Monoglycoconjugated phthalocyanines: effect of sugar and linkage on photodynamic activity.

BACKGROUND Click chemistry can be advantageously used to graft carbohydrates on phthalocyanines which are potent photosensitisers, but the effect of the presence of triazole moieties on photodynamic efficiency was not investigated systematically to date. The nature and linkage of the sugar were investigated in order to define structure-activity relationships. METHOD Two sets of monoglycoconjugated water-soluble phthalocyanines have been designed and their photodynamic activity and uptake investigated in HT-29 human colon adenocarcinoma cells. Carbohydrates: galactose, mannose or lactose were grafted onto Zn(II) phthalocyanines either by glycosylation or by click reaction. RESULTS The triazole linkage formed by click conjugation lowered the biological efficiency for mannose and galactose, compared to classical glycosylation grafting. The mannose conjugate formed by glycosylation was the most photodynamically active, without correlation with the photosensitiser cell uptake.

[1]  S. Ogura,et al.  Development of phthalocyanines for photodynamic therapy , 2006 .

[2]  Ross W. Boyle,et al.  Photodynamic Therapy and the Development of Metal-Based Photosensitisers , 2008, Metal-based drugs.

[3]  W. Fong,et al.  Effects of the number and position of the substituents on the in vitro photodynamic activities of glucosylated zinc(II) phthalocyanines. , 2009, Organic & biomolecular chemistry.

[4]  J. E. Lier,et al.  Preparation of amphiphilic glycerol-substituted zinc phthalocyanines using copper-free Sonogashira cross-coupling in aqueous medium , 2011 .

[5]  Á. Juarranz,et al.  Glycophthalocyanines as photosensitizers for triggering mitotic catastrophe and apoptosis in cancer cells. , 2012, Chemical research in toxicology.

[6]  J. V. van Lier,et al.  Metal complexes as photo- and radiosensitizers. , 1999, Chemical reviews.

[7]  M. Barberi-Heyob,et al.  Modulation of photosensitization processes for an improved targeted photodynamic therapy. , 2010, Current medicinal chemistry.

[8]  M. Barberi-Heyob,et al.  Phthalocyanines covalently bound to biomolecules for a targeted photodynamic therapy. , 2007, Current medicinal chemistry.

[9]  J. Blais,et al.  Synthesis, cellular internalization and photodynamic activity of glucoconjugated derivatives of tri and tetra(meta-hydroxyphenyl)chlorins. , 2003, Bioorganic & medicinal chemistry.

[10]  Marcel Garcia,et al.  Mannose-targeted mesoporous silica nanoparticles for photodynamic therapy. , 2009, Chemical communications.

[11]  C. M. Allen,et al.  Current status of phthalocyanines in the photodynamic therapy of cancer , 2001 .

[12]  T. Ziegler,et al.  The first example of anomeric glycoconjugation to phthalocyanines , 2006 .

[13]  M. Karabörk,et al.  SYNTHESIS AND CHARACTERIZATION OF PHTHALOCYANINES WITH NON-IONIC SOLUBILIZING GROUPS , 2002 .

[14]  J. Blais,et al.  Photodynamic efficiency of diethylene glycol-linked glycoconjugated porphyrins in human retinoblastoma cells. , 2006, Journal of medicinal chemistry.

[15]  F. Santoyo-González,et al.  Silica-based clicked hybrid glyco materials. , 2009, Chemical Society reviews.

[16]  P. Maillard,et al.  Microwave-mediated ‘click-chemistry’ synthesis of glycoporphyrin derivatives and in vitro photocytotoxicity for application in photodynamic therapy , 2011 .

[17]  T. Ziegler,et al.  Expeditious Synthesis of Glycosylated Phthalocyanines , 2007 .

[18]  J. Blais,et al.  In vitro phototoxicity of glycoconjugated porphyrins and chlorins in colorectal adenocarcinoma (HT29) and retinoblastoma (Y79) cell lines. , 2007, Photodiagnosis and photodynamic therapy.

[19]  Aijian Wang,et al.  Synthesis of Unsymmetrical Phthalocyanines: A Brief Overview , 2012 .

[20]  Jarod C Finlay,et al.  The role of photodynamic therapy (PDT) physics. , 2008, Medical physics.

[21]  V. Ahsen,et al.  Glycerol and galactose substituted zinc phthalocyanines. Synthesis and photodynamic activity , 2009, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

[22]  Erhong Hao,et al.  Synthesis of porphyrin-carbohydrate conjugates using "click" chemistry and their preliminary evaluation in human HEp2 cells , 2009 .

