Materials Today Bio,
Journal Year:
2025,
Volume and Issue:
32, P. 101781 - 101781
Published: April 17, 2025
Depression
and
cognitive
disorders
remain
major
challenges
in
healthcare,
with
conventional
treatments
often
facing
limitations
such
as
slow
onset,
side
effects,
poor
drug
delivery
to
the
brain.
Biomimetic
nanodelivery
systems,
including
nanozymes,
cell
membrane-based
exosomes,
have
emerged
promising
solutions
these
issues.
These
systems
leverage
natural
biological
processes
enhance
targeting,
improve
bioavailability,
regulate
complex
pathways.
Nanoenzymes,
their
catalytic
properties,
offer
antioxidant
anti-inflammatory
benefits,
while
membranes
exosomes
provide
efficient
targeting
immune
evasion.
However,
remain,
immaturity
of
large-scale
production
techniques,
stability
concerns,
incomplete
understanding
mechanisms
action.
Moreover,
long-term
safety,
pharmacokinetics,
toxicity
require
further
investigation.
Despite
obstacles,
potential
biomimetic
revolutionize
depression
treatment
is
significant.
Future
research
should
focus
on
optimizing
preparation,
improving
release,
ensuring
clinical
safety.
Multidisciplinary
collaboration
will
be
essential
for
advancing
from
laboratory
practice,
offering
new
therapeutic
avenues
other
neurological
disorders.
Acta Materia Medica,
Journal Year:
2025,
Volume and Issue:
4(1)
Published: Jan. 1, 2025
Cardiovascular
diseases
(CVDs)
pose
a
significant
threat
to
human
health
due
the
high
mortality
and
morbidity
rates.
Traditional
drugs
often
have
limited
efficacy
inherent
constraints,
such
as
low
bioavailability
notable
side
effects.
As
highly
regarded
therapeutic
strategy,
nanotechnology
offers
new
perspectives
means
for
treating
CVDs.
Nanozyme-based
targeted
specifically
address
biological
processes
in
areas
affected
by
CVDs,
thereby
achieving
precise
treatment.
Compared
traditional
drugs,
nanozymes
offer
advantages,
efficiency,
specificity,
controllability,
fewer
effects,
showing
great
This
paper
first
explores
design
strategies
mechanisms
of
nanozyme-based
therapy,
then
introduces
its
application
key
ischemic
stroke,
myocardial
infarction,
coronary
heart
disease.
Finally,
discusses
challenges
introducing
into
clinical
applications
future
development
prospects
treatment
Journal of Nanobiotechnology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Aug. 20, 2024
Ischemic
stroke
poses
significant
challenges
in
terms
of
mortality
and
disability
rates
globally.
A
key
obstacle
to
the
successful
treatment
ischemic
lies
limited
efficacy
administering
therapeutic
agents.
Leveraging
unique
properties
nanoparticles
for
brain
targeting
crossing
blood-brain
barrier,
researchers
have
engineered
diverse
nanoparticle-based
drug
delivery
systems
improve
outcomes
stroke.
This
review
provides
a
concise
overview
pathophysiological
mechanisms
implicated
stroke,
encompassing
oxidative
stress,
glutamate
excitotoxicity,
neuroinflammation,
cell
death,
elucidate
potential
targets
systems.
Furthermore,
outlines
classification
according
these
distinct
physiological
processes.
categorization
aids
identifying
attributes
commonalities
that
target
specific
pathways
thereby
facilitating
advancement
nanomedicine
development.
The
discusses
benefits
existing
associated
with
employing
offering
new
perspectives
on
designing
efficacious
enhance
outcomes.
Biomedical Technology,
Journal Year:
2024,
Volume and Issue:
7, P. 32 - 45
Published: July 16, 2024
Ischemic
stroke
(IS),
a
major
cause
of
death
and
disability
globally,
requires
innovative
therapeutic
approaches
due
to
its
complex
pathology.
