Aggregate,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 2, 2024
Abstract
Photodynamic
therapy
is
a
highly
recommended
alternative
treatment
for
solid
tumors,
such
as
cutaneous
or
luminal
in
clinical
practice.
However,
conventional
photosensitizers
(PSs)
often
induce
undesirable
phototoxic
effects
because
of
their
normal
tissue
distribution
and
reduction
antitumor
resulting
from
aggregation‐caused
quenching
effects.
The
present
study
developed
novel
nano‐formulated
aggregation‐induced
emission
(AIE)‐characteristic
PS,
nab‐TTVPHE,
which
composed
human
serum
albumin
carrier
TTVPHE
therapeutic
agent,
more
effective
cancer
with
lower
Notably,
the
reactive
oxygen
species
generated
by
were
shielded
nanoaggregate
structure,
photodynamic
activity
was
after
nanostructure
dissociation.
Nab‐TTVPHE
actively
internalized
tumor
cells
via
secreted
protein,
acidic
rich
cysteine
released
to
form
nanoaggregates.
accumulated
mitochondria,
where
it
triggered
mitochondrial
damage
under
light
irradiation
its
induced
pyroptosis
caspase‐3/gasdermin
E
(GSDME)
signaling
pathway
kill
cells.
Therefore,
this
AIE‐characteristic
PS
provides
an
innovative
strategy
effect
ability
boost
potential
immunity
GSDME‐mediated
pyroptosis.
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 13, 2025
Abstract
Photodynamic
therapy
holds
great
potentials
in
cancer
treatment,
yet
its
effectiveness
hypoxic
solid
tumor
is
limited
by
the
oxygen‐dependence
and
insufficient
oxidative
potential
of
conventional
type
II
reactive
oxygen
species
(ROS).
Herein,
study
reports
a
supramolecular
photosensitizer,
BSA@TPE‐BT‐SCT
NPs,
through
encapsulating
aggregation‐enhanced
emission
photosensitizer
bovine
serum
albumin
(BSA)
to
significantly
enhance
ROS,
particularly
less
oxygen‐dependent
I
ROS
for
photodynamic
immunotherapy.
The
abundant
generated
NPs
induce
multiple
forms
programmed
cell
death,
including
apoptosis,
pyroptosis,
ferroptosis.
These
multifaceted
deaths
synergistically
facilitate
release
damage‐associated
molecular
patterns
antitumor
cytokines,
thereby
provoking
robust
immunity.
Both
vitro
vivo
experiments
confirmed
that
elicited
immunogenic
dendritic
maturation,
activate
T
cell,
reduce
myeloid‐derived
suppressor
cells,
leading
inhibition
both
primary
distant
tumors.
Additionally,
BSA@TPE‐BT‐SCP
also
exhibited
excellent
performance
humanized
mice
model,
evidenced
reduction
senescent
cells
among
these
activated
cells.
findings
advance
development
photosensitizers
unveil
important
role
enhancing
immunogenicity.
Journal of Materials Chemistry A,
Journal Year:
2023,
Volume and Issue:
11(45), P. 24911 - 24917
Published: Jan. 1, 2023
We
have
designed
and
constructed
supramolecular
dimers
between
triphenylamine
derivatives
with
AIE
properties
CB[8]
through
host–guest
interactions,
which
can
be
used
as
photosensitizers
for
photooxidation
reactions
of
thioanisole.
Aggregate,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 2, 2024
Abstract
Photodynamic
therapy
is
a
highly
recommended
alternative
treatment
for
solid
tumors,
such
as
cutaneous
or
luminal
in
clinical
practice.
However,
conventional
photosensitizers
(PSs)
often
induce
undesirable
phototoxic
effects
because
of
their
normal
tissue
distribution
and
reduction
antitumor
resulting
from
aggregation‐caused
quenching
effects.
The
present
study
developed
novel
nano‐formulated
aggregation‐induced
emission
(AIE)‐characteristic
PS,
nab‐TTVPHE,
which
composed
human
serum
albumin
carrier
TTVPHE
therapeutic
agent,
more
effective
cancer
with
lower
Notably,
the
reactive
oxygen
species
generated
by
were
shielded
nanoaggregate
structure,
photodynamic
activity
was
after
nanostructure
dissociation.
Nab‐TTVPHE
actively
internalized
tumor
cells
via
secreted
protein,
acidic
rich
cysteine
released
to
form
nanoaggregates.
accumulated
mitochondria,
where
it
triggered
mitochondrial
damage
under
light
irradiation
its
induced
pyroptosis
caspase‐3/gasdermin
E
(GSDME)
signaling
pathway
kill
cells.
Therefore,
this
AIE‐characteristic
PS
provides
an
innovative
strategy
effect
ability
boost
potential
immunity
GSDME‐mediated
pyroptosis.