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Scientia Pharmaceutica is published by MDPI from Volume 84 Issue 3 (2015). Articles in this Issue were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence. Articles are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Austrian Pharmaceutical Society (Österreichische Pharmazeutische Gesellschaft, ÖPhG).
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Sci. Pharm. 2010, 78(3), 576; https://doi.org/10.3797/scipharm.cespt.8.LNT02 (registering DOI)

Development of Solid Lipid Nanoparticles for Praziquantel Delivery: Particle Size Characterization and Cell Toxicity Assessment

1
Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, UNESP, Araraquara, Brazil
2
Department of Biology and Environment, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal
3
Centre of Genomics and Biotechnology, IBB/CGB-UTAD, Vila-Real, Portugal
4
Centre for Research and Technology of Agro-Environmental and Biological Sciences, Vila Real, Portugal
5
Department of Pharmaceutical Technology, Faculty of Health Sciences, UFP, Porto, Portugal
*
Author to whom correspondence should be addressed.
Received: 12 July 2010 / Accepted: 12 July 2010 / Published: 12 July 2010
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Praziquantel (PZQ) is a drug active against all species of Schistosoma and it is the drug of choice for the treatment of schistosomiasis [1]. [...]
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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SOUZA, A.L.R.; ANDREANI, T.; DOKTOROVOVÁ, S.; SILVA, A.M.; SOUTO, E.B.; GREMIÃO, M.P.D. Development of Solid Lipid Nanoparticles for Praziquantel Delivery: Particle Size Characterization and Cell Toxicity Assessment. Sci. Pharm. 2010, 78, 576.

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