Pharmacia,
Journal Year:
2023,
Volume and Issue:
70(3), P. 758 - 796
Published: Sept. 18, 2023
Cardiovascular
disorder
is
the
leading
cause
death
in
world,
one
of
them
are
acute
myocardial
infarction
(AMI)
which
associated
with
hypertension
and
cardiac
remodeling.
ISO
may
inflammation,
enhance
production
oxidative
stress
while
decrease
antioxidant
defensive
system,
myocardium
impairment,
calcium
overload,
enhanced
cyclic
adenosine
monophosphate
level,
intracellular
acidosis,
altered
membrane
permeability.
Vernonia
amygdalina
(
VA
)
a
medicinal
plant
anti-inflammatory
properties.
This
study
investigated
potential
cardioprotective
effect
on
ISO-induced
toxicity
rats.
Male
Wistar
rats
were
randomly
divided
into
six
groups:
(ISO),
quercetin
100
mg/kg
plus
(ISO+QR),
ethanol
extract
100,
300,
500
(ISO+VA100,
ISO+VA300
ISO+VA500).
was
administered
subcutaneously
(85
mg/kg)
days
15
given
orally
for
14
days.
At
end
experiment,
blood
taken
from
heart
analyzed
markers
cardiac,
inflammation.
The
group
exhibited
significant
(p<0.05)
elevation
biomarkers
such
as
lactate
dehydrogenase
(LDH),
creatine
kinase-MB
(CK-MB),
troponin-T,
BNP
well
increased
malondialdehyde
(MDA)
reduced
enzyme
superoxide
dismutase
(SOD),
catalase
(CAT),
Glutathione
peroxidases
(GPx).
Additionally,
had
elevated
levels
pro-inflammatory
cytokines
interleukin-1
(IL-1),
interleukin-6
(IL-6),
Highly
sensitive
c
reactive
protein
(HsCRP)
tumor
necrosis
factor-alpha
(TNF-α).
Treatment
significantly
(p<0.001)
these
parameters
VA+ISO
compared
to
group.
These
findings
suggest
that
has
protective
against
cardiotoxicity
by
reducing
stress,
apoptosis,
(The
graphiccal
abstract
can
be
seen
Fig.
1).
Plants,
Journal Year:
2023,
Volume and Issue:
12(14), P. 2661 - 2661
Published: July 16, 2023
Transdermal
delivery
devices
and
wound
dressing
materials
are
constantly
improved
upgraded
with
the
aim
of
enhancing
their
beneficial
effects,
biocompatibility,
biodegradability,
cost
effectiveness.
Therefore,
researchers
in
field
have
shown
an
increasing
interest
using
natural
compounds
as
constituents
for
such
systems.
Plants,
important
source
so-called
“natural
products”
enormous
variety
structural
diversity
that
still
exceeds
capacity
present-day
sciences
to
define
or
even
discover
them,
been
part
medicine
since
ancient
times.
However,
benefits
just
at
beginning
being
fully
exploited
modern
dermal
transdermal
Thus,
plant-based
primary
compounds,
without
biological
activity,
contained
gums
mucilages,
traditionally
used
gelling
texturing
agents
food
industry,
now
explored
valuable
cost-effective
components
biomedical
field.
Their
non-toxicity
compensate
local
availability
compositional
variations.
Also,
secondary
metabolites,
classified
based
on
chemical
structure,
intensively
investigated
wide
pharmacological
toxicological
effects.
impact
is
highlighted
detail
through
most
recent
reported
studies.
Innovative
isolation
purification
techniques,
new
drug
systems,
advanced
evaluation
procedures
presented.
Gels,
Journal Year:
2024,
Volume and Issue:
10(6), P. 385 - 385
Published: June 5, 2024
A
combination
of
Poloxamer
407
(P407)
and
hydroxypropyl
methylcellulose
(HPMC)
hydrosols
is
proposed
as
an
in
situ
thermo-gelling
vehicle
for
the
nasal
drug
delivery
chlorhexidine–silver
nanoparticles
conjugates
(SN-CX).
Optimization
formulation
was
carried
out
by
applying
varying
ratios
P407
HPMC
presence
absence
SN-CX
so
that
gelation
would
occur
temperature
range
cavity
(30–34
°C).
Mechanisms
observed
phenomena
were
suggested
based
on
viscosimetry,
texture
analysis,
dynamic
light
scattering.
