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Poly(vinyl alcohol)-C60 nanohybrids for cancer photodynamic therapy

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Academic year: 2021

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Poly(vinyl alcohol)-C60 Nanohybrids for Cancer Photodynamic Therapy Hurtgen, M., Liège/B, Debuigne, A., Liège/B, Mouithys-Mickalad, A., Liège/B,

Jérôme, C., Liège/B, Detrembleur, C., Liège/B, Passirani, C., Angers/FR. Marie Hurtgen, University of Liège, Sart-Tilman B6A, B-4000 Liège

Among other relevant electronic properties, C60 is able to convert triplet oxygen (3O2)

into reactive oxygen species (ROS) upon irradiation. C60 has therefore been suggested

as potential medicine for photodynamic therapy (PDT), a cancer treatment involving photoinduced generation of ROS followed by tumor cells death. [1]

In order to make C60 water-soluble and biocompatible, poly(vinyl acetate) (PVAc) was

prepared by cobalt-mediated radical polymerization (CMRP) [2] and next grafted onto C60 by radical addition. [3] Cobalt traces were removed by further reaction with TEMPO,

a stable radical, or with 1-propanethiol. Methanolysis of the ester groups of PVAc-C60

led to water-soluble poly(vinyl alcohol)-C60 (PVOH-C60) nanohybrids, that turned out to

be interesting candidates for PDT. Indeed, these nanohybrids produced significant amounts of ROS upon red light irradiation, as assessed by the ADPA bleaching test. Moreover, they displayed marked toxicity towards human monocytic cells when subjected to light. PVOH-C60 nanohybrids were also submitted to a protein absorption

test (CH50) that revealed a significant activation of the complement system by the nanohybrids. Protein-repellent polymers (e.g. PEG) will be incorporated in the PVOH crown of the nanohybrid to improve its stealthy properties.

Finally, the key characteristic of these nanohybrids is the presence of many hydroxyl functions enabling their post-functionalization by targeting agents and/or anti-tumoral compounds that could increase the selectivity and the efficiency of the therapy.

Literature:

[1] P. Mroz, Photochem. Photobiol. Sci., 2007, 6, 1139. [2] A. Debuigne, Angew.

Chem., Int. Ed., 2005, 44, 1101. [3] C. Detrembleur, Macromol. Rapid Commun., 2006, 27, 498.

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