Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi

Detalhes bibliográficos
Autor(a) principal: Vieira,Cecilia Stahl
Data de Publicação: 2011
Outros Autores: Almeida,Diogo Burigo, Thomaz,André Alexandre de, Menna-Barreto,Rubem Figueredo Sadok, Santos-Mallet,Jacenir Reis dos, Cesar,Carlos Lenz, Gomes,Suzete Araujo Oliveira, Feder,Denise
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Memórias do Instituto Oswaldo Cruz
Texto Completo: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200007
Resumo: Semiconductor nanoparticles, such as quantum dots (QDs), were used to carry out experiments in vivo and ex vivo with Trypanosoma cruzi. However, questions have been raised regarding the nanotoxicity of QDs in living cells, microorganisms, tissues and whole animals. The objective of this paper was to conduct a QD nanotoxicity study on living T. cruzi protozoa using analytical methods. This was accomplished using in vitro experiments to test the interference of the QDs on parasite development, morphology and viability. Our results show that after 72 h, a 200 μM cadmium telluride (CdTe) QD solution induced important morphological alterations in T. cruzi, such as DNA damage, plasma membrane blebbing and mitochondrial swelling. Flow cytometry assays showed no damage to the plasma membrane when incubated with 200 μM CdTe QDs for up to 72 h (propidium iodide cells), giving no evidence of classical necrosis. Parasites incubated with 2 μM CdTe QDs still proliferated after seven days. In summary, a low concentration of CdTe QDs (2 μM) is optimal for bioimaging, whereas a high concentration (200 μM CdTe) could be toxic to cells. Taken together, our data indicate that 2 μM QD can be used for the successful long-term study of the parasite-vector interaction in real time.
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spelling Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruziCdTe quantum dotsTrypanosoma cruzinanotoxicitySemiconductor nanoparticles, such as quantum dots (QDs), were used to carry out experiments in vivo and ex vivo with Trypanosoma cruzi. However, questions have been raised regarding the nanotoxicity of QDs in living cells, microorganisms, tissues and whole animals. The objective of this paper was to conduct a QD nanotoxicity study on living T. cruzi protozoa using analytical methods. This was accomplished using in vitro experiments to test the interference of the QDs on parasite development, morphology and viability. Our results show that after 72 h, a 200 μM cadmium telluride (CdTe) QD solution induced important morphological alterations in T. cruzi, such as DNA damage, plasma membrane blebbing and mitochondrial swelling. Flow cytometry assays showed no damage to the plasma membrane when incubated with 200 μM CdTe QDs for up to 72 h (propidium iodide cells), giving no evidence of classical necrosis. Parasites incubated with 2 μM CdTe QDs still proliferated after seven days. In summary, a low concentration of CdTe QDs (2 μM) is optimal for bioimaging, whereas a high concentration (200 μM CdTe) could be toxic to cells. Taken together, our data indicate that 2 μM QD can be used for the successful long-term study of the parasite-vector interaction in real time.Instituto Oswaldo Cruz, Ministério da Saúde2011-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200007Memórias do Instituto Oswaldo Cruz v.106 n.2 2011reponame:Memórias do Instituto Oswaldo Cruzinstname:Fundação Oswaldo Cruzinstacron:FIOCRUZ10.1590/S0074-02762011000200007info:eu-repo/semantics/openAccessVieira,Cecilia StahlAlmeida,Diogo BurigoThomaz,André Alexandre deMenna-Barreto,Rubem Figueredo SadokSantos-Mallet,Jacenir Reis dosCesar,Carlos LenzGomes,Suzete Araujo OliveiraFeder,Deniseeng2020-04-25T17:50:57Zhttp://www.scielo.br/oai/scielo-oai.php0074-02761678-8060opendoar:null2020-04-26 02:17:30.311Memórias do Instituto Oswaldo Cruz - Fundação Oswaldo Cruztrue
dc.title.none.fl_str_mv Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
title Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
spellingShingle Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
Vieira,Cecilia Stahl
CdTe quantum dots
Trypanosoma cruzi
nanotoxicity
title_short Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
title_full Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
title_fullStr Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
