Natural enzyme cascade bimetallic sulfide MoCuSx nanozyme for synergistic photothermal/photodynamic enhanced chemodynamic antimicrobial therapy of wound infection
Caiyun Xu,
No information about this author
Junqin Li,
No information about this author
Chunlei Ou
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2024,
Volume and Issue:
unknown, P. 156170 - 156170
Published: Sept. 1, 2024
Language: Английский
A pH/GSH Dual‐Responsive Triple Synergistic Bimetallic Nanocatalyst for Enhanced Tumor Chemodynamic Therapy
Lu Zhang,
No information about this author
Huan Shen,
No information about this author
Tingting Liu
No information about this author
et al.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Abstract
Chemodynamic
therapy
(CDT)
has
garnered
significant
attention
in
the
field
of
tumor
due
to
its
ability
convert
overexpressed
hydrogen
peroxide
(H
2
O
)
tumors
into
highly
toxic
hydroxyl
radicals
(•OH)
through
metal
ion‐mediated
catalysis.
However,
effectiveness
CDT
is
hindered
by
low
catalyst
efficiency,
insufficient
intra‐tumor
H
level,
and
excessive
glutathione
(GSH).
In
this
study,
a
pH/GSH
dual
responsive
bimetallic
nanocatalytic
system
(CuFeMOF@GOx@Mem)
developed
modifying
red
blood
cell
membranes
onto
glucose
oxidase
(GOx)‐loaded
Fe‐Cu
MOFs,
enhancing
efficacy
triple‐enhanced
way
self‐supply,
catalysts
self‐cycling,
GSH
self‐elimination.
Upon
accumulation
tissues
facilitated
membrane,
GOx
initiates
reaction
with
generate
gluconic
acid
situ.
Subsequently,
reduced
pH
triggers
release
Fe
3+
Cu
2+
from
CuFeMOF@GOx@Mem,
which
immediately
turned
+
GSH,
activating
‐mediated
Fenton
reaction.
More
importantly,
can
also
act
as
an
accelerator
/Fe
conversion,
meanwhile,
generated
be
further
GSH.
Consequently,
sustained
well
elimination
are
achieved
simultaneously,
providing
unique
approach
for
improving
anti‐tumor
CDT.
Language: Английский
H2O2‐Generating Advanced Nanomaterials for Cancer Treatment
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 21, 2025
Abstract
Tumor
cells
exploit
abnormal
redox
homeostasis
and
the
pro‐tumorigenic
effect
of
reactive
oxygen
species
(ROS)
to
enhance
their
survival
progression.
However,
excessively
high
levels
ROS
can
exceed
oxidative
stress
threshold
tumor
cells,
inducing
cell
death.
This
occur
by
selectively
elevating
concentration
H
2
O
in
through
both
endogenous
exogenous
mechanisms.
The
generated
serves
as
a
precursor
for
toxic
ROS,
such
•
OH
1
,
via
chemodynamic
photodynamic
therapy,
respectively,
leading
apoptosis,
necrosis,
ferroptosis.
Strategies
boost
include
direct
delivery
amplifying
generation
inhibiting
antioxidant
enzymes,
leveraging
glucose
oxidase,
employing
photocatalytic
therapy
(PCT),
utilizing
metal
peroxides.
Among
them,
peroxides
have
displayed
remarkable
performance
due
excellent
potential
elevate
within
while
simultaneously
normalizing
acidic
hypoxic
conditions
microenvironment
(TME).
Moreover,
these
nanostructures
sensitivity
complementary
treatments,
like
chemotherapy.
review
summarizes
advanced
perspectives
design,
synthesis,
comparative
analysis
‐generating
nanoplatforms,
emphasizing
capacity
treat
various
cancers.
