Custom‐Design of Multi‐Stimuli‐Responsive Degradable Silica Nanoparticles for Advanced Cancer‐Specific Chemotherapy
Small,
Journal Year:
2024,
Volume and Issue:
20(35)
Published: April 23, 2024
Chemotherapy
is
crucial
in
oncology
for
combating
malignant
tumors
but
often
encounters
obatacles
such
as
severe
adverse
effects,
drug
resistance,
and
biocompatibility
issues.
The
advantages
of
degradable
silica
nanoparticles
tumor
diagnosis
treatment
lie
their
ability
to
target
delivery,
minimizing
toxicity
normal
tissues
while
enhancing
therapeutic
efficacy.
Moreover,
responsiveness
both
endogenous
exogenous
stimuli
opens
up
new
possibilities
integrating
multiple
modalities.
This
review
scrutinizes
the
burgeoning
utility
combination
with
chemotherapy
other
Commencing
elucidation
synthesis
degradation
mechanisms,
emphasis
placed
on
these
materials
(e.g.,
pH,
redox
reactions,
hypoxia,
enzymes)
light
high-intensity
focused
ultrasound).
this
exploration
delves
into
strategies
harnessing
alone,
coupled
radiotherapy,
photothermal
therapy,
photodynamic
gas
immunotherapy,
starvation
chemodynamic
elucidating
multimodal
synergies.
Concluding
an
assessment
advances,
challenges,
constraints
oncology,
despite
hurdles,
future
investigations
are
anticipated
augment
role
cancer
therapy.
These
insights
can
serve
a
compass
devising
more
efficacious
combined
strategies.
Language: Английский
Biomimetic Trypsin-Responsive Structure-Bridged Mesoporous Organosilica Nanomedicine for Precise Treatment of Acute Pancreatitis
Yanan Wang,
No information about this author
Deyao Qian,
No information about this author
Xinyuan Wang
No information about this author
et al.
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(29), P. 19283 - 19302
Published: July 11, 2024
Developing
strategies
to
target
injured
pancreatic
acinar
cells
(PACs)
in
conjunction
with
primary
pathophysiology-specific
pharmacological
therapy
presents
a
challenge
the
management
of
acute
pancreatitis
(AP).
We
designed
and
synthesized
trypsin-cleavable
organosilica
precursor
bridged
by
arginine-based
amide
bonds,
leveraging
trypsin's
ability
selectively
identify
guanidino
groups
on
arginine
via
Asp189
at
active
S1
pocket
cleave
carboxy-terminal
(C-terminal)
bond
catalytic
triads.
The
precursors
were
incorporated
into
framework
mesoporous
silica
nanoparticles
(MSNs)
for
encapsulating
membrane-permeable
Ca
Language: Английский
Glutathione-responsive polypeptide nanogel encapsulates Shikonin for breast cancer therapy
Siqi Li,
No information about this author
Qingshuang Wang,
No information about this author
Zhilin Li
No information about this author
et al.
Nanomedicine Nanotechnology Biology and Medicine,
Journal Year:
2025,
Volume and Issue:
64, P. 102802 - 102802
Published: Jan. 7, 2025
Language: Английский
Recent Advances in Silica-Based Nanomaterials for Enhanced Tumor Imaging and Therapy
ACS Applied Bio Materials,
Journal Year:
2024,
Volume and Issue:
7(11), P. 7133 - 7169
Published: Nov. 4, 2024
Cancer
remains
a
formidable
challenge,
inflicting
profound
physical,
psychological,
and
financial
burdens
on
patients.
In
this
context,
silica-based
nanomaterials
have
garnered
significant
attention
for
their
potential
in
tumor
imaging
therapy
owing
to
exceptional
properties,
such
as
biocompatibility,
customizable
porosity,
versatile
functionalization
capabilities.
This
review
meticulously
examines
the
latest
advancements
application
of
therapy.
It
underscores
enhancing
various
cancer
modalities,
including
fluorescence
imaging,
magnetic
resonance
computed
tomography,
positron
emission
ultrasound
multimodal
approaches.
Moreover,
delves
into
therapeutic
efficacy
chemotherapy,
radiotherapy,
phototherapy,
immunotherapy,
gas
therapy,
sonodynamic
chemodynamic
starvation
gene
Critical
evaluations
biosafety
profiles
degradation
pathways
these
within
biological
environments
are
also
presented.
By
discussing
current
challenges
prospects,
aims
provide
nuanced
perspective
clinical
translation
nanomaterials,
thereby
highlighting
promise
revolutionizing
diagnostics,
enabling
real-time
monitoring
responses,
advancing
personalized
medicine.
Language: Английский
Magnesium-ion-doped silica nanosheets as degradable drug carriers with enhanced antibacterial activity and cellular uptake
Ruohan Liao,
No information about this author
Chengdong Zhang,
No information about this author
Z.G Wang
No information about this author
et al.
