Advanced Functional Materials,
Год журнала:
2020,
Номер
30(43)
Опубликована: Авг. 7, 2020
Abstract
Cancer
immunotherapy
has
received
tremendous
attention
in
the
past
decade
owing
to
its
clinical
successes
with
use
of
immune‐checkpoint
inhibition
and
chimeric
antigen
receptor
T
cell
therapy.
However,
only
a
small
proportion
patients
have
benefited
from
these
immunotherapeutic
drugs,
which
raised
concerns
about
low
response
rate
immune‐related
adverse
events.
Nanomedicines
served
as
paradigm
for
preferential
tumor
accumulation
but
still
confront
issues
such
poor
circulation
insufficient
accumulation.
By
virtue
coating
nanoparticles
membranes
diverse
sources,
active
proteins
on
can
impart
variety
desired
functionalities
or
supplementary
therapeutic
effects
nanoparticles,
providing
ways
enhanced
cancer
immunotherapy.
In
this
review,
recent
advances
membrane
camouflaged
applied
improved
are
discussed
basis
different
sources
corresponding
working
mechanisms.
These
biomimetic
potentially
deliver
agents
designated
sites
actively
engage
particular
stages
immunity
cycle,
eliciting
antitumor
less
off‐target
toxicities.
Advanced Materials,
Год журнала:
2020,
Номер
32(40)
Опубликована: Авг. 28, 2020
Macrophages
play
an
important
role
in
cancer
development
and
metastasis.
Proinflammatory
M1
macrophages
can
phagocytose
tumor
cells,
while
anti-inflammatory
M2
such
as
tumor-associated
(TAMs)
promote
growth
invasion.
Modulating
the
immune
microenvironment
through
engineering
is
efficacious
therapy.
target
cancerous
cells
and,
therefore,
be
used
drug
carriers
for
Herein,
strategies
to
engineer
immunotherapy,
inhibition
of
macrophage
recruitment,
depletion
TAMs,
reprograming
blocking
CD47-SIRPα
pathway,
are
discussed.
Further,
recent
advances
delivery
using
macrophages,
macrophage-derived
exosomes,
macrophage-membrane-coated
nanoparticles
elaborated.
Overall,
there
still
significant
room
macrophage-mediated
modulation
delivery,
which
will
further
enhance
current
therapies
against
various
malignant
solid
tumors,
including
drug-resistant
tumors
metastatic
tumors.
Angewandte Chemie International Edition,
Год журнала:
2020,
Номер
59(29), С. 11717 - 11731
Опубликована: Март 5, 2020
Optical
imaging
plays
a
crucial
role
in
biomedicine.
However,
due
to
strong
light
scattering
and
autofluorescence
biological
tissue
between
650-900
nm,
conventional
optical
often
has
poor
signal-to-background
ratio
shallow
penetration
depth,
which
limits
its
ability
deep-tissue
vivo
imaging.
Second
near-infrared
fluorescence,
chemiluminescence,
photoacoustic
modalities
mitigate
these
issues
by
their
respective
advantages
of
minimized
scattering,
eliminated
external
excitation,
ultrasound
detection.
To
enable
disease
detection,
activatable
molecular
probes
(AMPs)
with
the
change
second
or
signals
response
biomarker
have
been
developed.
This
Minireview
summarizes
design
strategies,
sensing
mechanisms,
applications
AMPs.
The
potential
challenges
perspectives
AMPs
are
also
discussed.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Ноя. 3, 2023
Abstract
Smart
nanoparticles,
which
can
respond
to
biological
cues
or
be
guided
by
them,
are
emerging
as
a
promising
drug
delivery
platform
for
precise
cancer
treatment.
The
field
of
oncology,
nanotechnology,
and
biomedicine
has
witnessed
rapid
progress,
leading
innovative
developments
in
smart
nanoparticles
safer
more
effective
therapy.
In
this
review,
we
will
highlight
recent
advancements
including
polymeric
dendrimers,
micelles,
liposomes,
protein
cell
membrane
mesoporous
silica
gold
iron
oxide
quantum
dots,
carbon
nanotubes,
black
phosphorus,
MOF
others.