Language: Английский
Bifunctional cobalt ferrite/reduced graphene oxide heterojunction enhances the antibacterial and osteogenic activities of scaffold
Applied Surface Science,
Journal Year:
2025,
Volume and Issue:
unknown, P. 162942 - 162942
Published: March 1, 2025
Language: Английский
FeS embedded bioreactor collaborate with artesunate for cascade-catalytic tumor ferroptosis
Journal of Colloid and Interface Science,
Journal Year:
2025,
Volume and Issue:
unknown, P. 137479 - 137479
Published: March 1, 2025
Language: Английский
Lipid acid metabolism reprogramming nanoagent induces ferroptosis storm and cGAS-STING activation for metal-immunotherapy of triple negative breast cancer
Dawei Zhou,
No information about this author
Gaorui Zhang,
No information about this author
J. Zhu
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 162048 - 162048
Published: April 1, 2025
Language: Английский
Targeted and intelligent nano-drug delivery systems for colorectal cancer treatment
Meihong Chai,
No information about this author
Shihua Wang,
No information about this author
Yuxin Chen
No information about this author
et al.
Frontiers in Bioengineering and Biotechnology,
Journal Year:
2025,
Volume and Issue:
13
Published: April 25, 2025
Colorectal
cancer
(CRC)
remains
a
highly
heterogeneous
malignancy
with
significant
morbidity
and
mortality
worldwide.
Despite
advancements
in
surgery,
chemotherapy,
immunotherapy,
targeted
therapy,
treatment
efficacy
is
often
hampered
by
drug
resistance
systemic
toxicity.
In
recent
years,
nano-drug
delivery
systems
(NDDS)
have
emerged
as
promising
strategy
to
enhance
therapeutic
precision,
reduce
adverse
effects,
overcome
CRC
treatment.
This
review
discusses
the
NDDS
for
treatment,
focusing
on
optimization
of
oral
systems,
development
tumor-specific
targeting
strategies,
design
intelligent
responsive
tumor
microenvironment
(TME).
Furthermore,
we
summarize
current
challenges
translation
explore
future
research
directions
enhancing
their
clinical
feasibility
impact.
Language: Английский
Controllable All-in-One Biomimetic Hollow Nanoscaffold Initiating Pyroptosis-Mediated Antiosteosarcoma Targeted Therapy and Bone Defect Repair
Qiming Ma,
No information about this author
Shenglin Xu,
No information about this author
Qian Wang
No information about this author
et al.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(49), P. 67424 - 67443
Published: Nov. 27, 2024
Pyroptosis
has
gained
attention
for
its
potential
to
reinvigorate
the
immune
system
within
tumor
microenvironment.
However,
current
approaches
employing
pyroptosis
inducers
suffer
from
limitations.
They
primarily
rely
on
single
agents,
lack
precise
targeting,
and
potentially
disrupt
intricate
bone
formation
microenvironment,
hindering
local
repair
of
tumor-induced
defects.
Therefore,
a
therapeutic
strategy
is
urgently
needed
that
can
effectively
trigger
while
simultaneously
promoting
regeneration.
This
research
introduces
an
all-in-one
construct
designed
address
these
It
combines
cell-camouflaged
shell
with
autosynergistic
reactive
oxygen
species
(ROS)
generating
polymer.
incorporates
hollow
core
manganese
dioxide
(HMnO2)
embedded
photosensitizer
IR780
disguised
by
cell
membrane
M1
macrophage.
The
macrophage
grants
stealth-like
properties,
enabling
it
accumulate
selectively
at
site.
Upon
laser
irradiation,
acts
as
exogenous
ROS
generation
converting
light
energy
into
heat.
Additionally,
structure
HMnO2
serves
efficient
carrier
IR780.
Furthermore,
Mn4+
ions
released
deplete
glutathione
(GSH)
tumor,
further
amplifying
production.
synergistic
cascade
ultimately
culminates
in
induction
through
caspase-3-mediated
cleavage
gasdermin
E
(GSDME)
upon
activation.
