Abstract | AIM: The present study was conducted to overcome the disadvantages associated with the poor water solubility and low bioavailability of curcumin by synthesizing nanotized curcumin and demonstrating its efficacy in treating malaria. MATERIALS AND METHODS: Nanotized curcumin was prepared by a modified emulsion-diffusion-evaporation method and was characterized by means of transmission electron microscopy, atomic force microscopy, dynamic light scattering, Zetasizer, Fourier transform infrared spectroscopy, and differential thermal analysis. The novelty of the prepared nanoformulation lies in the fact that it was devoid of any polymeric matrices used in conventional carriers. The antimalarial efficacy of the prepared nanotized curcumin was then checked both in vitro and in vivo. RESULTS: The nanopreparation was found to be non-toxic and had a particle size distribution of 20-50 nm along with improved aqueous dispersibility and an entrapment efficiency of 45%. Nanotized curcumin (half maximal inhibitory concentration [IC50]: 0.5 μM) was also found to be ten-fold more effective for growth inhibition of Plasmodium falciparum in vitro as compared to its native counterpart (IC50: 5 μM). Oral bioavailability of nanotized curcumin was found to be superior to that of its native counterpart. Moreover, when Plasmodium berghei-infected mice were orally treated with nanotized curcumin, it prolonged their survival by more than 2 months with complete clearance of parasites in comparison to the untreated animals, which survived for 8 days only. CONCLUSION:
|
Authors | Aparajita Ghosh, Tanushree Banerjee, Suman Bhandary, Avadhesha Surolia |
Journal | International journal of nanomedicine
(Int J Nanomedicine)
Vol. 9
Pg. 5373-87
( 2014)
ISSN: 1178-2013 [Electronic] New Zealand |
PMID | 25484584
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
|
Topics |
- Animals
- Antimalarials
(adverse effects, chemistry, pharmacology, toxicity)
- Cell Line
- Cell Survival
(drug effects)
- Curcumin
(adverse effects, chemistry, pharmacology, toxicity)
- Humans
- Kidney Function Tests
- Liver Function Tests
- Malaria
(parasitology)
- Mice
- Nanoparticles
(adverse effects, chemistry, toxicity)
- Particle Size
- Plasmodium berghei
(drug effects)
- Plasmodium falciparum
(drug effects)
|