Tests
sprayability,
washout
time,
vitro
release,
ex
vivo
permeation,
antimicrobial
activity.
When
applied
separately,
found
to
lower
(Tg),
whereas
increased
it.
However,
HPMC,
interfered
with
micellar
organization
a
principally
contrasting
way
while
leading
even
further
decrease
Tg.
SN-CX-loaded
formulations
composed
16%
0.1%
demonstrated
desired
at
31.9
°C,
good
sprayability
(52.95%
coverage
anterior
cavity),
mucoadhesion
70
min
under
simulated
clearance,
expedient
release
preserved
anti-infective
activity
against
seasonal
Influenza
virus
beta-coronavirus,
Pseudomonas
aeruginosa,
Klebsiella
pneumoniae,
Staphylococcus
aureus
other
pathogens.
Our
findings
suggest
current
development
could
be
considered
potential
protective
spray
respiratory
infections.
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(3), P. 366 - 366
Published: March 4, 2025
Background/Objectives:
This
study
aims
to
gain
insights
into
the
antimicrobial
and
antiherpetic
activity
of
hyperforin-rich
Hypericum
perforatum
L.
(HP)
extract
using
nanostructured
lipid
carriers
(NLCs)
as
delivery
platforms.
Methods:
Two
established
NLC
specimens,
comprising
glyceryl
behenate
almond
oil
or
borage
oil,
their
extract-loaded
counterparts
(HP-NLCs)
were
utilized.
Their
minimal
bactericidal/fungicidal
concentrations
(MBC;
MFC)
investigated
against
Escherichia
coli
ATCC
25922,
Staphylococcus
aureus
25923,
Pseudomonas
aeruginosa
10145,
Klebsiella
pneumoniae
10031,
Candida
albicans
10231.
The
anti-herpesvirus
(HSV-1)
potential
was
evaluated
concerning
antiviral
virucidal
impact
on
viral
adsorption.
Results:
oil-based
nanodispersion
(HP-NLC2)
exhibited
pronounced
microbicidal
S.
(MBC
6.3
mg/mL),
K.
97.7
µg/mL),
C.
(MFC
<
48.8
unlike
oil-containing
sample
(HP-NLC1),
which
showed
only
weak
inhibition
fungal
growth.
HP-NLC2
found
be
less
cytotoxic
suppress
HSV-1
replication
slightly
more
than
HP-NLC1,
but
generally,
effects
weak.
Neither
empty
nanoparticles
nor
HP
expressed
E.
coli,
P.
aeruginosa,
extracellular
virions,
adhesion.
Conclusions:
It
could
concluded
that
both
HP-NLC
samples
revealed
minor
extract,
demonstrated
significant
antibacterial
antimycotic
activity.
Therefore,
latter
featured
a
convenient
HP-carrier
system
for
nano-designed
dermal
pharmaceutical
formulations.
Such
thorough
investigation
hyperforin-determined
anti-HSV-1
properties,
being
first
its
kind,
contributes
fundamental
knowledge
reveals
new
perspectives
utilization,
limitations,
therapeutic
designation
non-polar
components.
Journal of Dispersion Science and Technology,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 31
Published: March 26, 2025
In
recent
years,
bigels
(BGs)
have
garnered
increasing
attention
as
an
innovative
class
of
semisolid
formulations,
distinguished
by
their
unique
ability
to
combine
two
immiscible
gels
through
high
shear
mixing,
resulting
in
a
uniform
dispersion.
This
distinctive
composition
imparts
BGs
with
wide
range
advantageous
properties.
They
not
only
facilitate
the
delivery
both
hydrophilic
and
lipophilic
drugs
but
also
demonstrate
rapid
spreadability
easy
washability,
which
are
crucial
for
patient
comfort
compliance.
Furthermore,
noted
capacity
enhance
skin
hydration,
particularly
within
stratum
corneum,
thereby
potentially
improving
therapeutic
outcomes.
review
aims
comprehensively
explore
classification,
advantages,
limitations,
various
preparation
methods,
characterization
techniques
employed
BGs.
Key
analytical
approaches
discussed
include
microscopy
detailed
structural
analysis,
droplet
size
distribution
assessments,
Fourier
transform
infrared
spectroscopy
examine
chemical
properties,
mechanical
tests
such
viscosity,
spreadability,
texture
evaluations.
irritation
determination
zone
inhibition
assess
antimicrobial
activity
ensure
safety
efficacy
formulations.
