Nanosonosensitizer Optimization for Enhanced Sonodynamic Disease Treatment
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 23, 2024
Low-intensity
ultrasound-mediated
sonodynamic
therapy
(SDT),
which,
by
design,
integrates
sonosensitizers
and
molecular
oxygen
to
generate
therapeutic
substances
(e.g.,
toxic
hydroxyl
radicals,
superoxide
anions,
or
singlet
oxygen)
at
disease
sites,
has
shown
enormous
potential
for
the
effective
treatment
of
a
variety
diseases.
Nanoscale
play
crucial
role
in
SDT
process
because
their
structural,
compositional,
physicochemical,
biological
characteristics
are
key
determinants
efficacy.
In
particular,
advances
materials
science
nanotechnology
have
invigorated
series
optimization
strategies
augmenting
efficacy
nanosonosensitizers.
This
comprehensive
review
systematically
summarizes,
discusses,
highlights
state-of-the-art
studies
on
current
achievements
nanosonosensitizer
enhanced
treatment,
with
an
emphasis
general
design
principles
nanosonosensitizers
strategies,
mainly
including
organic
inorganic
Additionally,
recent
advancements
optimized
applications
aimed
treating
various
diseases,
such
as
cancer,
bacterial
infections,
atherosclerosis,
autoimmune
clarified
detail.
Furthermore,
effects
improved
versatile
thoroughly
discussed.
The
concludes
highlighting
challenges
future
opportunities
this
rapidly
evolving
research
field
expedite
its
practical
clinical
translation
application.
Language: Английский
Self‐Assembled Aza‐Boron‐Dipyrromethene‐Based H2S Prodrug for Synergistic Ferroptosis‐Enabled Gas and Sonodynamic Tumor Therapies
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(30)
Published: June 13, 2024
Glioblastoma
multiforme
(GBM)
is
the
most
aggressive
and
lethal
subtype
of
gliomas
central
nervous
system.
The
efficacy
sonodynamic
therapy
(SDT)
against
GBM
significantly
reduced
by
expression
apoptosis-inhibitory
proteins
in
cells.
In
this
study,
an
intelligent
nanoplatform
(denoted
as
Aza-BD@PC
NPs)
based
on
aza-boron-dipyrromethene
dye
phenyl
chlorothionocarbonate-modified
DSPE-PEG
molecules
developed
for
synergistic
ferroptosis-enabled
gas
(GT)
SDT
GBM.
Once
internalized
cells,
NPs
showed
effective
cysteine
(Cys)
consumption
Cys-triggered
hydrogen
sulfide
(H
Language: Английский
NaHS@Cy5@MS@SP nanoparticles improve rheumatoid arthritis by inactivating the Hedgehog signaling pathway through sustained and targeted release of H2S into the synovium
Xuexue Zhu,
No information about this author
An‐Jing Xu,
No information about this author
Weiwei Cai
No information about this author
et al.
Journal of Nanobiotechnology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: March 8, 2025
Aberrant
proliferation
and
inflammation
of
fibroblast-like
synoviocytes
(FLSs)
significantly
contribute
to
the
pathogenesis
rheumatoid
arthritis
(RA).
Deficiency
hydrogen
sulfide
(H2S)
is
a
driving
force
for
development
RA,
short
half-life
H2S-releasing
donor
sodium
hydrosulfide
(NaHS)
limits
its
clinical
application
in
RA
therapy.
Designing
targeted
delivery
system
with
slow-release
properties
FLSs
could
offer
novel
strategies
treating
RA.
Herein,
we
designed
strategy
achieve
slow
release
H2S
synovium,
which
was
accomplished
by
synthesizing
NaHS-CY5@mesoporous
silic@LNP
peptide
Dil
(NaHS@Cy5@MS@SP)
nanoparticles.
Our
results
demonstrated
that
NaHS@Cy5@MS@SP
effectively
targets
FLSs,
upregulates
its-producing
enzyme
cystathionine-γ-lyase
(CSE)
joints
arthritic
mice.
