Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(31)
Published: April 5, 2024
Abstract
4D
(bio‐)printing
endows
3D
printed
(bio‐)materials
with
multiple
functionalities
and
dynamic
properties.
materials
have
been
recently
used
in
biomedical
engineering
for
the
design
fabrication
of
devices,
such
as
stents,
occluders,
microneedles,
smart
3D‐cell
engineered
microenvironments,
drug
delivery
systems,
wound
closures,
implantable
medical
devices.
However,
success
printing
relies
on
rational
objects,
selection
materials,
availability
appropriate
types
external
(multi‐)stimuli.
Here,
this
work
first
highlights
different
stimuli,
strategies
(bio‐)printing.
Then,
it
presents
a
critical
review
applications
discusses
future
directions
research
exciting
area,
including
vivo
tissue
regeneration
studies,
implementation
reversible
shape
memory
behaviors,
creation
fast
shape‐transformation
responses,
ability
to
operate
at
microscale,
untethered
activation
control,
application
(machine
learning‐based)
modeling
approaches
predict
structure–property
design–shape
transformation
relationships
(bio)printed
constructs.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(21)
Published: Feb. 7, 2024
Single-atom
nanozymes
(SAzymes)
showcase
not
only
uniformly
dispersed
active
sites
but
also
meticulously
engineered
coordination
structures.
These
intricate
architectures
bestow
upon
them
an
exceptional
catalytic
prowess,
thereby
captivating
numerous
minds
and
heralding
a
new
era
of
possibilities
in
the
biomedical
landscape.
Tuning
microstructure
SAzymes
on
atomic
scale
is
key
factor
designing
targeted
with
desirable
functions.
This
review
first
discusses
summarizes
three
strategies
for
their
impact
reactivity
biocatalysis.
The
effects
choices
carrier,
different
synthesis
methods,
modulation
first/second
shell,
type
number
metal
centers
enzyme-like
activity
are
unraveled.
Next,
attempt
made
to
summarize
biological
applications
tumor
therapy,
biosensing,
antimicrobial,
anti-inflammatory,
other
from
mechanisms.
Finally,
how
designed
regulated
further
realization
diverse
reviewed
prospected.
It
envisaged
that
comprehensive
presented
within
this
exegesis
will
furnish
novel
perspectives
profound
revelations
regarding
SAzymes.
Advanced Healthcare Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Sonodynamic
therapy
(SDT),
which
is
non-invasive
and
controllable
has
the
potential
to
treat
triple-negative
breast
cancer
(TNBC).
However,
hypoxia
immunosuppressive
tumor
microenvironment
(TME)
often
block
production
of
reactive
oxygen
species
induction
SDT-activated
immunogenic
cell
death,
thus
limiting
activation
adaptive
immune
responses.
To
alleviate
these
challenges,
we
proposed
development
a
multifunctional
biomimetic
nanoplatform
(mTSeIR),
was
designed
with
diselenide-conjugated
sonosensitizers
tirapazamine
(TPZ),
encapsulated
within
M1
macrophage
membrane.
This
utilized
hypoxia-induced
chemotherapy
improve
efficacy
SDT,
further
enhance
immunotherapy
by
activating
innate
immunity
remodeling
TME.
Firstly,
prodrug
TPZ
activated
due
increased
consumption
associated
SDT.
Subsequently,
mTSeIR
enhanced
repolarization
M2
macrophages
phenotype.
The
diselenide
component
in
effectively
natural
killer
cell-mediated
antitumor
response.
Ultimately,
vivo
studies
indicated
that
mTSeIR+US
good
biosafety
achieved
over
98%
inhibition
immunotherapy.
research
presents
an
efficient
approach
addressed
limitations
SDT
achieves
simultaneous
both
immunotherapy,
resulting
significant
anti-metastatic
TNBC.
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(33), P. 22153 - 22171
Published: Aug. 9, 2024
cGAS/STING
pathway,
which
is
highly
related
to
tumor
hypoxia,
considered
as
a
potential
target
for
remodeling
the
immunosuppressive
microenvironment
of
solid
tumors.
Metal
ions,
such
Mn2+,
activate
but
their
efficacy
in
cancer
therapy
limited
by
insufficient
effect
on
immunogenic
cell
death
single
ion.
Here,
we
evaluate
association
between
hypoxia
and
inhibition
report
polymetallic-immunotherapy
strategy
based
large
mesoporous
trimetal-based
nanozyme
(AuPdRh)
coordinated
with
Mn2+
(Mn2+@AuPdRh)
signaling
robust
adaptive
antitumor
immunity.
Specifically,
inherent
CAT-like
activity
this
polymetallic
Mn2+@AuPdRh
decomposes
endogenous
H2O2
into
O2
relieve
induced
suppression
signaling.
Moreover,
displays
potent
near-infrared-II
photothermal
strong
POD-mimic
activity;
generated
hyperthermia
•OH
radicals
synergistically
trigger
tumors,
releasing
abundant
dsDNA,
while
delivered
augments
sensitivity
cGAS
dsDNA
activates
cGAS-STING
thereby
triggering
downstream
immunostimulatory
signals
kill
primary
distant
metastatic
Our
study
demonstrates
metal-based
STING-mediated
may
inspire
development
more
effective
strategies
immunotherapy.
