In vitro evaluation of permeation, toxicity and effect of praziquantel-loaded solid lipid nanoparticles against Schistosoma mansoni as a strategy to improve efficacy of the schistosomiasis treatment

• Published in: International journal of pharmaceutics 2014-03, Vol.463 (1), p.31-37
• Main Authors: Souza, Ana Luiza Ribeiro de, Andreani, Tatiana, de Oliveira, Rosimeire Nunes, Kiill, Charlene Priscila, Santos, Fernanda Kolenyak dos, Allegretti, Silmara Marques, Chaud, Marco Vinícius, Souto, Eliana B., Silva, Amélia M., Gremião, Maria Palmira Daflon
• Format: Article
• Language: English
• Subjects: Animals; Anthelmintics - administration & dosage; Anthelmintics - chemistry; Cell Survival - drug effects; Cytotoxicity; Delayed-Action Preparations - administration & dosage; Delayed-Action Preparations - chemistry; Female; Hep G2 Cells; HepG2 cells; Humans; In Vitro Techniques; Intestinal Absorption; Intestines - metabolism; Lipids - chemistry; Nanoparticles - administration & dosage; Nanoparticles - chemistry; Praziquantel; Praziquantel - administration & dosage; Praziquantel - chemistry; Rats; Schistosoma mansoni; Schistosoma mansoni - drug effects; Schistosomiasis; Schistosomiasis - drug therapy; Solid lipid nanoparticles
• ISSN: 0378-5173; 1873-3476
• DOI: 10.1016/j.ijpharm.2013.12.022

Adult worms of Schistosoma mansoni exposed to praziquantel (PZQ) in: (a) PBS (25μgmL−1); (b) PBS (50μgmL−1); (c) SLN (Eq. 25μgmL−1); (d) SLN (Eq. 50μgmL−1); (e) PZQ-SLN (25μgmL−1 of PZQ); (f) PZQ-SLN (50μgmL−1 of PZQ). Arrows indicate nanoparticles in worm tegument (magnification of 100×). Solid lipid nanoparticles (SLN) are a promising drug delivery system for oral administration of poorly-water soluble drugs because of their capacity to increase the solubility of drug molecules when loaded in their lipid matrices, with the resulting improvement of the drug bioavailability. In the present work, we have developed praziquantel (PZQ)-loaded SLN and explored the biological applications of this system for intestinal permeation of PZQ. The effect in vitro on Schistosoma mansoni culture and the cytotoxicity in HepG2 line cell were also evaluated. The results showed a significant decrease in the intestinal absorption of PZQ loaded in SLN compared to free PZQ, suggesting that the SLN matrix could act as reservoir system. In culture of S. mansoni, we observed that PZQ-loaded SLN were more effective than free PZQ, leading the death of the parasites in less time. The result was proportional to doses of PZQ (25 and 50μgmL−1) and lipid concentration. Regarding cytotoxicity, the encapsulation of PZQ into SLN decreased the toxicity in HepG2 cells in comparison to the free PZQ. From the obtained results, PZQ-loaded SLN could be a new drug delivery system for the schistosomiasis treatment especially in marginalized communities, improving the therapeutic efficacy and reducing the toxic effects of PZQ.