Chemical Society Reviews,
Journal Year:
2020,
Volume and Issue:
49(24), P. 9057 - 9094
Published: Jan. 1, 2020
This
review
provides
a
comprehensive
overview
of
the
recent
advances
in
nanoplatform-based
cascade
engineering
for
cancer
therapy,
by
concentrating
on
design
smart
nanoplatforms
and
implementation
specific
processes.
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.
Chemical Society Reviews,
Journal Year:
2021,
Volume and Issue:
50(16), P. 9152 - 9201
Published: Jan. 1, 2021
Photodynamic
therapy
(PDT)
has
been
extensively
investigated
for
decades
tumor
treatment
because
of
its
non-invasiveness,
spatiotemporal
selectivity,
lower
side-effects,
and
immune
activation
ability.
Accounts of Chemical Research,
Journal Year:
2020,
Volume and Issue:
53(4), P. 752 - 762
Published: Feb. 6, 2020
Cancer
therapy
is
routinely
performed
in
the
clinic
to
cure
cancer
and
control
its
progression,
wherein
therapeutic
agents
are
generally
used.
To
reduce
side
effects,
protherapeutic
that
can
be
activated
by
overexpressed
biomarkers
under
development.
However,
these
still
face
certain
extent
of
off-target
activation
normal
tissues,
stimulating
interest
design
external-stimuli
activatable
protherapeutics.
In
this
regard,
photoactivatable
have
been
utilized
for
treatments.
because
intrinsic
features
photolabile
moieties,
most
only
respond
ultraviolet-visible
light,
limiting
their
vivo
applications.
Thus,
near-infrared
(NIR)
light
with
minimal
phototoxicity
increased
tissue
penetration
highly
desired.In
Account,
we
summarize
our
semiconducting
polymer
nanomaterials
(SPNs)
as
NIR
treatment.
SPNs
transformed
from
π-conjugated
polymers
efficiently
convert
into
heat
or
singlet
oxygen
(1O2).
With
photothermal
photodynamic
properties,
directly
used
photomedicine
serve
transducers
activate
1O2-responsive
agents.The
heat-activatable
SPN-based
developed
loading
conjugating
(e.g.,
agonist,
gene,
enzyme).
For
instance,
photothermally
triggered
release
agonists
specifically
activates
protein
ion
channels
on
cellular
membrane,
leading
overinflux
induced
mitochondria
dysfunction
consequently
apoptosis
cells.
Moreover,
temperature-sensitive
bromelain
promote
situ
degradation
collagens
(the
major
components
extracellular
matrix),
resulting
an
improved
accumulation
tumor
tissues
thus
amplified
outcome.The
1O2-activatable
constructed
through
covalent
conjugation
caged
via
hypoxia-
1O2-cleavable
linkers.
Upon
photoirradiation,
consume
generate
1O2,
which
leads
(PDT),
meanwhile
breaks
linkers
on-demand
molecules
chemodrug,
enzyme,
inhibitor).
Such
remote
applied
induce
DNA
damage,
ribonucleic
acid
degradation,
inhibition
biosynthesis,
immune
system
tumors
living
animals.
By
synergizing
PDT
photoactivation
those
biological
actions,
effectively
eliminate
even
fully
inhibit
metastasis.This
Account
highlights
potential
construction
versatile
protherapeutics
treat
at
designated
times
locations
high
outcome
precision.
Journal of the American Chemical Society,
Journal Year:
2020,
Volume and Issue:
142(8), P. 3939 - 3946
Published: Jan. 23, 2020
Metal-organic
frameworks
(MOFs)
have
shown
great
potential
as
nanophotosensitizers
(nPSs)
for
photodynamic
therapy
(PDT).
The
use
of
such
MOFs
in
PDT,
however,
is
limited
by
the
shallow
depth
tissue
penetration
short-wavelength
light
and
oxygen-dependent
mechanism
that
renders
it
inadequate
hypoxic
tumors.
Here,
to
combat
limitations,
we
rationally
designed
core-shell
upconversion
nanoparticle@porphyrinic
(UCSs)
combinational
against
UCSs
were
synthesized
high
yield
through
conditional
surface
engineering
UCNPs
subsequent
seed-mediated
growth
strategy.
heterostructure
allows
efficient
energy
transfer
from
UCNP
core
MOF
shell,
which
enables
near-infrared
(NIR)
light-triggered
production
cytotoxic
reactive
oxygen
species.
A
hypoxia-activated
prodrug
tirapazamine
(TPZ)
was
encapsulated
nanopores
shell
heterostructures
final
construct
TPZ/UCSs.
We
demonstrated
TPZ/UCSs
represent
a
promising
system
achieving
improved
cancer
treatment
vitro
vivo
via
combination
NIR
light-induced
PDT
chemotherapy.
Furthermore,
integration
nanoplatform
with
antiprogrammed
death-ligand
1
(α-PD-L1)
promotes
abscopal
effect
completely
inhibit
untreated
distant
tumors
generating
specific
tumor
infiltration
T
cells.
Collectively,
this
work
highlights
robust
combining
chemotherapy
immunotherapy
current
limitations
treatment.
Theranostics,
Journal Year:
2021,
Volume and Issue:
12(1), P. 434 - 458
Published: Dec. 15, 2021
Cancer
immunotherapy
has
made
tremendous
clinical
progress
in
advanced-stage
malignancies.
