posted on 2024-01-25, 01:05authored byMichal Skowicki, Dimitri Hürlimann, Shabnam Tarvirdipour, Myrto Kyropoulou, Cora-Ann Schoenenberger, Sandrine Gerber-Lemaire, Cornelia G. Palivan
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-<i>b</i>-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 α (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.