Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(26)
Published: Feb. 27, 2024
Abstract
Reactive
oxygen
species
(ROS)‐induced
endoplasmic
reticulum
(ER)
stress
in
sonodynamic
therapy
(SDT)
can
elicit
immunogenic
cell
death
(ICD)‐initiated
antitumor
immunity
for
augmented
sono‐immunotherapy.
However,
unsatisfactory
activity
and
mediocre
ER
induction
ability
of
sonosensitizers
essentially
restrict
SDT
efficacy
ICD
stimulation.
Herein,
a
versatile
ER‐targeting
Iridium(III)
nanosonosensitizer
is
developed
as
superior
inducer
boosted
tumor
An
ingenious
cholic
acid
(CA)‐functionalized
sonosensitizer
Ir‐CA
well‐designed
skillfully
crosslinked
with
human
serum
albumin
(HSA)
to
form
HSA@Ir‐CA.
With
high
stability,
favorable
tumor‐targeting
ability,
reduction‐responsiveness,
HSA@Ir‐CA
preferentially
accumulates
sites
enhanced
cellular
uptake,
followed
by
rapid
disassembly
responding
intracellular
reductive
environment.
The
uncaged
selectively
accumulate
precisely
disrupt
situ
produced
type
I
II
ROS
upon
US
irradiation
high‐efficiency
SDT.
Moreover,
the
maximized
eminently
amplifies
evoke
robust
systemic
immunity,
inhibiting
growths
primary/distant
tumor,
lung
metastasis,
recurrence.
This
combined
immune
checkpoint
inhibitor
(αPD‐L1)
further
achieves
reinforced
therapeutic
outcome
against
immunologically
“cold”
tumor.
study
presents
an
effective
paradigm
optimize
amplify
ICD‐initiated
responses
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(10)
Published: Dec. 18, 2022
Conventional
sonodynamic
therapy
is
unavoidably
limited
by
the
tumor
microenvironment,
although
many
sonosensitizers
have
been
developed
to
improve
them
a
certain
extent.
Given
this,
concept
of
sonocatalytic
hydrogen
evolution
proposed,
which
defined
as
an
oxygen-independent
therapeutics.
To
demonstrate
feasibility
concept,
narrow-bandgap
semiconductor
bismuth
sulfide
(Bi2
S3
)
selected
sonocatalyst
and
platinum
(Pt)
nanoparticles
are
grown
in
situ
optimize
their
catalytic
performance.
In
this
nanocatalytic
system,
Pt
help
capture
sonoexcited
electrons,
whereas
intratumoral
overexpressed
glutathione
(GSH),
natural
hole
sacrificial
agent,
can
consume
holes,
greatly
improves
charge-separation
efficiency
promotes
controllable
sustainable
H2
generation.
Even
under
hypoxic
conditions,
Pt-Bi2
also
produce
sufficient
ultrasound
irradiation.
Mechanistically,
mitochondrial
dysfunction
caused
redox
homeostasis
destruction
GSH
depletion
synergistically
damage
DNA
induce
cells
apoptosis.
At
same
time,
holes
trigger
decomposition
peroxide
into
O2
relieve
hypoxia,
thus
being
synergistic
with
reverse
immunosuppressive
microenvironment.
The
proposed
sonocatalysis-mediated
will
provide
new
direction
realize
facile
efficient
cancer
therapy.
Advanced Functional Materials,
Journal Year:
2022,
Volume and Issue:
32(29)
Published: April 28, 2022
Abstract
The
combination
of
apoptosis
and
ferroptosis
is
highly
appealing
in
addressing
the
tumor
heterogeneity‐induced
therapy
resistance.
Reactive
oxygen
species
(ROS)‐based
cancer
nanomedicine
can
assemble
multiple
cell
death
modalities
a
single
platform,
but
potency
induction
limited.
Here,
novel
mechano‐responsive
polymeric
micellar
system
for
selective
boosting
ROS
sensitization
reported.
mechanophore,
ferrocene
(Fc)
key
to
such
design,
ultrasound
speed
up
dissociation
Fc
release
Fe
2+
hydroxyl
radical
presence
elevated
H
2
O
microenvironment.
Fc‐conjugated
amphiphilic
copolymers
self‐assemble
into
nanoscale
micelles
wherein
model
sonosensitizer,
protoporphyrin
IX
physically
encapsulated.
