Relationship between structure and photoactivity of porphyrins derived from protoporphyrin IX


Autoria(s): UCHOA, Adjaci F.; OLIVEIRA, Carla S.; BAPTISTA, Mauricio S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Protoporphyrin (Pp IX) derivatives were prepared to study the relationship between photosensitizer structure and photoactivity, with an emphasis on understanding the role of membrane interactions in the efficiency of photosensitizers used in photodynamic therapy (PDT). The synthetic strategies described here aimed at changing protoporphyrin periferic groups, varying overall charge and oil/water partition, while maintaining their photochemical properties. Three synthetic routes were used: (1) modification of Pp IX at positions 3(1) and 8(1) by addition of alkyl amine groups of different lengths (compounds 2-5), (2) change of Pp IX at positions 13(3) and 17(3), generating alkyl amines (compounds 6 and 7), a phosphate amine (compound 8), and quarternary ammonium compounds (compounds 9 and 10), and (3) amine-alkylation of Hematoporphyrin IX (Hp IX) at positions 3(1), 8(1), 13(3) and 17(3) (compound 12). Strategy 1 leads to hydrophobic compounds with low photocytotoxicity. Strategy 2 leads to compounds 6-10 that have high levels of binding/incorporation in vesicles, mitochondria and cells, which are indicative of high bioavailability. Addition of the phosphate group (compound 8), generates an anionic compound that has low liposome and cell incorporation, plus low photocytotoxicity. Compound 12 has intermediate incorporation and photocytotoxic properties. Compound modification is also associated with changes in their sub-cellular localization: 30% of 8 (anionic) is found in mitochondria as compared to 95% of compound 10 (cationic). Photocytotoxicity was shown to be highly correlated with membrane affinity, which depends on the asymmetrical and amphiphilic characters of sens, as well as with sub-cellular localization.

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP (Fundacao de Amparo a Pequisa do Estado de Sao Paulo)

CNPq (Conselho Nacional de Pesquisa)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

CAPES

Identificador

JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, v.14, n.9, p.832-845, 2010

1088-4246

http://producao.usp.br/handle/BDPI/30967

10.1142/S108842461000263X

http://dx.doi.org/10.1142/S108842461000263X

Idioma(s)

eng

Publicador

WORLD SCI PUBL CO INC

Relação

Journal of Porphyrins and Phthalocyanines

Direitos

restrictedAccess

Copyright WORLD SCI PUBL CO INC

Palavras-Chave #photodynamic therapy #PDT #synthesis #membrane #logP #singlet oxygen #photosensitizer #bioavailability #mitochondria #organelle targeting #sub-cellular distribution #SINGLET OXYGEN GENERATION #CARCINOMA-CELL-LINE #PHOTODYNAMIC THERAPY #PHOTOCHEMICAL PROPERTIES #IN-SITU #TRIARYLMETHANE DYES #METHYLENE-BLUE #MITOCHONDRIA #LOCALIZATION #FLUORESCENCE #Chemistry, Multidisciplinary
Tipo

article

original article

publishedVersion