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  4. FAP Targeting of Photosensitizer-Loaded Polymersomes for Increased Light-Activated Cell Killing
 
research article

FAP Targeting of Photosensitizer-Loaded Polymersomes for Increased Light-Activated Cell Killing

Skowicki, Michal
•
Hurlimann, Dimitri
•
Tarvirdipour, Shabnam
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January 24, 2024
Biomacromolecules

As current chemo- and photodynamic cancer therapies are associated with severe side effects due to a lack of specificity and to systemic toxicity, innovative solutions in terms of targeting and controlled functionality are in high demand. Here, we present the development of a polymersome nanocarrier equipped with targeting molecules and loaded with photosensitizers for efficient uptake and light-activated cell killing. Polymersomes were self-assembled in the presence of photosensitizers from a mixture of nonfunctionalized and functionalized PDMS-b-PMOXA diblock copolymers, the latter designed for coupling with targeting ligands. By encapsulation inside the polymersomes, the photosensitizer Rose Bengal was protected, and its uptake into cells was mediated by the nanocarrier. Inhibitor of fibroblast activation protein alpha (FAPi), a ligand for FAP, was attached to the polymersomes' surface and improved their uptake in MCF-7 breast cancer cells expressing relatively high levels of FAP on their surface. Once internalized by MCF-7, irradiation of Rose Bengal-loaded FAPi-polymersomes generated reactive oxygen species at levels high enough to induce cell death. By combining photosensitizer encapsulation and specific targeting, polymersomes represent ideal candidates as therapeutic nanocarriers in cancer treatment.

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Type
research article
DOI
10.1021/acs.biomac.3c00943
Web of Science ID

WOS:001161575800001

Author(s)
Skowicki, Michal
Hurlimann, Dimitri
Tarvirdipour, Shabnam
Kyropoulou, Myrto
Schoenenberger, Cora-Ann
Gerber-Lemaire, Sandrine  
Palivan, Cornelia G.
Date Issued

2024-01-24

Publisher

American Chemical Society

Published in
Biomacromolecules
Volume

25

Issue

2

Start page

754

End page

766

Subjects

Life Sciences & Biomedicine

•

Physical Sciences

•

Photodynamic Therapy

•

Cancer

•

Delivery

•

Nanoparticles

•

Nanoreactors

•

Strategies

•

Liposomes

•

Protein

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
SCI-SB-SG  
FunderGrant Number

Universit?t Basel

NCCR Molecular Systems Engineering, University of Basel

Available on Infoscience
February 23, 2024
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/205556
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