ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(17), P. 21400 - 21414
Published: April 19, 2024
Morin,
a
naturally
occurring
bioactive
compound
shows
great
potential
as
an
antioxidant,
anti-inflammatory
agent,
and
regulator
of
blood
glucose
levels.
However,
its
low
water
solubility,
poor
lipid
limited
bioavailability,
rapid
clearance
in
vivo
hinder
application
regulation.
To
address
these
limitations,
we
report
enzymatically
synthesized
nanosized
morin
particle
(MNs)
encapsulated
sodium
alginate
microgels
(M@SA).
This
approach
significantly
enhances
morin's
delivery
efficiency
therapeutic
efficacy
Utilizing
horseradish
peroxidase,
MNs
averaging
305.7
±
88.7
nm
size.
These
were
then
via
electrohydrodynamic
microdroplet
spraying
to
form
M@SA
microgels.
In
studies
revealed
that
demonstrated
prolonged
intestinal
retention
superior
compared
with
unmodified
alone.
Moreover,
notably
improved
uptake
HepG2
cells.
Furthermore,
effectively
regulated
glucose,
profiles,
oxidative
stress
diabetic
mice
while
mitigating
liver,
kidney,
pancreatic
damage
enhancing
responses.
Our
findings
propose
promising
strategy
for
the
oral
administration
natural
compounds
regulation,
implications
broader
applications.
Journal of Drug Delivery Science and Technology,
Journal Year:
2024,
Volume and Issue:
96, P. 105699 - 105699
Published: April 22, 2024
Microfluidic-based
nanoscale
drug
delivery
systems
have
risen
to
prominence
in
the
field
of
precision
nanomedicine
recent
years.
This
intriguing
innovation
could
provide
unique
therapeutic
prospects
treatment
serious
disorders
as
traumatic
brain
injury,
a
potentially
fatal
condition
that
is
widespread
during
childhood.
According
current
scientific
study,
neurotrophins
are
vital
for
healing
injured
parenchyma,
and
brain-derived
neurotrophic
factor
(BDNF)
particular
may
significant
regenerative
effects.
To
address
BDNF-related
pharmacokinetic
constraints,
microfluidic-assisted
manufacturing
BDNF-loaded
solid
lipid
nanoparticles
(BDNF-SLNs)
was
carried
out,
following
evaluation,
formulation
demonstrated
optimum
characteristics
terms
size
(190.3
±
10.1
nm),
PDI
(0.180
0.023),
ζ-potential
(–
39.2
1.30
mV).
Short-term
stability
studies
haemolysis
assay
verified
formulation's
biocompatibility,
while
an
vitro
permeability
analysis
revealed
increase
Papp
encapsulated
BDNF
(1.27x10-5
cm/sec)
compared
plain
(9.31x10-6
cm/sec).
The
mimicked
neuroinflammatory
model
enhanced
decrease
nitrite
production
Nos
mRNA
levels
using
BDNF-SLNs
control,
validating
proficiency
microfluidic-based
pioneering
valuable
approaches
biologicals.
Nanomaterials,
Journal Year:
2022,
Volume and Issue:
12(13), P. 2224 - 2224
Published: June 29, 2022
The
impact
of
nanotechnology
on
the
exponential
growth
several
research
areas,
particularly
nanomedicine,
is
undeniable.
ability
to
deliver
active
molecules
desired
site
could
significantly
improve
efficiency
medical
treatments.
One
nanocarriers
developed
which
has
drawn
researchers'
attention
are
cubosomes,
nanosized
dispersions
lipid
bicontinuous
cubic
phases
in
water,
consisting
a
lipidic
interior
and
aqueous
domains
folded
lattice.
They
stand
out
due
their
incorporate
hydrophobic,
hydrophilic,
amphiphilic
compounds,
tortuous
internal
configuration
that
provides
sustained
release,
capacity
protect
safely
molecules.
Several
approaches
can
be
taken
prepare
this
structure,
as
well
different
lipids
like
monoolein
or
phytantriol.
This
review
paper
describes
methods
nanocarriers.
As
it
known,
physicochemical
properties
very
important,
they
influence
pharmacokinetics
Therefore,
an
extensive
characterization
essential
obtain
effect.
result,
we
have
extensively
described
most
common
techniques
characterize
exceptional
cubosomes
make
them
suitable
used
applications
biomedical
field,
from
cancer
therapeutics
imaging,
will
described.
