HPB@LA@PDA nanoplatform ameliorates osteoarthritis by scavenging reactive oxygen species and remodelling the inflammatory microenvironment: An in vitro and in vivo study
Dongze Ren,
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Mingjie Liu,
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Min Cao
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et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 160592 - 160592
Published: Feb. 1, 2025
Language: Английский
Regulator of oxidative balance: Research progress of nanozymes in ROS-related diseases
Materials Today Chemistry,
Journal Year:
2025,
Volume and Issue:
44, P. 102540 - 102540
Published: Jan. 22, 2025
Language: Английский
Multiscale Metal-based Nanocomposites for Bone and Joint Disease Therapies
Yuwen Wang,
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Hasnain Jan,
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Zhong Zheng
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et al.
Materials Today Bio,
Journal Year:
2025,
Volume and Issue:
32, P. 101773 - 101773
Published: April 17, 2025
Bone
and
joint
diseases
are
debilitating
conditions
that
can
result
in
significant
functional
impairment
or
even
permanent
disability.
Multiscale
metal-based
nanocomposites,
which
integrate
hierarchical
structures
ranging
from
the
nanoscale
to
macroscale,
have
emerged
as
a
promising
solution
this
challenge.
These
materials
combine
unique
properties
of
nanoparticles
(MNPs),
such
enzyme-like
activities,
stimuli
responsiveness,
photothermal
conversion,
with
advanced
manufacturing
techniques,
3D
printing
biohybrid
systems.
The
integration
MNPs
within
polymer
ceramic
matrices
offers
degree
control
over
mechanical
strength,
antimicrobial
efficacy,
manner
drug
delivery,
whilst
concomitantly
promoting
processes
osteogenesis
chondrogenesis.
This
review
highlights
breakthroughs
stimulus-responsive
(e.g.,
photo-,
magnetically-,
pH-activated
systems)
for
on-demand
therapy
their
biocomposite
hybrids
containing
cells
extracellular
vesicles
mimic
native
tissue
microenvironment.
applications
these
composites
extensive,
bone
defects,
infections,
tumors,
degenerative
diseases.
emphasizes
enhanced
load-bearing
capacity,
bioactivity,
be
achieved
through
designs.
Notwithstanding
potential
applications,
barriers
progress
persist,
including
challenges
related
long-term
biocompatibility,
regulatory
hurdles,
scalable
manufacturing.
Finally,
we
propose
future
directions,
machine
learning-guided
design
patient-specific
biomanufacturing
accelerate
clinical
translation.
bridge
innovations
macroscale
functionality,
revolutionary
force
field
biomedical
engineering,
providing
personalized
regenerative
solutions
Language: Английский
A novel metal‐organic framework encapsulated iridium oxide nanozyme enhanced antisense oligonucleotide combo for osteoarthritis synergistic therapy
Aggregate,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 16, 2024
Abstract
Osteoarthritis
(OA)
is
associated
with
metabolic
imbalance
of
articular
cartilage
and
an
increase
intracellular
reactive
oxygen
species
(ROS).
Synergistic
therapy
based
on
the
codelivery
ROS
scavengers
antisense
oligonucleotides
(ASO)
into
chondrocytes
has
potential
to
effectively
treat
OA.
Here,
we
developed
a
novel
biocompatible
metal‐organic
framework
(MOF)‐encapsulated
nanozyme/ASO
delivery
platform
(miR/IrO
2
@ZIF‐8)
for
OA
treatment.
IrO
nanoparticles
catalytic
activities
superoxide
dismutase/catalase
were
synthesized
using
hydrothermal
method,
resulting
in
excellent
scavenging
performance.
was
further
loaded
zeolitic
imidazolate
framework‐8
(ZIF‐8)
maintain
its
efficacy
regulate
size,
surface
charge,
biocompatibility
enhance
therapeutic
effect
platform.
As
effective
ASO
carrier,
@ZIF‐8
exhibited
high
antagomiR‐181a
loading
lysosomal
escape
capacity,
enabling
it
rebalance
metabolism.
In
vitro
experiments
showed
that
miR/IrO
could
restore
levels,
mitochondrial
membrane
potential,
lipid
peroxidation
chondrocytes.
At
same
time,
expression
levels
proinflammatory
markers
(IL‐1β,
IL‐6,
COX‐2)
as
well
extracellular
matrix
degrading
enzymes
(ADAMTS‐5
MMP13)
downregulated,
indicating
antioxidant,
anti‐inflammatory,
anticartilage
degradation
effects.
Notably,
able
deliver
tissue
at
depth
up
1.5
mm,
thus
solving
problems
poor
permeability
difficult
retention
drugs
tissue.
This
improves
synergistic
by
inhibiting
degradation.
The
combination
MOF‐encapsulated
nanozymes
OA,
offering
promising
translational
medicine
paradigm.
Language: Английский
Nanozyme‐Engineered Hyaluronic Acid Adhesives Loading Platelet‐Rich Plasma for Multilayered Osteoarthritis Treatment with Pain‐Relief Effect
Yiyang Zhao,
No information about this author
Wanglin Duan,
No information about this author
Bin Zhu
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 23, 2024
Abstract
Osteoarthritis
(OA)
is
the
most
common
degenerative
joint
disease,
causing
pain,
disability,
and
economic
strain.
Combining
nanozymes
with
dopamine
(DOPA)‐based
adhesives
offers
a
promising
approach
to
effectively
modulate
microenvironment
of
OA‐affected
tissues.
However,
traditional
fabrication
methods
DOPA‐based
often
involve
external
oxidants
or
curing
agents,
which
can
introduce
additional
oxidative
stress,
posing
systemic
risks.
Here,
different
enzyme‐catalyzed
activities
platinum–copper
(PtCu)
at
pH
values
are
utilized
directly
catalyze
cross‐linking
DOPA‐modified
hyaluronic
acid
(HAD),
representing
new
polymerization
method
for
phenol‐based
bioadhesives.
The
resulting
adhesive
(HAD/PtCu/platelet‐rich
plasma
(PRP)),
when
combined
PRP,
mitigates
generation
proinflammatory
factors,
scavenges
reactive
oxygen
species,
boosts
hypoxic
chemotaxis
chondrocytes,
stimulates
chondrocyte
proliferation
migration,
protects
interleukin‐1β‐treated
human
articular
C28/I2
cells
from
further
OA
advancement.
Additionally,
in
vivo
assessments
show
that
HAD/PtCu/PRP
significantly
alleviates
pain
improves
knee
osteoarthritic
rats.
These
findings
suggest
provides
alternative
therapy.
Language: Английский