Processes,
Journal Year:
2024,
Volume and Issue:
12(12), P. 2772 - 2772
Published: Dec. 5, 2024
This
study
introduces
a
novel
approach
for
enhancing
the
functional
properties
of
cotton
fibers
through
complexation
copper
sulfate,
and
subsequent
combination
with
chitosan
(COT-CuSO4-CTS).
Our
preliminary
investigations
focused
on
development
composites
as
candidate
materials
coatings
antimicrobial
properties.
The
were
thoroughly
characterized
via
scanning
electron
microscopy
(SEM)
optical
microscopy,
providing
insights
into
their
structural
features
composition.
findings
show
that
modified
exhibit
potent
activity.
Specifically,
COT-CuSO4
COT-CuSO4-CTS
samples
demonstrated
zones
inhibition
against
both
Gram-positive
Staphylococcus
aureus
Gram-negative
Escherichia
coli,
confirming
ability
to
reduce
microbial
growth
significantly.
incorporation
layer
significantly
enhanced
Ultraviolet
Protection
Factor
(UPF)
fabric
from
3.37
over
50,
indicating
exceptional
UV
shielding
capabilities,
while
copper(II)
oxide
treatment
provided
moderate
UPF
value
14.56.
Blood
compatibility
studies
further
revealed
fabrics
influence
coagulation
parameters,
marked
prolongation
in
activated
partial
thromboplastin
time
(aPTT)
prothrombin
(PT)
compared
untreated
cotton.
anticoagulant
effect
is
primarily
linked
presence
copper,
although
addition
modulates
this
response,
slightly
reducing
clotting
times
alone.
Cytotoxicity
genotoxicity
assessments
using
Peripheral
Mononuclear
(PBM)
cells
indicated
was
non-toxic
non-genotoxic.
However,
displayed
reduction
cell
viability
induced
DNA
damage,
highlighting
potential
cytotoxic
genotoxic
effects.
Notably,
showed
lower
cytotoxicity
than
COT-CuSO4-CTS,
suggesting
reduces
overall
composite.
Furthermore,
plasmid
relaxation
assays
interact
DNA,
exhibiting
stronger
interaction
consistent
PBM
cells.
Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
13(29)
Published: Aug. 12, 2024
Triple-negative
breast
cancer
(TNBC)
is
the
most
common
primary
tumor
of
with
limited
effectual
drug
availability.
Therefore,
aim
study
to
develop
an
innovative
phyto-nanomedicine
(PNM)
cure
TNBC
least
genotoxicity.
Hereinafter,
sea
buckthorn'
extracted
polyphenols
(SBP),
combine
metformin
(MET),
are
synthesized
as
a
novel
PNM
evaluate
its
anti-tumor
properties,
effectiveness,
and
mechanism
action
in
vitro
vivo
models.
The
SBP
exhibits
16
new
kinds
that
been
reported
earlier
which
regulated
cell
development,
proliferation,
programmed
death
(PCD)
effectively.
SBP-MET
inhibits
MDA-MB-231
(47%),
MDA-MB-436
(46%),
4T1
(46%)
proliferation
but
does
not
affect
L929
normal
murine
development
successfully
induce
PCD
(73.19%)
cells.
Mechanistically,
proteome
expression
profiling
reveals
upregulation
proapoptotic
Bax
protein
activation
Fas
signaling
pathways
convince
downstream
Daxx
FADD
proteins,
further
triggers
Caspase-3
prompts
apoptosis
human
cells
by
cleaving
PARP-1
protein.
Current
findings
establish
highly
biocompatible
has
significant
potential
inhibit
growth
(RCD)
model,
thereby
opening
arena
for
therapy.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 28, 2024
AbstractBackground
Osteoarthritis
(OA)
is
considered
an
advancing
chronic
degenerative
joint
disease,
leading
to
severe
physical
functional
impairment
of
patients.
Its
development
closely
related
increased
inflammation
and
oxidative
stress
within
the
joint.
Ginkgetin
(GK),
a
natural
non-toxic
chemical,
has
proven
anti-inflammatory,
antioxidant,
anti-tumor,
neuroprotective
effects.Methods
First,
this
study
utilizes
network
pharmacology
explore
intrinsic
connection
between
GK
OA.
In
vitro,
SW1353
human
cartilage
cells
were
stimulated
with
Tert-butyl
hydrogen
peroxide
(TBHP),
different
concentrations
pre-treated
evaluate
its
protective
effects.
GK's
anti-inflammatory
antioxidative
effects
comprehensively
assessed
via
MTT
assay,
western
blot,
cell
immunofluorescence,
ELISA,
transcriptome
sequencing.
Potential
underlying
mechanisms
also
explored.
vivo,
OA
was
induced
in
rats
anterior
cruciate
ligament
transection
(ACLT),
impact
on
protection
further
histological
analysis
blot.Results
Network
revealed
that
regulates
several
key
pathways,
especially
NF-κB,
HIF-1,
PI3K-AKT,
substances
like
reactive
oxygen
species.
vitro
experiments
showed
effectively
reverses
damage
from
TBHP,
inhibits
inflammatory
factor
release,
protects
cellular
matrix
(ECM)
degradation.
These
functions
may
be
achieved
NF-κB
MAPK
signaling
pathways.
vivo
significantly
reduced
proteoglycan
loss
ACLT
inhibited
metalloproteinase
13
(MMP13)
glycan
protease
5
(ADAMTS5)
production,
preventing
degeneration
rats.Conclusion
The
research
findings
indicate
novel
approach
for
treatment
Processes,
Journal Year:
2024,
Volume and Issue:
12(12), P. 2772 - 2772
Published: Dec. 5, 2024
This
study
introduces
a
novel
approach
for
enhancing
the
functional
properties
of
cotton
fibers
through
complexation
copper
sulfate,
and
subsequent
combination
with
chitosan
(COT-CuSO4-CTS).
Our
preliminary
investigations
focused
on
development
composites
as
candidate
materials
coatings
antimicrobial
properties.
The
were
thoroughly
characterized
via
scanning
electron
microscopy
(SEM)
optical
microscopy,
providing
insights
into
their
structural
features
composition.
findings
show
that
modified
exhibit
potent
activity.
Specifically,
COT-CuSO4
COT-CuSO4-CTS
samples
demonstrated
zones
inhibition
against
both
Gram-positive
Staphylococcus
aureus
Gram-negative
Escherichia
coli,
confirming
ability
to
reduce
microbial
growth
significantly.
incorporation
layer
significantly
enhanced
Ultraviolet
Protection
Factor
(UPF)
fabric
from
3.37
over
50,
indicating
exceptional
UV
shielding
capabilities,
while
copper(II)
oxide
treatment
provided
moderate
UPF
value
14.56.
Blood
compatibility
studies
further
revealed
fabrics
influence
coagulation
parameters,
marked
prolongation
in
activated
partial
thromboplastin
time
(aPTT)
prothrombin
(PT)
compared
untreated
cotton.
anticoagulant
effect
is
primarily
linked
presence
copper,
although
addition
modulates
this
response,
slightly
reducing
clotting
times
alone.
Cytotoxicity
genotoxicity
assessments
using
Peripheral
Mononuclear
(PBM)
cells
indicated
was
non-toxic
non-genotoxic.
However,
displayed
reduction
cell
viability
induced
DNA
damage,
highlighting
potential
cytotoxic
genotoxic
effects.
Notably,
showed
lower
cytotoxicity
than
COT-CuSO4-CTS,
suggesting
reduces
overall
composite.
Furthermore,
plasmid
relaxation
assays
interact
DNA,
exhibiting
stronger
interaction
consistent
PBM
cells.