Biology,
Journal Year:
2024,
Volume and Issue:
13(12), P. 1024 - 1024
Published: Dec. 7, 2024
The
National
Cancer
Institute
(NCI)
recognizes
the
potential
of
technologies
based
on
use
nanoparticles
(NPs)
in
revolutionizing
clinical
approaches
to
diagnosis
and
prognosis
cancer.
Recent
research
suggests
that
once
NPs
come
into
contact
with
biological
fluid
cancer
patients,
they
are
covered
by
proteins,
forming
a
“protein
corona”
composed
hundreds
plasma
proteins.
concept
personalized,
disease-specific
protein
corona,
demonstrating
substantial
differences
NP
corona
profiles
between
patients
without
cancer,
has
been
introduced.
We
developed
design
an
experimental
prospective
single-center
study
allocated
1:1:1
ratio
one
three
arms:
untreated
benign
prostatic
hyperplasia
(BPH),
non-metastatic
prostate
(PCa),
metastatic
starting
systemic
therapies
new
androgen-targeted
agents
or
taxanes.
protocol
aims
develop
implement
sensitive
nanotools
two
distinct
objectives:
First,
capable
selectively
binding
detecting
biomarkers
order
build
predictive
diagnostic
model
effectively
discriminate
patient
sera
affected
BPH
PCa.
Secondly,
within
population
PCa,
case
initial
advanced
diagnosis,
objective
is
find
predicting
response
treatments
improve
precision
efficiency
monitoring
treatment
outcomes.
For
metabolite
experiments,
we
cross-reactive
sensor
array
platform
detection
capacity
made
liposomal
formulations
different
surface
charges.
proteomic-NP
studies,
proteins
were
identified
quantified
using
nano-high-performance
LC
(nanoHPLC)
coupled
MS/MS
(nanoHPLC−MS/MS).
Metabolites
instead
analyzed
untargeted
metabolomic
approach.
Compared
previous
review
articles,
novelty
this
represented
analysis
possible
applications
focused
PCa
presentation
phase
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(10), P. 5171 - 5171
Published: May 9, 2024
Nanoparticles
(NPs)
are
extremely
important
tools
to
overcome
the
limitations
imposed
by
therapeutic
agents
and
effectively
biological
barriers.
Smart
designed/tuned
nanostructures
can
be
effective
for
cancer
treatment.
The
selection
design
of
adjustment
size
surface
properties
important,
especially
some
precision
treatments
drug
delivery
(DD).
By
designing
specific
methods,
an
era
opened
in
biomedical
field
personalized
precise
Here,
we
focus
on
advances
nanostructures,
as
well
how
structure
shape,
size,
charge,
fluids
(BFs)
affected.
We
discussed
applications
specialized
therapy
head
neck
(HNC),
which
is
a
difficult
aggressive
type
treat,
give
impetus
novel
treatment
approaches
this
field.
also
comprehensively
touched
shortcomings,
current
trends,
future
perspectives
when
using
cancer.
Cancer
is
among
the
leading
causes
of
death
worldwide.
Therefore,
timely
diagnosis
and
appropriate
treatment
are
very
important.
There
many
disadvantages
that
come
with
traditional
cancer
treatments,
such
as
chemotherapy
radiotherapy.
In
these
specific
drug
concentration
affects
not
only
tumor
site
but
also
healthy
tissues
or
organs.
One
foremost
promising
uses
nanotechnology
in
field
medical
technology
targeting
can
be
achieved
due
to
manipulation
materials
at
a
nanometric
scale.
Nanotechnology
offers
benefits
terms
therapy
by
enhancing
it
reducing
its
adverse
effects
guiding
drugs
selectively
target
cells.
addition,
use
minute
amounts
medicine
lead
cost
savings.
Furthermore,
nanoparticles
used
imaging
agents
improve
diagnostics,
therapeutics,
management.
Thus,
this
review
has
focused
on
different
types
therapy,
their
action
mechanisms,
applications
diagnosis,
imaging,
treatment.
This
sums
up
parameters
need
considered
when
designing
systems
for
while
considering
desired
characteristics
from
biological
point
view.
Microorganisms,
Journal Year:
2025,
Volume and Issue:
13(5), P. 956 - 956
Published: April 22, 2025
The
transformative
effect
of
nanotechnology
is
revolutionizing
medicine
by
introducing
new
therapeutic
approaches.
