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Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi

Chagas is a neglected tropical disease caused by Trypanosoma cruzi, and affects about 25 million people worldwide. N, N’-Squaramide 17 (S) is a trypanocidal compound with relevant in vivo effectiveness. Here, we produced, characterized, and evaluated cytotoxic and trypanocidal effects of macrophage-...

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Autores principales: Quijia, Christian Rafael, Bonatto, Cínthia Caetano, Silva, Luciano Paulino, Andrade, Milene Aparecida, Azevedo, Clenia Santos, Lasse Silva, Camila, Vega, Manel, de Santana, Jaime Martins, Bastos, Izabela Marques Dourado, Carneiro, Marcella Lemos Brettas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730638/
https://www.ncbi.nlm.nih.gov/pubmed/33276688
http://dx.doi.org/10.3390/ma13235505
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author Quijia, Christian Rafael
Bonatto, Cínthia Caetano
Silva, Luciano Paulino
Andrade, Milene Aparecida
Azevedo, Clenia Santos
Lasse Silva, Camila
Vega, Manel
de Santana, Jaime Martins
Bastos, Izabela Marques Dourado
Carneiro, Marcella Lemos Brettas
author_facet Quijia, Christian Rafael
Bonatto, Cínthia Caetano
Silva, Luciano Paulino
Andrade, Milene Aparecida
Azevedo, Clenia Santos
Lasse Silva, Camila
Vega, Manel
de Santana, Jaime Martins
Bastos, Izabela Marques Dourado
Carneiro, Marcella Lemos Brettas
author_sort Quijia, Christian Rafael
collection PubMed
description Chagas is a neglected tropical disease caused by Trypanosoma cruzi, and affects about 25 million people worldwide. N, N’-Squaramide 17 (S) is a trypanocidal compound with relevant in vivo effectiveness. Here, we produced, characterized, and evaluated cytotoxic and trypanocidal effects of macrophage-mimetic liposomes from lipids extracted of RAW 264.7 cells to release S. As results, the average hydrodynamic diameter and Zeta potential of mimetic lipid membranes containing S (MLS) was 196.5 ± 11 nm and −61.43 ± 2.3 mV, respectively. Drug entrapment efficiency was 73.35% ± 2.05%. After a 72 h treatment, MLS was observed to be active against epimastigotes in vitro (IC(50) = 15.85 ± 4.82 μM) and intracellular amastigotes (IC(50) = 24.92 ± 4.80 μM). Also, it induced low cytotoxicity with CC(50) of 1199.50 ± 1.22 μM towards VERO cells and of 1973.97 ± 5.98 μM in RAW 264.7. MLS also induced fissures in parasite membrane with a diameter of approximately 200 nm in epimastigotes. MLS showed low cytotoxicity in mammalian cells and high trypanocidal activity revealing this nanostructure a promising candidate for the development of Chagas disease treatment.
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spelling pubmed-77306382020-12-12 Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi Quijia, Christian Rafael Bonatto, Cínthia Caetano Silva, Luciano Paulino Andrade, Milene Aparecida Azevedo, Clenia Santos Lasse Silva, Camila Vega, Manel de Santana, Jaime Martins Bastos, Izabela Marques Dourado Carneiro, Marcella Lemos Brettas Materials (Basel) Article Chagas is a neglected tropical disease caused by Trypanosoma cruzi, and affects about 25 million people worldwide. N, N’-Squaramide 17 (S) is a trypanocidal compound with relevant in vivo effectiveness. Here, we produced, characterized, and evaluated cytotoxic and trypanocidal effects of macrophage-mimetic liposomes from lipids extracted of RAW 264.7 cells to release S. As results, the average hydrodynamic diameter and Zeta potential of mimetic lipid membranes containing S (MLS) was 196.5 ± 11 nm and −61.43 ± 2.3 mV, respectively. Drug entrapment efficiency was 73.35% ± 2.05%. After a 72 h treatment, MLS was observed to be active against epimastigotes in vitro (IC(50) = 15.85 ± 4.82 μM) and intracellular amastigotes (IC(50) = 24.92 ± 4.80 μM). Also, it induced low cytotoxicity with CC(50) of 1199.50 ± 1.22 μM towards VERO cells and of 1973.97 ± 5.98 μM in RAW 264.7. MLS also induced fissures in parasite membrane with a diameter of approximately 200 nm in epimastigotes. MLS showed low cytotoxicity in mammalian cells and high trypanocidal activity revealing this nanostructure a promising candidate for the development of Chagas disease treatment. MDPI 2020-12-02 /pmc/articles/PMC7730638/ /pubmed/33276688 http://dx.doi.org/10.3390/ma13235505 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Quijia, Christian Rafael
Bonatto, Cínthia Caetano
Silva, Luciano Paulino
Andrade, Milene Aparecida
Azevedo, Clenia Santos
Lasse Silva, Camila
Vega, Manel
de Santana, Jaime Martins
Bastos, Izabela Marques Dourado
Carneiro, Marcella Lemos Brettas
Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi
title Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi
title_full Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi
title_fullStr Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi
title_full_unstemmed Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi
title_short Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N’-Squaramide 17 towards Trypanosoma cruzi
title_sort liposomes composed by membrane lipid extracts from macrophage cell line as a delivery of the trypanocidal n,n’-squaramide 17 towards trypanosoma cruzi
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730638/
https://www.ncbi.nlm.nih.gov/pubmed/33276688
http://dx.doi.org/10.3390/ma13235505
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