26th International Conference on Optical Fiber Sensors,
Journal Year:
2023,
Volume and Issue:
unknown, P. Th5.1 - Th5.1
Published: Jan. 1, 2023
The
paper
provides
an
overall
picture
of
the
technological
roadmap
aimed
to
develop
Lab
on
fiber
(LOF)
assisted
needles
for
in-vivo
liquid
and
tissue
biopsy
support
light
localized
therapies
precision
medicine.
Journal of Hepatocellular Carcinoma,
Journal Year:
2024,
Volume and Issue:
Volume 11, P. 1265 - 1278
Published: July 1, 2024
Abstract:
Ferroptosis
is
a
type
of
cell
death
that
relies
on
iron
and
distinguished
by
the
occurrence
lipid
peroxidation
buildup
reactive
oxygen
species.
has
been
demonstrated
to
have
significant
impact
advancement
resistance
treatment
hepatocellular
carcinoma
(HCC),
thereby
highlighting
its
potential
as
viable
therapeutic
target.
was
observed
in
HCC
tissues
contrast
normal
liver
tissue.
The
inhibition
ferroptosis
found
increase
viability
cells
decrease
their
susceptibility
various
anticancer
therapies,
including
chemotherapy,
radiotherapy,
immune
checkpoint
blockade.
administration
drugs
directly
modulate
regulators
or
induce
excessive
production
lipid-reactive
species
enhance
responsiveness
drug-resistant
treatment.
However,
precise
mechanism
underlying
this
phenomenon
remains
ambiguous.
This
review
presents
comprehensive
overview
crucial
role
played
enhancing
efficacy
for
(HCC).
main
aim
study
examine
feasibility
utilizing
approach
improve
overcome
drug
resistance.
Keywords:
ferroptosis,
carcinoma,
tyrosine
kinase
inhibitor,
immunosuppressive
therapy,
radiotherapy
Nanomaterials,
Journal Year:
2023,
Volume and Issue:
14(1), P. 47 - 47
Published: Dec. 23, 2023
To
develop
a
potential
cancer
treatment,
we
formulated
novel
drug
delivery
platform
made
of
poly(lactic-co-glycolic)
acid
(PLGA)
and
used
combination
an
emerging
siRNA
technology
extracted
natural
substance
called
catechins.
The
synthesized
materials
were
characterized
to
determine
their
properties,
including
morphology,
hydrodynamic
size,
charge,
particle
stability,
release
profile.
therapeutic
effect
AFP-siRNA
epigallocatechin
gallate
(EGCG)
was
revealed
have
remarkable
cytotoxicity
towards
HepG2
when
in
soluble
formulation.
Notably,
the
killing
enhanced
by
co-treatment
AFP-siRNA-loaded
PLGA
EGCG.
Cell
viability
significantly
dropped
59.73
±
6.95%
after
treatment
with
12.50
μg/mL
EGCG
AFP-siRNA-PLGA.
Meanwhile,
80%
viable
cells
observed
monotherapy.
reduction
survival
is
clear
indication
complementary
action
both
active
PLGA.
corresponding
cell
death
involved
apoptosis,
as
evidenced
increased
caspase-3/7
activity.
combined
exhibited
2.5-fold
increase
Moreover,
nanoparticles
internalized
time-dependent
manner,
indicating
appropriate
use
carrier.
Accordingly,
system
effective
strategy.
This
study
was
to
designed
develop
sorafenib-loaded
polymeric
nanoparticles,
surface-modified
with
pluronic
F-127
for
the
effective
treatment
of
hepatocellular
(HCC)
and
renal
cell
carcinomas
(RCC).
Poly
lactic
coglycolic
acid
(PLGA)
used
encapsulate
different
concentrations
sorafenib
by
a
simple
modified
solvent
evaporation
method
applying
as
surfactant
coating
agent.
The
preformulation
characterization
studies
were
conducted
evaluate
incompatibilities
among
sorafenib,
PLGA
F-127,
physicochemical
properties
formulations,
respectively.
sizes
coated
plain
nanoparticles
~140
±
14.7
nm
~
120
10.1
nm,
It
has
been
confirmed
from
in
vitro
release
that
sustained
avoiding
initial
burst
release,
while
vivo
demonstared
have
greater
affinity
target
aorgans
than
free
drug
keeping
dose
constant
(20
mg/kg
body
weight).
delivery
into
tissues
their
pharmacokinetic
parameters
improved
significantly
compared
reported
formulations.
International Journal of Applied Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
unknown, P. 135 - 141
Published: July 7, 2024
Objective:
The
purpose
of
this
study
was
to
develop,
characterize,
and
optimize
sorafenib-loaded
Poly
(lactic-co-glycolic
acid)
PLGA
polymeric
nanoparticles
for
prolonged
delivery
sorafenib
improved
hepatic
cancer
treatment
Methods:
drug-excipient
interaction
explored
by
molecular
docking
studies
within
silico
tools.
drug-loaded
were
prepared
single
emulsion
solvent
evaporation
method
using
box-bhenkan
design
characterized
particle
size,
zeta
potential,
entrapment
efficiency.
Shape
surface
morphology
analysed
Transmission
Electron
Microscopy
(TEM).
In
vitro
drug
release
performed
a
diffusion
membrane.
Results:
analysis
inferred
that
the
has
interacted
well
with
PF-68,
which
could
prevent
crystal
formation.
optimized
had
size
175
nm,
Entrapment
Efficiency
(EE)
85.1%
potential
of-23.8mV
found
be
95%
CI
predicted
value,
is
acceptable.
TEM
showed
formed
smooth,
spherical
in
shape
uniform
size.
formulation
extended
sorafenib.
Conclusion:
Based
on
computational
studies,
developed
Sorafenib
loaded
promising
oral
liver
cancer.
Open Life Sciences,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: Jan. 1, 2024
Abstract
Hepatocellular
carcinoma
(HCC)
is
among
the
most
common
malignant
liver
tumors.
Despite
progress
in
anticancer
drugs
and
surgical
approaches,
early
detection
of
HCC
remains
challenging,
often
leading
to
late-stage
diagnosis
where
rapid
disease
progression
precludes
intervention,
leaving
chemotherapy
as
only
option.
However,
systemic
toxicity,
low
bioavailability,
significant
adverse
effects
lead
resistance,
rendering
treatments
ineffective
for
many
patients.
This
article
outlines
how
nanoparticles,
following
functional
modification,
offer
high
sensitivity,
reduced
drug
extended
duration
action,
enabling
precise
targeting
tissues.
Combined
with
other
therapeutic
modalities
imaging
techniques,
this
significantly
enhances
diagnosis,
treatment,
long-term
prognosis
HCC.
The
advent
nanomedicine
provides
new
methodologies
strategies
integrated
treatment
26th International Conference on Optical Fiber Sensors,
Journal Year:
2023,
Volume and Issue:
unknown, P. Th5.1 - Th5.1
Published: Jan. 1, 2023
The
paper
provides
an
overall
picture
of
the
technological
roadmap
aimed
to
develop
Lab
on
fiber
(LOF)
assisted
needles
for
in-vivo
liquid
and
tissue
biopsy
support
light
localized
therapies
precision
medicine.