Studies
on
vitro
drug
release,
ex
vivo
permeation
experiments,
stability
assessments
understanding
performance
pharmaceutical
cosmetic
applications.
release
studies
help
predicting
kinetics
from
BGs,
while
experiments
provide
insights
into
deliver
skin.
Stability
including
physical,
chemical,
microbiological
stability,
essential
long-term
effectiveness
bigel
Despite
yet
being
commercially
available,
research
has
shown
be
effective
carriers
controlled
topical,
transdermal,
buccal,
vaginal
systems.
Their
incorporate
makes
them
versatile
promising
candidates
variety
Moving
forward,
hold
substantial
promise
platforms
experience
diverse
properties
multifunctional
capabilities
could
revolutionize
field
delivery,
paving
way
more
patient-friendly
treatments.
Pharmaceuticals,
Journal Year:
2024,
Volume and Issue:
17(5), P. 575 - 575
Published: April 30, 2024
Hydrogels
consist
of
a
network
highly
porous
polymeric
chains
with
the
potential
for
use
as
wound
dressing.
Propolis
is
natural
product
several
biological
properties
including
anti-inflammatory,
antibacterial
and
antioxidant
activities.
This
study
was
aimed
at
synthesizing
characterizing
polyacrylamide/methylcellulose
hydrogel
containing
propolis
an
active
ingredient,
to
serve
dressing
alternative,
treatment
skin
lesions.
The
hydrogels
were
prepared
using
free
radical
polymerization,
characterized
scanning
electron
microscopy,
infrared
spectroscopy,
thermogravimetry,
differential
calorimetry,
swelling
capacity,
mechanical
rheological
properties,
UV-Vis
activity
by
DPPH,
ABTS
FRAP
assays
biocompatibility
determined
in
Vero
cells
J774
macrophages
MTT
assay.
showed
foliaceous
structure
well-defined
network,
good
ability
absorb
water
aqueous
solutions
simulating
body
fluids
well
desirable
pseudoplastic
behavior.
In
1.0
2.5%
propolis,
contents
total
polyphenols
24.74
±
1.71
mg
GAE/g
32.10
1.01
those
flavonoids
8.01
0.99
QE/g
13.81
0.71
QE/g,
respectively,
addition
all
three
methods
used.
Therefore,
extract,
may
promising
alternative
lesions,
due
their
anti-oxidant
low
cost
availability.
Gels,
Journal Year:
2024,
Volume and Issue:
10(5), P. 341 - 341
Published: May 17, 2024
The
wound-healing
effect
of
St.
John’s
Wort
(SJW)
is
mainly
attributed
to
hyperforin
(HP),
but
its
low
stability
restricts
topical
administration.
This
study
investigates
how
“free”
HP-rich
SJW
extract
(incorporated
into
a
bigel;
B/SJW)
and
“protected”
by
nanostructured
lipid
carriers
(also
included
in
biphasic
semisolid;
B/NLC-SJW)
affect
tissue
regeneration
rat
skin
excision
wound
model.
Wound
diameter,
histological
changes,
gene
expression
levels
fibronectin
(Fn),
matrix
metalloproteinase
8
(MMP8),
tumor
necrosis
factor-alpha
(TNF-α)
were
employed
quantify
the
healing
progress.
A
significant
size
reduction
was
achieved
after
applying
both
extract-containing
semisolids,
21-day
application
period,
smallest
observed
B/NLC-SJW-treated
animals.
However,
inflammatory
response
affected
more
favorably
bigel
containing
extract,
as
evidenced
studies.
Moreover,
B/SJW,
Fn,
MMP8,
TNF-α
significantly
higher
than
positive
control.
In
conclusion,
formulations
exhibited
beneficial
effects
on
skin,
B/SJW
restoration
processes
comprehensive
efficient
way.
Gels,
Journal Year:
2024,
Volume and Issue:
10(12), P. 770 - 770
Published: Nov. 26, 2024
The
therapeutic
potential
of
Cannabis
sativa
L.
extract
has
gained
significant
attention
due
to
its
diverse
medical
applications.
Sublingual
administration
remains
a
common
delivery
method
cannabinoids;
however,
challenges
often
arise
the
inconvenient
form
and
taste.
