Nanotechnology-Enhanced siRNA Delivery: Revolutionizing Cancer Therapy
ACS Applied Bio Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 12, 2025
RNA
interference
(RNAi)
has
emerged
as
a
transformative
approach
for
cancer
therapy,
enabling
precise
gene
silencing
through
small
interfering
(siRNA).
However,
the
clinical
application
of
siRNA-based
treatments
faces
challenges
such
rapid
degradation,
inefficient
cellular
uptake,
and
immune
system
clearance.
Nanotechnology-enhanced
siRNA
delivery
revolutionized
therapy
by
addressing
these
limitations,
improving
stability,
tumor-specific
targeting,
therapeutic
efficacy.
Recent
advancements
in
nanocarrier
engineering
have
introduced
innovative
strategies
to
enhance
safety
precision
therapies,
offering
new
opportunities
personalized
medicine.
This
review
highlights
three
key
innovations
nanotechnology-enhanced
delivery:
artificial
intelligence
(AI)-driven
design,
multifunctional
nanoparticles
combined
strategies,
biomimetic
nanocarriers
enhanced
biocompatibility.
AI-driven
utilize
machine
learning
algorithms
optimize
nanoparticle
properties,
drug
release
profiles
minimizing
off-target
effects.
Multifunctional
integrate
with
chemotherapy,
immunotherapy,
or
photothermal
synergistic
treatment
approaches
that
outcomes
reduce
resistance.
Biomimetic
nanocarriers,
including
exosome-mimicking
systems
cell-membrane-coated
nanoparticles,
improve
circulation
time,
evasion,
targeted
tumor
delivery.
These
collectively
precision,
efficiency,
therapies.
The
scope
novelty
lie
their
ability
overcome
primary
barriers
while
paving
way
clinically
viable
solutions.
provides
comprehensive
analysis
latest
developments
fabrication,
preclinical
studies,
assessments.
By
integrating
multifunctionality,
biomimicry,
holds
immense
potential
future
therapy.
Language: Английский
High‐Efficiency Ocular Delivery of Brain‐Derived Neurotrophic Factor and Oligomycin for Neuroprotection in Glaucoma
Yuheng Cao,
No information about this author
Xue Yin,
No information about this author
Lanrong Wu
No information about this author
et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 13, 2025
Abstract
Glaucoma
is
a
retinal
neurodegenerative
disease
characterized
by
progressive
apoptosis
of
ganglion
cells
(RGCs)
and
irreversible
visual
impairment.
Current
therapies
rarely
offer
direct
protection
for
RGCs,
highlighting
the
need
new
neuroprotective
approaches.
Although
viral
delivery
brain‐derived
neurotrophic
factor
(BDNF)
has
shown
potential,
concerns
about
inflammation
limited
applicability
persist.
Meanwhile,
non‐viral
vectors
remain
inefficient
in
vivo
ocular
gene
delivery.
Here,
highly
biocompatible
nanoplatform—PBAE‐PLGA‐Oligomycin‐pBDNF
nanoparticles
(PPOB
NPs)
reported—that
co‐delivers
oligomycin
(an
ATP
inhibitor)
BDNF
plasmid
to
Müller
vivo.
This
nanoplatform
attains
an
unprecedented
transfection
efficiency
64.26%
cells,
thereby
overcoming
limitations
monotherapeutic
approaches
that
fail
inhibit
overproduction
attendant
inflammatory
responses.
In
chronic
hypertension
rat
model,
effectively
mitigated
RGC
damage
suppressing
cell
hyperactivation
excessive
production
under
elevated
intraocular
pressure.
Concurrently,
it
synergistically
enhanced
expression
achieving
robust
RGCs
preservation
optic
nerve
function.
These
findings
underscore
promise
PPOB
NPs
as
dual‐functional
platform,
featuring
high
biocompatibility
efficient
delivery,
multifaceted
against
glaucoma
other
diseases.
Language: Английский