Taking
consideration
outstanding
application
fields
envisaged.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2023,
Volume and Issue:
11(19), P. 7288 - 7300
Published: April 24, 2023
Acute
kidney
injury
(AKI)
is
a
common
and
lethal
complication
for
inpatients
in
the
intensive
care
unit.
Accumulative
evidence
suggests
that
severe
inflammation
oxidative
stress
are
major
causes
of
AKI.
Natural
polyphenols
with
potent
antioxidative
anti-inflammation
activities
promising
treatment
AKI,
but
low
bioavailability
reduces
their
therapeutic
efficacy
vivo.
Herein,
we
reported
novel
polyphenol-based
nanomedicine
comprising
tea
polyphenol
nanocarrier
insoluble
small-molecule
drug
curcumin
targeted
sepsis-induced
AKI
therapy.
Tea
nanoparticles
(TP-NPs)
were
synthesized
oligomers,
then
curcumin-containing
(Cur-NPs)
prepared
by
loading
into
TP-NPs.
In
vitro
experiments
proved
capability
Cur-NPs
to
scavenge
free
radicals,
protect
normal
cells
from
damage,
suppress
expression
proinflammatory
factors.
Furthermore,
these
nanomedicines
effectively
alleviated
septic
suppressing
response
restoring
oxidant-redox
homeostasis
The
further
exhibited
carrier-enhanced
due
effects
inornate
conclusion,
phytochemical
provide
an
attractive
strategy
therapy
herald
prospective
future
development
natural
reproducible
resource-derived
various
diseases
related
inflammation.
ACS Applied Nano Materials,
Journal Year:
2023,
Volume and Issue:
6(19), P. 17581 - 17592
Published: Sept. 20, 2023
The
development
of
efficient
drug
formulations
for
Parkinson's
disease
(PD)
treatment
is
challenged
by
achieving
pharmacokinetic
profiles,
reduced
side
effects,
and
better
permeability
through
the
blood–brain
barrier
(BBB).
As
nanoparticles
may
facilitate
delivery
drugs
in
brain
due
to
their
high-loading
capacity
ability
cross
biological
barriers,
we
designed
two
different
types
selenium
(SeNPs)
that
increase
transport
across
BBB
act
as
antioxidants
at
site
action.
SeNPs
were
functionalized
with
polyvinylpyrrolidone
(PVP)
polysorbate
20
(Tween)
characterized
terms
size,
size
distribution,
shape,
surface
charge,
colloidal
stability
relevant
media.
Their
drug-loading
was
tested
using
dopamine
l-DOPA
therapeutically
active
agents
PD.
Thermodynamic
analysis
revealed
binding
processes
occurred
spontaneously
hydrogen
bond/van
der
Waals
interactions
or
electrostatic
interactions.
strongest
interaction
observed
between
PVP-SeNPs
dopamine,
which
a
constant
several
orders
magnitude
higher
than
Tween-SeNPs.
However,
addition
human
transferrin
model
plasma
protein
significantly
this
difference,
indicates
crucial
role
corona
formation
design
nanodelivery
systems.
In
vitro
evaluation
cell-free
cellular
transwell
models
showed
internalization
SeNP-loaded
l-DOPA/dopamine
endothelial
cells,
while
facilitated
l-DOPA,
achieved
PVP-SeNPs.
Overall,
high
potential
drug-delivery
vehicles
PD
demonstrated.
Processes,
Journal Year:
2025,
Volume and Issue:
13(2), P. 460 - 460
Published: Feb. 8, 2025
Solid
lipid
microparticles
(SLMs)
are
multi-compartment
drug
carriers
that
can
be
used
in
various
forms
via
many
routes
of
administration,
primarily
to
obtain
prolonged
release,
protect
the
substance
or
mask
its
taste.
It
is
practically
impossible
theoretically
predict
effectiveness
incorporation
and
distribution
active
pharmaceutical
ingredients
(APIs)
SLMs,
these
fundamental
features
determine
key
properties
dosage
form.
The
possibility
an
effective
assessment
by
selecting
developing
sensitive,
universal
methods,
therefore,
conditions
further
development
practical
use
this
carrier.
