Journal of Colloid and Interface Science,
Год журнала:
2024,
Номер
664, С. 338 - 348
Опубликована: Март 5, 2024
Combination
therapies
demand
co-delivery
platforms
with
efficient
entrapment
of
distinct
payloads
and
specific
delivery
to
cells
possibly
organelles.
Herein,
we
introduce
the
combination
two
therapeutic
modalities,
gene
photodynamic
therapy,
in
a
purely
peptidic
platform.
The
simultaneous
formation
cargo
loading
multi-micellar
platform
is
governed
by
self-assembly
at
nanoscale.
architecture
nanocarrier
positive
charge
its
constituent
micelles
offer
controlled
dual
capacity
locations
for
hydrophobic
photosensitizer
(PS)
negatively
charged
antisense
oligonucleotides
(ASOs).
Moreover,
nuclear
localization
signal
(NLS)
sequence
built-in
peptide
targets
PS
+
ASO-loaded
nanocarriers
nucleus.
Breast
cancer
treated
demonstrated
photo-triggered
enhancement
radical
oxygen
species
(ROS)
associated
increased
cell
death.
Besides,
ASO
resulted
up
90
%
knockdown
Bcl-2,
an
inhibitor
apoptosis
that
overexpressed
more
than
half
all
human
cancers.
Simultaneous
elicited
synergistic
extent
could
not
be
reached
singly
loaded
or
free
form
drugs.
Both,
location
compounds
prevents
them
from
interfering
each
other,
highly
cellular
support
great
potential
this
versatile
therapy.
Communications Materials,
Год журнала:
2024,
Номер
5(1)
Опубликована: Авг. 27, 2024
Osteosarcoma,
the
predominant
bone
malignancy,
poses
significant
challenges
due
to
its
high
metastatic
potential
and
recurrence
rates.
Accounting
for
a
substantial
percentage
of
malignant
tumors,
osteosarcoma
particularly
affects
children
adolescents.
Despite
standard
treatment
combining
surgery
multi-drug
chemotherapy,
systemic
drug
administration
presents
limitations,
leading
compromised
patient
quality
life
severe
side
effects.
New
strategies
are
needed
address
these
enhance
efficacy
while
minimizing
toxicity.
Here,
we
explore
delivery
platforms
in
context
treatment.
We
delve
into
both
local
approaches,
highlighting
recent
advances
controlled
release
triggered
by
various
stimuli,
modifications
targeted
delivery,
co-delivery
chemotherapeutics
using
nano-platforms.
Additionally,
discuss
innovations
methods,
including
implantable
nanoparticles,
injectable
hydrogels,
scaffolds.
advancements,
limitations
persist,
emphasizing
need
continued
research.
conclude
offering
perspectives
on
multifunctional
scaffolds
revolutionizing
thereby
paving
way
improved
survival
enhanced
life.
Drug
combatting
osteosarcoma,
which
accounts
large
proportion
tumors.
This
Review
highlights
progress
nanoparticle-based
such
as
scaffolds,
addressing
ongoing
future
research
needs.
Scientific Reports,
Год журнала:
2024,
Номер
14(1)
Опубликована: Июль 5, 2024
Drug
delivery
is
the
process
or
method
of
delivering
a
pharmacological
product
to
have
therapeutic
effects
on
humans
animals.
The
use
nanoparticles
deliver
medications
cells
driving
present
surge
in
interest
improving
human
health.
Green
nanodrug
methods
are
based
chemical
processes
that
acceptable
for
environment
natural
biomaterials
such
as
plant
extracts
and
microorganisms.
In
this
study,
zinc
oxide-superparamagnetic
iron
oxide-silver
nanocomposite
was
synthesized
via
green
synthesis
using
Fusarium
oxysporum
fungi
mycelia
then
loaded
with
sorafenib
drug.
nanocomposites
were
characterized
by
UV-visibile
spectroscopy,
FTIR,
TEM
SEM
techniques.
Sorafenib
cancer
treatment
also
known
its
brand
name,
Nexavar.
only
systemic
medication
available
world
treat
hepatocellular
carcinoma.
Sorafenib,
like
many
other
chemotherapeutics,
has
side
restrict
effectiveness,
including
toxicity,
nausea,
mucositis,
hypertension,
alopecia,
hand-foot
skin
reaction.
our
40
male
albino
rats
given
single
dose
diethyl
nitrosamine
(DEN)
60
mg/kg
b.wt.,
followed
carbon
tetrachloride
2
ml/kg
b.wt.
twice
week
one
month.
aim
study
nanocarrier
enhancement
anticancer
effect.
