Advanced Healthcare Materials,
Год журнала:
2024,
Номер
14(1)
Опубликована: Ноя. 14, 2024
Abstract
Tirapazamine
(TPZ),
an
antitumor
prodrug,
can
be
activated
in
hypoxic
environment.
It
specifically
targets
the
microenvironment
of
tumors
and
produces
toxic
free
radicals.
However,
due
to
tumor
is
not
completely
hypoxic,
TPZ
often
fails
effectively
treat
entire
tissue,
resulting
suboptimal
therapeutic
outcomes.
Herein,
a
low
pathogenic
Escherichia
coli
TOP10
utilized
selectively
colonize
tissues,
disrupt
blood
vessels,
induce
thrombus
formation,
leading
expansion
region
improving
effect
TPZ.
Additionally,
thermosensitive
hydrogel
constructed
by
Pluronic
F‐127
(F127),
which
undergoes
gelation
situ
at
site,
sustained
release
To
monitor
process,
it
genetically
modified
integrating
bioluminescent
system
luxCDABE
(TOP10‐Lux).
The
signal
associated
with
hypoxia
enhancement
beneficial
for
monitoring
bioluminescence
imaging.
In
murine
colon
cancer
model,
TOP10‐Lux
combined
TPZ‐loaded
F127
suppressed
growth,
treatment
process
efficiently
monitored.
Together,
this
work
employs
enhance
efficacy
providing
effective
strategy
bacteria‐based
tumor‐targeted
chemotherapy
monitoring.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Март 25, 2023
Abstract
Nanomedicine
holds
great
promise
to
enhance
cancer
therapy.
However,
low
active
pharmaceutical
ingredient
(API)
loading
content,
unpredictable
drug
release,
and
potential
toxicity
from
excipients
limit
their
translational
capability.
We
herein
report
a
full-API
nanodrug
composed
of
FDA-approved
5-aminolevulinic
acid
(ALA),
human
essential
element
Fe
3+
,
natural
bioactive
compound
curcumin
with
an
ideal
API
content
pH-responsive
release
profile
for
continuous
spatiotemporal
therapy
achieved
by
multi-step
tandem
endogenous
biosynthesis.
First,
ALA
enzymatically
converts
into
photosensitizer
protoporphyrin
IX
(PpIX).
Afterward,
multiple
downstream
products
including
carbon
monoxide
(CO),
2+
biliverdin
(BV),
bilirubin
(BR)
are
individually
biosynthesized
through
the
PpIX-heme-CO/Fe
/BV-BR
metabolic
pathway,
further
cooperating
released
curcumin,
ultimately
eliciting
mitochondria
damage,
membrane
disruption,
intracytoplasmic
injury.
This
work
not
only
provides
paradigm
exploiting
diversified
metabolites
tumor
suppression,
but
also
presents
safe
efficient
nanodrug,
facilitating
practical
translation
nanodrugs.
Journal of Nanobiotechnology,
Год журнала:
2023,
Номер
21(1)
Опубликована: Ноя. 6, 2023
Pancreatic
cancer
is
a
highly
aggressive
malignancy
with
limited
treatment
options
and
poor
prognosis.
Trophoblast
cell
surface
antigen
2
(TROP2),
overexpressed
in
the
tumors
of
more
than
half
pancreatic
patients,
has
been
identified
as
potential
target
for
antibody-drug
conjugates
(ADCs).
Almost
all
reported
TROP2-targeted
ADCs
are
IgG
type
have
poorly
studied
cancer.
Here,
we
aimed
to
develop
novel
nanobody-drug
conjugate
(NDC)
targeting
TROP2
cancer.In
this
study,
developed
NDC,
HuNbTROP2-HSA-MMAE,
TROP2-positive
HuNbTROP2-HSA-MMAE
characterized
by
use
nanobodies
against
human
serum
albumin
(HSA)
drug-antibody
ratio
1.
exhibited
specific
binding
was
internalized
into
tumor
cells
high
endocytosis
efficiency
within
5
h,
followed
intracellular
translocation
lysosomes
release
MMAE
induce
apoptosis
through
caspase-3/9
pathway.
