A supramolecular approach for modulated photoprotection, lysosomal delivery, and photodynamic activity of a photosensitizer

Full text not archived in this repository.

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Roy, I., Bobbala, S., Young, R. M., Beldjoudi, Y., Nguyen, M. T., Cetin, M. M., Cooper, J. A. orcid id iconORCID: https://orcid.org/0000-0002-3981-9246, Allen, S., Anamimoghadam, O., Scott, E. A., Wasielewski, M. R. and Stoddart, J. F. (2019) A supramolecular approach for modulated photoprotection, lysosomal delivery, and photodynamic activity of a photosensitizer. Journal of the American Chemical Society, 141 (31). pp. 12296-12304. ISSN 0002-7863 doi: 10.1021/jacs.9b03990

Abstract/Summary

Prompted by a knowledge of the photoprotective mechanism operating in photosystem supercomplexes and bacterial antenna complexes by pigment binding proteins, we have appealed to a boxlike synthetic receptor (ExBox·4Cl) that binds a photosensitizer, 5,15-diphenylporphyrin (DPP), to provide photoprotection by regulating light energy. The hydrophilic ExBox4+ renders DPP soluble in water and modulates the phototoxicity of DPP by trapping it in its cavity and releasing it when required. While trapping removes access to the DPP triplet state, a pH-dependent release of diprotonated DPP (DPPH22+) restores the triplet deactivation pathway, thereby activating its ability to generate reactive oxygen species. We have employed the ExBox4+-bound DPP complex (ExBox4+⊃DPP) for the safe delivery of DPP into the lysosomes of cancer cells, imaging the cells by utilizing the fluorescence of the released DPPH22+ and regulating photodynamic therapy to kill cancer cells with high efficiency.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/113515
Identification Number/DOI 10.1021/jacs.9b03990
Refereed Yes
Divisions No Reading authors. Back catalogue items
Publisher American Chemical Society
Download/View statistics View download statistics for this item

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar