Physicochemical characterization and in vivo assessment of novel apixaban-loaded polymeric nano-aggregates
Journal of Pharmaceutical Investigation,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 31, 2024
Language: Английский
A Quaternary Solid Dispersion System for Improving the Solubility of Olaparib
Tae-Han Yun,
No information about this author
Jeong-Gyun Lee,
No information about this author
Kyu-Ho Bang
No information about this author
et al.
Solids,
Journal Year:
2025,
Volume and Issue:
6(1), P. 1 - 1
Published: Jan. 2, 2025
To
improve
the
low
solubility
of
poorly
water
soluble
olaparib,
in
following
study,
we
prepared
olaparib-loaded
quaternary
solid
dispersions
with
hypromellose,
Tween
20
or
Labrasol,
and
colloidal
silica.
The
olaparib
various
types
surfactants
was
evaluated
to
select
most
suitable
surfactant
effectively
enhance
its
solubility,
subsequently,
were
through
spray
drying.
physicochemical
properties
investigated
using
scanning
electron
microscopy,
flowability,
powder
X-ray
diffraction,
Fourier-transform
infrared
spectroscopy.
particle
size
smaller
more
spherical
compared
drug
maintained
an
amorphous
state,
exhibited
no
intermolecular
interactions
other
excipients
within
dispersion.
Additionally,
they
enhanced
flow
powder.
results
subsequent
kinetic
tests
dissolution
demonstrated
that
influenced
enhancement
release
olaparib.
Therefore,
dispersions,
characterized
by
will
be
beneficial
for
oral
delivery
Language: Английский
Study on Dispersion Technology of Pigment Powder and Its Interaction Based on Octenyl Succinate Starch and Arabic Gum Complex
Starch - Stärke,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 24, 2025
ABSTRACT
High
concentrations
of
pigment
powders
present
significant
challenges
for
dispersion
stability
in
cosmetic
formulations,
the
iron
oxide
yellow
paste
may
lead
to
flocculation,
reducing
its
stability.
This
study
employed
octenyl
succinate
starch
(OSA
starch)
and
Arabic
gum
(AG)
as
composite
wall
materials
encapsulate
optimize
system
water‐soluble
powders.
Transmission
electron
microscopy
(TEM)
scanning
(SEM)
confirmed
formation
a
well‐structured
microcapsule,
significantly
smaller
than
original
particles.
Accelerated
tests
indicated
that
microcapsule
structure
enhanced
stability,
with
improved
performance
observed
at
higher
OAF
solution
concentrations.
The
contact
angle
measurements,
which
were
consistently
below
90°,
demonstrated
wettability
hydrophilicity
solution,
thereby
improving
skin
adhesion.
encapsulation
using
OSA
AG
underscores
potential
application
natural
hydrocolloids
modified
starches
cosmetics
industry.
Language: Английский
Development of a Carvedilol-Loaded Solid Self-Nanoemulsifying System with Increased Solubility and Bioavailability Using Mesoporous Silica Nanoparticles
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(4), P. 1592 - 1592
Published: Feb. 13, 2025
This
study
developed
a
solid
self-nanoemulsifying
drug
delivery
system
(S-SNEDDS)
to
improve
the
oral
bioavailability
of
poorly
soluble
carvedilol
using
mesoporous
silica
nanoparticles
(MSNs).
The
liquid
(L-SNEDDS)
consisted
carvedilol,
Peceol,
Tween
80,
and
Labrasol
in
weight
ratio
10:25:50:25.
SNEDDS
was
suspended
MSN
at
various
ratios
spray-dried
produce
S-SNEDDS.
emulsion
size,
PDI,
solubility,
dissolution
were
evaluated
make
optimal
S-SNEDDS,
manufactured
L-SNEDDS
1000
500,
formed
nanoemulsion
achieved
efficient
supersaturation
compared
alone,
which
significantly
improved
solubility
(approximately
400
times),
5.7
times
60
min),
area
under
curve
(AUC)
(21.7
maximum
plasma
concentration
(Cmax)
(15.7
times).
In
addition,
physicochemical
properties
S-SNEDDS
by
differential
scanning
calorimetry
(DSC),
X-ray
powder
diffraction
(XRD),
Fourier
transform
infrared
(FT-IR),
particle
electron
microscopy
(SEM)
images.
showed
smaller
size
than
crystalline
transformed
into
an
amorphous
substance,
resulting
encapsulation
MSN.
These
results
suggest
that
can
be
novel
biocompatible
carrier
contributing
safer
more
effective
system.
Language: Английский
Principle of Tibetan medicine fluoritum processing by vinegar based on the change of microstructure and chemical composition
Yuzhou Zhuo,
No information about this author
Chang Lin,
No information about this author
Jing Hu
No information about this author
et al.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: March 4, 2025
Traditional
Chinese
medicine
(TCM)
processing
is
a
cultural
treasure
of
the
nation.
The
vinegar-quenched
method
mineral
an
important
part
traditional
theory.
Fluoritum
commonly
used
clinical
drug
in
medicine.