In
xenograft
model
cancer,
doses
0.2
mg/kg
1
demonstrated
significant
antitumor
effects,
dose
even
eradicated
tumor.HuNbTROP2-HSA-MMAE
desirable
affinity,
internalization
activity.
It
holds
promise
therapeutic
option
Self-assembled
prodrug
nanoparticles
with
tumor-responsive
capacity
have
great
potential
in
tumor
visualization
and
treatment.
However,
the
nanoparticle
formulas
usually
contain
multiple
components,
especially
polymeric
materials,
which
result
various
issues.
Herein,
we
report
an
indocyanine
green
(ICG)-driven
assembly
of
paclitaxel
prodrugs
integrating
near-infrared
fluorescence
imaging
tumor-specific
chemotherapy.
By
feat
hydrophilic
merit
ICG,
dimer
could
form
more
uniformly
monodispersed
nanoparticles.
This
two-in-one
strategy
reinforces
complementary
advantages,
resulting
superior
behavior,
robust
colloidal
stability,
enhanced
accumulation
as
well
desirable
vivo
feedback
The
experiments
validated
activation
at
sites
evidenced
by
intensity,
potent
growth
suppression,
reduced
systemic
toxicity
compared
commercial
Taxol.
universality
ICG
potentiated
toward
photosensitizers
dyes
was
confirmed.
presentation
provides
deep
insight
into
feasibility
constructing
clinical-close
alternatives
for
improving
antitumor
efficacy.
Abstract
Prodrug‐based
self‐assembled
nanoparticles
(PSNs)
with
tailored
responses
to
tumor
microenvironments
show
a
significant
promise
for
chemodynamic
therapy
(CDT)
by
generating
highly
toxic
reactive
oxygen
species
(ROS).
However,
the
insufficient
level
of
intracellular
ROS
and
limited
drug
accumulation
remain
major
challenges
further
clinical
transformation.
In
this
study,
PSNs
delivery
artesunate
(ARS)
are
demonstrated
designing
pH‐responsive
ARS‐4‐hydroxybenzoyl
hydrazide
(HBZ)‐5‐amino
levulinic
acid
(ALA)
(AHA
NPs)
self‐supplied
excellent
chemotherapy
CDT.
The
greatly
improved
loading
capacity
generation
from
endoperoxide
bridge
using
electron
withdrawing
group
attached
directly
C10
site
artesunate.
ALA
ARS‐HBZ
could
be
released
AHA
NPs
under
cleavage
hydrazone
bonds
triggered
acidic
surroundings.
Besides,
increased
heme
in
mitochondria,
promoting
lipid
peroxidation
anti‐tumor
effects.
Our
study
ARS
through
chemical
modification,
pointing
out
potential
applications
fields.
International Journal of Nanomedicine,
Год журнала:
2024,
Номер
Volume 19, С. 1867 - 1886
Опубликована: Фев. 1, 2024
Abstract:
Although
the
frequency
of
bone
metastases
from
breast
cancer
has
increased,
effective
treatment
is
lacking,
prompting
development
nanomedicine,
which
involves
use
nanotechnology
for
disease
diagnosis
and
treatment.
Nanocarrier
drug
delivery
systems
offer
several
advantages
over
traditional
methods,
such
as
higher
reliability
biological
activity,
improved
penetration
retention,
precise
targeting
delivery.
Various
nanoparticles
that
can
selectively
target
tumor
cells
without
causing
harm
to
healthy
or
organs
have
been
synthesized.
Recent
advances
in
enabled
prevention
metastatic
diseases
well
ability
deliver
complex
molecular
"cargo"
particles
regions.
Nanoparticles
modulate
systemic
biodistribution
enable
targeted
accumulation
therapeutic
agents.
