Journal of Materials Chemistry B,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
An
uncomplicated
template
method
was
employed
to
produce
sulfur
vacancies
(V
S
)-doped
hollow
Co
9
8
nanocages
(Co
8−
x
)
endow
a
single-component
nanomaterial
with
simultaneous
catalytic
activity
and
NIR-II
photothermal
property.
Advanced Materials,
Год журнала:
2024,
Номер
36(25)
Опубликована: Март 16, 2024
The
immunosuppressive
tumor
microenvironment
(TME)
is
a
huge
hurdle
in
immunotherapy.
Sono-immunotherapy
new
treatment
modality
that
can
reverse
TME,
but
the
sonodynamic
effects
are
compromised
by
overexpressed
glutathione
(GSH)
and
hypoxia
TME.
Herein,
this
work
reports
sono-immunotherapy
strategy
using
Pd
Advanced Materials,
Год журнала:
2024,
Номер
36(30)
Опубликована: Май 4, 2024
Abstract
Low
efficacy
of
immunotherapy
due
to
the
poor
immunogenicity
most
tumors
and
their
insufficient
infiltration
by
immune
cells
highlights
importance
inducing
immunogenic
cell
death
activating
system
for
achieving
better
treatment
outcomes.
Herein,
ferroelectric
Bi
2
CuO
4
nanoparticles
with
rich
copper
vacancies
(named
BCO‐V
Cu
)
are
rationally
designed
engineered
ferroelectricity‐enhanced
apoptosis,
cuproptosis,
subsequently
evoked
immunotherapy.
In
this
structure,
suppressed
recombination
electron–hole
pairs
band
bending
polarization
lead
high
catalytic
activity,
triggering
reactive
oxygen
species
bursts
apoptosis.
The
fragments
produced
apoptosis
serve
as
antigens
activate
T
cells.
Moreover,
generated
charge
catalysis,
nanomedicine
can
act
“a
smart
switch”
open
membrane,
promote
nanomaterial
endocytosis,
shut
down
+
outflow
pathway
evoke
thus
a
strong
response
is
triggered
reduced
content
adenosine
triphosphate.
Ribonucleic
acid
transcription
tests
reveal
pathways
related
activation.
Thus,
study
firstly
demonstrates
feasible
strategy
enhancing
using
single
semiconductor‐induced
cuproptosis.
Nanoscale,
Год журнала:
2024,
Номер
16(9), С. 4434 - 4483
Опубликована: Янв. 1, 2024
Metal-organic
frameworks
have
become
promising
stimuli-responsive
agents
to
release
the
loaded
therapeutic
in
target
site
achieve
more
precise
drug
delivery
due
their
high
loading,
excellent
biocompatibility,
and
stimuli-responsiveness.
Advanced Materials,
Год журнала:
2024,
Номер
36(27)
Опубликована: Март 29, 2024
Cancer
treatment
requires
precise
tumor-specific
targeting
at
specific
sites
that
allows
for
high-resolution
diagnostic
imaging
and
long-term
patient-tailorable
cancer
therapy;
while,
minimizing
side
effects
largely
arising
from
non-targetability.
This
can
be
realized
by
harnessing
exogenous
remote
stimuli,
such
as
tissue-penetrative
ultrasound,
magnetic
field,
light,
radiation,
enable
local
activation
therapy
in
deep
tumors.
A
myriad
of
nanomedicines
efficiently
activated
when
the
energy
stimuli
transformed
into
another
type
energy.
review
discusses
control
transformation
targetable,
efficient,
therapy.
Such
ultrasonic,
magnetic,
photonic,
radiative,
radioactive
mechanical,
thermal,
chemical,
radiative
to
a
variety
modalities.
The
current
article
describes
multimodal
where
serial
cascade
or
multiple
types
occur.
includes
not
only
hyperthermia,
radiation
but
also
emerging
thermoelectric,
pyroelectric,
piezoelectric
therapies
treatment.
It
illustrates
resonance,
fluorescence,
computed
tomography,
photoluminescence,
photoacoustic
imaging-guided
therapies.
highlights
afterglow
eliminate
autofluorescence
sustained
signal
emission
after
excitation.
Abstract
Ferroptosis
is
a
new
form
of
regulated
cell
death
featuring
iron‐dependent
lipid
peroxides
accumulation
to
kill
tumor
cells.
A
growing
body
evidence
has
shown
the
potential
ferroptosis‐based
cancer
therapy
in
eradicating
refractory
malignancies
that
are
resistant
apoptosis‐based
conventional
therapies.
In
recent
years,
studies
have
reported
number
ferroptosis
inducers
can
increase
vulnerability
cells
by
regulating
ferroptosis‐related
signaling
pathways.
Encouraged
rapid
development
ferroptosis‐driven
therapies,
interdisciplinary
fields
combine
ferroptosis,
pharmaceutical
chemistry,
and
nanotechnology
focused.
First,
prerequisites
metabolic
pathways
for
briefly
introduced.