[23]  R. Boyle,et al.  Strategies for selective delivery of photodynamic sensitisers to biological targets , 2004 .

[24]  V. Ahsen,et al.  Click chemistry: the emerging role of the azide-alkyne Huisgen dipolar addition in the preparation of substituted tetrapyrrolic derivatives , 2011 .

[25]  F. Santoyo-González,et al.  Azide–Alkyne 1,3-Dipolar Cycloadditions: a Valuable Tool in Carbohydrate Chemistry , 2007 .

[26]  V. Ahsen,et al.  Light-triggered liposomal release: membrane permeabilization by photodynamic action. , 2010, Langmuir : the ACS journal of surfaces and colloids.

[27]  Tebello Nyokong,et al.  Synthetic pathways to water-soluble phthalocyanines and close analogs , 2010 .

[28]  Y. Hagiya,et al.  Current states and future views in photodynamic therapy , 2011 .

[29]  P. Maillard,et al.  A strategy for the targeting of photosensitizers. Synthesis, characterization, and photobiological property of porphyrins bearing glycodendrimeric moieties. , 2011, The Journal of organic chemistry.

[30]  A. Davies,et al.  Synthesis and biological evaluation of a library of glycoporphyrin compounds. , 2012, Chemistry.

[31]  Jian‐Dong Huang,et al.  Glycosylated zinc(II) phthalocyanines as efficient photosensitisers for photodynamic therapy. Synthesis, photophysical properties and in vitro photodynamic activity. , 2008, Organic & biomolecular chemistry.

[32]  F. Dumoulin Design and Conception of Photosensitisers , 2011 .

[33]  D. Filippov,et al.  SOLID-SUPPORT SYNTHESIS OF DI- AND TETRAMANNOSYLATED TETRATHYMIDYLIC ACID , 2010 .

[34]  A. J. Blake,et al.  Enantioselective conjugate addition nitro-Mannich reactions: solvent controlled synthesis of acyclic anti- and syn-β-nitroamines with three contiguous stereocenters. , 2011, The Journal of organic chemistry.

[35]  S. Franke,et al.  Ex post glycoconjugation of phthalocyanines. , 2010, The Journal of organic chemistry.

[36]  Laurence Raehm,et al.  Silica-based nanoparticles for photodynamic therapy applications. , 2010, Nanoscale.

[37]  Tianjun Liu,et al.  Synthesis, properties and near-infrared imaging evaluation of glucose conjugated zinc phthalocyanine via Click reaction , 2012 .

[38]  T. Basova,et al.  Amphiphilic carbohydrate–phthalocyanine conjugates obtained by glycosylation or by azide–alkyne click reaction , 2010 .

[39]  S. Penadés,et al.  Gold glyconanoparticles: synthetic polyvalent ligands mimicking glycocalyx-like surfaces as tools for glycobiological studies. , 2003, Chemistry.

[40]  T. Torres,et al.  Synthetic Advances in Phthalocyanine Chemistry , 2002 .

[41]  R. Field,et al.  Recent applications of the Cu(I)-catalysed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in carbohydrate chemistry. , 2007, Organic & biomolecular chemistry.

[42]  Vefa Ahsen,et al.  Monoglycoconjugated water-soluble phthalocyanines. Design and synthesis of potential selectively targeting PDT photosensitisers , 2010 .

[43]  P. McCarron,et al.  Antifungal photodynamic therapy. , 2008, Microbiological research.

[44]  Devrim Atilla,et al.  A set of highly water-soluble tetraethyleneglycol-substituted Zn(II) phthalocyanines: synthesis, photochemical and photophysical properties, interaction with plasma proteins and in vitro phototoxicity. , 2011, Dalton transactions.

[45]  J. Thiem,et al.  Glycoscience : chemistry and chemical biology , 2008 .

[46]  V. Ahsen,et al.  Comparative studies of photophysical and photochemical properties of solketal substituted platinum(II) and zinc(II) phthalocyanine sets , 2010 .

[47]  R. Boyle,et al.  Structure and Biodistribution Relationships of Photodynamic Sensitizers * , 1996, Photochemistry and photobiology.

[48]  J. Jacquinet,et al.  Total synthesis of the carbohydrate-protein linkage region common to several mammalian proteoglycans. , 1993, Carbohydrate research.

[49]  Tayyaba Hasan,et al.  Imaging and photodynamic therapy: mechanisms, monitoring, and optimization. , 2010, Chemical reviews.

[50]  A. Harris,et al.  An update on photodynamic therapy in age-related macular degeneration , 2002, Expert opinion on pharmacotherapy.