Advanced Functional Materials,
Journal Year:
2019,
Volume and Issue:
29(50)
Published: Oct. 7, 2019
Abstract
Fe‐based
Fenton
agents
can
generate
highly
reactive
and
toxic
hydroxyl
radicals
(·OH)
in
the
tumor
microenvironment
(TME)
for
chemodynamic
therapy
(CDT)
with
high
specificity.
However,
strict
condition
(lower
pH
environment:
3–4)
of
efficient
reaction
limits
its
practical
application
clinic.
Development
new
CDT
more
suitable
TME
is
significant
challenging.
A
Cu(I)‐based
agent,
copper(I)
phosphide
nanocrystals
(CP
NCs),
which
adaptable
to
value
than
agents,
thereby
producing
·OH
trigger
apoptosis
cancer
cells,
prepared.
Moreover,
excess
glutathione
(GSH)
reduce
Cu(II)
produced
by
a
Fenton‐like
Cu(I),
further
increasing
generation
rate
relieving
antioxidant
ability.
Furthermore,
owing
their
strong
absorption
NIR
II
region,
CP
NCs
exhibit
an
excellent
photothermal
conversion
effect,
improve
reaction.
What
more,
act
as
situ
self‐generation
magnetic
resonance
imaging
(MRI)
paramagnetic
response
H
2
O
TME.
These
properties
may
open
up
exploration
copper‐based
materials
clinical
imaging‐guided
synergetic
treatment.
Advanced Materials,
Journal Year:
2021,
Volume and Issue:
33(7)
Published: Jan. 4, 2021
Chemodynamic
therapy
(CDT)
is
an
emerging
method
that
kills
cancer
cells
by
converting
intracellular
hydrogen
peroxide
(H2
O2
)
into
highly
toxic
hydroxyl
radicals
(•
OH).
To
overcome
the
current
limitations
of
insufficient
endogenous
H2
and
high
concentration
glutathione
(GSH)
in
tumor
cells,
intelligent
nanocatalytic
theranostics
(denoted
as
PGC-DOX)
possesses
both
self-supply
GSH-elimination
properties
for
efficient
presented.
This
nanoplatform
constructed
a
facile
one-step
biomineralization
using
poly(ethylene
glycol)-modified
glucose
oxidase
(GOx)
template
to
form
biodegradable
copper-doped
calcium
phosphate
nanoparticles,
followed
loading
doxorubicin
(DOX).
As
enzyme
catalyst,
GOx
can
effectively
catalyze
generate
,
which
not
only
starves
but
also
supplies
subsequent
Fenton-like
reaction.
Meanwhile,
redox
reaction
between
released
Cu2+
ions
GSH
will
induce
depletion
reduce
Fenton
agent
Cu+
ions,
then
trigger
•
OH
-mediated
reaction,
resulting
enhanced
CDT
efficacy.
The
integration
GOx-mediated
starvation
therapy,
CDT,
DOX-induced
chemotherapy,
endow
PGC-DOX
with
effective
growth
inhibition
minimal
side
effects
vivo.
Chemical Reviews,
Journal Year:
2021,
Volume and Issue:
121(4), P. 1981 - 2019
Published: Jan. 25, 2021
Since
the
first
connection
between
Fenton
chemistry
and
biomedicine,
numerous
studies
have
been
presented
in
this
field.
Comprehensive
presentation
of
guidance
from
a
summary
its
representative
applications
cancer
therapy
would
help
us
understand
promote
further
development
This
comprehensive
review
supplies
basic
information
regarding
chemistry,
including
reactions
Fenton-like
reactions.
Subsequently,
current
progress
is
discussed,
with
some
corresponding
examples
presented.
Furthermore,
strategies
for
optimizing
performance
chemodynamic
guided
by
are
highlighted.
Most
importantly,
future
perspectives
on
combination
biomedicine
or
wider
range
catalytic
approaches
We
hope
that
will
attract
positive
attention
materials
science,
fields
tighten
their
connections.
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.
Journal of the American Chemical Society,
Journal Year:
2020,
Volume and Issue:
142(11), P. 5177 - 5183
Published: Feb. 26, 2020
The
insufficient
intracellular
H2O2
level
in
tumor
cells
is
closely
associated
with
the
limited
efficacy
of
chemodynamic
therapy
(CDT).
Despite
tremendous
efforts,
engineering
CDT
agents
a
straightforward
and
secure
supplying
ability
remains
great
challenge.
Inspired
by
balance
generation
elimination
cancer
cells,
herein,
nanozyme-based
homeostasis
disruptor
fabricated
to
elevate
through
facilitating
production
restraining
for
enhanced
CDT.
In
formulation,
superoxide
dismutase-mimicking
activity
can
convert
O2•–
H2O2,
promoting
H2O2.
Simultaneously,
suppression
catalase
depletion
glutathione
weaken
transformation
H2O.
Thus,
well-defined
system
could
perturb
give
rise
accumulation
cells.
raised
would
ultimately
amplify
Fenton-like
reaction-based
efficiency.
Our
work
not
only
paves
way
engineer
alternative
intensive
but
also
provides
new
insights
into
construction
bioinspired
materials.
Theranostics,
Journal Year:
2020,
Volume and Issue:
10(10), P. 4557 - 4588
Published: Jan. 1, 2020
In
recent
years,
much
progress
has
been
motivated
in
stimuli-responsive
nanocarriers,
which
could
response
to
the
intrinsic
physicochemical
and
pathological
factors
diseased
regions
increase
specificity
of
drug
delivery.
