Regenerative Biomaterials,
Journal Year:
2024,
Volume and Issue:
11
Published: Jan. 1, 2024
Tendinopathy
is
a
common
disorder
that
causes
local
dysfunction
and
reduces
quality
of
life.
Recent
research
has
indicated
alterations
in
the
inflammatory
microenvironment
play
vital
role
pathogenesis
tendinopathy.
Herein,
injectable
methacrylate
gelatin
(GelMA)
microspheres
(GM)
were
fabricated
loaded
with
heparin-dopamine
conjugate
(HDC)
hepatocyte
growth
factor
(HGF).
GM@HDC@HGF
designed
to
balance
by
inhibiting
oxidative
stress
inflammation,
thereby
regulating
extracellular
matrix
(ECM)
metabolism
halting
tendon
degeneration.
Combining
factors
heparin
was
expected
improve
encapsulation
rate
maintain
long-term
efficacy
HGF.
In
addition,
catechol
groups
on
dopamine
have
adhesion
antioxidant
properties,
allowing
potential
attachment
at
injured
site,
better
function
synergized
injected
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(19)
Published: March 13, 2024
Abstract
Efferocytosis,
an
intrinsic
regulatory
mechanism
to
eliminate
apoptotic
cells,
will
be
suppressed
due
the
delayed
apoptosis
process
in
aging‐related
diseases,
such
as
osteoarthritis
(OA).
In
this
study,
cartilage
lesion‐localized
hydrogel
microspheres
are
developed
remodel
situ
efferocytosis
reverse
senescence
and
recruit
endogenous
stem
cells
accelerate
repair.
Specifically,
aldehyde‐
methacrylic
anhydride
(MA)‐modified
hyaluronic
acid
(AHM),
loaded
with
pro‐apoptotic
liposomes
(liposomes
encapsulating
ABT263,
A‐Lipo)
PDGF‐BB,
namely
A‐Lipo/PAHM,
prepared
by
microfluidic
photo‐cross‐linking
techniques.
By
a
degraded
porcine
explant
OA
model,
lesion
location
experiment
illustrated
that
aldehyde‐functionalized
promote
affinity
for
cartilage.
vitro
data
showed
A‐Lipo
induced
of
senescent
chondrocytes
(Sn‐chondrocytes),
which
can
then
phagocytosed
macrophages,
remodeling
facilitated
protection
normal
maintained
chondrogenic
differentiation
capacity
MSCs.
vivo
experiments
confirmed
localized
reversed
promoted
repair
OA.
It
is
believed
strategy
great
significance
tissue
regeneration
diseases.
Exploration,
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 24, 2024
Immune-mediated
inflammatory
diseases
(IMIDs)
impose
an
immeasurable
burden
on
individuals
and
society.
While
the
conventional
use
of
immunosuppressants
disease-modifying
drugs
has
provided
partial
relief
control,
their
inevitable
side
effects
limited
efficacy
cast
a
shadow
over
finding
cure.
Promising
nucleic
acid
have
shown
potential
to
exert
precise
at
molecular
level,
with
different
classes
acids
having
regulatory
functions
through
varying
mechanisms.
For
better
delivery
acids,
safe
effective
viral
vectors
non-viral
systems
(including
liposomes,
polymers,
etc.)
been
intensively
explored.
Herein,
after
describing
range
categories
vectors,
we
focus
application
therapeutic
in
various
IMIDs,
including
rheumatoid
arthritis,
bowel
disease,
psoriasis,
multiple
sclerosis,
asthma,
ankylosing
spondylitis,
systemic
lupus
erythematosus,
uveitis.
Molecules
implicated
inflammation
immune
dysregulation
are
abnormally
expressed
series
meticulous
modulation
therapy
results
degrees
remission
improvement
these
diseases.
By
synthesizing
findings
centered
specific
targets,
this
review
delivers
systematic
elucidation
perspective
towards
advancing
utilization
therapeutics
for
managing
IMIDs.
Materials Today Bio,
Journal Year:
2024,
Volume and Issue:
26, P. 101044 - 101044
Published: April 4, 2024
Joint
injuries
are
among
the
leading
causes
of
disability.
Present
concentrations
were
focused
on
oral
drugs
and
surgical
treatment,
which
brings
severe
unnecessary
difficulties
for
patients.
Smart
patches
with
high
flexibility
intelligent
drug
control-release
capacity
greatly
desirable
efficient
joint
management.
Herein,
we
present
a
novel
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(30), P. 38989 - 39004
Published: July 22, 2024
Implant-associated
infections
and
excessive
immune
responses
are
two
major
postsurgical
issues
for
successful
implantation.
However,
conventional
strategies
including
antibiotic
treatment
inflammatory
regulation
always
compromised
due
to
the
comodification
of
various
biochemical
agents
instances
functional
interference.
It
is
imperative
provide
implant
surfaces
with
satisfactory
antibacterial
anti-inflammatory
properties.
Here,
a
dual-effect
nanostructured
polyetheretherketone
(PEEK)
surface
(NP@PDA/Zn)
bionic
mechano-bactericidal
nanopillars
immobilized
immunomodulatory
Zn2+
designed.
The
constructed
hybrid
display
remarkable
performance
against
Gram-negative
Gram-positive
strains
through
synergy
physical
chemical
bactericidal
effects
imposed
by
Zn2+.
