Frontiers in Chemistry,
Journal Year:
2024,
Volume and Issue:
12
Published: Oct. 3, 2024
Eliciting
anti-tumor
immune
responses
and
improving
the
tumor
microenvironment
crucial
for
boosting
effectiveness
of
anti-PD-1
immunotherapy.
Tumor-associated
macrophages
(TAMs),
primary
types
cells
infiltrating
tumors,
play
a
critical
role
in
formation
an
immunosuppressive
microenvironment.
In
this
study,
we
constructed
novel
Evans
Blue
(EB)-based
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(43), P. 29689 - 29703
Published: Oct. 14, 2024
Cold
exposure
(CE)
therapy
can
quickly
induce
tumor
starvation
by
brown
adipose
tissue
(BAT)
thermogenesis.
Exploring
the
combined
antitumor
mechanism
of
CE
and
traditional
therapies
(such
as
radiotherapy
(RT))
is
exciting
promising.
In
this
study,
we
investigated
effect
in
combination
with
nitric
oxide
(NO)
gas
on
sensitizing
tumors
to
RT
promoting
radio-immunotherapy.
We
first
constructed
a
liposome
(SL)
loaded
NO
prodrug
S-nitroso-N-acetylpenicillamine
(SNAP).
When
SL
injected,
glutathione
(GSH)
within
region
promotes
release
from
SNAP.
Subsequently,
superoxide
anion
produced
reacts
generate
peroxynitrite
(ONOO–),
which
has
strong
oxidative
properties
induces
cell
death.
Meanwhile,
mice
were
exposed
environment
4
°C.
CE-mediated
BAT
thermogenesis
induced
starvation,
led
decrease
ATP
GSH
content
well
an
improvement
hypoxic
microenvironment
myeloid-derived
suppressor
cells.
All
above
have
promoted
effectiveness
activated
systemic
immunity.
bilateral
experiment,
treatment
primary
inhibited
growth
distant
infiltration
CD8+
T
cells
into
tumor.
These
findings
reveal
that
synergy
CE,
therapy,
could
confer
high
effective
anticancer
effects,
providing
possibilities
personalized
cancer
treatment.
International Journal of Nanomedicine,
Journal Year:
2023,
Volume and Issue:
Volume 18, P. 7533 - 7541
Published: Dec. 1, 2023
Photothermal
therapy
(PTT)
has
a
significant
potential
for
its
application
in
precision
tumour
therapy.
However,
PTT-induced
hyperthermia
may
damage
healthy
tissues
and
trigger
the
expression
of
heat
shock
proteins
(HSPs),
thereby
compromising
long-term
therapeutic
efficacy
PTT.In
this
study,
biomimetic
drug
delivery
system
comprising
CuP
nanozymes
as
inner
core
platelet
membrane
(PM)
outer
shell
was
successfully
developed
administering
synergistic
chemodynamic
mild
PTT.
PM
is
encapsulated
on
to
form
nanoparticle
(PM-coated
nanoparticles,
PC).
PC
possesses
peroxidase
(POD)
activity,
can
facilitate
conversion
hydrogen
peroxide
into
·OH,
inhibiting
HSPs.Upon
exposure
low-power
laser
irradiation
(0.5
W/cm2,
1064
nm),
convert
near-infrared
II
energy
energy,
enabling
administration
enhanced
In
vitro
vivo
experiments
have
demonstrated
that
approach
induce
over
90%
eradication
with
favourable
biocompatibility.PC
exhibits
high
biocompatibility,
making
it
promising
candidate
future
applications.
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 1699 - 1707
Published: Feb. 1, 2024
Introduction:
The
presence
of
cancer
stem
cells
(CSCs)
significantly
limits
the
therapeutic
efficacy
radiotherapy
(RT).
Efficient
elimination
potential
CSCs
is
crucial
for
enhancing
effectiveness
RT.
Methods:
In
this
study,
we
developed
a
biomimetic
hybrid
nano-system
(PMC)
composed
MnCO
3
as
inner
core
and
platelet
membrane
(PM)
outer
shell.
By
exploiting
specific
recognition
properties
surface
proteins,
PMC
enables
precise
targeting
CSCs.