This
study
explores
the
utilization
aqueous
extract
from
mushroom
(Cortinarius
sp.)
used
as
a
reducing
agent
to
prepare
zinc
oxide
myco-nanoparticles
(ZnO-MNPs)
in
an
eco-friendly
manner.
synthesis
ZnO-MNPs
has
been
confirmed
various
characterization
studies,
including
UV-vis
spectroscopy,
which
revealed
absorption
peak
at
378
nm;
X-ray
diffraction
(XRD)
analysis,
wurtzite
hexagonal
structure;
and
Fourier
transform
infrared
spectra
(FTIR),
showed
stabilizing
agents
around
ZnO-MNPs.
effectiveness
anti-cancer
was
evaluated
monitoring
liver
biochemical
parameters
against
hepatotoxicity
caused
carbon
tetrachloride
(CCl4)
Balb
C
mice.
results
that
levels
catalase,
glutathione
(GSH),
total
protein
were
significantly
lower,
while
alanine
aminotransferase
(ALT),
aspartate
(ASAT),
alkaline
phosphatase
(ALP),
lactate
dehydrogenase
(LDH),
melanin
dialdehyde
(MDA),
bilirubin
(TB)
higher
each
CCl4
treatment
groups.
ZnO-MNP
reduced
toxicological
effects
but
did
not
completely
restore
accumulation.
antimicrobial
efficacy
investigated
potential
common
pathogens,
Bacillus
subtilis
(29.05
±
0.76),
meurellus
(27.05
0.5),
Acetobacter
rhizospherensis
(23.36
Escherichia
coli
(25.86
0.80),
antifungal
activity
relatively
lower.
Moreover,
2,2-diphenyl-1-picrylhydrazyl
(DPPH)
assay
are
strong
antioxidant
agents.
Overall,
these
findings
highlight
myco-synthesized
ZnO-NPs
combating
pathogenic
diseases,
their
promising
role
cancer
therapy,
biomaterial
option
for
future
applications.
Pharmaceutics,
Journal Year:
2025,
Volume and Issue:
17(3), P. 305 - 305
Published: Feb. 26, 2025
This
review
discusses
the
literature
data
on
synthesis,
physicochemical
properties,
and
cytotoxicity
of
composite
nanoparticles
bearing
mitochondrial
protein
cytochrome
c
(cytC),
which
can
act
as
a
proapoptotic
mediator
in
addition
to
its
main
function
an
electron
carrier
transport
chain.
The
introduction
exogenous
cytC
via
absorption
particles,
phagocytosis
colloid
particles
submicrometric
size,
or
receptor-mediated
endocytosis
cancer
cells,
initiates
process
apoptosis—a
multistage
cascade
biochemical
reactions
leading
complete
destruction
cells.
CytC–carrier
have
potential
for
use
treatment
neoplasms
with
superficial
localization:
skin,
mouth,
stomach,
colon,
etc.
approach
solve
two
problems
anticancer
therapy:
selectivity
non-toxicity.
Selectivity
is
based
incapability
normal
cell
absorb
(nano)particles,
except
cells
immune
system.
that
normally
functions
mitochondria
harmless
macroorganism.
In
this
review,
factors
limiting
ways
increase
it
are
discussed
from
point
view
properties
cytC–carrier
particles.
different
techniques
used
preparation
cytC-bearing
colloids
discussed.
Articles
reporting
achievement
high
each
critically
analyzed.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(16), P. 8934 - 8934
Published: Aug. 16, 2024
Anticancer
therapy
urgently
needs
the
development
of
novel
strategies.
An
innovative
molecular
target
is
represented
by
circular
RNAs
(circRNAs),
single-strand
RNA
molecules
with
5'
and
3'
ends
joined,
characterized
a
high
stability.
Although
circRNA
properties
biological
functions
have
only
been
partially
elucidated,
their
relationship
involvement
in
onset
progression
cancer
emerged.
Specific
targeting
circRNAs
may
be
obtained
antisense
oligonucleotides
silencing
RNAs.
Nanotechnology
at
forefront
research
for
perfecting
delivery.
Continuous
efforts
made
to
develop
nanoparticles
(NPs)
improve
performance,
materials,
regarding
biocompatibility
capabilities.
Applications
various
fields,
from
imaging
gene
therapy,
explored.
This
review
sums
up
smart
strategies
developed
directly
fruitful
application
NPs
this
context.
Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
16(9), P. 1181 - 1181
Published: Sept. 7, 2024
The
programmed
death-1/programmed
death-ligand
1
(PD-1/PD-L1)
immune
checkpoint
constitutes
an
inhibitory
pathway
best
known
for
its
regulation
of
cluster
differentiation
8
(CD8)+
T
cell-mediated
responses.
Engagement
PD-L1
with
PD-1
expressed
on
CD8+
cells
activates
downstream
signaling
pathways
that
culminate
in
cell
exhaustion
and/or
apoptosis.