Meanwhile,
immunoregulatory
property
evaluated
investigation
macrophage
polarization
both
in
vitro
vivo,
results
reveal
that
NP@PDA/Zn
could
downregulate
expression
M1-related
cytokines
decrease
M1
recruitment
lower
response.
Notably,
exhibited
exceptional
biocompatibility
discerning
biocidal
activity
between
bacterial
mammalian
cells
antioxidant
effectively
scavenges
ROS,
minimizing
potential
cytotoxicity.
Taken
together,
presents
convenient
promising
strategy
combining
synergistic
without
any
mutual
interference,
which
can
support
development
multifunctional
implant-associated
materials.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 2, 2025
High
transductive
loss
at
tissue
injury
sites
impedes
repair.
The
high
dissipation
characteristics
in
the
electromechanical
conversion
of
piezoelectric
biomaterials
pose
a
challenge.
Therefore,
supramolecular
engineering
and
microfluidic
technology
is
utilized
to
introduce
slide-ring
polyrotaxane
conductive
polypyrrole
construct
stress-electric
coupling
hydrogel
microspheres.
molecular
slippage
mechanism
structure
stores
releases
mechanical
energy,
reducing
loss,
barium
titanate
enables
stress-electricity
conversion,
conjugated
π-electron
movement
network
improves
internal
electron
transfer
efficiency
microspheres,
thereby
for
first
time.
Compared
traditional
low-dissipation
microspheres
increased
by
2.3
times,
energy
decreased
43%.
At
cellular
level,
electrical
signals
generated
triggered
Ca
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 9, 2025
Abstract
Efferocytosis
in
macrophages
typically
engages
an
anti‐inflammatory
positive
feedback
regulatory
mechanism.
In
osteoarthritis
(OA),
characterized
by
imbalanced
inflammatory
homeostasis,
the
proinflammatory
state
of
immune
microenvironment
can
be
reversed
through
enhanced
efferocytosis.
This
study
develops
situ
proefferocytosis
hydrogel
microsphere
(macrophage
polarity
converter,
H‐C@IL)
for
OA
treatment.
Immunoliposomes
(IL),
CD16/32
antibody‐modified
clodronate
liposomes,
are
initially
prepared
using
Re‐emulsion
method.
Then,
IL
is
loaded
into
CCL19‐modified
HAMA
microspheres
microfluidic
technology.
vitro,
H‐C@IL
specifically
recruit
M0
and
M1
via
CCL19,
induce
apoptosis
secondary
targeting
with
IL,
provide
“Find/Eat‐me”
signals
to
enhance
Additionally,
it
promotes
macrophage
polarization
toward
M2
phenotype.
vivo,
behavioral,
imaging,
histological
analyses
demonstrate
that
effectively
facilitates
M2,
inhibits
inflammation,
cartilage
regeneration.
Mechanistically,
enhances
efferocytosis
activating
proteins
such
as
PROS1
TIMD4
macrophages.
Concurrently,
signaling
pathways,
including
PQLC2‐Arg‐Rac1
Pbx1/IL‐10,
activated
drive
from
M2.
summary,
situ,
restores
regeneration,
offering
a
comprehensive
treatment
strategy
OA.
Inflammation
and
cartilage
degeneration
are
critical
challenges
in
osteoarthritis
(OA)
treatment.
Achieving
sustained
drug
efficacy
while
mitigating
the
adverse
effects
of
inflammation
reactive
oxygen
species
remains
a
significant
challenge.
This
study
synthesizes
gallic
acid-magnesium
(GA-Mg)
metal–organic
framework
(MOF)
as
carrier
for
puerarin
(PA).
The
PA-loaded
GA-Mg
MOF
(pGM)
is
encapsulated
within
chondroitin
sulfate
methacrylate,
forming
monodisperse
hybrid
microspheres
(CM@pGM)
under
ultraviolet
light
using
microfluidic
technology.
pGM
physically
confined
through
network
structural
obstructions
noncovalent
interactions.
During
degradation,
GA
Mg2+
ions
release
from
pGM,
improving
inflammatory
microenvironment
articular
cavity
oxidative
stress.
PA
supports
chondrocyte
anabolism
facilitates
repair.
In
vitro
studies
confirm
that
injectable
extend
period
to
over
2
weeks.
vivo
experiments
demonstrate
CM@pGM
significantly
reduces
osteophyte
formation,
alleviates
degenerative
changes
cartilage,
delays
OA
progression.
conclusion,
CM@pGM,
delivery
platform
ameliorates
microenvironment,
stress,
promotes
repair,
holds
potential
Regenerative Biomaterials,
Journal Year:
2023,
Volume and Issue:
10
Published: Jan. 1, 2023
Bone
defects
are
a
persistent
challenge
in
clinical
practice.
Although
repair
therapies
based
on
tissue-engineered
materials,
which
known
to
have
crucial
role
defective
bone
regeneration,
gathered
increased
attention,
the
current
treatments
for
massive
several
limitations.
In
present
study,
immunomodulatory
inflammatory
microenvironment
properties
of
quercetin,
we
encapsulated
quercetin-solid
lipid
nanoparticles
(SLNs)
hydrogel.
Temperature-responsive
poly(ε-caprolactone-co-lactide)-b-poly(ethylene
glycol)-b-poly(ε-caprolactone-co-lactide)
modifications
were
coupled
main
chain
hyaluronic
acid
hydrogel,
constructing
novel,
injectable
hydrogel
scaffold.
Extensive