Sonodynamic
therapy
(SDT)
was
employed
using
manganese
carbonate
nanoparticles
(MnCO
NPs),
which
generate
abundant
reactive
oxygen
species
(ROS)
upon
ultrasound
(US)
irradiation,
thereby
impairing
CSC
self-renewal
capacity
eradicating
Subsequent
RT
effectively
eliminates
common
tumor
cells.
Results:
Both
in
vitro
cell
experiments
vivo
animal
studies
demonstrate
that
SDT
mediated
by
synergistically
enhances
to
selectively
combat
while
inhibiting
growth
without
noticeable
side
effects.
Discussion:
Our
findings
offer
novel
insights
safety
profiles
Keywords:
clearance,
radiosensitization,
membrane,
sonodynamic
therapy,
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 11923 - 11940
Published: Nov. 1, 2024
Ferroptosis-driven
tumor
ablation
strategies
based
on
nanotechnology
could
be
achieved
by
elevating
intracellular
iron
levels
or
inhibiting
glutathione
peroxidase
4
(GPX4)
activity.
However,
the
antioxidative
defense
mechanisms
endow
cells
with
ferroptosis
resistance
capacity.
The
purpose
of
this
study
was
to
develop
a
synergistic
therapeutic
platform
enhance
efficacy
ferroptosis-based
therapy.
In
study,
multifunctional
nano-catalytic
(mFeB@PDA-FA)
chemodynamic
therapy
(CDT)
and
photothermal
(PTT)
developed
effectively
trigger
in
tumor.
our
work,
iron-based
mesoporous
Fe3O4
nanoparticles
(mFe3O4
NPs)
were
employed
for
encapsulation
L-buthionine
sulfoximine
(BSO),
followed
modification
folic
acid-functionalized
polydopamine
(PDA)
coating
periphery.
Then,
antitumor
effect
mFeB@PDA-FA
NPs
evaluated
using
Human
OS
(MNNG/HOS)
subcutaneous
xenograft
model
osteosarcoma.
mFe3O4
harboring
multivalent
elements
(Fe2+/3+)
catalyze
hydrogen
peroxide
(H2O2)
into
highly
cytotoxic
˙OH,
while
microenvironment
(TME)-responsive
released
BSO
molecules
inhibit
biosynthesis
GSH,
thus
achieving
deactivation
GPX4
enhancement
ferroptosis.
Moreover,
thanks
remarkable
conversion
performance
PDA
shell,
PTT
further
synergistically
enhanced
CDT
facilitated
Both
vivo
vitro
experiments
confirmed
that
achieve
excellent
inhibition
effects.
nanotherapeutic
disrupted
redox
homeostasis
boosting
through
combination
CDT,
GSH
elimination,
which
provided
new
perspective
treatment
sensitive
tumors.
Nanotechnology,
Journal Year:
2023,
Volume and Issue:
35(11), P. 115102 - 115102
Published: Dec. 29, 2023
Abstract
Quercetin
(QU),
a
natural
flavonoid
with
potent
anti-inflammatory
and
antioxidant
properties,
holds
promise
in
treating
acute
liver
injury
(ALI).
Nonetheless,
its
limited
solubility
hampers
efficacy,
systemic
distribution
lacks
targeting,
leading
to
off-target
effects.
To
address
these
challenges,
we
developed
macrophage
membrane-coated
quercetin-loaded
PLGA
nanoparticles
(MVs-QU-NPs)
for
active
ALI
targeting.
The
resulting
MVs-QU-NPs
exhibited
spherical
morphology
clear
core–shell
structure.
average
size
zeta
potential
were
assessed
as
141.70
±
0.89
nm
–31.83
0.76
mV,
respectively.
Further
studies
revealed
sustained
drug
release
characteristics
from
over
continuous
period
of
24
h.
Moreover,
demonstrated
excellent
biocompatibility
when
tested
on
normal
cells.
results
biodistribution
analysis
mice
displayed
the
remarkable
ALI-targeting
ability
MVs-DiD-NPs,
highest
fluorescence
intensity
observed
tissue.
This
biomimetic
approach
combining
membranes
nanoparticle
delivery,
great
targeted
treatment.
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 9145 - 9160
Published: Sept. 1, 2024
Triple
negative
breast
cancer
(TNBC)
is
one
of
the
worst
prognosis
types
that
urgently
needs
effective
therapy
methods.
However,
a
complicated
disease
usually
requires
multiple
treatment
modalities.