Advanced Pharmaceutical Bulletin,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 15, 2024
Purpose:
Breast
cancer
is
a
prevalent
form
of
in
woman.
Vorinostat
(VOR)
chemotherapeutic
drug
that
has
been
utilized
for
treatment
breast
cancer,
but
its
effectiveness
limited
due
to
low
bioavailability
and
several
side
effects.
The
primary
aim
this
study
prepare
folic
acid
(FA)
conjugated
pegylated
bilosomes
containing
VOR
the
selective
targeting
cells
with
FA
receptor
expression.
Accordingly,
lithocholic
(LCA)
was
used
as
bile
anti-cancer
anti-proliferation
Methods:
loaded
were
prepared
using
thin-film
hydration
method
optimized
by
applying
two-level
fractional
factorial
design.
Various
properties
considered
bilosomes,
including
particle
size,
zeta
potential
(ZP),
polydispersity
index
(PdI),
encapsulation
efficiency
(EE)
%
loading
(DL)
%,
then
investigated
synthesized
FA-PEG-Cholesterol
incorporated
bilosomes.
efficacy
FA-PEG-
also
evaluated
vitro
MCF-7
4T1
cell
lines.
Furthermore,
drug-free
FA-PEG-bilosomes
biocompatibility
L929
line.
Results:
exhibited
spherical
particles
size
305.33
±
18.50
nm,
PdI
0.37
0.03,
-17.66
0.15
mV,
EE
92.91
0.22
DL%
23.64
0.04%.
Incorporation
FA-PEG-cholesterol
nanobilosomes
increased
absolute
value
potential.
In
cytotoxicity
revealed
FA-
PEG-bilosomes
demonstrated
greater
cytotoxic
effect,
compared
free
VOR-
both
cells.
Conclusion:
This
showed
could
be
promising
formulation
(+)
tumors.
Advanced Drug Delivery Reviews,
Journal Year:
2023,
Volume and Issue:
200, P. 115028 - 115028
Published: July 28, 2023
Lipid-based
nanocarriers
have
been
extensively
investigated
for
their
application
in
drug
delivery.
Particularly,
liposomes
are
now
clinically
established
treating
various
diseases
such
as
fungal
infections.
In
contrast,
extracellular
vesicles
(EVs)
-
small
cell-derived
nanoparticles
involved
cellular
communication
just
recently
sparked
interest
carriers
but
development
is
still
at
the
preclinical
level.
To
drive
this
further,
methods
and
technologies
exploited
context
of
liposome
research
should
be
applied
domain
EVs
to
facilitate
accelerate
clinical
translation.
One
crucial
steps
EV-based
therapeutics
designing
them
proper
dosage
forms
specific
applications.
This
review
offers
a
comprehensive
overview
state-of-the-art
polysaccharide-based
hydrogel
platforms
designed
artificial
natural
with
delivery
skin.
We
discuss
physicochemical
biological
properties
try
create
sound
basis
optimization
EV-embedded
hydrogels
versatile
therapeutic
avenues.
Gels,
Journal Year:
2024,
Volume and Issue:
10(2), P. 119 - 119
Published: Feb. 2, 2024
The
goal
of
this
investigation
is
to
improve
the
topical
delivery
medicine
by
preparing
and
maximizing
potential
a
nanotransferosome
gel
infused
with
Solanum
xanthocarpum
methanolic
extract
(SXE)
provide
localized
regulated
distribution.
Thin-film
hydration
was
used
create
SXE-infused
nanotransferosomes
(SXE-NTFs),
Box–Behnken
design
them.
Phospholipon
90G
(X1),
cholesterol
(X2)
sodium
cholate
(X3)
were
chosen
as
independent
variables,
their
effects
on
vesicle
size
(Y1),
polydispersity
index
(PDI)
(Y2)
percentage
entrapment
efficiency
(EE)
(Y3)
observed
both
individually
in
combination.
For
SXE-NTFs,
146.3
nm,
PDI
0.2594,
EE
82.24
±
2.64%,
drug-loading
capacity
8.367
0.07%
drug
release
rate
78.86
5.24%.
Comparing
antioxidant
activity
conventional
ascorbic
acid,
it
determined
be
83.51
3.27%.
Ex
vivo
permeation
tests
revealed
that
SXE-NTF
(82.86
2.38%)
considerably
outperformed
SXE
(35.28
1.62%)
terms
permeation.
In
addition,
seemed
from
confocal
laser
scanning
microscopy
(CLSM)
picture
Wistar
rat’s
skin
rhodamine-B-loaded
had
higher
penetration
capability
than
control.
Dermatokinetic
studies
showed
better
retention
gel.
According
experimental
results,
promising
successful
formulation.
Antibiotics,
Journal Year:
2023,
Volume and Issue:
12(10), P. 1550 - 1550
Published: Oct. 19, 2023
Itraconazole
(ITZ)
is
a
broad-spectrum
antifungal
for
superficial
subcutaneous
and
systemic
fungal
infections.
This
study
aimed
to
enhance
the
activity
of
ITZ
using
surfactin
A
(SA),
cyclic
lipopeptide
produced
by
SA-producing
Bacillus
strain
NH-100,
possessing
strong
activity.
SA
was
extracted,
ITZ-loaded
micelles
formulations
were
prepared
via
single-pot
rinsing
method
characterized
particle
size,
zeta
potential,
infrared
spectroscopy.
In
vitro
dissolution
at
pH
1.2,
as
well
hemolysis
studies,
also
carried
out.
The
fabricated
stable
non-spherical
in
shape,
with
an
average
size
about
179
nm,
FTIR
spectra
depicted
no
chemical
interaction
among
formulation
components.
showed
decreased
comparison
pure
ITZ.
drug
released
followed
Korsmeyer–Peppas
model,
having
R2
0.98
diffusion
release
mechanism.
acidic
buffer,
all
range
73–89%
2
h.
molecular
simulation
outstanding
binding
stability
profile
ITZ-SA
complex.
aromatic
ring
mediates
π-alkyl
contact
side
chain
SA.
It
can
be
concluded
that
micelles,
owing
significant
enhanced
up
6-fold
due
synergistic
effect
SA,
promising
delivery
platform
poorly
soluble