Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)

Detalhes bibliográficos
Autor(a) principal: Silva,André R. da
Data de Publicação: 2008
Outros Autores: Pelegrino,Alessandra C., Tedesco,Antonio C., Jorge,Renato A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000300017
Resumo: Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III) (InTPP) in vitro was investigated for possible use in photodynamic therapy (PDT). The quantum yield of singlet oxygen generation in DMSO of InTPP (F D = 0.72) was higher than 5,10,15,20-tetraphenylporphyrin (TPP) (F D = 0.52). Binding sites between photosensitizers and bovine serum albumin (BSA) are independent while binding sites with human red blood cells (RBC) are cooperatives, with one and four binding sites per molecule, respectively. Binding constants with BSA are (1.15 ± 0.07) × 10(5) and (2.6 ± 0.1) × 10(4) L mol-1 and with RBC are (2.40 ± 0.05) × 10(7) L mol-1 e (7.2 ± 0.2) × 10(4) L mol-1 for InTPP and Photofrin®, respectively. InTPP was more efficient than Photofrin® in the photooxidation of L-tryptophan(Trp) and BSA when higher concentrations (14 µmol L-1) of photosensitizers were used. InTPP was 1.37-1.5 times more effective in the photooxidation of RBC than Photofrin®. Our results indicate that InTPP should be used in future studies of PDT.
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spelling Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)indium(III)-meso-tetraphenylporphyrinPDTquantum yieldhemolysissinglet oxygenPhotodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III) (InTPP) in vitro was investigated for possible use in photodynamic therapy (PDT). The quantum yield of singlet oxygen generation in DMSO of InTPP (F D = 0.72) was higher than 5,10,15,20-tetraphenylporphyrin (TPP) (F D = 0.52). Binding sites between photosensitizers and bovine serum albumin (BSA) are independent while binding sites with human red blood cells (RBC) are cooperatives, with one and four binding sites per molecule, respectively. Binding constants with BSA are (1.15 ± 0.07) × 10(5) and (2.6 ± 0.1) × 10(4) L mol-1 and with RBC are (2.40 ± 0.05) × 10(7) L mol-1 e (7.2 ± 0.2) × 10(4) L mol-1 for InTPP and Photofrin®, respectively. InTPP was more efficient than Photofrin® in the photooxidation of L-tryptophan(Trp) and BSA when higher concentrations (14 µmol L-1) of photosensitizers were used. InTPP was 1.37-1.5 times more effective in the photooxidation of RBC than Photofrin®. Our results indicate that InTPP should be used in future studies of PDT.Sociedade Brasileira de Química2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000300017Journal of the Brazilian Chemical Society v.19 n.3 2008reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532008000300017info:eu-repo/semantics/openAccessSilva,André R. daPelegrino,Alessandra C.Tedesco,Antonio C.Jorge,Renato A.eng2008-05-27T00:00:00Zoai:scielo:S0103-50532008000300017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2008-05-27T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
title Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
spellingShingle Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
Silva,André R. da
indium(III)-meso-tetraphenylporphyrin
PDT
quantum yield
hemolysis
singlet oxygen
title_short Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
title_full Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
title_fullStr Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
title_full_unstemmed Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
title_sort Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
author Silva,André R. da
author_facet Silva,André R. da
Pelegrino,Alessandra C.
Tedesco,Antonio C.
Jorge,Renato A.
author_role author
author2 Pelegrino,Alessandra C.
Tedesco,Antonio C.
Jorge,Renato A.
author2_role author
author
author
dc.contributor.author.fl_str_mv Silva,André R. da
Pelegrino,Alessandra C.
Tedesco,Antonio C.
Jorge,Renato A.
dc.subject.por.fl_str_mv indium(III)-meso-tetraphenylporphyrin
PDT
quantum yield
hemolysis
singlet oxygen
topic indium(III)-meso-tetraphenylporphyrin
PDT
quantum yield
hemolysis
singlet oxygen
description Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III) (InTPP) in vitro was investigated for possible use in photodynamic therapy (PDT). The quantum yield of singlet oxygen generation in DMSO of InTPP (F D = 0.72) was higher than 5,10,15,20-tetraphenylporphyrin (TPP) (F D = 0.52). Binding sites between photosensitizers and bovine serum albumin (BSA) are independent while binding sites with human red blood cells (RBC) are cooperatives, with one and four binding sites per molecule, respectively. Binding constants with BSA are (1.15 ± 0.07) × 10(5) and (2.6 ± 0.1) × 10(4) L mol-1 and with RBC are (2.40 ± 0.05) × 10(7) L mol-1 e (7.2 ± 0.2) × 10(4) L mol-1 for InTPP and Photofrin®, respectively. InTPP was more efficient than Photofrin® in the photooxidation of L-tryptophan(Trp) and BSA when higher concentrations (14 µmol L-1) of photosensitizers were used. InTPP was 1.37-1.5 times more effective in the photooxidation of RBC than Photofrin®. Our results indicate that InTPP should be used in future studies of PDT.
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000300017
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532008000300017
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.19 n.3 2008
reponame:Journal of the Brazilian Chemical Society (Online)
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reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
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