To
address
these
issues,
novel
bigel
formulation
was
developed,
combining
water
oil
phases
enhance
stability
bioavailability.
This
incorporates
cannabidiol-rich
hemp
extract,
hyaluronic
acid
for
moisturizing
properties,
taste-masking
agent
improve
patient
compliance
comfort.
Using
standardized
rich
in
cannabinoids
well-characterized
terpene
profile,
printability
bigels
evaluated
through
3D
printing
technology.
A
printout
with
known
cannabidiol
(CBD)
cannabidiolic
(CBDA)
content
11.613
mg
±
0.192
CBD
4.732
0.280
CBDA
obtained.
In
addition,
release
profile
determine
efficiency
active
ingredient—dissolved
ingredient
levels
ranged
from
74.84%
0.50
80.87%
3.20
80.84
1.33
98.31
1.70
depending
on
formulation.
Rheological
studies
were
conducted
evaluate
viscosity
under
varying
temperature
conditions,
ensuring
their
usability.
Findings
suggest
that
this
3D-printed
could
significantly
cannabis
extracts,
offering
more
convenient
effective
option
patients.
research
underscores
importance
innovation
cannabinoid
therapies
paves
way
further
advancements
personalized
medicine.
Pharmacia,
Journal Year:
2023,
Volume and Issue:
70(3), P. 435 - 447
Published: July 6, 2023
St.
John’s
wort
is
a
medicinal
herb
well-known
for
its
antidepressant,
anti-inflammatory,
antimycotic,
and
wound-healing
properties.
Hyperforin,
the
major
phloroglucinol
derivative,
has
been
implicated
as
one
of
main
contributors
to
these
therapeutic
effects.
Because
high
reactivity,
this
phytochemical
can
cause
various
adverse
effects,
such
allergic
reactions,
dizziness,
dry
mouth,
fatigue.
To
predict
critical
parameters
hyperforin’s
possible
behavior
after
oral
administration,
in
silico
methods
were
applied.
The
pharmacokinetic
profile,
bioactivity,
toxicity
analyzed
by
applying
Molinspiration
cheminformatics,
SwissADME,
PreADME/Tox,
OECD
QSAR
Toolbox
software.
results
showed
adequate
absorption,
affinity
plasma
proteins,
prolonged
renal
excretion
acylphloroglucinol.
metabolic
activity,
reason
potential
cyto-
genotoxicity,
predicted
carcinogenicity
mutagenicity
hyperforin,
necessitate
further
vitro
vivo
tests.
This
study
aimed
to
investigate
the
toxicological
profile
of
hyperforin
(HP)
in
silico
and
assess
it
vivo
after
topical
application
an
HP-rich
St.
John's
wort
(SJW)
extract.
The
former
analysis
predicted
low
toxicity
because
HP's
inability
bind
DNA
or
proteins,
but
structural
alerts
for
skin
irritation/corrosion,
carcinogenicity,
mutagenicity
were
found.
Animal
studies
involved
treatment
excision
wounds
Wistar
rats
with
poloxamer
407/borage
oil
formulations
(bigels;
Bs)
containing
SJW
extract
previously
developed
by
us.
effects
semisolids
comprising
'free'
(B/SJW)
loaded
nanostructured
lipid
carriers
(B/NLC-SJW)
compared
positive
(commercial
herbal
product)
negative
(untreated)
controls
2-,
7-,
14-,
21-day
applications.
Malondialdehyde
(MDA)
ABTS
assays
evaluated
degree
oxidative
stress—treatment
bigels
did
not
affect
MDA
favorably
led
increased
radical-cation
scavenging
capacity
(compared
controls).
Gamma-glutamyl
transferase
(GGT),
aspartate
aminotransferase
(ASAT),
alanine
(ALAT),
lactate
dehydrogenase
(LDH)
enzyme
levels
measured
as
indicators
liver/tissue
damage.
Treatment
both
B/SJW
B/NLC-SJW
21
days
resulted
lower
GGT
ASAT
than
those
controls.
Two-day
biphasic
contributed
normalized
ALAT
(lower
controls),
same
trends
observed
LDH
a
7-day
treatment.
promising
results
obtained
suggest
that
this
drug
delivery
system
may
only
preserve
HP
effectively
also
'expose'
its
cyto-/hepatoprotective
potential.