the systemic delivery of siRNA.Nanomedicine (Lond). 2014 Jan;9(1):105-20. doi: 10.2217/nnm.13.192. Nanomedicine (Lond). 2014. PMID: 24354813 Review.
-
Physicochemical characterization techniques for lipid based delivery systems for siRNA.Int J Pharm. 2012 May 1;427(1):35-57. doi: 10.1016/j.ijpharm.2011.09.032. Epub 2011 Sep 29. Int J Pharm. 2012. PMID: 21979250 Review.
Cited by
-
Precise and efficient siRNA design: a key point in competent gene silencing.Cancer Gene Ther. 2016 Apr;23(4):73-82. doi: 10.1038/cgt.2016.4. Epub 2016 Mar 18. Cancer Gene Ther. 2016. PMID: 26987292 Review.
-
Molecular Mechanisms and Biological Functions of siRNA.Int J Biomed Sci. 2017 Jun;13(2):48-57. Int J Biomed Sci. 2017. PMID: 28824341 Free PMC article. Review.
-
Ligand-Targeted Delivery of Photosensitizers for Cancer Treatment.Molecules. 2020 Nov 14;25(22):5317. doi: 10.3390/molecules25225317. Molecules. 2020. PMID: 33202648 Free PMC article. Review.
-
Cancer Stem Cells and Nucleolin as Drivers of Carcinogenesis.Pharmaceuticals (Basel). 2021 Jan 13;14(1):60. doi: 10.3390/ph14010060. Pharmaceuticals (Basel). 2021. PMID: 33451077 Free PMC article. Review.
-
Nucleolin Overexpression Predicts Patient Prognosis While Providing a Framework for Targeted Therapeutic Intervention in Lung Cancer.Cancers (Basel). 2022 Apr 29;14(9):2217. doi: 10.3390/cancers14092217. Cancers (Basel). 2022. PMID: 35565346 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous