Materials Today Bio,
Journal Year:
2025,
Volume and Issue:
32, P. 101778 - 101778
Published: April 17, 2025
Osteoarthritis
(OA)
is
a
progressive
degenerative
disorder
which
severely
threatens
the
quality
of
life
older
individuals.
OA
progression
closely
related
to
heightened
levels
mitochondrial
reactive
oxygen
species
(mtROS).
Although
nanozymes
have
good
ROS-scavenging
effect,
they
cannot
precisely
scavenge
mtROS
because
immune
rejection
cell
membranes,
lysosomal
escape,
and
inability
conventional
directly
target
mitochondria.
Dual-target
were
engineered
in
chondrocytes.
We
used
chondrocyte
membrane-camouflaged
TPP-modified
hollow
Prussian
blue
subsequently
encapsulated
these
hybrid
glycyrrhizic
acid
hydrogel.
The
therapeutic
efficacy
underlying
mechanisms
assessed
vitro
vivo.
novel
enhanced
selectivity,
evasion
capabilities,
targeting.
dual-targeted
exerted
pronounced
impact
on
inflammatory
chondrocytes,
mitigated
mtDNA
leakage
by
scavenging
mtROS,
dampened
cGAS-STING-NF-κB
signaling,
function.
hydrogels
also
exhibited
improved
outcomes.
confirmed
beneficial
effects
nanozyme-hydrogel
combination
mice.
can
reduce
avoiding
suppressing
signaling
pathway,
thereby
decreasing
responses
alleviate
progression.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 29, 2024
Abstract
Intra‐articular
injection
of
drugs
is
an
effective
strategy
for
osteoarthritis
(OA)
treatment.
However,
the
complex
microenvironment
and
limited
joint
space
result
in
rapid
clearance
drugs.
Herein,
a
nanogel‐based
proposed
prolonged
drug
delivery
remodeling.
Nanogel
constructed
through
functionalization
hyaluronic
acid
(HA)
by
amide
reaction
on
surface
Kartogenin
(KGN)‐loaded
zeolitic
imidazolate
framework‐8
(denoted
as
KZIF@HA).
Leveraging
inherent
hydrophilicity
HA,
KZIF@HA
spontaneously
forms
nanogels,
ensuring
extended
release
OA
microenvironment.
exhibits
sustained
over
one
month,
with
low
leakage
risk
from
cavity
compared
to
KZIF,
enhanced
cartilage
penetration,
reparative
effects
chondrocytes.
Notably,
KGN
released
serves
promote
extracellular
matrix
(ECM)
secretion
hyaline
regeneration.
Zn
2+
reverses
progression
promoting
M2
macrophage
polarization
establish
anti‐inflammatory
Ultimately,
facilitates
regeneration
alleviation
within
three
months.
Transcriptome
sequencing
validates
that
stimulates
macrophages
secretes
IL‐10
inhibit
JNK
ERK
pathways,
chondrocytes
recovery
enhancing
ECM
This
pioneering
nanogel
system
offers
new
therapeutic
opportunities
release,
presenting
significant
stride
treatment
strategies.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 16, 2024
Nanotechnology-based
approaches
are
promising
for
the
treatment
of
musculoskeletal
(MSK)
disorders,
which
present
significant
clinical
burdens
and
challenges,
but
their
translation
requires
a
deep
understanding
complex
interplay
between
nanotechnology
MSK
biology.
Organ-on-a-chip
(OoC)
systems
have
emerged
as
an
innovative
versatile
microphysiological
platform
to
replicate
dynamics
tissue
microenvironment
studying
nanotechnology-biology
interactions.
This
review
first
covers
recent
advances
applications
OoCs
ability
mimic
biophysical
biochemical
stimuli
encountered
by
tissues.
Next,
integrating
into
OoCs,
cellular
responses
behaviors
may
be
investigated
precisely
controlling
manipulating
nanoscale
environment.
Analysis
disease
mechanisms,
particularly
bone,
joint,
muscle
degeneration,
drug
screening
development
personalized
medicine
greatly
facilitated
using
OoCs.
Finally,
future
challenges
directions
outlined
field,
including
advanced
sensing
technologies,
integration
immune-active
components,
enhancement
biomimetic
functionality.
By
highlighting
emerging
this
aims
advance
intricate
nanotechnology-MSK
biology
interface
its
significance
in
management,
therapeutic
interventional
strategies.
Nano Letters,
Journal Year:
2024,
Volume and Issue:
24(37), P. 11697 - 11705
Published: Sept. 3, 2024
Osteoarthritis
(OA)
is
a
degenerative
joint
disease
characterized
by
obscure
etiology
and
unsatisfactory
therapeutic
outcomes,
making
the
development
of
new
efficient
therapies
urgent.
Superfluous
reactive
oxygen
species
(ROS)
have
historically
been
considered
one
crucial
factors
inducing
pathological
progression
OA.
Ultrasmall
Prussian
blue
nanoparticles
(USPBNPs),
approximately
sub-5
nm
in
size,
are
developed
regulating
configuration
polyvinylpyrrolidone
chains.
USPBNPs
display
an
excellent
ROS
eliminating
capacity
catalase-like
activity,
capable
decomposing
hydrogen
peroxide
(H
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 8, 2024
Abstract
Osteoarthritis
is
a
common
degenerative
disease
characterized
by
continuous
detachment
of
lubrication
factors
from
damaged
cartilage
matrix.
This
study
proposes
paradigm
that
combines
natural
polyanionic
polysaccharides
(hyaluronic
acid,
HA)
with
dopamine
(DA)
to
design
synovial
factors‐recruiting
biomimetic
polyphenolized
system.
