Small,
Journal Year:
2020,
Volume and Issue:
16(31)
Published: June 15, 2020
Abstract
Fenton
reaction‐mediated
chemodynamic
therapy
(CDT)
can
kill
cancer
cells
via
the
conversion
of
H
2
O
to
highly
toxic
HO•.
However,
problems
such
as
insufficient
levels
in
tumor
tissue
and
low
reaction
efficiency
severely
limit
performance
CDT.
Here,
prodrug
tirapazamine
(TPZ)‐loaded
human
serum
albumin
(HSA)–glucose
oxidase
(GOx)
mixture
is
prepared
modified
with
a
metal–polyphenol
network
composed
ferric
ions
(Fe
3+
)
tannic
acid
(TA),
obtain
self‐amplified
nanoreactor
termed
HSA–GOx–TPZ–Fe
–TA
(HGTFT)
for
sustainable
cascade
exogenous
production
TA‐accelerated
Fe
/Fe
2+
conversion.
The
HGTFT
efficiently
convert
oxygen
into
HO•
CDT,
consume
glucose
starvation
therapy,
provide
hypoxic
environment
TPZ
radical‐mediated
chemotherapy.
Besides,
it
revealed
that
significantly
elevate
intracellular
reactive
species
content
hypoxia
level,
decrease
glutathione
content,
release
metal
tumors
ion
interference
(also
“ion‐interference
therapy”
or
“metal
therapy”).
Further,
also
increase
tumor’s
level
inhibit
growth.
It
believed
this
microenvironment‐regulable
anticancer
excellent
biosafety
represents
an
advance
nanomedicine.
Chemical Reviews,
Journal Year:
2021,
Volume and Issue:
121(21), P. 13454 - 13619
Published: Sept. 28, 2021
This
review
presents
a
robust
strategy
to
design
photosensitizers
(PSs)
for
various
species.
Photodynamic
therapy
(PDT)
is
photochemical-based
treatment
approach
that
involves
the
use
of
light
combined
with
light-activated
chemical,
referred
as
PS.
Attractively,
PDT
one
alternatives
conventional
cancer
due
its
noninvasive
nature,
high
cure
rates,
and
low
side
effects.
PSs
play
an
important
factor
in
photoinduced
reactive
oxygen
species
(ROS)
generation.
Although
concept
photosensitizer-based
photodynamic
has
been
widely
adopted
clinical
trials
bioimaging,
until
now,
our
surprise,
there
no
relevant
article
on
rational
designs
organic
PDT.
Furthermore,
most
published
articles
focused
nanomaterials
nanotechnology
based
traditional
PSs.
Therefore,
this
aimed
at
reporting
recent
strategies
develop
innovative
enhanced
therapy,
each
example
described
detail
instead
providing
only
general
overview,
typically
done
previous
reviews
PDT,
provide
intuitive,
vivid,
specific
insights
readers.
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.
ACS Nano,
Journal Year:
2019,
Volume and Issue:
13(4), P. 4267 - 4277
Published: March 22, 2019
The
integration
of
reactive
oxygen
species
(ROS)-involved
photodynamic
therapy
(PDT)
and
chemodynamic
(CDT)
holds
great
promise
for
enhanced
anticancer
effects.
Herein,
we
report
biodegradable
cancer
cell
membrane-coated
mesoporous
copper/manganese
silicate
nanospheres
(mCMSNs)
with
homotypic
targeting
ability
to
the
lines
ROS
generation
through
singlet
(1O2)
production
glutathione
(GSH)-activated
Fenton
reaction,
showing
excellent
CDT/PDT
synergistic
therapeutic
We
demonstrate
that
mCMSNs
are
able
relieve
tumor
hypoxia
microenvironment
by
catalytic
decomposition
endogenous
H2O2
O2
further
react
produce
toxic
1O2
a
635
nm
laser
irradiation.
GSH-triggered
biodegradation
can
simultaneously
generate
Fenton-like
Cu+
Mn2+
ions
deplete
GSH
efficient
hydroxyl
radical
(•OH)
production.
specific
recognition
cells
were
also
revealed.
Notably,
relieving
depletion
disrupts
(TME)
cellular
antioxidant
defense
system,
achieving
exceptional
cancer-targeting
effects
in
vitro
vivo.
growth
was
significantly
inhibited.
Moreover,
released
act
as
an
advanced
contrast
agent
magnetic
resonance
imaging
(MRI).
Thus,
together
photosensitizers,
provider
MRI
along
modulating
TME
allow
realize
MRI-monitored
therapy.
It
provides
paradigm
rationally
design
TME-responsive
ROS-involved
strategies
based
on
single
polymetallic
nanomaterial
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.
Advanced Materials,
Journal Year:
2019,
Volume and Issue:
31(21)
Published: March 25, 2019
Abstract
Over
the
past
3
years,
glucose
oxidase
(GOx)
has
aroused
great
research
interest
in
context
of
cancer
treatment
due
to
its
inherent
biocompatibility
and
biodegradability,
unique
catalytic
properties
against
β‐
d
‐glucose.
GOx
can
effectively
catalyze
oxidation
into
gluconic
acid
hydrogen
peroxide.
This
process
depletes
oxygen
levels,
resulting
elevated
acidity,
hypoxia,
oxidative
stress
tumor
microenvironment.
All
these
changes
be
readily
harnessed
develop
a
multimodal
synergistic
therapy
by
combining
with
other
therapeutic
approaches.
Herein,
representative
studies
GOx‐instructed
are
introduced,
their
mechanisms
discussed
systematically.
The
current
challenges
future
prospects
advance
development
GOx‐based
nanomedicines
this
cutting‐edge
area
highlighted.
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
ACS Nano,
Journal Year:
2019,
Volume and Issue:
13(12), P. 13985 - 13994
Published: Dec. 13, 2019
Glucose
oxidase
(GOx)
has
been
recognized
as
a
"star"
enzyme
catalyst
involved
in
cancer
treatment
the
past
few
years.
Herein,
GOx
is
mineralized
with
manganese-doped
calcium
phosphate
(MnCaP)
to
form
spherical
nanoparticles
(GOx-MnCaP
NPs)
by
an
situ
biomimetic
mineralization
method,
followed
loading
of
doxorubicin
(DOX)
construct
biodegradable,
biocompatible,
and
tumor
acidity-responsive
nanotheranostics
for
magnetic
resonance
imaging
(MRI)
cascade
reaction-enhanced
cooperative
treatment.
The
GOx-driven
oxidation
reaction
can
effectively
eliminate
intratumoral
glucose
starvation
therapy,
elevated
H2O2
then
converted
into
highly
toxic
hydroxyl
radicals
via
Mn2+-mediated
Fenton-like
chemodynamic
therapy
(CDT).
Moreover,
acidity
amplification
due
gluconic
acid
generation
will
turn
accelerate
degradation
nanoplatform
promote
Mn2+-H2O2
enhanced
CDT.
Meanwhile,
released
Mn2+
ions
be
used
MRI
monitor
process.
After
carrying
anticancer
drug,
DOX-loaded
GOx-MnCaP
integrate
CDT,
DOX-induced
chemotherapy
together,
which
showed
greatly
improved
therapeutic
efficacy
than
each
monotherapy.
Such
orchestrated
demonstrated
high-efficiency
suppression
on
4T1
tumor-bearing
mice
minimal
side
effects.
Our
findings
suggested
that
excellent
biodegradability
biocompatibility
hold
clinical
translation
potential
management.