We
focus
on
their
classification,
structures,
synthesis,
intelligent
features.
These
possess
the
ability
various
external
internal
stimuli,
such
enzymes,
pH,
temperature,
optics,
magnetism,
making
them
systems.
Additionally,
review
explore
latest
studies
tumor
targeting
functionalizing
surfaces
with
tumor-specific
ligands
like
antibodies,
peptides,
transferrin,
folic
acid.
also
summarize
different
types
options,
small
molecules,
proteins,
nucleic
acids,
even
living
cells,
potential
use
While
is
promising,
acknowledge
challenges
clinical
prospects
associated
use.
Finally,
propose
blueprint
that
involves
artificial
intelligence-powered
treatment
applications.
By
harnessing
aims
usher
new
era
personalized
therapy,
providing
patients
individualized
options.
Abstract
Although
cancer
immunotherapy
has
emerged
as
a
tremendously
promising
therapy
method,
it
remains
effective
only
for
several
cancers.
Photoimmunotherapy
(e.g.,
photodynamic/photothermal
therapy)
could
synergistically
enhance
the
immune
response
of
immunotherapy.
However,
excessively
generated
immunogenicity
will
cause
serious
inflammatory
syndrome.
Herein,
biomimetic
magnetic
nanoparticles,
Fe
3
O
4
‐SAS
@
PLT,
are
reported
novel
approach
to
sensitize
ferroptosis
and
generate
mild
immunogenicity,
enhancing
rate
non‐inflamed
tumors
‐SAS@PLT
built
from
sulfasalazine
(SAS)‐loaded
mesoporous
nanoparticles
(Fe
)
platelet
(PLT)
membrane
camouflage
triggered
ferroptotic
cell
death
via
inhibiting
glutamate‐cystine
antiporter
system
X
c
−
pathway.
PLT‐mediated
significantly
improves
efficacy
programmed
1
checkpoint
blockade
achieves
continuous
tumor
elimination
in
mouse
model
4T1
metastatic
tumors.
Proteomics
studies
reveal
that
not
induce
tumor‐specific
but
also
efficiently
repolarize
macrophages
immunosuppressive
M2
phenotype
antitumor
M1
phenotype.
Therefore,
concomitant
with
expected
provide
great
potential
clinical
treatment
metastasis.
Abstract
Nanotechnology
has
provided
great
opportunities
for
managing
neoplastic
conditions
at
various
levels,
from
preventive
and
diagnostic
to
therapeutic
fields.
However,
when
it
comes
clinical
application,
nanoparticles
(NPs)
have
some
limitations
in
terms
of
biological
stability,
poor
targeting,
rapid
clearance
the
body.
Therefore,
biomimetic
approaches,
utilizing
immune
cell
membranes,
are
proposed
solve
these
issues.
For
example,
macrophage
or
neutrophil
membrane
coated
NPs
developed
with
ability
interact
tumor
tissue
suppress
cancer
progression
metastasis.
The
functionality
particles
largely
depends
on
surface
proteins
cells
their
preserved
function
during
extraction
coating
process
NPs.
Proteins
outer
can
render
a
wide
range
activities
NPs,
including
prolonged
blood
circulation,
remarkable
competency
recognizing
antigens
enhanced
better
cellular
interactions,
gradual
drug
release,
reduced
toxicity
vivo.
In
this
review,
nano‐based
systems
cells‐derived
membranous
layers,
detailed
production
process,
applicability
treatment
discussed.
addition,
future
perspectives
challenges
translation
also
presented.
Cardiovascular
disease
is
the
leading
cause
of
mortality
worldwide.
Atherosclerosis,
one
most
common
forms
disease,
characterized
by
a
gradual
formation
atherosclerotic
plaque,
hardening,
and
narrowing
arteries.
Nanomaterials
can
serve
as
powerful
delivery
platforms
for
atherosclerosis
treatment.
However,
their
therapeutic
efficacy
substantially
limited
in
vivo
due
to
nonspecific
clearance
mononuclear
phagocytic
system.
