Synthesis and Application of Selenium Nanoparticles for the Modulation of Inflammatory Diseases
Nano Biomedicine and Engineering,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 1, 2025
Language: Английский
Maintaining cardiac homeostasis by translational selenium nanoparticles with rapid selenoproteins regulation to achieve radiation-induced heart prevention
Ke-wei Jin,
No information about this author
Sujiang Shi,
No information about this author
Dina Huang
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 160005 - 160005
Published: Jan. 1, 2025
Language: Английский
Mn-Specific Recognition of Guanidine Drives Selective Inhibition of Complex I
Fei Cai,
No information about this author
Jiaxin Dong,
No information about this author
Peng Xie
No information about this author
et al.
Journal of Medicinal Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 20, 2025
Developing
structurally
well-defined
targeted
drugs
is
an
effective
way
to
enhance
the
chemotherapy
efficacy.
Herein,
a
target
mitochondrial
complex
I
(complex
I)
inhibitor
was
developed
for
key
methylation
site
ARG-85
in
subunit
NDUFS2.
Based
on
unique
:NH═C-
group
of
guanidyl
and
surrounding
environment
ARG-85,
macrocyclic
bulky
manganese
porphyrin
[MnIII(TTPPC2-)]+
selected
insert
into
gap
Experimental
computational
analyses
revealed
that
planar
π
system
TTPPC2-
ligand
rotatable
benzene
ring
stably
bind
between
metal
center,
medium-strong
Lewis
acid.
The
Mn-specific
recognition
guanidine
drives
selective
inhibition
activity.
Further,
MnIII(TTPPC2-)]+
modified
nanoformulation
Mn
NPs.
In
vitro
vivo
experiments
confirmed
efficient
mechanism
activity,
offering
novel
strategy
drug
development.
Language: Английский
Recent Progress in Radiosensitive Nanomaterials for Radiotherapy-Triggered Drug Release
Renfeng Jiang,
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Qiong Fang,
No information about this author
Wenjun Liu
No information about this author
et al.
ACS Applied Materials & Interfaces,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 27, 2025
Benefiting
from
the
unique
properties
of
ionizing
radiation,
such
as
high
tissue
penetration,
spatiotemporal
resolution,
and
clinical
relevance
compared
with
other
external
stimuli,
radiotherapy-induced
drug
release
strategies
are
showing
great
promise
in
developing
effective
personalized
cancer
treatments.
However,
requirement
doses
X-ray
irradiation
to
break
chemical
bonds
for
limits
application
prodrug
activation
clinics.
Recent
advances
nanomaterials
offer
a
promising
approach
radiotherapy
sensitization
well
integrating
multiple
modalities
improved
therapy
outcomes.
In
particular,
catalytic
radiosensitization
that
utilizes
electrons
energy
generated
by
upon
has
demonstrated
excellent
potential
enhanced
radiotherapy.
this
Review,
we
summarize
design
principles
X-ray-responsive
controlled
release,
radiosensitization,
recent
progress
nanoradiosensitizers
integration
chemotherapy,
chemodynamic
therapy,
photodynamic
photothermal
gas
immunotherapy.
Finally,
discuss
challenges
heading
toward
possible
translation.
We
expect
emerging
based
on
radiotherapy-triggered
will
facilitate
frontier
accurate
near
future.
Language: Английский
Selenium nanoparticles activate selenoproteins to mitigate septic lung injury through miR-20b-mediated RORγt/STAT3/Th17 axis inhibition and enhanced mitochondrial transfer in BMSCs
Wan‐Jie Gu,
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Fengzhi Zhao,
No information about this author
Wei Huang
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et al.
Journal of Nanobiotechnology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: March 20, 2025
Sepsis-induced
acute
lung
injury
(ALI)
remains
a
critical
clinical
challenge
with
complex
inflammatory
pathogenesis.
While
bone
marrow
mesenchymal
stem
cells
(BMSCs)
demonstrate
therapeutic
potential
through
anti-inflammatory
and
cytoprotective
effects,
their
age-related
functional
decline
limits
utility.
This
study
developed
chitosan-functionalized
selenium
nanoparticles
(SeNPs@CS,
100
nm)
to
rejuvenate
BMSCs
miR-20b-mediated
selenoprotein
biosynthesis.
Mechanistic
investigations
revealed
that
SeNPs@CS-treated
exhibited
enhanced
mitochondrial
transfer
capacity,
delivering
mitochondria
damaged
alveolar
epithelial
(AECII)
for
cellular
repair.