International Journal of Nanomedicine,
Год журнала:
2024,
Номер
Volume 19, С. 3387 - 3404
Опубликована: Апрель 1, 2024
Abstract:
Cancer
immunotherapy
has
emerged
as
a
novel
therapeutic
approach
against
tumors,
with
immune
checkpoint
inhibitors
(ICIs)
making
significant
clinical
practice.
The
traditional
ICIs,
PD-1
and
PD-L1,
augment
the
cytotoxic
function
of
T
cells
through
inhibition
tumor
evasion
pathways,
ultimately
leading
to
initiation
an
antitumor
response.
However,
implementation
ICIs
encounters
obstacles
stemming
from
existence
immunosuppressive
microenvironment
inadequate
infiltration
CD8
+
cells.
Considerable
attention
been
directed
towards
advancing
immunogenic
cell
death
(ICD)
potential
solution
counteract
microenvironment.
This
holds
promise
in
transforming
"cold"
tumors
into
"hot"
that
exhibit
responsiveness
antitumor.
By
combining
ICD
synergistic
response
can
be
achieved.
combination
inducers
PD-1/PD-L1
is
hindered
by
issues
such
poor
targeting
uncontrolled
drug
release.
An
advantageous
presented
stimulus-responsive
nanocarrier
integrating
physicochemical
properties
inhibitors,
facilitating
precise
delivery
specific
tissues
for
optimal
therapy.
Moreover,
these
nanocarriers
leverage
distinct
features
accomplish
controlled
release
regulate
kinetics
delivery.
article
aims
investigate
advancement
co-delivery
utilizing
inhibitors.
Special
focus
dedicated
exploring
advantages
recent
advancements
this
system
enabling
inducers.
molecular
mechanisms
are
concisely
summarized.
In
conclusion,
we
examine
research
prospects
challenges
could
greatly
enhance
immunotherapeutic
approaches
cancer
treatment.
Keywords:
therapy,
death,
co-delivery,
immune-checkpoint
Macromolecular Bioscience,
Год журнала:
2024,
Номер
unknown
Опубликована: Май 11, 2024
Abstract
The
targeted
delivery
of
drugs
using
wireless
navigable
magnetic
robots
allows
the
drug
molecules
to
be
controlled
non
only
in
time
but
also
space,
improving
medical
outcomes.
main
disadvantages
behind
their
use
lies
low
amount
that
can
transported
and
single
nature
loaded
(hydrophilic
or
hydrophobic).
These
considerations
limit
co‐delivery
systems,
now
recognized
very
promising
for
many
different
pathologies.
A
bijel‐like
structure
is
developed
load
release
types
In
this
work,
ε‐caprolactone
explored,
which
polymerize,
forming
hydrophobic
domains
(oil
phase).
After
mixing
with
iron
oxide
nanoparticles
(NPs),
water
dispersion
creates
a
biphasic
porous
without
phase
separation.
resulting
device
shows
good
performance
both
actuation
as
system.
International Journal of Nanomedicine,
Год журнала:
2025,
Номер
Volume 20, С. 741 - 770
Опубликована: Янв. 1, 2025
Different
types
of
cancers
affect
the
gastrointestinal
tract
(GIT),
starting
from
oral
cavity
and
extending
to
colon.
In
general,
most
current
research
focuses
on
systemic
delivery
therapeutic
agents,
which
leads
undesired
side
effects
a
limited
enhancement
in
outcomes.
As
result,
localized
within
(GI)
is
favorable
overcoming
these
limitations.
However,
via
administration
faces
many
challenges
related
complex
structure
GIT
(varied
pH
levels
transit
times)
as
well
harsh
environment
tumor
cells
(hypoxia,
efflux
pumps,
acidity).
To
overcome
obstacles,
nano-drug
systems
(NDDs)
have
been
designed
proved
their
potential
by
exploiting
favor
offering
specific
desired
target.
The
review
begins
with
an
overview
different
GI
impact
globally.
Then,
it
discusses
treatment
approaches
corresponding
Additionally,
associated
drug
for
are
summarized.
Finally,
detail
recent
diagnostic
applications
NDDs
that
conducted
oral,
esophageal,
gastric,
colon,
liver
cancers,
aiming
offer
valuable
insights
into
future
state
utilizing
local
cancers.