In
order
address
this
limitation,
rapamycin
(RAP)-loaded
poly(lactic-
ACS Nano,
Год журнала:
2020,
Номер
14(9), С. 11017 - 11028
Опубликована: Авг. 13, 2020
Although
ferroptosis
therapy
has
been
proven
to
be
a
promising
strategy
for
cancer
treatment,
its
efficacy
still
might
limited
by
insufficient
H2O2
supply
in
tumor
tissue.
Herein,
we
designed
cell
membrane-cloaked
cascade
nanoreactor
based
on
ferric
metal–organic
frameworks
(MOF)
and
glucose
oxidase
(GOx)
decoration
synergistic
ferroptosis–starvation
anticancer
therapy.
The
GOx
can
catalyze
generate
sufficient
therapy,
the
consumption
caused
utilized
as
another
attractive
treatment
called
starvation
When
reached
sites,
high
concentration
of
GSH
reduced
Fe3+
trigger
structure
collapse
MOF
release
Fe2+
catalyzed
oxidation
H2O2.
Then
Fenton
reaction
happened
between
produce
hydroxyl
radicals
(•OH)
promoted
With
these
reactions,
was
realized.
Furthermore,
membrane
endows
homologous
targeting
immune
escaping
ability,
which
facilitated
accumulate
into
site
with
efficiency.
exhibits
efficiency
suppression
situ
consumed
produced
compounds,
promote
development
precise
cooperative
spatiotemporal
controllability.
Abstract
Cryopreservation
technology
has
developed
into
a
fundamental
and
important
supporting
method
for
biomedical
applications
such
as
cell‐based
therapeutics,
tissue
engineering,
assisted
reproduction,
vaccine
storage.
The
formation,
growth,
recrystallization
of
ice
crystals
are
the
major
limitations
in
cell/tissue/organ
cryopreservation,
cause
fatal
cryoinjury
to
cryopreserved
biological
samples.
Flourishing
anti‐icing
materials
strategies
can
effectively
regulate
suppress
crystals,
thus
reducing
damage
promoting
cryopreservation
efficiency.
This
review
first
describes
basic
cryodamage
mechanisms
process.
recent
development
chemical
ice‐inhibition
molecules,
including
cryoprotectant,
antifreeze
protein,
synthetic
polymer,
nanomaterial,
hydrogel,
their
summarized.
advanced
engineering
strategies,
trehalose
delivery,
cell
encapsulation,
bioinspired
structure
design
inhibition,
further
discussed.
Furthermore,
external
physical
field
technologies
used
inhibiting
both
cooling
thawing
processes
systematically
reviewed.
Finally,
current
challenges
future
perspectives
inhibition
high‐efficiency
proposed.
Nature Communications,
Год журнала:
2021,
Номер
12(1)
Опубликована: Сен. 30, 2021
Cell
membrane
coated
nanoparticles
(NPs)
have
recently
been
recognized
as
attractive
nanomedical
tools
because
of
their
unique
properties
such
immune
escape,
long
blood
circulation
time,
specific
molecular
recognition
and
cell
targeting.
However,
the
integrity
coating
on
NPs,
a
key
metrics
related
to
quality
these
biomimetic-systems
resulting
biomedical
function,
has
remained
largely
unexplored.
Here,
we
report
fluorescence
quenching
assay
probe
coating.
In
contradiction
common
assumption
perfect
coating,
uncover
that
up
90%
biomimetic
NPs
are
only
partially
coated.
Using
in
vitro
homologous
targeting
studies,
demonstrate
could
still
be
internalized
by
target
cells.
By
combining
simulations
with
experimental
analysis,
further
identify
an
endocytic
entry
mechanism
for
NPs.
We
unravel
high
degree
(≥50%)
enter
cells
individually,
whereas
low
(<50%)
need
aggregate
together
before
internalization.
This
quantitative
method
fundamental
understanding
how
will
enhance
rational
designing
nanosystems
pave
way
more
effective
cancer
nanomedicine.