Chemical Communications,
Journal Year:
2024,
Volume and Issue:
60(93), P. 13641 - 13652
Published: Jan. 1, 2024
Hypoxia
limits
the
phototherapeutic
efficacy
of
porphyrin-based
nMOFs;
loading
with
hypoxia-activated
drug
TPZ
enhances
combined
PDT
and
chemotherapy
effects.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(27)
Published: April 24, 2024
A
planar
conjugated
ligand
functionalized
with
bithiophene
and
its
Ru(II),
Os(II),
Ir(III)
complexes
have
been
constructed
as
single-molecule
platform
for
synergistic
photodynamic,
photothermal,
chemotherapy.
The
significant
two-photon
absorption
at
808
nm
remarkable
singlet
oxygen
superoxide
anion
production
in
aqueous
solution
cells
when
exposed
to
infrared
irradiation.
most
potent
Ru(II)
complex
Ru7
enters
tumor
via
the
rare
macropinocytosis,
locates
both
nuclei
mitochondria,
regulates
DNA-related
chemotherapeutic
mechanisms
intranuclearly
including
DNA
topoisomerase
RNA
polymerase
inhibition
their
effects
photoactivated
apoptosis,
ferroptosis
cleavage.
exhibits
high
efficacy
vivo
malignant
melanoma
cisplatin-resistant
non-small
cell
lung
cancer
tumors,
a
100
%
survival
rate
of
mice,
low
toxicity
normal
residual
rate.
Such
an
activatable
metal
may
contribute
new
generation
single-molecule-based
integrated
diagnosis
treatment
address
drug
resistance
clinical
practice
phototherapy
large,
deeply
located
solid
tumors.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(3), P. 1703 - 1703
Published: Jan. 30, 2024
This
work
was
aimed
at
the
complex
analysis
of
metabolic
and
oxygen
statuses
tumors
in
vivo
after
photodynamic
therapy
(PDT).
Studies
were
conducted
on
mouse
tumor
model
using
two
types
photosensitizers—chlorin
e6-based
drug
Photoditazine
predominantly
targeted
to
vasculature
genetically
encoded
photosensitizer
KillerRed
chromatin.
Metabolism
cells
assessed
by
fluorescence
lifetime
redox-cofactor
NAD(P)H,
imaging.
Oxygen
content
phosphorescence
macro-imaging
with
an
oxygen-sensitive
probe.
For
visualization
perfused
microvasculature,
optical
coherence
tomography-based
angiography
used.
It
found
that
PDT
induces
different
alterations
cellular
metabolism,
depending
degree
depletion.
Moderate
decrease
case
accompanied
increase
fraction
free
indicator
glycolytic
switch,
early
treatment.
Severe
hypoxia
resulted
from
a
vascular
shutdown
yielded
persistent
protein-bound
(mitochondrial)
NAD(P)H.
These
findings
improve
our
understanding
physiological
mechanisms
modes
can
be
useful
develop
new
approaches
monitoring
its
efficacy.
Materials Horizons,
Journal Year:
2024,
Volume and Issue:
11(23), P. 5815 - 5842
Published: Jan. 1, 2024
The
current
state-of-the
art
on
NIR-II-activated
photosensitizers
and
their
applications
for
the
deep
tumor
treatment,
as
well
recent
efforts
that
combine
NIR-II
activated
PDT
with
other
complementary
therapeutic
routes.
Advanced Healthcare Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 27, 2025
Abstract
The
combination
of
Ca
2+
overload
and
reactive
oxygen
species
(ROS)
production
for
cancer
therapy
offers
a
superior
solution
to
the
lack
specificity
in
traditional
antitumor
strategies.
However,
current
therapeutic
platforms
this
strategy
are
primarily
based
on
non‐targeting
nanomaterials,
leading
undesirable
off‐target
side
effects.
Additionally,
resistance
ROS
apoptosis
induced
by
hypoxic
tumor
microenvironment
(TME)
further
limits
efficiency.
Herein,
magnetic
microrobot
living
Spirulina
Platensis
(SP),
which
is
coated
with
double
layer
Fe
3
O
4
nanoparticles
(NPs)
CaCO
NPs.
microrobots
can
accumulate
regions
under
attraction,
produces
high‐Ca
environment
acidic
TME
facilitates
ultrasound
(US)
stimulation.
Meanwhile,
sufficient
(O
2
)
photosynthesis
helps
alleviate
hypoxia
promotes
situ
chlorophyll‐mediated
photodynamic
(PDT),
coordinate
induce
cell
apoptosis.
With
these
unique
properties,
SP‐based
offer
promising
microrobotics‐based
accumulation
production,
contributing
precise
effective
way
treatment.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(15)
Published: Feb. 16, 2024
Abstract
Developing
Type‐I
photosensitizers
provides
an
attractive
approach
to
solve
the
dilemma
of
inadequate
efficacy
photodynamic
therapy
(PDT)
caused
by
inherent
oxygen
consumption
traditional
Type‐II
PDT
and
anoxic
tumor
microenvironment.
The
challenge
for
exploration
PSs
is
facilitate
electron
transfer
ability
photosensitization
molecules
transforming
or
H
2
O
reactive
species
(ROS).