Materials Today Bio,
Journal Year:
2024,
Volume and Issue:
26, P. 101018 - 101018
Published: March 11, 2024
The
cGAS-STING
pathway
holds
tremendous
potential
as
a
regulator
of
immune
responses,
offering
means
to
reshape
the
tumor
microenvironment
and
enhance
immunotherapy.
Despite
emergence
STING
agonists,
their
clinical
viability
is
hampered
by
stability
delivery
challenges,
well
variations
in
expression
within
tumors.
In
this
study,
we
present
Mn-phenolic
networks
novel
carrier
for
ADU-S100,
hydrophilic
agonist,
aimed
at
bolstering
These
nanoparticles,
termed
TMA
NMs,
are
synthesized
through
coordination
tannic
acid
manganese
ions,
with
surface
modification
involving
bovine
serum
albumin
colloidal
stability.
NMs
exhibit
pH/GSH-responsive
disintegration
properties,
enabling
precise
drug
release.
This
effectively
addresses
issues
facilitates
efficient
intracellular
delivery.
Importantly,
synergistically
effects
ADU-S100
concurrent
release
Mn2+,
which
serves
sensitizer
pathway,
resulting
significant
activation.
Upon
systemic
administration,
these
nanoparticles
efficiently
accumulate
activation
pathways
not
only
induces
immunogenic
cell
death
(ICD)
cells
but
also
orchestrates
remodeling
immunosuppressive
microenvironment.
includes
promotion
cytokine
release,
dendritic
maturation,
T
infiltration,
leading
pronounced
suppression
growth.
Combining
excellent
biocompatibility
biodegradability,
Mn-based
nanocarrier
represents
promising
strategy
enhancing
immunotherapy
pathway.
Immunological Reviews,
Journal Year:
2023,
Volume and Issue:
321(1), P. 181 - 198
Published: July 5, 2023
Summary
Immunogenic
cell
death
(ICD)
is
a
special
pattern
of
tumor
death,
enabling
to
elicit
tumor‐specific
immune
response
via
the
release
damage‐associated
molecular
patterns
and
tumor‐associated
antigens
in
microenvironment.
ICD‐induced
immunotherapy
holds
promise
for
completely
eliminating
tumors
long‐term
protective
antitumor
response.
Increasing
ICD
inducers
have
been
discovered
boosting
immunity
evoking
ICD.
Nonetheless,
utilization
remains
insufficient
owing
serious
toxic
reactions,
low
localization
efficiency
within
microenvironmental
niche,
etc.
For
overcoming
such
limitations,
stimuli‐responsive
multifunctional
nanoparticles
or
nanocomposites
with
developed
improving
immunotherapeutic
lowering
toxicity,
which
represent
prospective
scheme
fostering
immunotherapy.
This
review
outlines
advances
near‐infrared
(NIR)‐,
pH‐,
redox‐,
pH‐
NIR‐
microenvironment‐responsive
nanodelivery
systems
induction.
Furthermore,
we
discuss
their
clinical
translational
potential.
The
progress
settings
depends
upon
development
biologically
safer
drugs
tailored
patient
needs.
Moreover,
an
in‐depth
comprehending
biomarkers,
immunosuppressive
microenvironment,
may
accelerate
advance
smarter
further
amplify
Analytical Chemistry,
Journal Year:
2023,
Volume and Issue:
95(38), P. 14402 - 14412
Published: Sept. 12, 2023
Nitroreductase
(NTR)
is
an
enzyme
that
upregulated
under
tumor-depleted
oxygen
conditions.
The
majority
of
studies
have
been
conducted
on
NTR,
but
many
existing
fluorescent
imaging
tools
for
monitoring
NTR
inevitably
suffer
from
weak
targeting,
low
sensitivity,
and
simple
tumor
models.
Research
diagnosing
lung
tumors
has
very
popular
in
recent
years,
targeting
assays
orthotopic
still
great
research
value,
as
such
models
better
mimic
the
reality
cancer
organism.
Here,
we
developed
a
novel
near-infrared
(NIR)
probe
IR-ABS
jointly
targets
carbonic
anhydrase
IX
(CAIX).
excellent
sensitivity
selectivity
shows
exceptional
response
spectroscopic
tests.
measurements
ensured
this
good
biosafety
both
cells
mice.
A
was
found
hypoxic
at
cellular
level,
distinguishing
normal
cells.
In
vivo
experiments
demonstrated
achieves
zebrafish
level
enables
rapid
accurate
margin
distinguishment
different
mouse
More
importantly,
successfully
applied
detection
models,
further
combined
with
tracheal
inhalation
drug
delivery
to
improve
targeting.
To
best
our
knowledge,
present
first
time
method
cancerous
situ
via
delivery,
contrast
reported
literature.
This
NIR
fluorescence
diagnostic
strategy
holds
exciting
potential
clinical
aid
diagnosis.