Therefore,
unlike
already
available
review
papers
on
aim
mini-review
focus
solely
issues
API
SLMs
their
release.
For
purpose,
most
important
observations
results
our
own
research
were
collected
summarized,
then
attempt
was
made
confront
them
with
literature
data.
Among
methods
describing
critical
attributes
instrumental
(DSC,
AFM,
Raman
spectroscopy
NMR),
quantitative
studies
for
assessing
(including
entrapment
efficiency
drug-loading
parameters)
as
well
different
release
techniques
(without
a
membrane,
dialysis
bag
horizontal
chambers,
taking
into
account
physiological
factors)
characterized
compared.
facilitate
understanding
SLM
assess
ability
achieve
intended
effect
vivo,
standardize
such
carriers,
facilitating
comparison
between
centers.
Frontiers in Medical Engineering,
Journal Year:
2025,
Volume and Issue:
3
Published: March 21, 2025
Lipid
bicontinuous
cubic
phases
are
precursors
to
cubosomes–a
promising
type
of
nanoparticle
for
the
delivery
multicomponent
biomolecular
mixtures
applications
in
health
such
as
regenerative
medicine
and
wound
healing.
In
this
study,
we
showed
that
secretome
mesenchymal
stem
cells
(MSCs),
a
complex
mixture
growth
factors,
cytokines,
extracellular
vesicles,
other
cell-secreted
molecules
with
therapeutic
potential,
can
be
fully
incorporated
into
phytantriol
monoolein.
When
was
added
dry
lipid
films,
resulting
partial
phase
diagrams
these
lipid-secretome
systems,
although
more
complex,
resemble
those
their
lipid-water
analogs.
Remarkably,
visual
inspections
Small-Angle
X-ray
Scattering
(SAXS)
studies
composition
regions
homogeneous
solid-like
mesophases
without
excess
liquid
phase-separation.
This
indicates
diverse
components,
even
varied
sizes
structures,
integrated
phases.
SAXS
patterns
dominated
by
structural
parameters
close
systems.
suggests
water-soluble
proteins
likely
localize
within
water
channels
phase,
which
must
exhibit
flexibility
accommodate
sizes,
through
formation
locally
disordered
channels.
Extracellular
vesicles
associated
membrane
proteins,
on
hand,
fusing
integrating
membranes.
These
findings
underscore
potential
crystalline
materials
matrices
entire
secretome,
paving
way
future
secretome-based
cell-free
therapeutics
tissue
regeneration,
neuroprotective
anti-inflammatory
treatments.
Foods,
Journal Year:
2023,
Volume and Issue:
12(10), P. 2045 - 2045
Published: May 18, 2023
Curcumin-loaded
solid
lipid
nanoparticles
(Cur-SLN)
were
prepared
using
medium-
and
long
chain
diacylglycerol
(MLCD)
or
glycerol
tripalmitate
(TP)
as
matrix
three
kinds
of
surfactants
including
Tween
20
(T20),
quillaja
saponin
(SQ)
rhamnolipid
(Rha).
The
MLCD-based
SLNs
had
a
smaller
size
lower
surface
charge
than
TP-SLNs
with
Cur
encapsulation
efficiency
87.54–95.32%
the
Rha-based
exhibited
small
but
low
stability
to
pH
decreases
ionic
strength.
Thermal
analysis
X-ray
diffraction
results
confirmed
that
different
cores
showed
varying
structures,
melting
crystallization
profiles.
emulsifiers
slightly
impacted
crystal
polymorphism
MLCD-SLNs
largely
influenced
TP-SLNs.
Meanwhile,
transition
was
less
significant
for
MLCD-SLNs,
which
accounted
better
stabilization
particle
higher
during
storage.
In
vitro
studies
emulsifier
formulation
greatly
on
bioavailability,
whereby
T20-SLNs
much
digestibility
bioavailability
SQ-
Rha-SLNs
possibly
due
difference
in
interfacial
composition.
Mathematical
modeling
membrane
release
further
mainly
released
from
intestinal
phase
faster
rate
compared
other
formulations.
This
work
contributes
understanding
performance
MLCD
lipophilic
compound-loaded
has
important
implications
rational
design
nanocarriers
instructing
their
application
functional
food
products.