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Polymeric Photosensitizer Prodrugs for Photodynamic Therapy

Authors

  • Marino A. Campo,

    1. Laboratory of Pharmaceutics and Biopharmaceutics, Section of Pharmaceutical Sciences, Université Lausanne, Université Geneva, Geneva, Switzerland
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  • Doris Gabriel,

    1. Laboratory of Pharmaceutics and Biopharmaceutics, Section of Pharmaceutical Sciences, Université Lausanne, Université Geneva, Geneva, Switzerland
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  • Pavel Kucera,

    1. Institut de Physiologie, Faculté de Médicine, Université de Lausanne, Lausanne, Switzerland
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  • Robert Gurny,

    1. Laboratory of Pharmaceutics and Biopharmaceutics, Section of Pharmaceutical Sciences, Université Lausanne, Université Geneva, Geneva, Switzerland
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  • Norbert Lange

    Corresponding author
    1. Laboratory of Pharmaceutics and Biopharmaceutics, Section of Pharmaceutical Sciences, Université Lausanne, Université Geneva, Geneva, Switzerland
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Corresponding author email: norbert.lange@pharm.unige.ch (Norbert Lange)

ABSTRACT

A targeting strategy based on the selective enzyme-mediated activation of polymeric photosensitizer prodrugs (PPP) within pathological tissue has led to the development of agents with the dual ability to detect and treat cancer. Herein, a detailed study of a simple model system for these prodrugs is described. We prepared “first-generation” PPP by directly tethering the photosensitizer (PS) pheophorbide a to poly-(l)-lysine via epsilon amide links and observed that by increasing the number of PS on a polymer chain, energy transfer between PS units improved leading to better quenching efficiency. Fragmentation of the PPP backbone by trypsin digestion gave rise to a pronounced fluorescence increase and to more efficient generation of reactive oxygen species upon light irradiation. In vitro tests using the T-24 bladder carcinoma cell line and ex vivo experiments using mouse intestines illustrated the remarkable and selective ability of these PPP to fluoresce and induce phototoxicity upon enzymatic activation. This work elucidated the basic physicochemical parameters, such as water solubility and quenching/activation behavior, required for the future elaboration of more adaptable “second-generation” PPP, in which the PS is tethered to a proteolytically stable polymer backbone via enzyme-specific peptide linkers. This polymer architecture offers great flexibility to tailor make the PPP to target any pathological tissue known to over-express a specific enzyme.

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