Angewandte Chemie International Edition,
Journal Year:
2020,
Volume and Issue:
59(24), P. 9491 - 9497
Published: Feb. 26, 2020
Abstract
Chaos
and
the
natural
evolution
of
tumor
systems
can
lead
to
failure
therapies.
Herein,
we
demonstrate
that
iridium
oxide
nanoparticles
(IrO
x
)
possess
acid‐activated
oxidase
peroxidase‐like
functions
wide
pH‐dependent
catalase‐like
properties.
The
integration
glucose
(GOD)
unlocked
peroxidase
activities
IrO
by
production
gluconic
acid
from
GOD
catalysis
in
cancer
cells,
produced
H
2
O
was
converted
into
compensate
its
consumption
owing
function
nanozyme,
thus
resulting
continual
self‐supply
substrates
generate
superoxide
anion
hydroxyl
radical.
Moreover,
constantly
consume
glutathione
(GSH)
self‐cyclic
valence
alternation
Ir
IV
III
.
These
cascade
reactions
a
“butterfly
effect”
initial
starvation
therapy
subsequent
pressure
multiple
reactive
oxygen
species
(ROS)
completely
break
self‐adaption
cells.
Chemical Society Reviews,
Journal Year:
2020,
Volume and Issue:
50(2), P. 1111 - 1137
Published: Nov. 27, 2020
This
review
summarizes
the
recent
development
of
second
near-infrared
photothermal
combinational
nanotheranostics
for
cancer,
infectious
diseases
and
regenerative
medicine.
Angewandte Chemie International Edition,
Journal Year:
2021,
Volume and Issue:
60(23), P. 12971 - 12979
Published: March 27, 2021
Abstract
Photothermal
therapy
(PTT)
is
an
extremely
promising
tumor
therapeutic
modality.
However,
excessive
heat
inevitably
injures
normal
tissues
near
tumors,
and
the
damage
to
cancer
cells
caused
by
mild
hyperthermia
easily
repaired
stress‐induced
shock
proteins
(HSPs).
Thus,
maximizing
PTT
efficiency
minimizing
healthy
simultaneously
adopting
appropriate
temperatures
imperative.
Herein,
innovative
strategy
reported:
ferroptosis‐boosted
based
on
a
single‐atom
nanozyme
(SAzyme).
The
Pd
SAzyme
with
atom‐economical
utilization
of
catalytic
centers
exhibits
peroxidase
(POD)
glutathione
oxidase
(GSHOx)
mimicking
activities,
photothermal
conversion
performance,
which
can
result
in
ferroptosis
featuring
up‐regulation
lipid
peroxides
(LPO)
reactive
oxygen
species
(ROS).
accumulation
LPO
ROS
provides
powerful
approach
for
cleaving
HSPs,
enables
SAzyme‐mediated
mild‐temperature
PTT.
Chemical Society Reviews,
Journal Year:
2021,
Volume and Issue:
50(10), P. 6013 - 6041
Published: Jan. 1, 2021
In
this
review,
we
systematically
survey
the
most
recent
progress
in
engineering
nanomedicine
for
intracellular
glutathione
consumption-augmented
cancer
therapy.
Advanced Materials,
Journal Year:
2020,
Volume and Issue:
32(42)
Published: Sept. 11, 2020
Abstract
Nanocatalytic
therapy,
using
artificial
nanoscale
enzyme
mimics
(nanozymes),
is
an
emerging
technology
for
therapeutic
treatment
of
various
malignant
tumors.
However,
the
relatively
deficient
catalytic
activity
nanozymes
in
tumor
microenvironment
(TME)
restrains
their
biomedical
applications.
Here,
a
versatile
and
bacteria‐like
PEG/Ce‐Bi@DMSN
nanozyme
developed
by
coating
uniform
Bi
2
S
3
nanorods
(NRs)
with
dendritic
mesoporous
silica
(Bi
@DMSN)
then
decorating
ultrasmall
ceria
into
large
mesopores
@DMSN.
The
exhibit
dual
enzyme‐mimic
activities
(peroxidase‐mimic
catalase‐mimic)
under
acidic
conditions
that
can
regulate
TME,
is,
simultaneously
elevate
oxidative
stress
relieve
hypoxia.
In
addition,
effectively
consume
overexpressed
glutathione
(GSH)
through
redox
reaction.
Photothermal
therapy
(PTT)
introduced
to
synergistically
improve
enzyme‐mimicking
depletion
GSH
tumors
photonic
hyperthermia.
This
achieved
taking
advantage
desirable
light
absorbance
second
near‐infrared
(NIR‐II)
window
nanozymes.
Subsequently
reactive
oxygen
species
(ROS)‐mediated
efficiency
significantly
improved.
Therefore,
this
study
provides
proof
concept
hyperthermia‐augmented
multi‐enzymatic
ablation.
ACS Nano,
Journal Year:
2021,
Volume and Issue:
15(3), P. 5735 - 5751
Published: March 11, 2021
As
next-generation
artificial
enzymes,
nanozymes
have
shown
great
promise
for
tumor
catalytic
therapy.
