Nucleoside–Lipid-Based Nanoparticles for Cisplatin Delivery
Source abstract
Abstract
The use of delivery vehicles to selectively transport anticancer agents to tumors is very attractive to address both toxicity and efficacy issues. We report a novel approach based on hybrid nucleoside-lipids allowing the efficient encapsulation and delivery of cisplatin. We demonstrate that the nucleoside polar heads guide the self-assembly of the aggregates into highly loaded and stable nanoparticles. The nanoparticles, which are efficient vehicles for the delivery of cisplatin into different sensitive and resistant cancer cell lines, can overcome the disadvantages and limitations of drug delivery systems previously reported.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoparticle-Based Drug Delivery · Advanced biosensing and bioanalysis techniques · RNA Interference and Gene Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
INSERM U869, Bordeaux F-33076, France
Université de Bordeaux, Bordeaux F-33076, France
CINaM, Université de la méditerranée, 13288 Marseille cedex 9, France
CHU Amiens-Picardie, 80054 Amiens Cedex, France
References (32)
Show source-provided references
1. Rosenberg B. · Nature · 1969 · 222 · 38510.1038/222385a0 ↗
2. Jamieson E. R. · Chem. Rev. · 1999 · 99 · 246710.1021/cr980421n ↗
3. Galanski M. · Curr. Med. Chem. · 2005 · 12 · 207510.2174/0929867054637626 ↗
4. Stordal B. · IUBMB Life · 2007 · 59 · 69610.1080/15216540701636287 ↗
5. Yao X. · Am. J. Med. Sci. · 2007 · 334 · 11510.1097/MAJ.0b013e31812dfe1e ↗
6. Van den Bent M. J. · Eur. J. Cancer · 2002 · 38 · 38710.1016/S0959-8049(01)00381-1 ↗
7. Duncan R. · Nat. Rev. Cancer · 2006 · 6 · 68810.1038/nrc1958 ↗
8. Wagner V. · Nat. Biotechnol. · 2006 · 24 · 121110.1038/nbt1006-1211 ↗
9. Ferrari M. · Nat. Rev. Cancer · 2005 · 5 · 16110.1038/nrc1566 ↗
10. Brigger I. · Adv. Drug Delivery Rev. · 2002 · 54 · 63110.1016/S0169-409X(02)00044-3 ↗
11. Peer D. · Nat. Nanotechnol. · 2007 · 2 · 75110.1038/nnano.2007.387 ↗
12. Boulikas T. · Oncol. Rep. · 2004 · 12 · 3
13. Burger K. N. J. · Nat. Med. · 2002 · 8 · 8110.1038/nm0102-81 ↗
14. Uchino H. · Br. J. Cancer · 2005 · 93 · 67810.1038/sj.bjc.6602772 ↗
15. Santosh A. · ACS Nano · 2010 · 4 · 25110.1021/nn9014032 ↗
16. Tian Y. · J. Controlled Release · 2007 · 121 · 13710.1016/j.jconrel.2007.05.010 ↗
17. Kaida S. · Cancer Res. · 2010 · 70 · 703110.1158/0008-5472.CAN-10-0303 ↗
18. Boulikas T. · Oncol. Rep. · 2004 · 11 · 559
19. Dhar S. · Proc. Natl. Acad. Sci. U.S.A. · 2008 · 105 · 1735610.1073/pnas.0809154105 ↗
20. Dhar S. · Proc. Natl. Acad. Sci. U.S.A. · 2011 · 108 · 185010.1073/pnas.1011379108 ↗
21. Paraskar A. S. · Proc. Natl. Acad. Sci. U.S.A. · 2010 · 107 · 1243510.1073/pnas.1007026107 ↗
22. Gissot A. · Org. Biomol. Chem. · 2008 · 6 · 132410.1039/b719280k ↗
23. Barthélémy P. · CR Chimie · 2009 · 12 · 17110.1016/j.crci.2008.09.015 ↗
24. Khiati S. · Bioconjugate Chem. · 2009 · 20 · 176510.1021/bc900163s ↗
25. Chabaud P. · Bioconjugate Chem. · 2006 · 17 · 46610.1021/bc050162q ↗
26. Burger K. N. · Nat. Med. · 2002 · 8 · 8110.1038/nm0102-81 ↗
27. Legendre F. · Chem.—Eur. J. · 2000 · 6 · 200210.1002/1521-3765(20000602)6:11<2002::AID-CHEM2002>3.0.CO;2-H ↗
28. Chupin V. · J. Am. Chem. Soc. · 2004 · 42 · 1381610.1021/ja0468933 ↗
29. Zwelling L. A. · Cancer Res. · 1978 · 38 · 1762
30. Kelland L. · Nat. Rev. Cancer · 2007 · 7 · 57310.1038/nrc2167 ↗
31. Kartalou M. · Mutat. Res. · 2001 · 478 · 2310.1016/S0027-5107(01)00141-5 ↗
32. Siddik Z. H. · Oncogene · 2003 · 22 · 726510.1038/sj.onc.1206933 ↗