Evaluation of liposomal nanosystems as oncological treatment and diagnostic agents.

Authors

DOI:

https://doi.org/10.35954/SM2015.34.1.3

Keywords:

Cancer Diagnostics; Nanotechnology; Breast Neoplasms; Drug Delivery Systems

Abstract

Curcumin is a natural polyphenol molecule derived from the plant Curcuma longa that exhibits anticancer, antifungal, antiviral, antioxidative, anti-inflammatory and antiploriferative properties.  Curcumin is widely available in the world, is safe, inexpensive and has multiple cancer-fighting functions that justify its development as a drug for cancer treatment. However, several basic and clinical studies have elucidated its limited efficacy due to its low solubility, high metabolism rate and low bioavailability.  In order to target curcumin more selectively to tumor formations and to overcome all the aforementioned disadvantages, various liposomal strategies such as "nanocarriers" for curcumin encapsulation were studied. There fore, in order to enhance the action and delivery of curcumin as an antineoplastic, a liposomal curcumin nanosystem was developed. The in vitro antitumor effect of curcumin and liposomal curcumin was evaluated in 4T1 murine mammary tumor cells and ex vivo studies were performed in a murine model of mammary tumor induced with 4T1 cells.  The results obtained have been very encouraging, we have achieved the encapsulation of curcumin, with an encapsulation efficiency of 31 %. Stable liposomal formulations were obtained, which could be characterized, showing that they had a manometric size (240 nm).  Both curcumin and the developed nanosystem, at the concentrations studied, were shown to be cytotoxic in murine 4T1 breast cancer cells.  Therefore, the developed nanosystem has potential for the development of liposomal formulations in tumor targeting applications for imaging and oncological treatment.

 

Received for evaluation: January 2015
Accepted for publication: May 2015
Correspondence: Radiopharmacy Laboratory, Nuclear Research Center, Faculty of Sciences, Universidad de la Republica. Mataojo 2055, C.P. 11400, Montevideo, Uruguay. Tel: (+598)25250901/108; fax: (+598)25250895.
Contact e-mail: pcabral@cin.edu.uy

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

(1) Maheshwari R, Singh A, Gaddipati J, Srimal R. Multiple biological activities of curcumin: A short review. Life Sci 2006; 78(18):2081-7.

(2) Anand P, Kunnumakkara A, Newman R, Aggarwal B. Bioavailability of curcumin: Problems and promises. Mal Pharm 2007; 4(6):807-18.

(3) Lopez-Lazaro M. Anticancer and carcinogenic properties of curcumin: Considerations for its clinical development as a cancer chemopreventive and chemotherapeutic agent. Mol Nutr Food Res 2008; 52(Suppl.1):103-27.

(4) Shenoy D, Amiji M. Poly(ethylene oxide)-modified poly(??-caprolactone) nanoparticles for targeted delivery of tamoxifen in breast cancer. Int J Pharm 2005; 293(1- 2):261-70.

(5) Akbarzadeh A, Rezaei-Sadabady R, Davaran S, Joo SW, Zarghami N, Hanifehpour Y, et.al. Liposome: classification, preparation, and applications. Nanoscale Res Lett 2013; 8(1):102.

(6) Fan Y, Zhang Q. Development of liposomal formulations: From concept to clinical investigations. Asian J Pharm Sci 2013; 8(2):81-87.

(7) Angius F, Floris A. Toxicology in Vitro Liposomes and MTT cell viability assay : An incompatible affair. Toxicol Vitr 2015; 29(2):314-9.

(8) Bozzuto G, Molinari A. Liposomes as nanomedical devices. lntJ Nanomedicine 2015; 2(10):975-99.

(9) Gregoriadis G, Florence A. Liposomes in drug delivery. Clinical, diagnostic and ophthalmic potential. Drugs 1993; 45(1):15-28.

(10) Johnston M, Semple S, Klimuk S, Ansell S, Maurer N, Cullis P. Characterization of the drug retention and pharmacokinetic properties of liposomal nanoparticles containing dihydrosphingomyelin. Biochim Biophys Acta 2007; 1768(5):1121-7.

(11) Noble C, Guo Z, Hayes M, Marks J, Park J, Benz C, et.al. Characterization of highly stable liposomal and immunoliposomal formulations of vincristine and vinblastine. Cancer Chemother Pharmacol 2009; 64(4):741-51.

(12) Samad A, Sultana Y, Aqil M. Liposomal drug delivery systems: an update review. Curr Drug Deliv 2007; 4(4):297-305.

Published

2015-06-30

How to Cite

1.
Lecot N, Oddone N, Fernández M, Benech J, Gambini JP, Cabral P. Evaluation of liposomal nanosystems as oncological treatment and diagnostic agents. Salud Mil [Internet]. 2015 Jun. 30 [cited 2026 Apr. 16];34(1):19-25. Available from: https://revistasaludmilitar.uy/ojs/index.php/Rsm/article/view/196

Issue

Section

Original Articles

        PlumX Metrics

Most read articles by the same author(s)

1 2 > >>