Physiologically,
these
immunosuppressive
effects
exist
to
prevent
autoimmunity,
but
cancer
exploit
this
by
overexpressing
facilitate
escape.
Intravenously
(IV)
administered
inhibitors
(ICIs)
block
the
interaction
between
PD-1/PD-L1
have
achieved
great
success
reversing
and
promoting
tumor
regression
various
malignancies.
However,
ICIs
can
cause
immune-related
adverse
events
(irAEs)
due
off-tumor
toxicities
which
limits
their
therapeutic
potential.
Therefore,
considerable
effort
has
been
channeled
into
exploring
alternative
delivery
strategies
enhance
tumor-directed
reduce
irAEs.
Here,
we
briefly
describe
PD-1/PD-L1-targeted
immunotherapy
associated
We
then
provide
a
detailed
review
approaches,
including
locoregional
(LDD)-,
oncolytic
virus
(OV)-,
nanoparticle
(NP)-,
ultrasound
microbubble
(USMB)-mediated
are
currently
under
investigation
enhancing
tumor-specific
minimize
toxic
effects.
conclude
commentary
key
challenges
methods
potential
mitigate
them.
Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
16(11), P. 1452 - 1452
Published: Nov. 14, 2024
Background:
Graphene
Oxide
(GO)
has
shown
great
potential
in
biomedical
applications
for
cancer
therapeutics.
The
biosafety
and
stability
issues
of
GO
biological
media
have
been
addressed
by
functionalization
with
polyethylene
glycol
(PEG).
Methods:
In
this
work,
carboxylated,
nanosized
(nCGO)
was
evaluated
as
a
carrier
paclitaxel
(PCT).
effect
PEG
characteristics
on
particle
size
surface
charge,
colloidal
stability,
drug,
release,
the
hemolytic
nCGO,
investigated.
Optimum
PEG-nCGO/PCT
formulations
based
above
properties
were
their
anticancer
activity
(cytotoxicity
apoptosis
induction)
A549
lung
cell
line.
Results:
An
increase
length
linear
chains
use
branched
(4-arm)
instead
resulted
decrease
hydrodynamic
diameter
an
ζ
pegylated
nCGO
particles.
Pegylated
exhibited
high
phosphate-buffered
saline
culture
low
effect,
even
at
relatively
concentration
1
mg/mL.
molecular
weight
branching
adversely
affected
PCT
loading.
increased
rate
release
acidic
pH
6.0
compared
to
physiological
7.4
observed
all
types
nCGO/PCT.
lower
cytotoxicity
apoptotic
than
non-pegylated
nCGO.
Cellular
uptake
incubation
time
cells
leading
time,
which
became
higher
that
free
24
48
h
incubation.
Conclusions:
biocompatibility
enhanced
are
desirable
regard
clinical
application
nanomedicine.
Molecules,
Journal Year:
2024,
Volume and Issue:
29(22), P. 5327 - 5327
Published: Nov. 12, 2024
Chemoresistance
encountered
using
conventional
chemotherapy
demands
novel
treatment
approaches.
Asplatin
(Asp),
a
platinum
(IV)
prodrug
designed
to
release
cisplatin
and
aspirin
in
reductive
environment,
has
demonstrated
high
cytotoxicity
at
reduced
drug
resistance.
Herein,
we
investigated
the
ability
of
green-synthesized
nanocarriers
enhance
Asp’s
efficacy.
Zinc
oxide
nanoparticles
(ZnO-NPs)
were
synthesized
green
microwave-assisted
method
with
reducing
capping
agent
gambogic
acid
(GA).
These
then
loaded
Asp,
yielding
Asp@ZnO-NPs.
Transmission
electron
microscopy
was
utilized
study
morphological
features
ZnO-NPs.
Cell
viability
studies
conducted
on
MDA-MB-231
breast
cancer
cells
Asp@ZnO-NPs
significantly
decrease
half-maximal
inhibitory
concentration
(IC50)
(5
±
1
µg/mL).
This
further
flow
cytometric
analysis
that
revealed
capacity
increase
late
apoptotic
fractions.
Furthermore,
vivo
carried
out
solid
Ehrlich
carcinoma-bearing
mice
showed
significant
tumor
volume
reduction
(156.3
7.6
mm3),
compared
Asp
alone
(202.3
8.4
mm3)
untreated
controls
(342.6
10.3
mm3).
The
histopathological
increased
necrosis
Asp@ZnO-NPs-treated
group.
Asp@ZnO-NPs,
an
eco-friendly
approach,
enhanced
anticancer
activity,
offering
sustainable
solution
for
potent
formulations.