The
lubricants
can
use
DA's
polarity
and
hydrophilic
groups
as
specific
binding
sites
type
II
collagen's
stably
bind
surface,
further
utilize
molecular
interaction
recruit
detached,
joint
endogenous
or
chondrocytes
expressed
factors,
continuously
forming
supramolecular
complex
onto
matrix
induce
lubrication.
Simultaneously,
the
biolubricants
also
catechol
eliminate
anionic
free
radicals
resist
reactive
oxygen
species
invasion
in
early
stages
failure.
prepared
exhibit
low
coefficient
friction
(µ
<
0.08),
which
attributed
fluid
hydration
provided
HA
DA
side
chains
through
dynamic
effect
interfacial
adsorption.
Cell
animal
experiments
demonstrate
polyphenolic
have
good
biocompatibility
promote
regeneration.
Therefore,
developed
lubricants‐recruiting
potential
for
treating
osteoarthritis,
provide
theoretical
basis
other
biological
tissues
problems.
Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 23, 2024
Osteoarthritis
(OA)
of
the
knee
is
most
prevalent
degenerative
joint
condition
that
places
a
substantial
financial
and
medical
burden
on
society.
However,
due
to
drawbacks
such
as
inefficiency,
adverse
effects,
brief
duration
action,
clinical
efficacy
current
major
therapies
for
OA
largely
restricted.
Therefore,
novel
medication
development
highly
required
address
these
issues.
Numerous
studies
in
recent
years
have
established
nanomaterials
can
be
potential
effective
way
overcome
challenges.
In
this
review,
anatomical
distinctions
between
healthy
joints,
well
advances
field
treatment
are
summarized.
The
limits
present
therapeutic
strategies
treating
also
highlighted,
prospects
future.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(22)
Published: March 30, 2024
Abstract
Cellular
senescence
is
a
significant
contributor
to
intervertebral
disc
aging
and
degeneration.
However,
the
application
of
senotherapies,
such
as
senomorphics
targeting
markers
senescence‐associated
secretory
phenotype
(SASP),
remains
limited
due
challenges
in
precise
delivery.
Given
that
natural
killer
group
2D
(NKG2D)
ligands
are
increased
on
surface
senescent
nucleus
pulposus
(NP)
cells,
NKG2D‐overexpressing
NP
cell
membranes
(NNPm)
constructed,
which
expected
achieve
dual
effect
toward
cells
based
homologous
membrane
fusion
NKG2D‐mediated
immunosurveillance
mechanism.
Then,
mesoporous
silica
nanoparticles
carrying
peroxisome
proliferator‐activated
receptor‐ɣ
coactivator
1α
(PGC1α)inducer
(SP)
coated
with
NNPm
(SP@NNPm)
it
found
SP@NNPm
selectively
targets
SP
cores
exhibit
pH‐responsive
drug
release.
Moreover,
effectively
induces
PGC1α‐mediated
mitochondrial
biogenesis
mitigates
induced
by
oxidative
stress
SASP,
thereby
alleviating
puncture‐induced
This
dual‐targeting
nanotherapeutic
system
represents
novel
approach
delivery
for
degeneration
treatment.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(38)
Published: March 19, 2024
Abstract
Mesenchymal
stem
cells
(MSCs)
play
a
crucial
role
in
maintaining
bone
homeostasis
and
are
extensively
explored
for
cell
therapy
various
bone‐related
diseases.
In
addition
to
direct
therapy,
the
secretion
of
extracellular
vesicles
(EVs)
by
MSCs
has
emerged
as
promising
alternative
approach.
MSC‐derived
EVs
(MSC‐EVs)
offer
equivalent
therapeutic
efficacy
while
mitigating
potential
risks.
These
possess
unique
properties
that
enable
them
traverse
biological
barriers
deliver
bioactive
cargos
target
cells.
Furthermore,
employing
modification
engineering
strategies,
effects
tissue
targeting
specificity
MSC‐EVs
can
be
further
enhanced
meet
specific
needs.
this
review,
mechanisms
advantages
MSC‐EV
diseased
tissues
highlighted.
Through
simple
isolation
techniques,
MSC‐EV‐based
biomaterials
have
demonstrated
great
promise
regeneration.
Finally,
future
perspectives
on
presented,
envisioning
development
next‐generation
regenerative
materials
agents
clinical
translation
field
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(43), P. 29864 - 29879
Published: Oct. 18, 2024
Therapeutic
efficacy
of
skeletal
diseases
is
usually
limited
by
unfavorable
drug
delivery
due
to
incapable
bone
targeting
and
low
affinity
conventional
carriers,
as
well
relatively
reduced
vascularization
dense
structure
tissues.
Due
CXC
chemokine
receptor
4
(CXCR4)/CXC
ligand
12
(CXCL12)
signal
axis-guided
recruitment,
osteoprogenitor
cells
(OPCs)
can
actively
migrate
disease
nidus.
Here,
drugs-loaded
nanoliposomes
are
prepared
decorated
onto
OPCs
biotin–streptavidin
linkage
for
precise
effective
delivery.
In
mouse
models
tibia
defect
orthotopic
osteosarcoma,
superior
property
OPCs-based
systems
toward
diseased
niduses
verified.
By
encapsulating
antitumor
antiosteoporosis
drugs
into
nanoliposomes,
effectively
inhibit
development
restore
destruction
in
osteosarcoma
ovariectomized
osteoporosis.
This
study
reveals
a
cell-based
system
highly
delivery,
which
will
find
great
potential
universal
platform
treatment
various
diseases.