Meanwhile,
depletion
GSH
microenvironment
(TME)
leads
Mn2+
ions.
These
establish
supportive
milieu,
which
promotes
transformation
marrow
mesenchymal
stem
cells
(BMSCs)
mature
cells.
This,
turn,
defects
rat
femurs.
Our
findings
strongly
indicate
may
be
osteosarcoma
treatment,
presents
robust
versatile
approach
targeted
therapy
tissue
regeneration
this
patient
population.
Language: Английский
Precise Carrier-Free Pt(IV)-Nanobombs for Apoptosis/Ferroptosis Synergistic Tumor Therapy: A New Effective Method to Obtain Good Chemotherapy and Low Toxicity
Xu Guo,
No information about this author
Xin Liang,
No information about this author
Jiale Liu
No information about this author
et al.
Journal of Medicinal Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 16, 2024
The
emerged
apoptosis/ferroptosis
synergistic
platinum-based
therapy
has
attracted
a
lot
of
attention
but
is
far
from
clinic
use
due
to
high
systemic
toxicity.
Herein,
series
novel
precise
carrier-free
self-assembled
platinum(IV)
nanoparticles
with
lipid
regulation
effect
named
FSPNPs
(5NPs–8NPs)
were
constructed
via
connecting
fenofibrate
acid
(FA)
cisplatin
or
oxaliplatin-derived
platinum(IV)-intermediates
disulfide
bonds.
can
be
stimulated
by
high-glutathione/ascorbic
and
acidity
environment
produce
an
"explosion-like"
cascade
release
process.
Cell-activity
showed
precision
FSPNPs,
which
accumulated
more
in
tumor
cells
inhibited
cell
proliferation.
Especially,
5NPs
have
higher
selectivity
than
cisplatin.
downregulated
glutathione/glutathione
peroxidase
4,
increased
reactive
oxygen
species/lipid
peroxidation/malondialdehyde,
induced
DNA
damage/S-phase
arrest,
regulated
p53/Bcl-2/Bax
trigger
the
hybrid
pathway.
released
FA
derivates
docked
into
peroxisome
proliferator-activated
receptor
α
activating
cholesterol
metabolism
destroy
membrane
integrity.
also
good
biocompatibility
superior
antitumor
activity
no
observable
tissue
damage.
Language: Английский
Excessive glutathione intake contributes to chemotherapy resistance in breast cancer: a propensity score matching analysis
Zhiyuan Zhang,
No information about this author
Jian Gao,
No information about this author
Linjiao Jia
No information about this author
et al.
World Journal of Surgical Oncology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Dec. 21, 2024
We
aim
to
explore
the
impact
of
excessive
glutathione
(GSH)
intake
on
chemotherapy
sensitivity
in
breast
cancer.
Clinicopathological
data
were
collected
from
460
cancer
patients
who
underwent
adjuvant
January
2016
December
2019
Zhengzhou
University
People's
Hospital.
The
clinicopathological
characteristics
following
GSH
treatment
and
compared
with
those
Non-GSH
group
after
1:2
propensity
score
matching
(PSM).
Intracellular
levels
expression
antioxidant
enzymes
(NRF2,
GPX4
SOD1)
evaluated
tumor
tissues
51
receiving
neoadjuvant
chemotherapy.
recurrence
rate
was
significantly
higher
(n
=
28,
31.8%)
than
that
39,
22.2%;
P
0.010).
Additionally,
HGSH
(high
intake,
≥
16
days)
exhibited
an
elevated
LGSH
(low
<
15
(46.8%)
vs.
n
52
(22.4%);
0.003).
Cox
regression
revealed
High
Ki67
30%,
Triple
negative
Lymphovascular
invasion
independent
risk
factors
progression
Among
chemotherapy,
intracellular
resistant
substantially
(P
0.001).
Excessive
may
contribute
resistance
cancer,
are
indicating
standardization
assist
reducing
resistance.
Language: Английский