RSC Advances,
Journal Year:
2025,
Volume and Issue:
15(5), P. 3183 - 3191
Published: Jan. 1, 2025
The
synthesis
of
degradable
magnesium-ion-doped
silica
nanosheets
(MgMSNs)
that
exhibit
antibacterial
activity
and
cellular
uptake
capability
positions
them
as
promising
candidates
for
drug
delivery
systems.
Language: Английский
Harnessing stimuli-responsive NO nanomaterials for advanced multi-disease therapy
Coordination Chemistry Reviews,
Journal Year:
2025,
Volume and Issue:
533, P. 216540 - 216540
Published: Feb. 27, 2025
Language: Английский
Artesunate loaded core-shell nanoplatform for the chemo-chemodynamic-photothermal synergistic cancer therapy
Z.H. Gan,
No information about this author
Chang Liu,
No information about this author
Shaopeng Li
No information about this author
et al.
Colloids and Surfaces B Biointerfaces,
Journal Year:
2025,
Volume and Issue:
254, P. 114810 - 114810
Published: May 17, 2025
Language: Английский
Nanostructured mesoporous silica carriers for platinum-based conjugates with anti-inflammatory agents
Biomaterials Advances,
Journal Year:
2024,
Volume and Issue:
165, P. 213998 - 213998
Published: Aug. 19, 2024
This
review
discusses
the
relationship
between
inflammation
and
cancer
initiation
progression,
which
has
prompted
research
into
anti-inflammatory
approaches
for
prevention
treatment.
Specifically,
it
focuses
on
use
of
inflammation-reducing
agents
to
enhance
effectiveness
tumor
treatment
methods.
These
are
combined
with
platinum(II)-based
antitumor
drugs
create
multifunctional
platinum(IV)
prodrugs,
allowing
simultaneous
delivery
cells
in
a
specific
ratio.
Once
inside
subjected
intracellular
reduction,
both
components
can
act
parallel
through
distinct
pathways.
Motivated
by
objective
reducing
systemic
toxicity
associated
contemporary
chemotherapy,
aim
leveraging
passive
enhanced
permeability
retention
effect
exhibited
nanostructured
materials
improve
their
accumulation
within
tissues,
complexes
have
been
efficiently
loaded
mesoporous
silica
SBA-15
material.
The
resulting
capable
providing
controlled
release
conjugates
when
simulated
plasma
conditions.
feature
suggests
potential
extended
circulation
body
vivo,
minimal
premature
drug
before
reaching
intended
target
site.
primary
emphasis
this
is
that
integrates
these
two
develop
chemotherapeutic
treatments
more
efficient
less
harmful.
Language: Английский
Gadolinium ion-loaded mesoporous organosilica nanoplatform for enhanced radiotherapy in breast tumor treatment
Colloids and Surfaces B Biointerfaces,
Journal Year:
2024,
Volume and Issue:
246, P. 114374 - 114374
Published: Nov. 13, 2024
Language: Английский
Self-Augmented Reactive Oxygen Species-Responsive Nanoformulation with Efficient Curcumin Delivery for Inhibiting Triple-Negative Breast Cancer Cell Growth and Migration
ACS Applied Polymer Materials,
Journal Year:
2024,
Volume and Issue:
6(9), P. 5516 - 5529
Published: April 24, 2024
Triple-negative
breast
cancer
(TNBC)
remains
the
second
most-life-threatening
carcinoma
to
women
worldwide.
Compared
conventional
chemotherapeutic
drugs,
natural
compounds,
especially
curcumin
(CUR),
have
been
proven
therapeutical
potential
in
TNBC
treatment.
To
improve
accumulation
of
CUR
at
tumor
sites,
a
reactive
oxygen
species
(ROS)-responsive
nanocarrier
was
developed
(CUR@Bio/PE-NPs)
with
entrapment
and
biotin
conjugation,
exhibiting
strong
affinity
for
cells.
CUR@Bio/PE-NPs
demonstrated
particle
size
142.9
nm,
good
stability,
an
encapsulation
efficiency
63.67%,
while
realizing
positive
feedback
loop
ROS-accelerated
release
CUR-induced
ROS
generation
In
vitro
studies
revealed
that
induced
effectively
promoted
∼1.30-
1.36-fold
cellular
uptake
Nile
red@Bio/PE-NPs
compared
nontargeted
nanoparticles
MDA-MB-231
4T1
cells,
respectively.
addition,
suppressed
their
proliferation
(IC50,
MDA-MB-231:3.277
μg/mL,
4T1:5.259
μg/mL)
increased
apoptosis
cell
cycle
arrest
preventing
cell-migration
invasion.
Importantly,
xenografted
mice
model,
nanoformulation
prolonged
modulated
immune
microenvironment
prevented
growth
lung
metastases
without
significant
toxicity.
short,
vivo
results
suggested
as
promising
strategy
therapy.
Language: Английский