Molecularly Engineered NIR-II Emitting Carbon Dots Assemblies for Unprecedented High-Resolution Angiography and Synergistic Photodynamic/Photothermal Tumor Therapy
Xiaokuang Xue,
Jian Li,
Tiejin Chen
и другие.
Chemical Engineering Journal,
Год журнала:
2025,
Номер
505, С. 159356 - 159356
Опубликована: Янв. 7, 2025
Язык: Английский
Nanotheranostics with Radionuclides for Cancer Diagnosis and Therapy
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 9, 2025
Abstract
Anti‐tumor
theranostic
radionuclide
nanosystems
have
gained
significant
attention
as
an
emerging
therapeutic
strategy.
This
review
systematically
elucidates
the
concept
and
recent
advances
of
anti‐tumor
nanotheranostic
systems
with
radionuclides,
a
focus
on
design
nanocarriers,
precise
selection
their
advantages
limitations
in
clinical
translation.
also
explores
integration
imaging
various
treatment
modalities,
including
photodynamic
therapy,
photothermal
sonodynamic
immunotherapy.
Furthermore,
combination
therapy
fluorescence
magnetic
resonance
technologies,
which
broadens
application
nanotheranostics,
is
discussed.
Finally,
outlooks
future
development
nanotheranostics
radionuclides
proposes
key
research
focus.
Язык: Английский
A Smart Visualized Phototherapy Switch: From NIR‐I Imaging‐Guided Photodynamic Therapy to NIR‐II‐Guided Photothermal Therapy for Enhanced Cascade Tumor Photoablation
Aggregate,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 11, 2025
ABSTRACT
Imaging‐guided
phototherapy
holds
promise
for
precision
cancer
treatment.
However,
most
photosensitizers
have
only
a
singular
modality
of
photodynamic
therapy
(PDT)
or
photothermal
(PTT),
which
make
their
therapeutic
efficacy
severely
limited
by
the
hypoxic
and
complex
tumor
microenvironment
(TME).
In
this
article,
we
provide
smart
platform
design
(BOD‐D)
based
on
visualized
light‐triggered
phototherapeutic
switch
transforming
from
near‐infrared
(NIR)‐I
imaging‐guided
PDT
to
activatable
NIR‐II‐guided
PTT
while
releasing
nitric
oxide
(NO)
gas
(GT).
BOD‐D
releases
native
NIR
one‐region
fluorescence
signals
in
tumors,
is
used
direct
robust
killing.
As
administered,
decreasing
oxygen
content
TME
becomes
progressively
insufficient
maintain
its
excellent
cell‐killing
effect.
Subsequently,
light
triggers
dissociation
NO
BOD‐D,
activating
agent
BOD‐T
that
emits
NIR‐II
fluorescence,
subsequent
PTT.
Notably,
not
light‐mediated
mechanism
can
be
switched
NIR‐I‐guided
PTT,
but
also
released
during
process
will
GT
sensitize
above
Our
study
contributes
intelligent
cascade
photoablation.
Язык: Английский
A cyanine fluorophore for imaging-guided tumor photodynamic and photothermal therapy under NIR-II light activation
Science China Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 10, 2025
Язык: Английский
Immunomodulating Platelet-mimicking Nanoparticles for AIE-based Enhanced Photodynamic Immunotherapy against Lung Cancer
Materials Today Bio,
Год журнала:
2025,
Номер
unknown, С. 101683 - 101683
Опубликована: Март 1, 2025
Язык: Английский
Ultrasound‐Triggered Cascade Delivery via Poly‐Oxaliplatin Nanoparticles for Immunotherapy
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 26, 2025
Abstract
Oxaliplatin
(OXA),
a
third‐generation
platinum‐based
chemotherapeutic
agent,
is
widely
utilized
in
cancer
treatment
due
to
its
potent
cytotoxic
effects
and
ability
induce
immunogenic
cell
death
(ICD).
However,
the
clinical
application
of
OXA
significantly
hindered
by
inefficient
drug
delivery.
To
address
these
challenges,
cascade
delivery
system
that
integrates
ultrasound
(US)
activation
with
Poly‐Oxaliplatin
nanoparticles
(OXA‐Ce6
NP)
developed
enhance
therapeutic
efficacy
overcome
resistance
mechanisms
OXA.