Journal of drug targeting,
Год журнала:
2025,
Номер
unknown, С. 1 - 43
Опубликована: Фев. 19, 2025
In
the
dynamic
arena
of
cancer
therapeutics,
chemoimmunotherapy
has
shown
tremendous
promise,
especially
for
aggressive
forms
breast
like
triple-negative
(TNBC).
This
review
delves
into
significant
role
liposomes
in
enhancing
effectiveness
by
leveraging
cancer-specific
mechanisms
such
as
induction
immunogenic
cell
death
(ICD),
reprogramming
tumor
microenvironment
(TME),
and
enabling
sequential
drug
release.
We
examine
innovative
dual-targeting
that
capitalize
on
heterogeneity,
well
pH-sensitive
formulations
offer
improved
control
over
delivery.
Unlike
prior
analyses,
this
directly
links
advancements
preclinical
research-such
PAMAM
dendrimer-based
nanoplatforms
RGD-decorated
liposomes-to
clinical
trial
results,
highlighting
their
potential
to
revolutionize
TNBC
treatment
strategies.
Additionally,
we
address
ongoing
challenges
related
scalability,
toxicity,
regulatory
compliance,
propose
future
directions
personalized,
immune-focused
nanomedicine.
work
not
only
synthesizes
latest
research
but
also
offers
a
framework
translating
liposomal
from
laboratory
practice.
Molecular Diversity,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 8, 2025
Novel
quinoline-based
derivatives
2a-e
and
4a-j
have
been
designed
synthesized
as
potential
antiproliferative
agents.
The
compounds
were
screened
for
their
activity
against
sixty
cell
lines
according
to
NCI
protocol.
promising
hybrids
4d-g
are
by
MTT
assays
on
three
cancer
lines:
leukemia
(MOLT-4),
lung
(HOP-92),
breast
(T47D),
with
IC50
values
ranging
from
4.982
±
0.2
36.52
1.46
µM
compared
Staurosporine,
compound
4e
being
the
most
effective.
Derivatives
evaluated
inhibitory
EGFR
BRAFV600E.
Compound
exhibited
highest
activities,
of
0.055
0.002
μM
0.068
0.003
BRAFV600E,
reference
drugs
erlotinib
(IC50
0.06
μM)
vemurafenib
0.035
0.001
μM),
respectively.
Cell
cycle
analysis
HOP-92
manifested
that
pre-G1
apoptosis
signaling
took
place
after
treatment.
Docking
simulations
employed
analyze
modes
scores
respect
results
revealed
strong
affinity
both
BRAFV600E
-
3.226
3.474
kcal/mol,
Journal of Translational Medicine,
Год журнала:
2025,
Номер
23(1)
Опубликована: Март 31, 2025
Abstract
Background
Breast
cancer
remains
one
of
the
leading
causes
death
among
women
globally,
with
traditional
therapies
often
limited
by
challenges
such
as
drug
resistance
and
significant
side
effects.
Combination
therapies,
coupled
nanotechnology-based
co-delivery
systems,
offer
enhanced
efficacy
targeting
multiple
pathways
in
progression.
In
this
study,
we
developed
an
injectable,
stimuli-responsive
nanosystem
using
a
chitosan
hydrogel
embedded
mesoporous
silica
nanoparticles
for
co-administration
5-fluorouracil
everolimus.
This
approach
aims
to
optimize
controlled
release,
enhance
synergistic
anticancer
effect,
overcome
associated
co-loading
different
therapeutic
agents.
Methods
Various
techniques
were
employed
characterize
hydrogel.
Cell
uptake,
apoptosis,
proliferation
4T1
breast
cells
evaluated
flow
cytometry
Resazurin
assay,
respectively.
The
Balb/C
mice
model
cancer,
which
received
therapeutical
nanoplatforms
subcutaneously
near
tumoral
region
was
used
examine
tumor
size
lung
metastases.
Results
results
revealed
that
had
suitable
loading
capacity
high
cellular
uptake.
release
pH-sensitive
synergistic.
By
incorporating
into
hydrogel,
cell
rate
apoptosis
increased
significantly,
due
effects
co-delivered
drugs.
Additionally,
combination
treatment
groups
showed
reduction
metastasis
compared
monotherapy
control
groups.
Conclusions
These
findings
underscore
potential
nanocomposite
develop
novel
system
outcomes,
reduce
effects,
provide
promising
new
strategy
future
treatments.