Photodynamic activity of chloro(5,10,15,20-tetraphenylporphyrinato)indium(III)
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , |
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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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 |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000300017 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000300017 |
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 |
eu_rights_str_mv |
openAccess |
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) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
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) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
_version_ |
1750318168655527936 |