This
sono‐responsive
platform
consists
an
amphiphilic
polymer
incorporating
OXA(IV)
prodrug
(Poly‐OXA(IV))
sonosensitizer
chlorin
e6
(Ce6),
enabling
US‐triggered
cascade.
Upon
US
exposure,
this
facilitates
1)
enhanced
cellular
uptake
via
increased
membrane
permeability,
2)
situ
through
electron
transfer,
3)
augmented
formation
OXA‐DNA
adducts,
thereby
intensifying
DNA
damage
effects.
Moreover,
US‐induced
reactive
oxygen
species
(ROS)
further
potentiate
ICD,
remodeling
tumor
immune
microenvironment
promoting
systemic
antitumor
immunity.
By
leveraging
as
external
stimulus,
enhances
outcome
while
mitigating
toxicity.
strategy
provides
versatile
approach
optimizing
chemotherapy
integrating
immunotherapy,
offering
promising
avenue
for
improving
treatments.
Язык: Английский
Ultrasound-Energized OX40L-Expressing Biohybrid for Multidimensional Mobilization of Sustained T Cell-Mediated Antitumor Immunity and Potent Sono-Immunotherapy
Mengyun Liang,
Xiaoying Kang,
Hanwen Liu
и другие.
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 9, 2025
Harnessing
immunostimulation
to
reinvigorate
antitumor
effector
immune
cells
represents
a
promising
strategy
for
tumor
eradication.
However,
achieving
durable
clinical
outcomes
necessitates
multidimensional
activation
sustain
robust
responses.
Here,
we
present
an
ultrasound-empowered
living
biohybrid
that
strategically
mobilizes
T-cell-mediated
immunity
potent
sono-immunotherapy.
Through
synthetic
biology,
engineer
bacteria
express
fusion
protein
encoding
the
costimulatory
OX40
ligand
(OX40L),
and
further
functionalize
them
with
high-performance
polymer
sonosensitizer
tethered
via
reactive
oxygen
species-cleavable
linker.
Upon
ultrasound
irradiation,
sono-activated
nanocargoes
detach
from
bacterial
surface,
facilitating
cellular
entry
exposing
immune-stimulating
OX40L.
The
sonodynamic
effects,
coupled
native
immunogenicity
of
bacteria,
promotes
tumor-associated
antigen
release,
fosters
proinflammatory
microenvironment,
drives
dendritic
cell
maturation,
thereby
priming
cytotoxic
T-cell
activation.
OX40L
expressed
by
engineered
amplifies
sustains
activity,
orchestrating
response.
This
cascade-amplified
effectively
suppresses
growth,
induces
long-lasting
memory,
provides
protection
against
metastasis
recurrence,
significantly
enhancing
survival
outcomes.
By
integrating
ultrasound-energized
nanoadjuvants
boosters,
this
hybrid
biotherapeutic
platform
offers
versatile
powerful
activation,
advancing
frontier
cancer
Язык: Английский
Novel Mitochondria-Targeted Asymmetric Heptamethine Cyanine Dye for Cancer Targeted NIR Imaging and Potent Necrosis and Senescence Induction with Prolonged Retention
Journal of Medicinal Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 11, 2025
Developing
small
molecules
that
inherently
integrate
highly
tumor-targeted
near-infrared
fluorescence
(NIRF)
imaging
with
potent
therapeutic
effects
remains
challenging
in
anticancer
theranostics.
Here,
we
synthesized
and
characterized
a
series
of
heptamethine
cyanine
PSs
symmetric
asymmetric
structures.
Among
them,
first
discovered
structures
significantly
enhanced
tumor
targeting.
Also,
novel
mitochondria-targeted
compound
17
exhibited
superior
NIRF
capability,
exceptional
selectivity
(TNR
=
8.54),
strong
antitumor
activity.
Compound
selectively
accumulates
mitochondria,
driven
by
MMP,
where
it
generates
ROS,
induces
DNA
damage,
triggers
senescence,
apoptosis,
necrosis.
Its
efficacy
was
demonstrated
across
multiple
models,
including
patient-derived
xenograft
(PDX),
allowed
precise
visualization,
suppressed
growth
single
administration,
showed
no
detectable
toxicity.
Notably,
the
single-dye
molecule
retained
tumors
for
over
120
h,
enabling
prolonged
imaging,
targeted
therapy,
drug
delivery
integrated
treatment.
Язык: Английский