However,
patients
with
various
tumors
exhibit
a
low
response
rate
to
because
of
powerful
immunosuppressive
tumor
microenvironment
(TME)
and
insufficient
immunogenicity
tumors.
Photodynamic
therapy
(PDT)
can
not
only
directly
kill
cells,
but
also
elicit
immunogenic
cell
death
(ICD),
providing
antitumor
immunity.
Unfortunately,
limitations
from
the
inherent
nature
complex
TME
significantly
reduce
efficiency
PDT.
Recently,
smart
nanomedicine-based
strategies
could
subtly
modulate
pharmacokinetics
therapeutic
compounds
optimize
both
PDT
immunotherapy,
resulting
an
improved
effect.
Here,
emerging
nanomedicines
for
PDT-driven
cancer
are
reviewed,
including
hypoxia-reversed
nanomedicines,
nanosized
metal-organic
frameworks,
subcellular
targeted
nanoparticles
(NPs).
Moreover,
we
highlight
synergistic
nanotherapeutics
used
amplify
immune
responses
combined
against
Lastly,
challenges
future
expectations
field
discussed.
Journal of the American Chemical Society,
Journal Year:
2020,
Volume and Issue:
142(11), P. 5380 - 5388
Published: Feb. 27, 2020
Tumor
hypoxia
has
proven
to
be
the
major
bottleneck
of
photodynamic
therapy
(PDT)
clinical
transformation.
Different
from
traditional
O2
delivery
approaches,
here
we
describe
an
innovative
binary
O2-economizer
(PDOE)
tactic
reverse
hypoxia-driven
resistance
by
designing
a
superoxide
radical
(O2•–)
generator
targeting
mitochondria
respiration,
termed
SORgenTAM.
This
PDOE
system
is
able
block
intracellular
consumption
and
down-regulate
HIF-1α
expression,
which
successfully
rescues
cancer
cells
becoming
hypoxic
relieves
intrinsic
burden
tumors
in
vivo,
thereby
sparing
sufficient
endogenous
for
PDT
process.
Photosensitization
mechanism
studies
demonstrate
that
SORgenTAM
ideal
intersystem
crossing
rate
triplet
excited
state
lifetime
generating
O2•–
through
type-I
photochemistry,
generated
can
further
trigger
biocascade
reduce
PDT's
demand
O2-recycble
manner.
Furthermore,
also
serves
activate
AMPK
metabolism
signaling
pathway
inhibit
cell
repair
promote
death.
Consequently,
using
this
two-step
O2-economical
strategy,
under
relatively
low
light
dose
irradiation,
excellent
therapeutic
responses
toward
are
achieved.
study
offers
conceptual
while
practical
paradigm
overcoming
pitfalls
phototherapeutics.
Angewandte Chemie International Edition,
Journal Year:
2019,
Volume and Issue:
58(36), P. 12680 - 12687
Published: July 6, 2019
Abstract
In
this
study,
an
organic
semiconducting
pro‐nanostimulant
(OSPS)
with
a
near‐infrared
(NIR)
photoactivatable
immunotherapeutic
action
for
synergetic
cancer
therapy
is
presented.
OSPS
comprises
polymer
nanoparticle
(SPN)
core
and
immunostimulant
conjugated
through
singlet
oxygen
(
1
O
2
)
cleavable
linkers.
Upon
NIR
laser
irradiation,
generates
both
heat
to
exert
combinational
phototherapy
not
only
ablate
tumors
but
also
produce
tumor‐associated
antigens.
More
importantly,
irradiation
triggers
the
cleavage
of
‐cleavable
linkers,
triggering
remote
release
immunostimulants
from
modulate
immunosuppressive
tumor
microenvironment.
Thus,
released
antigens
in
conjunction
activated
induce
synergistic
antitumor
immune
response
after
OSPS‐mediated
phototherapy,
resulting
inhibited
growth
primary/distant
lung
metastasis
mouse
xenograft
model,
which
observed
sole
phototherapy.
Advanced Materials,
Journal Year:
2020,
Volume and Issue:
33(4)
Published: Dec. 16, 2020
Abstract
Immunotherapy
has
offered
new
treatment
options
for
cancer;
however,
the
therapeutic
benefits
are
often
modest
and
desired
to
be
improved.
A
semiconducting
polymer
nanoadjuvant
(SPN
II
R)
with
a
photothermally
triggered
cargo
release
second
near‐infrared
(NIR‐II)
photothermal
immunotherapy
is
reported
here.
SPN
R
consists
of
nanoparticle
core
as
an
NIR‐II
converter,
which
doped
toll‐like
receptor
(TLR)
agonist
adjuvant
coated
thermally
responsive
lipid
shell.
Upon
photoirradiation,
effectively
generates
heat
not
only
ablate
tumors
induce
immunogenic
cell
death
(ICD),
but
also
melt
layers
on‐demand
TLR
agonist.
The
combination
ICD
activation
TLR7/TLR8
enhances
maturation
dendritic
cells,
amplifies
anti‐tumor
immune
responses.
Thus,
single
R‐mediated
inhibits
growth
both
primary
distant
eliminates
lung
metastasis
in
murine
mouse
model.
This
study
thus
provides
remote‐controlled
smart
delivery
system
synergize
photomedicine
enhanced
cancer
treatment.