title_full_unstemmed Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
title_sort Studying nanotoxic effects of CdTe quantum dots in Trypanosoma cruzi
author Vieira,Cecilia Stahl
author_facet Vieira,Cecilia Stahl
Almeida,Diogo Burigo
Thomaz,André Alexandre de
Menna-Barreto,Rubem Figueredo Sadok
Santos-Mallet,Jacenir Reis dos
Cesar,Carlos Lenz
Gomes,Suzete Araujo Oliveira
Feder,Denise
author_role author
author2 Almeida,Diogo Burigo
Thomaz,André Alexandre de
Menna-Barreto,Rubem Figueredo Sadok
Santos-Mallet,Jacenir Reis dos
Cesar,Carlos Lenz
Gomes,Suzete Araujo Oliveira
Feder,Denise
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Vieira,Cecilia Stahl
Almeida,Diogo Burigo
Thomaz,André Alexandre de
Menna-Barreto,Rubem Figueredo Sadok
Santos-Mallet,Jacenir Reis dos
Cesar,Carlos Lenz
Gomes,Suzete Araujo Oliveira
Feder,Denise
dc.subject.por.fl_str_mv CdTe quantum dots
Trypanosoma cruzi
nanotoxicity
topic CdTe quantum dots
Trypanosoma cruzi
nanotoxicity
dc.description.none.fl_txt_mv Semiconductor nanoparticles, such as quantum dots (QDs), were used to carry out experiments in vivo and ex vivo with Trypanosoma cruzi. However, questions have been raised regarding the nanotoxicity of QDs in living cells, microorganisms, tissues and whole animals. The objective of this paper was to conduct a QD nanotoxicity study on living T. cruzi protozoa using analytical methods. This was accomplished using in vitro experiments to test the interference of the QDs on parasite development, morphology and viability. Our results show that after 72 h, a 200 μM cadmium telluride (CdTe) QD solution induced important morphological alterations in T. cruzi, such as DNA damage, plasma membrane blebbing and mitochondrial swelling. Flow cytometry assays showed no damage to the plasma membrane when incubated with 200 μM CdTe QDs for up to 72 h (propidium iodide cells), giving no evidence of classical necrosis. Parasites incubated with 2 μM CdTe QDs still proliferated after seven days. In summary, a low concentration of CdTe QDs (2 μM) is optimal for bioimaging, whereas a high concentration (200 μM CdTe) could be toxic to cells. Taken together, our data indicate that 2 μM QD can be used for the successful long-term study of the parasite-vector interaction in real time.
description Semiconductor nanoparticles, such as quantum dots (QDs), were used to carry out experiments in vivo and ex vivo with Trypanosoma cruzi. However, questions have been raised regarding the nanotoxicity of QDs in living cells, microorganisms, tissues and whole animals. The objective of this paper was to conduct a QD nanotoxicity study on living T. cruzi protozoa using analytical methods. This was accomplished using in vitro experiments to test the interference of the QDs on parasite development, morphology and viability. Our results show that after 72 h, a 200 μM cadmium telluride (CdTe) QD solution induced important morphological alterations in T. cruzi, such as DNA damage, plasma membrane blebbing and mitochondrial swelling. Flow cytometry assays showed no damage to the plasma membrane when incubated with 200 μM CdTe QDs for up to 72 h (propidium iodide cells), giving no evidence of classical necrosis. Parasites incubated with 2 μM CdTe QDs still proliferated after seven days. In summary, a low concentration of CdTe QDs (2 μM) is optimal for bioimaging, whereas a high concentration (200 μM CdTe) could be toxic to cells. Taken together, our data indicate that 2 μM QD can be used for the successful long-term study of the parasite-vector interaction in real time.
publishDate 2011
dc.date.none.fl_str_mv 2011-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200007
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0074-02762011000200007
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Instituto Oswaldo Cruz, Ministério da Saúde
publisher.none.fl_str_mv Instituto Oswaldo Cruz, Ministério da Saúde
dc.source.none.fl_str_mv Memórias do Instituto Oswaldo Cruz v.106 n.2 2011
reponame:Memórias do Instituto Oswaldo Cruz
instname:Fundação Oswaldo Cruz
instacron:FIOCRUZ
reponame_str Memórias do Instituto Oswaldo Cruz
collection Memórias do Instituto Oswaldo Cruz
instname_str Fundação Oswaldo Cruz
instacron_str FIOCRUZ
institution FIOCRUZ
repository.name.fl_str_mv Memórias do Instituto Oswaldo Cruz - Fundação Oswaldo Cruz
repository.mail.fl_str_mv
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