In
particular,
their
peroxidase-like
activity
has
been
employed
to
catalyze
hydrogen
peroxide
(H2O2)
produce
highly
toxic
hydroxyl
radicals
(•OH)
kill
cells.
However,
limited
by
the
low
affinity
between
with
H2O2
and
level
of
in
microenvironment,
peroxidase
usually
produced
insufficient
•OH
cells
therapeutic
purposes.
Herein,
we
present
a
pyrite
nanozyme
ultrahigh
affinity,
resulting
4144-
3086-fold
increase
compared
that
classical
Fe3O4
natural
horseradish
peroxidase,
respectively.
We
found
also
possesses
intrinsic
glutathione
oxidase-like
activity,
which
catalyzes
oxidation
reduced
accompanied
generation.
Thus,
dual-activity
constitutes
self-cascade
platform
generate
abundant
deplete
glutathione,
induces
apoptosis
as
well
ferroptosis
Consequently,
it
killed
apoptosis-resistant
harboring
KRAS
mutation
inducing
ferroptosis.
The
exhibited
favorable
tumor-specific
cytotoxicity
biodegradability
ensure
its
biosafety.
These
results
indicate
high-performance
is
an
effective
reagent
may
aid
development
nanozyme-based
Small,
Journal Year:
2020,
Volume and Issue:
16(22)
Published: April 27, 2020
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.
Advanced Materials,
Journal Year:
2020,
Volume and Issue:
33(4)
Published: Dec. 2, 2020
Abstract
The
past
decades
have
witnessed
hyperthermia
therapy
(HTT)
as
an
emerging
strategy
against
malignant
tumors.
Nanomaterial‐based
photothermal
(PTT)
and
magnetic
(MHT),
highly
effective
noninvasive
treatment
models,
offer
advantages
over
other
strategies
in
the
of
different
types
However,
both
PTT
MHT
cannot
completely
cure
cancer
due
to
recurrence
distal
metastasis.
In
recent
years,
immunotherapy
has
attracted
widespread
attention
owing
its
capability
activate
body's
own
natural
defense
identify,
attack,
eradicate
cells.
Significant
efforts
been
devoted
studying
activated
immune
responses
caused
by
hyperthermia‐ablated
this
article,
synergistic
mechanism
HTT
immunotherapy,
including
immunogenic
cell
death
reversal
immunosuppressive
tumor
microenvironment
is
discussed.
reports
combination
or
HTT‐based
multimodal
with
immunoadjuvant
exploitation,
checkpoint
blockade
therapy,
adoptive
cellular
are
summarized.
As
highlighted,
these
could
achieve
synergistically
enhanced
therapeutic
outcomes
primary
tumors
metastatic
lesions,
prevent
recurrence,
prolong
survival
period.
Finally,
current
challenges
prospective
developments
HTT‐synergized
also
reviewed.
Advanced Materials,
Journal Year:
2021,
Volume and Issue:
33(48)
Published: Sept. 27, 2021
Chemodynamic
therapy
(CDT)
uses
the
tumor
microenvironment-assisted
intratumoral
Fenton
reaction
for
generating
highly
toxic
hydroxyl
free
radicals
(•OH)
to
achieve
selective
treatment.
However,
limited
efficiency
restricts
therapeutic
efficacy
of
CDT.
Recent
years
have
witnessed
impressive
development
various
strategies
increase
reaction.
The
introduction
these
reinforcement
can
dramatically
improve
treatment
CDT
and
further
promote
enhanced
(ECDT)-based
multimodal
anticancer
treatments.
In
this
review,
authors
systematically
introduce
strategies,
from
their
basic
working
principles,
mechanisms
representative
clinical
applications.
Then,
ECDT-based
is
discussed,
including
how
integrate
emerging
accelerating
therapy,
as
well
synergistic
ECDT
other
methods.
Eventually,
future
direction
challenges
therapies
are
elaborated,
highlighting
key
scientific
problems
unsolved
technical
bottlenecks
facilitate
translation.
Angewandte Chemie International Edition,
Journal Year:
2020,
Volume and Issue:
59(38), P. 16381 - 16384
Published: June 2, 2020
Abstract
Despite
the
widespread
applications
of
manganese
oxide
nanomaterials
(MONs)
in
biomedicine,
intrinsic
immunogenicity
MONs
is
still
unclear.
MnO
x
nanospikes
(NSs)
as
tumor
microenvironment
(TME)‐responsive
nanoadjuvants
and
immunogenic
cell
death
(ICD)
drugs
are
proposed
for
cancer
nanovaccine‐based
immunotherapy.
NSs
with
large
mesoporous
structures
show
ultrahigh
loading
efficiencies
ovalbumin
fragment.
The
combination
ICD
via
chemodynamic
therapy
ferroptosis
inductions,
well
antigen
stimulations,
presents
a
better
synergistic
immunopotentiation
action.
Furthermore,
obtained
nanovaccines
achieve
TME‐responsive
magnetic
resonance/photoacoustic
dual‐mode
imaging
contrasts,
while
effectively
inhibiting
primary/distal
growth
metastasis.