Its
microstructure
and
chemical
composition
will
change
after
vinegar
quenching,
which
reduce
its
toxicity
enhance
efficacy.
However,
study
changes
during
quenching
insufficient.
purpose
our
to
compare
differences
fluoritum
processed
products
from
aspects
microstructure,
content
main
trace
elements,
organic
elements.
carbon
nitrogen
elements
were
observed
by
thermal
field
emission
scanning,
energy
spectrum,
element
analyzer,
X-ray
fluorescence
spectrometer
inductively
coupled
plasma
mass
spectrometer.
results
showed
that
particles
quenched
water
flying
product
became
more
finer
uniform
than
other
(RSD
=
18.9%).
contents
are
0.185%
0.028%,
their
increased
nearly
4
5
times
raw
product,
respectively.
There
was
no
significant
CaF2
different
1.61%),
but
iron
has
doubled.
show
very
230%).
whose
significantly
Li,
V,
Zn,
Ga,
Cr
80%,RSD
84.2%,Zn
never
been
detected
11.3
μg.g-1,
RSD
62.3%,
51.3%).
with
decreased
Tl,
W
25.4%,
79.5%).
can
be
listed
as
best
for
because
it
make
smaller
uniform,
increase
matter
remove
toxic
harmful
metal
decrease
grain
size,
carbon,
U
may
reasons
enhancement
efficiency
reduction
processing.
Language: Английский
Enhancing Bioavailability Of Water-Soluble Drugs through Precision Electrostatic Spraying
Nisha D Barole,
No information about this author
Sunil N. Thitame,
No information about this author
Ashwini Aher
No information about this author
et al.
Journal of Pharmacy And Bioallied Sciences,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 1, 2025
A
BSTRACT
The
problem
of
the
bioavailability
water-soluble
drugs
can
be
staggering
in
formulation
when
drug
dissolves
readily
body
fluids.
Electrostatic
spraying,
a
sophisticated
particle
engineering
technology,
has
been
identified
as
one
most
potential
methods
managing
size
these
to
improve
their
bioavailability.
In
this
review,
author
discusses
principles
and
mechanisms
that
are
fundamental
electrostatic
spraying
and,
more
importantly,
possibility
adjusting
dimensions
particles
so
important
for
dissolution,
absorption,
Due
nanoscale
processing
drugs,
it
is
achievable
extend
time
small
intestine,
increase
absorption
by
biological
membranes,
maintain
stable
release
characteristics.
This
article
will
critically
discuss
parameters
affecting
formation
during
solvents
used,
spray
parameters,
environmental
etc.
Examples
case
studies
experimental
works
validate
use
technique
improvement
presented.
possible
limitations
structure,
issues
scaling
up,
prospects
refining
future
also
discussed.
present
analysis
aims
offer
comprehensive
understanding
achieving
barriers
advance
domains
delivery
systems.
Language: Английский
Molecular Mechanisms for Stabilizing Biologics in the Solid State
Journal of Pharmaceutical Sciences,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 1, 2024
Language: Английский
A Systematic Review of Spironolactone Nano-Formulations for Topical Treatment of Skin Hyperandrogenic Disorders and Chronic Wounds
Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
17(1), P. 27 - 27
Published: Dec. 27, 2024
Background/Objectives:
Spironolactone
(SP),
an
aldosterone
inhibitor
widely
used
to
treat
androgen-dependent
disorders
such
as
acne,
hirsutism,
and
alopecia,
has
demonstrated
therapeutic
potential
in
both
oral
topical
formulations.
However,
SP's
low
solubility
poor
bioavailability
conventional
formulations
have
driven
the
development
of
novel
nanocarriers
enhance
its
efficacy.
This
review
systematically
examines
recent
advancements
SP-loaded
nanocarriers,
including
lipid
nanoparticles
(LNPs),
vesicular
(VNPs),
polymeric
(PNPs),
nanofibers
(NFs).
Methods:
A
search
strategy
was
developed,
relevant
literature
searched
using
databases
Scopus,
PubMed,
Google
Scholar.
The
process,
screening,
inclusion,
exclusion
criteria,
adhered
Preferred
Reporting
Items
for
Systematic
Reviews
Meta-Analyses
(PRISMA)
guidelines.
Results:
comprehensive
analysis
13
eligible
research
articles,
corresponding
15
studies,
highlights
key
aspects
encapsulation
efficiency,
stability,
particle
size,
vitro
vivo
Six
studies
focused
on
solid
(SLNs)
nanostructured
carriers
(NLCs),
which
were
found
improve
skin
permeation.
Another
six
investigated
ethosomes
niosomes,
demonstrating
superior
targeting
penetration
capabilities.
Two
(PNPs)
showed
effectiveness
delivering
SP
hair
follicles
treatment
alopecia
acne.
Additionally,
one
study
indicated
significant
rosacea
therapy.
Conclusions:
nanocarrier
systems
represent
promising
targeted
further
clinical
are
required
optimize
their
safety,
efficacy,
delivery
mechanisms.
Language: Английский