Currently,
numerous
nanocarriers
have
engineered
with
changes
responding
external
stimuli,
such
as
ultrasound,
thermal,
light
magnetic
field,
well
internal
including
pH,
redox
potential,
hypoxia
enzyme,
etc.
Nanocarriers
respond
stimuli
tumor
microenvironments
or
inside
cancer
cells
for
on-demanded
delivery
accumulation,
controlled
release,
activation
bioactive
compounds,
probes
targeting
ligands,
size,
charge
conformation
conversion,
etc.,
leading
sensing
signaling,
overcoming
multidrug
resistance,
accurate
diagnosis
precision
therapy.
This
review
summarized
general
strategies
developing
advances,
presented
their
applications
delivery,
imaging,
therapy
theranostics,
illustrated
clinical
translation
made
prospects.
Nature Communications,
Journal Year:
2020,
Volume and Issue:
11(1)
Published: April 8, 2020
Abstract
The
therapeutic
effect
of
reactive
oxygen
species
(ROS)-involved
cancer
therapies
is
significantly
limited
by
shortage
oxy-substrates,
such
as
hypoxia
in
photodynamic
therapy
(PDT)
and
insufficient
hydrogen
peroxide
(H
2
O
)
chemodynamic
(CDT).
Here,
we
report
a
H
/O
self-supplying
nanoagent,
(MSNs@CaO
-ICG)@LA,
which
consists
manganese
silicate
(MSN)-supported
calcium
(CaO
indocyanine
green
(ICG)
with
further
surface
modification
phase-change
material
lauric
acid
(LA).
Under
laser
irradiation,
ICG
simultaneously
generates
singlet
emits
heat
to
melt
the
LA.
exposed
CaO
reacts
water
produce
for
hypoxia-relieved
ICG-mediated
PDT
-supplying
MSN-based
CDT,
acting
an
open
source
strategy
ROS
production.
Additionally,
MSNs-induced
glutathione
depletion
protects
from
scavenging,
termed
reduce
expenditure.
This
expenditure
effective
inhibiting
tumor
growth
both
vitro
vivo,
improves
generation
efficiency
multi-level
ROS-involved
therapies.
Small,
Journal Year:
2021,
Volume and Issue:
18(6)
Published: Nov. 2, 2021
Abstract
Chemodynamic
therapy
(CDT),
a
novel
cancer
therapeutic
strategy
defined
as
the
treatment
using
Fenton
or
Fenton‐like
reaction
to
produce
•OH
in
tumor
region,
was
first
proposed
by
Bu,
Shi,
and
co‐workers
2016.
Recently,
with
rapid
development
of
nanomaterials,
CDT
has
attracted
tremendous
attention
because
its
unique
advantages:
1)
It
is
tumor‐selective
low
side
effects;
2)
process
does
not
depend
on
external
field
stimulation;
3)
it
can
modulate
hypoxic
immunosuppressive
microenvironment;
4)
cost
low.
In
addition
Fe‐involved
strategies,
reaction‐mediated
strategies
have
also
been
proposed,
which
are
based
many
other
metal
elements
including
copper,
manganese,
cobalt,
titanium,
vanadium,
palladium,
silver,
molybdenum,
ruthenium,
tungsten,
cerium,
zinc.
Moreover,
combined
therapies
like
chemotherapy,
radiotherapy,
phototherapy,
sonodynamic
therapy,
immunotherapy
for
achieving
enhanced
anticancer
effects.
Besides,
there
studies
that
extend
application
antibacterial
field.
This
review
introduces
latest
advancements
nanomaterials‐involved
from
2018
present
proposes
current
limitations
well
future
research
directions
related
Advanced Materials,
Journal Year:
2019,
Volume and Issue:
32(6)
Published: Dec. 13, 2019
The
clinical
application
of
chemotherapy
is
impeded
by
the
unsatisfactory
efficacy
and
severe
side
effects.
Chemodynamic
therapy
(CDT)
has
emerged
as
an
efficient
strategy
for
cancer
treatment
utilizing
Fenton
chemistry
to
destroy
cells
converting
endogenous
H2
O2
into
highly
toxic
reactive
oxygen
species.
Apart
from
chemotherapeutic
effect,
cisplatin
able
act
artificial
enzyme
produce
CDT
through
cascade
reactions,
thus
remarkably
improving
anti-tumor
outcomes.
Herein,
organic
theranostic
nanomedicine
(PTCG
NPs)
constructed
with
high
loading
capability
using
epigallocatechin-3-gallate
(EGCG),
phenolic
platinum(IV)
prodrug
(Pt-OH),
polyphenol
modified
block
copolymer
(PEG-b-PPOH)
building
blocks.
stability
PTCG
NPs
during
circulation
stems
their
strong
metal-polyphenol
coordination
interactions,
drug
release
realized
after
cellular
internalization.
activated
elevates
intracellular
level
reactions.
This
further
utilized
species
catalyzed
iron-based
reaction.
In
vitro
in
vivo
investigations
demonstrate
that
combination
chemodynamic
achieves
excellent
anticancer
efficacy.
Meanwhile,
systemic
toxicity
faced
platinum-based
drugs
avoided
this
nanoformulation.
work
provides
a
promising
develop
advanced
therapy.