A luminum-phthalocyanine chloride associated to poly(methyl vinyl ether-co-maleic anhydride) nanoparticles as a new third-generation photosensitizer for anticancer photodynamic therapy

被引:70
作者
Muehlmann, Luis Alexandre [1 ]
Ma, Beatriz Chiyin [1 ]
Figueiro Longo, Joao Paulo [1 ]
Menezes, Maria de Fatima [1 ]
Santos, Almeida [1 ]
Azevedo, Ricardo Bentes [1 ]
机构
[1] Univ Brasilia, Inst Biol Sci, Dept Genet & Morphol, Brasilia, DF, Brazil
关键词
third-generation photosensitizer; nanoparticles; cancer; photodynamic therapy; drug delivery systems; CELL-DEATH; DELIVERY-SYSTEM; IN-VITRO; ZINC PHTHALOCYANINE; NECROSIS; AGGREGATION; MECHANISMS; APOPTOSIS; GROWTH; ASSAY;
D O I
10.2147/IJN.S57420
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Photodynamic therapy is generally considered to be safer than conventional anticancer therapies, and it is effective against different kinds of cancer. However, its clinical application has been significantly limited by the hydrophobicity of photosensitizers. In this work, a system composed of the hydrophobic photosensitizer aluminum-phthalocyanine chloride (AlPc) associated with water dispersible poly(methyl vinyl ether-co-maleic anhydride) nanoparticles is described. AlPc was associated with nanoparticles produced by a method of solvent displacement. This system was analyzed for its physicochemical characteristics, and for its photodynamic activity in vitro in cancerous (murine mammary carcinoma cell lineage 4T1, and human mammary adenocarcinoma cells MCF-7) and noncancerous (murine fibroblast cell lineage NIH/3T3, and human mammary epithelial cell lineage MCF-10A) cell lines. Cell viability and the elicited mechanisms of cell death were evaluated after the application of photodynamic therapy. This system showed improved photophysical and photochemical properties in aqueous media in comparison to the free photosensitizer, and it was effective against cancerous cells in vitro.
引用
收藏
页码:1199 / 1213
页数:15
相关论文
共 51 条
[1]   The roles of therapy-induced autophagy and necrosis in cancer treatment [J].
Amaravadi, Ravi K. ;
Thompson, Craig B. .
CLINICAL CANCER RESEARCH, 2007, 13 (24) :7271-7279
[2]   Influence of the surface characteristics of PVM/MA nanoparticles on their bioadhesive properties [J].
Arbós, P ;
Campanero, MA ;
Arnangoa, MA ;
Renedo, MJ ;
Irache, JM .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (01) :19-30
[3]   Gantrez® AN as a new polymer for the preparation of ligand-nanoparticle conjugates [J].
Arbós, P ;
Wirth, M ;
Arangoa, MA ;
Gabor, F ;
Irache, JM .
JOURNAL OF CONTROLLED RELEASE, 2002, 83 (03) :321-330
[4]   Improved size-tunable preparation of polymeric nanoparticles by microfluidic nanoprecipitation [J].
Bally, Florence ;
Garg, Dhiraj Kumar ;
Serra, Christophe A. ;
Hoarau, Yannick ;
Anton, Nicolas ;
Brochon, Cyril ;
Parida, Dambarudhar ;
Vandamme, Thierry ;
Hadziioannou, Georges .
POLYMER, 2012, 53 (22) :5045-5051
[5]   Molecular effectors of multiple cell death pathways initiated by photodynamic therapy [J].
Buytaert, Esther ;
Dewaele, Michael ;
Agostinis, Patrizia .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2007, 1776 (01) :86-107
[6]   Photodynamic therapy and anti-tumour immunity [J].
Castano, Ana P. ;
Mroz, Pawel ;
Hamblin, Michael R. .
NATURE REVIEWS CANCER, 2006, 6 (07) :535-545
[7]   Mechanisms in photodynamic therapy: part one-photosensitizers, photochemistry and cellular localization [J].
Castano, Ana P. ;
Demidova, Tatiana N. ;
Hamblin, Michael R. .
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2004, 1 (04) :279-293
[8]  
CHAN WS, 1990, CANCER RES, V50, P4533
[9]   Current clinical and preclinical photosensitizers for use in photodynamic therapy [J].
Detty, MR ;
Gibson, SL ;
Wagner, SJ .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (16) :3897-3915
[10]   Comparison of the photophysics of an aggregating and non-aggregating aluminium phthalocyanine system incorporated into unilamellar vesicles [J].
Dhami, S ;
Phillips, D .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1996, 100 (1-3) :77-84