Nature
medicine
(NM)
offers
promising
treatments
through
bioactive
compounds,
which
target
the
multifaceted
nature
stroke-induced
damage.
However,
clinical
application
NM
is
limited
by
challenges
in
bioavailability
specificity.
This
review
article
presents
an
advanced
perspective
on
integrating
nanotechnology
with
create
potent
nanodelivery
systems
for
ischemic
treatment.
We
highlight
pathological
underpinnings
stroke,
including
oxidative
stress,
inflammation,
apoptosis,
discuss
how
compounds
offer
targeted
mitigation
strategies.
By
incorporating
platforms,
such
as
liposomes
nanoparticles,
these
-based
can
achieve
enhanced
targeting,
solubility,
controlled
release,
significantly
improving
outcomes
while
reducing
side
effects.
Despite
developments,
translation
nano-enhanced
into
practice
faces
obstacles,
manufacturing
scalability,
regulatory
approval,
safety
evaluations.
emphasizes
potential
combining
advance
therapy,
calling
integrated
research
efforts
overcome
existing
barriers
fully
realize
benefits
this
approach.
Chemical Engineering Journal,
Journal Year:
2024,
Volume and Issue:
494, P. 153210 - 153210
Published: June 16, 2024
β-Amyloid
(Aβ)
aggregation
and
oxidative
stress
are
primary
pathological
features
of
Alzheimer's
disease
(AD).
Combination
therapies
that
target
brain
tissue
corporately
address
these
main
factors
required
for
effective
AD
treatment.
Here,
we
developed
a
multifunctional
liposome
delivery
system
(KLVFF@LIP-CeO2)
co-delivery
Aβ-targeted
KLVFF
reactive
oxygen
species
(ROS)-responsive
Ceria
(CeO2)
through
intranasal
administration.
After
Aβ1-42-induced
ROS
apoptosis
in
HT22
cells,
KLVFF@LIP-CeO2
exhibited
significant
protective
effects
by
inhibiting
Aβ
scavenging
multi-ROS.
With
features,
verified
the
therapeutic
effectiveness
APPswe/PSEN1dE9
(APP/PS1)
model
mice.
administration,
demonstrated
sufficient
rapid
accumulation
significantly
alleviated
deposition
stress,
contributing
to
rescue
cognitive
impairment
APP/PS1
These
results
highlight
clinical
potential
multi-targeted
nanoparticles
synergistic
therapy
AD.
Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(37), P. 14944 - 14952
Published: Aug. 29, 2024
The
long-term
operation
feature
of
enzymatic
biofuel
cell-based
self-powered
biosensor
(EBFC-SPB)
endows
them
with
the
potential
to
execute
dual-signal
biosensing
without
having
integrate
an
extra
signal
acquisition
device.
Herein,
cobalt
and
manganese
codoped
CeO2
nanospheres
(CoMn-CeO2
NSs)
glucose-oxidase-like
peroxidase-like
activities
have
been
developed
as
substrate-switched
dual-channel
transduction
components
in
EBFC-SPB
for
a
assay
aflatoxin
B1
(AFB1).
CoMn-CeO2
NSs
modified
aptamer
are
anchored
complementary
DNA-attached
bioanode
by
base
pairing,
which
catalyze
glucose
oxidation
together
oxidase
(GOx)
on
bioanode.
Once
AFB1
appears,
will
be
released
from
due
binding
specificity
aptamer,
resulting
decreased
catalytic
efficiency
first
declining
stage
EBFC-SPB.
Accompanied
introduction
H2O2,
residual
switch
activity
mediate
production
benzo-4-chlorohexadienone
(4-CD)
precipitate,
increases
steric
hindrance
yields
another
By
assessing
variation
amplitudes
during
these
two
stages,
has
realized
satisfying
results.
This
work
not
only
breaks
ground
bioassays
but
also
deepens
application
nanozymes