Overexpression
CSE
inhibited
proliferation,
migration,
upon
lipopolysaccharide
(LPS)
exposure,
effects
were
mimicked
NaHS@Cy5@MS@SP.
In
vivo
studies
showed
achieved
threefold
higher
AUCinf
than
free
NaHS,
improving
bioavailability
NaHS.
Further,
synovial
hyperplasia
reduced
bone
cartilage
erosion
DBA/1J
mouse
model
collagen-induced
(CIA),
superior
RNA
sequencing
molecular
validated
inactivated
Hedgehog
signaling
pathway
as
evidenced
reductions
protein
expression
SHH,
SMO,
GLI1
phosphorylated
p38/MAPK.
This
study
highlights
promising
controlled
synoviocytes,
offering
potential
management.
Language: Английский
Glutathione/Cysteine Dual‐Consuming Prodrug Nanoassemblies for Potentiated Gas‐Photodynamic Therapy
Ning Tang,
No information about this author
Fan Tong,
No information about this author
Pin-Yi Wu
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 14, 2025
Abstract
Tuning
the
oxidative
stress‐defense
system
plays
a
vital
role
in
treatment
of
breast
tumors.
In
this
study,
pyropheophorbide‐a
(PPa)‐based
prodrug
nanoassembly
is
constructed
by
linking
PPa
with
furoxan,
cysteine‐depleting
nitric
oxide
(NO)
donor,
through
disulfide
bond.
The
as‐prepared
(NOSP)
can
assemble
distearoyl
phosphoethanolamine‐PEG
2000
(DSPE‐PEG
)
to
form
nanoassemblies
aqueous
media.
Following
internalization
tumor
cells,
NOSP
respond
cysteine
(Cys)
and
induce
NO
release
activate
endogenous
matrix
metalloproteinases
(MMP‐1,
‐2),
leading
collagen
degradation
improved
drug
delivery.
addition,
Cys
consumption
impede
biosynthesis
glutathione
(GSH),
while
react
high
levels
intracellular
GSH
within
seconds,
thus
synergizing
photodynamic
therapy
against
tumors
distant
metastasis.
Language: Английский
A General Strategy for Tumor-Specific In Situ Synthesis of Copper Sulfide for Gas Therapy and Surface Plasmon Resonance Enhanced Phototherapy
Wei Cheng,
No information about this author
Ying Wu,
No information about this author
Bowen Li
No information about this author
et al.
ACS Materials Letters,
Journal Year:
2024,
Volume and Issue:
7(1), P. 181 - 192
Published: Dec. 9, 2024
Language: Английский
ROS Regulation in CNS Disorder Therapy: Unveiling the Dual Roles of Nanomedicine
Zhengyang Quan,
No information about this author
Sa Wang,
No information about this author
Huanhuan Xie
No information about this author
et al.
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 15, 2024
Abstract
The
treatment
of
brain
diseases
has
always
been
the
focus
attention.
Due
to
presence
blood‐brain
barrier
(BBB),
most
small
molecule
drugs
are
difficult
reach
brain,
leading
undesirable
therapeutic
outcomes.
Recently,
nanomedicines
that
can
cross
BBB
and
precisely
target
lesion
sites
have
emerged
as
thrilling
tools
enhance
early
diagnosis
treat
various
intractable
disorders.
Extensive
research
shown
reactive
oxygen
species
(ROS)
play
a
crucial
role
in
occurrence
progression
diseases,
including
tumors
neurodegenerative
(NDDs)
such
Alzheimer's
disease,
Parkinson's
stroke,
or
traumatic
injury,
making
ROS
potential
target.
In
this
review,
on
structure
function
well
mechanisms
first
elaborated
through
which
nanomedicine
traverses
it.
Then,
recent
studies
production
summarized
photodynamic
therapy
(PDT),
chemodynamic
(CDT),
sonodynamic
(SDT)
for
treating
tumors,
depletion
NDDs.
This
provides
valuable
guidance
future
design
ROS‐targeted
disease
treatment.
ongoing
challenges
perspectives
developing
nanomedicine‐based
management
also
discussed
outlined.
Language: Английский