Concurrently,
miR-20b
upregulation
suppressed
the
RORγt/STAT3/Th17
axis,
reducing
pro-inflammatory
Th17
cell
differentiation
in
CD4+
T
lymphocytes.
The
dual-target
mechanism
integrates
immunomodulation
via
pathway
inhibition
rejuvenation
therapy,
representing
paradigm-shifting
approach
ALI
management.
These
engineered
mitigated
markers
murine
models,
demonstrating
superior
efficacy
conventional
BMSC
therapies.
Our
findings
establish
SeNPs@CS-modified
as
novel
platform
combining
nanotechnology-enhanced
engineering
precision
immunometabolic
regulation,
providing
new
avenues
treatment
of
sepsis-induced
ALI.
Language: Английский
Boosting Peroxidase-Mimetic Activity of FeMn-NCe Dual-Atom Radiosensitizing Nanozymes for Augmented Radiodynamic Immunotherapy
Bo Chen,
No information about this author
Yinggang Wang,
No information about this author
Min Mu
No information about this author
et al.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 7, 2025
Dual-atom
nanozymes
(DAzymes)
have
garnered
considerable
attention
as
catalysts
for
reactive
oxygen
species
(ROS)-based
therapies,
effectively
leveraging
ROS
generation
within
the
tumor
microenvironment
(TME).
Herein,
we
introduce
FeMn-NCe
DAzymes,
which
are
meticulously
engineered
enhanced
peroxidase
(POD)-mimetic
activity
and
potent
radiosensitization
to
advance
radioimmunotherapy.
Density
functional
theory
(DFT)
calculations
reveal
that
DAzymes
lower
energy
barrier
increase
substrate
affinity,
enabling
highly
efficient
catalytic
performance.
Within
TME,
these
efficiently
convert
overexpressed
hydrogen
peroxide
(H2O2)
into
hydroxyl
radicals
(•OH),
potentially
activating
cGAS-STING
immune
pathway.
This
POD-mimetic
catalysis
is
further
accelerated
under
X-ray
irradiation,
significantly
enhancing
radiosensitization.
Additionally,
a
uniform
coating
of
ultrasmall
gold
nanoparticles
on
enhances
absorption
cancer
cells.
The
incorporation
STING
agonist
diABZI
onto
induces
long-term
antitumor
immunity,
reprograms
immunosuppressive
suppresses
growth
metastasis
following
single
low-dose
treatment.
work
highlights
valuable
strategy
designing
radiodynamic
immunotherapy.
Language: Английский
Translational selenium nanoparticles enhance NKG2D-mediated cytotoxicity of NK cells against malignant pleural mesothelioma cells through the TrxR1-pSTAT3 pathway
Nano Today,
Journal Year:
2025,
Volume and Issue:
62, P. 102720 - 102720
Published: March 28, 2025
Language: Английский
Light-Responsive Ru–Se Coordinated Nanoreactor Spatiotemporally Relieves Hypoxia for Photodynamic Therapy of Bladder Cancer
ACS Applied Materials & Interfaces,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 9, 2025
Photodynamic
therapy
(PDT)
has
been
employed
as
a
noninvasive
treatment
option
for
bladder
cancer
due
to
its
controllability
and
minimal
toxicity.
However,
the
efficacy
of
PDT
is
often
compromised
by
hypoxic
microenvironment
solid
tumors.
To
address
this
challenge,
our
research
dedicated
developing
Ru-Se-Ce6
nanoreactor
that
combines
photoresponsiveness
Ru-Se
coordination
bonds
reactive
oxygen
species
(ROS)
triggered
diselenide
bonds,
achieving
dual-controlled
release
photosensitizer
enhance
effectiveness.
The
photoresponsive
catalytic
characteristics
were
validated
through
synchrotron
radiation
density
functional
theory
calculations.
Under
laser
irradiation,
metal-to-ligand
charge
transfer
(MLCT)
within
ruthenium
complex
leads
cleavage
bond,
resulting
in
liberation
complex,
which
significantly
improves
O2
generation
from
H2O2
tumor
(TME).
In
vivo
assessments
demonstrated
disrupted
mitochondrial
membrane
potential
via
excessive
ROS
production,
leading
cell
cycle
arrest
apoptosis.
Additionally,
revealed
significant
suppression
subcutaneous
orthotopic
models
while
exhibiting
good
biocompatibility.
These
findings
propose
potent
innovative
approach
therapy.
Language: Английский