Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.14814/phy2.13190 http://hdl.handle.net/11449/159460 |
Resumo: | Infectious pneumonia is a major cause of morbidity/mortality, mainly because of the increasing rate of microorganisms resistant to antibiotics. Photodynamic Therapy (PDT) is emerging as a promising approach, as effects are based on oxidative stress, preventing microorganism resistance. In two previous studies, the in vitro inactivation of Streptococcus pneumoniae using indocyanine green (ICG) and infrared light source was a success killing 5 log10 colony-forming units (CFU/mL) with only 10 lmol/L ICG. In this work, a proof-of-principle protocol was designed to treat lung infections by PDT using extracorporeal illumination with a 780 nm laser device and also ICG as photosensitizer. Hairless mice were infected with S. pneumoniae and PDT was performed two days after infection. For control groups, CFU recovery ranged between 10(3)-10(4) / mouse. For PDT group, however, no bacteria were recovered in 80% of the animals. Based on this result, animal survival was evaluated separately over 50 days. No deaths occurred in PDT group, whereas 60% of the control group died. Our results indicate that extracorporeal PDT has the potential for pneumonia treatment, and pulmonary decontamination with PDT may be used as a single therapy or as an antibiotics adjuvant. |
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Repositório Institucional da UNESP |
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Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental modelExtracorporeal illuminationindocyanine greenphotodynamic therapypneumoniaStreptococcus pneumoniaeInfectious pneumonia is a major cause of morbidity/mortality, mainly because of the increasing rate of microorganisms resistant to antibiotics. Photodynamic Therapy (PDT) is emerging as a promising approach, as effects are based on oxidative stress, preventing microorganism resistance. In two previous studies, the in vitro inactivation of Streptococcus pneumoniae using indocyanine green (ICG) and infrared light source was a success killing 5 log10 colony-forming units (CFU/mL) with only 10 lmol/L ICG. In this work, a proof-of-principle protocol was designed to treat lung infections by PDT using extracorporeal illumination with a 780 nm laser device and also ICG as photosensitizer. Hairless mice were infected with S. pneumoniae and PDT was performed two days after infection. For control groups, CFU recovery ranged between 10(3)-10(4) / mouse. For PDT group, however, no bacteria were recovered in 80% of the animals. Based on this result, animal survival was evaluated separately over 50 days. No deaths occurred in PDT group, whereas 60% of the control group died. Our results indicate that extracorporeal PDT has the potential for pneumonia treatment, and pulmonary decontamination with PDT may be used as a single therapy or as an antibiotics adjuvant.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Sao Paulo, Sao Carlos, SP, BrazilUniv Fed Sao Carlos, Sao Carlos, SP, BrazilSao Paulo State Univ, Araraquara, BrazilSt Michaels Hosp, Keenan Res Ctr, Toronto, ON, CanadaSao Paulo State Univ, Araraquara, BrazilFAPESP: 13/07276-1CAPES: 99999.003154/2015-07Wiley-BlackwellUniversidade de São Paulo (USP)Universidade Federal de São Carlos (UFSCar)Universidade Estadual Paulista (Unesp)St Michaels HospGeralde, Mariana C.Leite, Ilaiali S.Inada, Natalia M.Salina, Ana Carolina G. [UNESP]Medeiros, Alexandra I. [UNESP]Kuebler, Wolfgang M.Kurachi, CristinaBagnato, Vanderlei S.2018-11-26T15:43:53Z2018-11-26T15:43:53Z2017-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article7application/pdfhttp://dx.doi.org/10.14814/phy2.13190Physiological Reports. Hoboken: Wiley, v. 5, n. 5, 7 p., 2017.2051-817Xhttp://hdl.handle.net/11449/15946010.14814/phy2.13190WOS:000397433300008WOS000397433300008.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPhysiological Reportsinfo:eu-repo/semantics/openAccess2023-11-07T06:08:42Zoai:repositorio.unesp.br:11449/159460Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:04:11.087160Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model |
title |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model |
spellingShingle |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model Geralde, Mariana C. Extracorporeal illumination indocyanine green photodynamic therapy pneumonia Streptococcus pneumoniae |
title_short |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model |
title_full |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model |
title_fullStr |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model |
title_full_unstemmed |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model |
title_sort |
Pneumonia treatment by photodynamic therapy with extracorporeal illumination - an experimental model |
author |
Geralde, Mariana C. |
author_facet |
Geralde, Mariana C. Leite, Ilaiali S. Inada, Natalia M. Salina, Ana Carolina G. [UNESP] Medeiros, Alexandra I. [UNESP] Kuebler, Wolfgang M. Kurachi, Cristina Bagnato, Vanderlei S. |
author_role |
author |
author2 |
Leite, Ilaiali S. Inada, Natalia M. Salina, Ana Carolina G. [UNESP] Medeiros, Alexandra I. [UNESP] Kuebler, Wolfgang M. Kurachi, Cristina Bagnato, Vanderlei S. |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Federal de São Carlos (UFSCar) Universidade Estadual Paulista (Unesp) St Michaels Hosp |
dc.contributor.author.fl_str_mv |
Geralde, Mariana C. Leite, Ilaiali S. Inada, Natalia M. Salina, Ana Carolina G. [UNESP] Medeiros, Alexandra I. [UNESP] Kuebler, Wolfgang M. Kurachi, Cristina Bagnato, Vanderlei S. |
dc.subject.por.fl_str_mv |
Extracorporeal illumination indocyanine green photodynamic therapy pneumonia Streptococcus pneumoniae |
topic |
Extracorporeal illumination indocyanine green photodynamic therapy pneumonia Streptococcus pneumoniae |
description |
Infectious pneumonia is a major cause of morbidity/mortality, mainly because of the increasing rate of microorganisms resistant to antibiotics. Photodynamic Therapy (PDT) is emerging as a promising approach, as effects are based on oxidative stress, preventing microorganism resistance. In two previous studies, the in vitro inactivation of Streptococcus pneumoniae using indocyanine green (ICG) and infrared light source was a success killing 5 log10 colony-forming units (CFU/mL) with only 10 lmol/L ICG. In this work, a proof-of-principle protocol was designed to treat lung infections by PDT using extracorporeal illumination with a 780 nm laser device and also ICG as photosensitizer. Hairless mice were infected with S. pneumoniae and PDT was performed two days after infection. For control groups, CFU recovery ranged between 10(3)-10(4) / mouse. For PDT group, however, no bacteria were recovered in 80% of the animals. Based on this result, animal survival was evaluated separately over 50 days. No deaths occurred in PDT group, whereas 60% of the control group died. Our results indicate that extracorporeal PDT has the potential for pneumonia treatment, and pulmonary decontamination with PDT may be used as a single therapy or as an antibiotics adjuvant. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-03-01 2018-11-26T15:43:53Z 2018-11-26T15:43:53Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.14814/phy2.13190 Physiological Reports. Hoboken: Wiley, v. 5, n. 5, 7 p., 2017. 2051-817X http://hdl.handle.net/11449/159460 10.14814/phy2.13190 WOS:000397433300008 WOS000397433300008.pdf |
url |
http://dx.doi.org/10.14814/phy2.13190 http://hdl.handle.net/11449/159460 |
identifier_str_mv |
Physiological Reports. Hoboken: Wiley, v. 5, n. 5, 7 p., 2017. 2051-817X 10.14814/phy2.13190 WOS:000397433300008 WOS000397433300008.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Physiological Reports |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
7 application/pdf |
dc.publisher.none.fl_str_mv |
Wiley-Blackwell |
publisher.none.fl_str_mv |
Wiley-Blackwell |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128749607059456 |