Volume 11, Issue 47 pp. 6338-6346
Full Paper

Immobilization of ALA-ZnII Coordination Polymer Pro-photosensitizers on Magnetite Colloidal Supraparticles for Target Photodynamic Therapy of Bladder Cancer

Jing Tan

Jing Tan

State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Polymers and Polymer Composite Materials, Department of Macromolecular Science and Laboratory of Advanced Materials, Fudan University, Shanghai, 200433 P. R. China

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Chuanyu Sun

Chuanyu Sun

Department of Urology, Huashan Hospital, Fudan University, Shanghai, 200040 P. R. China

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Ke Xu

Corresponding Author

Ke Xu

Department of Urology, Huashan Hospital, Fudan University, Shanghai, 200040 P. R. China

E-mail: [email protected], [email protected]Search for more papers by this author
Changchun Wang

Changchun Wang

State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Polymers and Polymer Composite Materials, Department of Macromolecular Science and Laboratory of Advanced Materials, Fudan University, Shanghai, 200433 P. R. China

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Jia Guo

Corresponding Author

Jia Guo

State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Polymers and Polymer Composite Materials, Department of Macromolecular Science and Laboratory of Advanced Materials, Fudan University, Shanghai, 200433 P. R. China

E-mail: [email protected], [email protected]Search for more papers by this author
First published: 30 October 2015
Citations: 27

Abstract

5-Aminolevulinic acid (ALA) is a widely used photodynamic therapy (PDT) prodrug in the clinic. It can be metalized to the photosensitizer PpIX, which produces toxic singlet oxygen to kill cancer cells upon visible light irradiation. Herein, a core/shell-structured vehicle is designed to comprise magnetite colloidal supraparticles (MCSPs) as cores and ALA-ZnII coordination polymers as shells (Fe3O4@ALA-ZnII) for target pro-photosensitizer delivery. The coordination polymers with 2D layered structures are locally deposited on the MCSPs by the complexation of the ALA and ZnII ions, and are readily controlled by varying the feed precursors and reaction temperatures. The maximum conjugated ALA amount is up to 17%. The Fe3O4@ALA-ZnII microspheres exhibit pH-sensitive release of ALA in acidic environment and rapid magnetic responsiveness. Cytotoxicity results demonstrate that Fe3O4@ALA-ZnII shows a significant inhibitory effect to T24 cells and is nontoxic to 293T normal cells as exposed to the 630 nm visible light for a very short time, which may due to the selective accumulation of ALA-induced PpIX in T24 cancer cells. Compared to the ALA used alone, the coordination polymer form is more efficient because of the bioactivity of incorporated Zn ions despite underlying the same apoptosis mechanism as ALA agent.

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