Upon
triggering,
produce
both
singlet
apoptotic
murine
breast
line
(4T1).
also
depletes
intracellular
glutathione
thioredoxin,
which
together
with
heightened
level
boosts
lipid
peroxidation
hence
ferroptotic
death.
interactive
further
demonstrated
4T1
tumor‐bearing
mice
negligible
adverse
effects.
current
work
provides
approach
simultaneously
sensitize
efficient
on‐demand
therapy.
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
33(32)
Published: May 5, 2023
Sonodynamic
therapy
(SDT),
which
uses
ultrasound
to
trigger
a
sonosensitizer
generate
reactive
oxygen
species
(ROS),
is
promising
form
of
cancer
with
outstanding
tissue
penetration
depth.
However,
the
may
inevitably
spread
surrounding
healthy
beyond
tumor,
resulting
in
undesired
side
effects
under
an
stimulus.
Herein,
as
glutathione
(GSH)
overexpressed
tumor
microenvironment,
GSH-activatable
prodrug
was
designed
by
attaching
quencher
tetraphydroxy
porphyrin
for
therapy.
The
exhibited
poor
fluorescence
and
low
ROS
generation
capacity
irradiation
but
it
can
be
activated
GSH
simultaneously
switch
on
emission
site.
Compared
non-quenched
sonosensitizer,
significantly
higher
tumor/healthy
organ
ratios,
due
specific
activation
tumor.
Finally,
efficient
growth
inhibition
irradiation,
further
demonstrating
its
promise
GSH-activated
highly
effective
treatment.
Advanced Healthcare Materials,
Journal Year:
2023,
Volume and Issue:
12(22)
Published: April 25, 2023
Abstract
Platinum
drugs
with
manifest
therapeutic
effects
are
widely
used,
but
their
systemic
toxicity
and
the
drug
resistance
acquired
by
cancer
cells
limit
clinical
applications.
Thus,
exploration
on
appropriate
methods
strategies
to
overcome
limitations
of
traditional
platinum
becomes
extremely
necessary.
Combination
therapy
can
inhibit
tumor
growth
metastasis
in
an
additive
or
synergistic
manner,
potentially
reduce
platinum‐resistance.
This
review
summarizes
various
modalities
current
progress
platinum‐based
combination
therapy.
The
synthetic
some
anticancer
complexes
gene
editing,
ROS‐based
therapy,
thermal
immunotherapy,
biological
modelling,
photoactivation,
supramolecular
self‐assembly
imaging
modality
briefly
described.
Their
potential
challenges
prospects
also
discussed.
It
is
hoped
that
this
will
inspire
researchers
have
more
ideas
for
future
development
highly
effective
anti‐cancer
complexes.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(2), P. 1644 - 1656
Published: Jan. 4, 2024
Photodynamic
therapy
(PDT),
an
emergent
noninvasive
cancer
treatment,
is
largely
dependent
on
the
presence
of
efficient
photosensitizers
(PSs)
and
a
sufficient
oxygen
supply.
However,
therapeutic
efficacy
PSs
greatly
compromised
by
poor
solubility,
aggregation
tendency,
depletion
within
solid
tumors
during
PDT
in
hypoxic
microenvironments.
Despite
potential
PS-based
metal–organic
frameworks
(MOFs),
addressing
hypoxia
remains
challenging.
Boron
dipyrromethene
(BODIPY)
chromophores,
with
excellent
photostability,
have
exhibited
great
bioimaging.
their
practical
application
suffers
from
limited
chemical
stability
under
harsh
MOF
synthesis
conditions.
Herein,
we
report
first
example
Zr-based
MOF,
namely,
69-L2,
exclusively
constructed
BODIPY-derived
ligands
via
single-crystal
to
post-synthetic
exchange,
where
direct
solvothermal
method
not
applicable.
To
increase
performance
hypoxia,
modify
69-L2
fluorinated
phosphate-functionalized
methoxy
poly(ethylene
glycol).
The
resulting
69-L2@F
carrier,
enabling
tumor
oxygenation
simultaneously
acting
as
PS
for
reactive
species
(ROS)
generation
LED
irradiation.
We
demonstrate
that
has
enhanced
effect
triple-negative
breast
MDA-MB-231
cells
both
normoxia
hypoxia.
Following
positive
results,
evaluated
vivo
activity
hydrogel,
local
mice
model
achieving
exceptional
antitumor
only
2
days.
envision
BODIPY-based
Zr-MOFs
provide
solution
relief
maximize
PDT,
offering
new
insights
into
design
promising
MOF-based
tumors.