Then,
detail
emerging
designed
boost
ferroptosis‐induced
therapy,
including
metal
complexes,
metal‐based
nanoparticles,
metal‐free
nanoparticles
summarized.
Subsequently,
application
synergistic
strategies
with
apoptosis
other
emphasis
on
use
both
cuproptosis
induce
redox
dysregulation
intracellular
bimetallic
copper/iron
metabolism
disorders
during
treatment
discussed.
Finally,
challenges
associated
clinical
translation
future
directions
potentiating
therapies
highlighted.
Advanced Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Авг. 3, 2024
Compared
with
conventional
therapies,
photoimmunotherapy
offers
precise
targeted
cancer
treatment
minimal
damage
to
healthy
tissues
and
reduced
side
effects,
but
its
efficacy
may
be
limited
by
shallow
light
penetration
the
potential
for
tumor
resistance.
Here,
an
acceptor-donor-acceptor
(A-D-A)-structured
nanoaggregate
is
developed
dual
phototherapy,
including
photodynamic
therapy
(PDT)
photothermal
(PTT),
triggered
single
near-infrared
(NIR)
light.
Benefiting
from
strong
intramolecular
charge
transfer
(ICT),
A-D-A-structured
nanoaggregates
exhibit
broad
absorption
extending
NIR
region
effectively
suppressed
fluorescence,
which
enables
deep
efficient
conversion
(η
=
67.94%).
A
suitable
HOMO-LUMO
distribution
facilitates
sufficient
intersystem
crossing
(ISC)
convert
ground-state
oxygen
(
Advanced Materials,
Год журнала:
2024,
Номер
36(24)
Опубликована: Фев. 28, 2024
Abstract
The
insufficient
exposure
sites
and
active
site
competition
of
multienzyme
are
the
two
main
factors
to
hinder
its
therapeutic
effect.
Here,
a
phase‐junction
nanomaterial
(amorphous‐crystalline
Cu
x
S–Ag
2
S)
is
designed
prepared
through
simple
room
temperature
ion‐exchange
process.
A
small
amount
Ag
+
added
into
7
S
4
nanocrystals,
which
transforms
amorphous
phased
produces
crystalline
simultaneously.
In
this
structure,
overhanging
bonds
on
surface
provide
abundant
for
optimizing
activity.
Meanwhile,
state
enhances
photothermal
effect
non‐radiative
relaxation,
due
low
thermal
resistance,
forms
significant
gradient
unlock
optimized
thermo‐electrodynamic
therapy.
Furthermore,
benefiting
from
high
asymmetry
state,
material
spin‐polarized
that
can
effectively
inhibit
electron–hole
recombination.
way,
thermoelectric
facilitate
enzyme‐catalyzed
cycle
by
providing
electrons
holes,
enabling
an
enhanced
coupling
therapy
with
activity,
induces
excellent
anti‐tumor
performance.
More
importantly,
catalytic
process
simulated
density‐functional
theory
proves
alleviates
burden
favorable
adsorption
O
prevents
competition.
Advanced Materials,
Год журнала:
2024,
Номер
36(48)
Опубликована: Окт. 13, 2024
Phototherapy,
such
as
photothermal
therapy
(PTT)
and
photodynamic
(PDT)
has
been
a
powerful
strategy
to
combat
bacterial
infection.
However,
the
compact
cell
membranes
of
pathogenic
bacteria,
especially
drug-resistant
significantly
diminish
efficiency
heat
conduction
impede
entrance
reactive
oxygen
species
(ROS)
into
cells,
resulting
in
unsatisfactory
sterilization.
Enlightened
by
membrane
feature
competent
herein
MXene/CaO
Nanozyme-based
metabolic
regulation
triggered
by
tumor-specific
endogenous
stimuli
has
emerged
as
a
promising
therapeutic
strategy
for
tumors.
The
current
efficacy,
however,
is
constrained
the
limited
concentration
of
substrates
and
plasticity
Consequently,
implementation
efficient
in
tumor
therapy
urgently
needed.
Herein,
versatile
nanozyme-based
nicotinamide
adenine
dinucleotide
(NADH)
circulating
oxidation
nanoreactor
reported.
First,
synthesized
cobalt-doped
hollow
carbon
spheres
(Co-HCS)
possess
NADH
oxidase
(NOX)-mimicking
activity
to
disrupt
oxidative
phosphorylation
(OXPHOS)
pathway
cells.
Second,
substrate-cycle
manner
Co-HCS
can
be
used
overcome
limitation
substrate
deficiency.
Finally,
2-Deoxy-D-glucose
(2-DG)
6-aminonicotinamide
(6-AN)
are
introduced
block
glycolysis
pentose
phosphate
(PPP),
thus
creating
(Co-HCS/D/A)
through
triple
cellular
metabolism
disruption.
In
vitro
vivo
results
demonstrate
that
designed
not
only
enhances
catalytic
efficiency
but
also
disrupts
homeostasis,
leading
outcome.
This
study
develops
novel
disruption,
which
addresses
limitations
therapy.