Molecular Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
21(11), P. 5864 - 5879
Published: Oct. 8, 2024
Despite
the
advancements
in
cancer
therapy,
delivering
active
pharmaceutical
ingredients
(APIs)
using
nanoparticles
remains
challenging
due
to
failed
conveyance
of
required
drug
payload,
poor
targeting
ability,
and
biodistribution,
hampering
their
clinical
translation.
Recently,
appropriate
design
materials
with
intrinsic
therapeutic
functionalities
has
garnered
enormous
interest
development
various
intelligent
nanoplatforms.
In
this
study,
we
demonstrate
fabrication
transition
metal
(molybdenum,
Mo)-doped
manganese
dioxide
(MnO2)
nanoarchitectures,
exhibiting
diagnostic
(magnetic
resonance
imaging,
MRI)
(chemodynamic
CDT)
functionalities.
The
facile
hydrothermal
approach-assisted
Mo-doped
MnO2
flower-like
nanostructures
offered
tailorable
morphologies
altered
dimensions,
precise
effects,
exceptional
biocompatibility,
biodegradability
tumor
microenvironment.
resultant
defects
doped
Mo
species
exhibited
peroxidase
oxidase
activities,
improving
glutathione
(GSH)
oxidation.
two
sets
variable
valence
ion
pairs
(Mn2+/Mn4+
Mo5+/Mo6+)
interplay
could
substantially
improve
Fenton-like
reaction
generate
toxic
hydroxyl
radicals
(•OH),
thus
achieving
CDT-assisted
antitumor
effects.
As
inherent
T1-MRI
agents,
these
displayed
excellent
MRI
efficacy
vitro.
Together,
believe
that
conformational
nanoarchitectures
states
potentiate
drugless
therapy
pharmaceutics.
ACS Applied Bio Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 8, 2025
Development
of
nanoplatforms
with
in
situ
activation
for
chemotherapy
represents
a
promising
modality
biomedical
application.
Herein,
multifunctional
nanoplatform,
CMS@DTC@PDA@RuNO@FA
(abbreviated
as
CDPNF
NPs),
was
developed
highly
efficient
antitumor
therapy,
which
diethyldithiocarbamate
(DTC)-loaded
mesoporous
Cu2MoS4
(CMS)
nanoparticles
were
covered
by
polydopamine
(PDA)
layers
and
further
covalently
modified
NO
donor
(RuNO)
folic
acid
(FA)-directing
moiety.
Under
the
mild
acidic
tumor
microenvironment
(TME),
NPs
co-liberated
DTC
Cu2+
site,
where
formation
cytotoxic
Cu(DTC)2
complex
effectively
killed
cells.
Furthermore,
under
near-infrared
(NIR)
light
irradiation,
could
deliver
nitric
oxide
(NO)
produce
superoxide
anions
(O2•-),
followed
more
toxic
peroxynitrite
(ONOO-),
led
to
promoted
cell
apoptosis.
1064
nm
NIR
vivo
experiments
demonstrated
an
impressively
high
inhibition
rate
(∼97%)
while
good
biocompatibility.
This
work
activated
approach
precision
medicine
that
might
imply
its
potential
clinical
applications.
Molecular Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
21(11), P. 5864 - 5879
Published: Oct. 8, 2024
Despite
the
advancements
in
cancer
therapy,
delivering
active
pharmaceutical
ingredients
(APIs)
using
nanoparticles
remains
challenging
due
to
failed
conveyance
of
required
drug
payload,
poor
targeting
ability,
and
biodistribution,
hampering
their
clinical
translation.
Recently,
appropriate
design
materials
with
intrinsic
therapeutic
functionalities
has
garnered
enormous
interest
development
various
intelligent
nanoplatforms.
In
this
study,
we
demonstrate
fabrication
transition
metal
(molybdenum,
Mo)-doped
manganese
dioxide
(MnO2)
nanoarchitectures,
exhibiting
diagnostic
(magnetic
resonance
imaging,
MRI)
(chemodynamic
CDT)
functionalities.
The
facile
hydrothermal
approach-assisted
Mo-doped
MnO2
flower-like
nanostructures
offered
tailorable
morphologies
altered
dimensions,
precise
effects,
exceptional
biocompatibility,
biodegradability
tumor
microenvironment.
resultant
defects
doped
Mo
species
exhibited
peroxidase
oxidase
activities,
improving
glutathione
(GSH)
oxidation.
two
sets
variable
valence
ion
pairs
(Mn2+/Mn4+
Mo5+/Mo6+)
interplay
could
substantially
improve
Fenton-like
reaction
generate
toxic
hydroxyl
radicals
(•OH),
thus
achieving
CDT-assisted
antitumor
effects.
As
inherent
T1-MRI
agents,
these
displayed
excellent
MRI
efficacy
vitro.
Together,
believe
that
conformational
nanoarchitectures
states
potentiate
drugless
therapy
pharmaceutics.