Herein,
we
propose
electronic
acceptor‐triggered
photoinduced
(a‐PET)
strategy
promoting
separation
electron‐hole
pairs
marriage
two
organic
semiconducting
a
non‐fullerene
scaffold‐based
photosensitizer
perylene
diimide
that
significantly
boost
pathway
produce
plentiful
ROS,
especially,
inducing
3.5‐fold
2.5‐fold
amplification
hydroxyl
(OH⋅)
superoxide
(O
−
⋅)
generation.
Systematic
mechanism
reveals
intermolecular
intramolecular
charge
after
photoirradiation
generate
competent
production
radical
ion
promote
process
theoretical
calculation
ultrafast
femtosecond
transient
absorption
(fs‐TA)
spectroscopy.
By
complementary
diagnosis
with
photoacoustic
imaging
second
near‐infrared
fluorescence
imaging,
this
as‐prepared
nanoplatform
exhibits
fabulous
photocytotoxicity
in
harsh
hypoxic
conditions
terrific
cancer
revoked
abilities
living
mice.
We
envision
work
will
broaden
insight
into
high‐efficiency
phototheranostics.
Nanomaterials,
Journal Year:
2024,
Volume and Issue:
14(7), P. 648 - 648
Published: April 8, 2024
Nanodynamic
therapy
(NDT)
exerts
its
anti-tumor
effect
by
activating
nanosensitizers
to
generate
large
amounts
of
reactive
oxygen
species
(ROS)
in
tumor
cells.
NDT
enhances
tumor-specific
targeting
and
selectivity
leveraging
the
microenvironment
(TME)
mechanisms
that
boost
immune
responses.
It
also
minimizes
damage
surrounding
healthy
tissues
cytotoxicity
cells,
showing
promise
cancer
treatment,
with
significant
potential.
This
review
covers
research
progress
five
major
nanodynamic
therapies:
photodynamic
(PDT),
electrodynamic
(EDT),
sonodynamic
(SDT),
radiodynamic
(RDT),
chemodynamic
(CDT),
emphasizing
role
advanced
nanotechnology
development
for
purposes.
The
mechanisms,
effects,
challenges
faced
these
NDTs
are
discussed,
along
their
respective
solutions
enhancing
efficacy,
such
as
pH
response,
delivery,
combined
immunotherapy.
Finally,
this
briefly
addresses
clinical
translation
NDT.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(14), P. 17313 - 17322
Published: March 27, 2024
Glucose
oxidase
(Gox)-mediated
starvation
therapy
offers
a
prospective
advantage
for
malignancy
treatment
by
interrupting
the
glucose
supply
to
neoplastic
cells.
However,
negative
charge
of
Gox
surface
hinders
its
enrichment
in
tumor
tissues.
Furthermore,
Gox-mediated
infiltrates
large
amounts
hydrogen
peroxide
(H2O2)
surround
normal
tissues
and
exacerbate
intracellular
hypoxia.
In
this
study,
cascade-catalyzed
nanogel
(A-NE)
was
developed
boost
antitumor
effects
consumption
cascade
reactive
release
nitric
oxide
(NO)
relieve
First,
cross-linking
structure
A-NE
can
serve
as
bioimmobilization
Gox,
ensuring
stability
while
improving
encapsulation
efficiency.
Then,
efficiently
inhibited
proliferation
cells
generating
H2O2.
addition,
covalent
l-arginine
(l-Arg)
consumed
H2O2
derived
from
decomposition
generate
NO,
which
augmented
on
metastatic
tumors
alleviating
Eventually,
both
vivo
vitro
studies
indicated
that
nanogels
remarkably
situ
growth
hindered
recurrence,
offering
an
alternative
possibility
clinical
intervention.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(2), P. 2166 - 2179
Published: Jan. 3, 2024
Hypoxia
is
a
pervasive
feature
of
solid
tumors,
which
significantly
limits
the
therapeutic
effect
photodynamic
therapy
(PDT)
and
further
influences
immunotherapy
efficiency
in
breast
cancer.
However,
transient
alleviation
tumor
hypoxia
fails
to
address
underlying
issue
increased
oxygen
consumption,
resulting
from
rapid
proliferation
cells.
At
present,
studies
have
found
that
reduction
consumption
rate
(OCR)
by
cytochrome
C
oxidase
(COX)
inhibition
induced
oxidative
phosphorylation
(OXHPOS)
suppression
was
able
solve
proposed
problem.
Herein,
we
developed
specific
mitochondrial-targeting
nanotrapper
(I@MSN-Im-PEG),
exhibited
good
copper
chelating
ability
inhibit
COX
for
reducing
OCR.
The
results
proved
alleviated
hypoxic
microenvironment
chelation
mitochondria
enhanced
PDT
vitro
vivo.
Meanwhile,
improved
photoimmunotherapy
through
both
enhancing
PDT-induced
immunogenetic
cell
death
(ICD)
effects
reversing
Treg-mediated
immune
on
4T1
tumor-bearing
mice.
provided
novel
efficacious
strategy
enhance
amplify