Several
strategies
are
used
treat
metastases,
including
untargeted
delivery,
bone-targeted
cell-targeted
Combining
agents
with
enhances
selective
payloads
lesions,
providing
multiple
In
this
review,
we
describe
recent
nanoparticle
treating
metastases.
Keywords:
cancer,
metastasis,
nanoparticle,
Advanced Functional Materials,
Год журнала:
2024,
Номер
34(30)
Опубликована: Март 21, 2024
Abstract
The
combination
of
chemotherapy
and
immunotherapy
holds
great
potential
in
clinical
treatment
advanced
cancers.
Whereas,
the
therapeutic
outcome
chemotherapeutic
immune
regulator
is
suboptimal
due
to
their
poor
tumor
availability
severe
off‐target
toxicity.
Herein,
self‐carrier
nanoparticles
(PSMT
NPs)
integrating
a
paclitaxel
(PTX)
prodrug
indoleamine
2,3‐dioxygenase
1
(IDO)
inhibitor
(1‐methyl‐tryptophan,
1MT)
for
tumor‐specific
chemo‐immunotherapy
constructed.
After
internalization
by
cancer
cells,
PSMT
NPs
can
respond
endogenous
redox
stimulus,
release
PTX
1MT.
released
not
only
promote
cell
apoptosis
via
intervention
mitosis
but
also
initiate
immunogenic
death
facilitate
recruitment
activation
tumor‐infiltrating
cytotoxic
T
lymphocytes.
concomitant
1MT
inhibit
IDO
activity
exhaust
regulatory
thereby
synergistically
activating
exhibit
potentiated
antitumor
output
toward
triple‐negative
breast
negligible
systemic
This
facile
versatile
nanoplatform
provides
promising
strategy
cooperatively
activate
immunity
chemo‐immunotherapy.
ACS Applied Bio Materials,
Год журнала:
2024,
Номер
7(8), С. 5121 - 5135
Опубликована: Июль 23, 2024
Indocyanine
green
J-aggregates
(ICG-Jagg)
have
emerged
as
a
significant
subject
of
interest
in
biomedical
applications
due
to
their
unique
optical
properties,
tunable
size,
and
excellent
biocompatibility.
This
comprehensive
review
aims
provide
an
in-depth
exploration
ICG-Jagg,
with
focus
on
elucidating
the
diverse
facets
preparation
factors
that
influence
process.
Additionally,
discusses
diagnostics,
such
imaging
contrast
agents,
well
utilization
drug
delivery
various
phototherapeutic
interventions.
Engineering
advanced
therapeutic
and
diagnostic
nano-bio-platforms
(NBPFs)
have
emerged
as
rapidly-developed
pathways
against
a
wide
range
of
challenges
in
antitumor,
antipathogen,
tissue
regeneration,
bioimaging,
biosensing
applications.
Emerged
2D
materials
attracted
extensive
scientific
interest
fundamental
building
blocks
or
nanostructures
among
material
scientists,
chemists,
biologists,
doctors
due
to
their
advantageous
physicochemical
biological
properties.
This
timely
review
provides
comprehensive
summary
creating
NBPFs
via
emerging
(2D-NBPFs)
with
unique
insights
into
the
corresponding
molecularly
restructured
microenvironments
biofunctionalities.
First,
it
is
focused
on
an
up-to-date
overview
synthetic
strategies
for
designing
2D-NBPFs
cross-comparison
advantages
disadvantages.
After
that,
recent
key
achievements
are
summarized
tuning
biofunctionalities
programmed
microenvironments,
including
physiological
stability,
biocompatibility,
bio-adhesiveness,
specific
binding
pathogens,
broad-spectrum
pathogen
inhibitors,
stimuli-responsive
systems,
enzyme-mimetics.
Moreover,
representative
applications
also
discussed
detailed
disclosure
critical
design
principles
parameters.
Finally,
current
future
research
directions
discussed.
Overall,
this
will
provide
cutting-edge
multidisciplinary
guidance
accelerating
developments
therapeutic/diagnostic
2D-NBPFs.