Cisplatin-loaded SLN produced by coacervation technique

Journal of Drug Delivery Science and Technology

Volumn 20, Issue 5, 2010, Pages 343-347

  Gallarate, M ^a   Trotta, M ^a   Battaglia, L ^a   Chirio, D ^a  

^a UNIVERSITY OF TURIN   (Italy)

Author keywords

Cisplatin; Coacervation; Ion pairs; SLN

Indexed keywords

CISPLATIN; DOCUSATE SODIUM; SOLID LIPID NANOPARTICLE; STEARATE SODIUM; STEARIC ACID; UNCLASSIFIED DRUG;

ARTICLE; COACERVATION; DRUG FORMULATION; DRUG RELEASE; ENCAPSULATION; MICELLE; PARTICLE SIZE; SOLUBILIZATION;

EID: 78349241054     PISSN: 17732247     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1773-2247(10)50057-1     Document Type: Article

References (26)

1. Müller R.H., Mäder K., Gohla S. - Solid lipid nanoparticles (SLN) for controlled drug delivery - a review of the state of the art. - Eur. J. Pharm. Biopharm., 50, 161-177, 2000.
2. Müller R.H., Lucks J.S. - Arzneistoffträger aus festen Lipid-Teilchen, Feste Lipidnanosphären (SLN). - Eur. Patent No. 06055497, 16 May 1996.
3. Gasco M.R. - Method for producing solid lipid microspheres having a narrow size distribution - US Patent No. 5250236, 5 October 1993.
4. Mumper R.J., Jay M. - Microemulsions as precursors to solid lipid nanoparticles - US Patent No. 7153525, 26 December 2006.
5. Siekmann B., Westesen K. - Investigation on solid lipid nanoparticles prepared by precipitation in o/w emulsion. - Eur. J. Pharm. Biopharm., 43, 104-109, 1996.
6. Schubert M.A., Müller-Goymann C.C. - Solvent injection as a new approach for manufacturing lipid nanoparticles - evaluation of the method and process parameters. - Eur. J. Pharm. Biopharm., 55, 125-131, 2003.
7. Battaglia L., Trotta M., Gallarate M., Carlotti M.E., Zara G.P., Bargoni A. - Solvent lipid nanoparticles formed by solvent-in-water emulsion diffusion technique: development and influence of insulin stability. - J. Microencaps., 14, 672-684, 2007.
8. Gallarate M., Trotta M., Battaglia L., Chirio D. - Preparation of solid lipid nanoparticles from w/o/w emulsions: preliminary studies on insulin encapsulation.-J. Microencaps., 26, 394-402, 2009.
9. Battaglia L., Gallarate M., Cavalli R., Trotta M. - Solid lipid nanoparticles produced through a coacervation method. - J. Microencaps., 27, 78-85, 2010.
10. Bianco M.A., Gallarate M., Trotta M., Battaglia L. - Amphotericin B loaded SLN prepared with the coacervation technique. - J. Drug Del. Sci. Tech., 20, 187-191, 2010.
11. Rouzes C., Durand A., Leonard M., Dellacherie E. - Surface activity and emulsification properties of hydrophobically modified dextrans - J. Colloid Interface Sci., 253, 217-223, 2002.
12. Rebik C.A., Dolan M.E. - Molecular mechanisms of resistance and toxicity associated with platinating agents. - Cancer Treat. Rev., 33, 9-13, 2007.
13. Young-Il J., Seong-Taek K., Shu-Guang J., Hyang-Hwa R., Yong-Hao J., Tae-Young J., In-Young K., Shin J. - Cisplatin-incorporated hyaluronic acid nanoparticles based on ion-complex formation. - J. Pharm. Sci., 97, 1268-1276, 2008.
14. Avgoustakis K., Beletsi A., Panagi Z., Klepetsanis P., Karydas A.G., Ithakissios D.S. - PLGA-mPEG nanoparticles of cisplatin: in vitro nanoparticle degradation, in vitro drug release and in vivo drug residence in blood properties. - J. Control. Rel., 79, 123-135, 2002.
15. Gryparis E.C., Hatziapostolou M., Papadimitriou E., Avgoustakis K. - Anticancer activity of cisplatin-loaded PLGA-mPEG nanoparticles on LNCaP prostate cancer cells. - Eur. J. Pharm. Biopharm., 67, 1-8, 2007.
16. Peisheng X., Van Kirk E.A., Shiyan L., Murdoch W.J., Ren J., Hussain M.D., Radosz M., Youqing S. - Highly stable core-surface crosslinked nanoparticles as cisplatin carriers for cancer chemotherapy. - Colloids and Surfaces B: Biointerfaces, 48, 50-57, 2006.
17. Cohen M.S., Cai S., Xie Y., Forrest M.L. - A novel intralymphatic nanocarrier delivery system for cisplatin therapy in breast cancer with improved tumor efficacy and lower systemic toxicity in vivo - Am. J. Surg., 198, 781-786, 2009.
18. Moreno D., Zalba S., Navarro I., Tros De Ilarduya C., Garrido M. J. - Pharmacodynamics of cisplatin-loaded PLGA nanoparticles administered to tumor-bearing mice - Eur. J. Pharm. Biopharm., 74, 265-274, 2010.
19. Feng L., De Dille A., Jameson V.J., Smith L., Dernell W.S., Manning M.C. - Improved potency of cisplatin by hydrophobic ion pairing - Cancer Chemother. Pharmacol., 54, 441-448, 2004.
20. Raghavan R., Burchett M., Loffredo D., Mulligan J.A. - Low-Level (PPB) Determination of cisplatin in cleaning validation (Rinse Water) samples. II. A high-performance liquid chromatographic method. - Drug Dev. Ind. Pharm., 6, 429-440, 2000.
21. Sato K. - Solvent effects on crystallization of polymorphic modifications of lipids, morphology and growth unit of crystals. - Tokyo, Terrapub., 1989, p. 513.
22. Siekmann B., Westesen K. - Thermoanalysis of the recrystallization process of melt-homogenized glyceride nanoparticles - Colloid Surf. B, 3, 159-175, 1994.
23. Hunter R.J. - Foundation of Colloidal Science. - Oxford, Oxford University Press, 1986.
24. Hou D., Xie C., Huang K., Zhu C. - The production and characteristics of solid lipid nanoparticles (SLN) - Biomaterials, 24, 1781-1785, 2003.
25. Liu J., Gong T., Wang C., Zhong Z., Zhang Z. - Solid lipid nanoparticles loaded with insulin by sodium cholate-phosphatidylcholine-based mixed micelles. Preparation and characterisation - Int. J. Pharm., 340, 153-162, 2007.
26. Goto M., Asada E. - The crystal structure of the B-form of stearic acid - Bull. Chem. Soc. Jap., 51, 2456-2459, 1978.