Development of Mn3O4 nanoparticles and Justicia adhatoda extract incorporated Carboxymethyl cellulose/Carbopol hydrogels: Rheological and in vitro bioactivity for sustained drug delivery system
International Journal of Biological Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown, P. 141713 - 141713
Published: March 1, 2025
Language: Английский
Design and Application of Stimuli‐Responsive Nanocomposite Hydrogels: A Review
Xiaohan Guo,
No information about this author
Huan Liu,
No information about this author
Aminov Nail
No information about this author
et al.
Macromolecular Rapid Communications,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Abstract
In
order
to
improve
the
disadvantages
of
traditional
hydrogels
such
as
low
mechanical
strength
and
lack
responsiveness,
different
types
nanoparticles
or
nanostructures
are
added
into
hydrogel
network
through
in
situ
polymerization,
self‐assembly
techniques,
other
strategies,
giving
a
variety
special
properties,
stimulation
sensitivity,
optical
electrical
reversibility.
With
development
nano
materials
synthesis
technology,
nanocomposite
have
shown
great
potential
drug
delivery,
tissue
engineering,
motion
detection,
wastewater
treatment,
been
extensively
studied
recent
years.
This
review
comprehensively
elucidates
state‐of‐the‐art
preparation
strategies
underlying
response
mechanisms
diverse
stimulus‐responsive
hydrogels,
spanning
temperature,
pH,
humidity,
electrical,
light
responses.
It
systematically
dissects
their
applications
biomedicine,
environmental
remediation,
flexible
sensing,
composite
phase
change
materials.
Moreover,
it
delves
future
prospects
challenges,
emphasizing
need
for
continuous
innovation
unlock
full
emerging
fields
address
existing
limitations.
Language: Английский
Evaluation of Dual Drug Delivery Efficiency of Nanocomposite Hydrogel Containing Pectin for Combating Cancer
Polymers for Advanced Technologies,
Journal Year:
2025,
Volume and Issue:
36(3)
Published: March 1, 2025
ABSTRACT
Traditional
chemotherapeutic
approaches
for
cancer
treatment
often
face
challenges,
such
as
limited
bioavailability
and
efficacy
of
anticancer
drugs
due
to
a
lack
specificity
quick
metabolism.
In
this
study,
nanocomposite
hydrogel,
namely
pectin‐
graft
‐poly(4‐acryloylmorpholine‐
co
‐2‐acrylamido‐2‐methyl‐1‐propanesulphonic
acid)
embedded
with
silver
nanoparticles
(Pec‐
g
‐poly(AcM‐
‐AMPS)‐SNPs)
was
developed
dual
drug
delivery
system
treatment.
The
the
neat
gel
without
(SNPs)
were
characterized
using
various
techniques
evaluated
their
efficiencies
co‐delivery
5‐fluorouracil
(5‐FU)
doxorubicin
(DOX)
model
drugs.
exhibited
pH‐responsive
swelling
behavior,
comparatively
higher
observed
nanocomposite,
maximum
at
pH
7.4.
process
obeyed
pseudo‐second‐order
kinetic
model.
A
similar
observation
made
regarding
release
drugs,
significantly
About
83.9%
5‐FU
73.3%
DOX
released
from
7.4
during
8
h.
profile
adhered
first‐order
Higuchi‐square
root
models.
transport
incorporated
out
matrix
into
dissolution
medium
be
Fickian
diffusion
process.
has
been
proven
cytocompatible,
demonstrated
by
cytotoxicity
study
carried
MCF‐10A
cells,
suggesting
its
suitability
oral
combating
cancer.
Language: Английский
Development of Pectin‐graft‐poly(4‐acryloylmorpholine) Embedded with Silver Nanoparticles as a Dual Drug Delivery System for Sustained Release of 5‐Fluorouracil and Curcumin
Macromolecular Chemistry and Physics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 22, 2025
Abstract
This
study
reports
the
preparation
of
pectin‐
graf
t‐poly(4‐acryloylmorpholine)
silver
nanocomposite
hydrogel
(Pec‐
g
‐PAcM‐AgNPs)
as
a
dual
drug
delivery
system
(DDDS)
for
sustained
release
5‐fluorouracil
(5‐FU)
and
curcumin
(CUR).
The
matrix
material
was
made
in
aqueous
medium
characterized
by
various
techniques.
Higher
swelling
were
observed
at
pH
7.4
than
1.2.
loading
efficiency
determined
to
be
39.1
mg
−1
5‐FU
42.8
CUR.
About
93.9%
72.2%
CUR
released
from
during
24
h.
kinetics
mechanism
best
fitted
first‐order
kinetic
Higuchi
square
rootmodels,
respectively.
adhered
Fickian
non‐Fickian
diffusion
mechanism,
cell
viability
drug‐loaded
above
85%,
indicating
cytocompatibility
developed
polymer
matrix.
results
highlight
potential
prepared
suitable
DDDS
enhancing
bioavailability
gastrointestinal
tract
cancer
therapy.
Language: Английский
Locust bean gum-based silver nanocomposite hydrogel as a drug delivery system and an antibacterial agent
International Journal of Biological Macromolecules,
Journal Year:
2024,
Volume and Issue:
unknown, P. 137097 - 137097
Published: Oct. 1, 2024
Language: Английский
Polymers Enhance Chlortetracycline Hydrochloride Solubility
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(19), P. 10591 - 10591
Published: Oct. 1, 2024
Chlortetracycline
hydrochloride
(CTC)
is
a
broad-spectrum
tetracycline
antibiotic
with
wide
range
of
antibacterial
activities.
Due
to
low
solubility,
poor
stability,
and
bioavailability,
clinical
preparation
development
limited.
We
sought
improve
these
solubility
dissolution
rates
by
preparing
solid
dispersions.
A
hydrophilic
polymer
was
selected
as
the
carrier,
dispersion
prepared
using
medium
grinding
method,
samples
characterized
scanning
electron
microscopy
(SEM),
differential
calorimetry
(DSC),
thermogravimetric
analysis
(TGA),
powder
X-ray
diffraction
(PXRD),
Fourier-transform
infrared
spectroscopy
(FT-IR),
particle
size
distribution
(PSD).
To
maximize
CTC
different
types
optimal
drug-to-polymer
ratios
were
screened.
The
optimized
povidone
K30
(PVPK30)
(1/0.75,
w/w)-,
hydroxypropyl-β-cyclodextrin
(HP-β-CD)
(1/2,
gelatin
(1/1,
w/w)-based
dispersions
6.25-,
7.7-,
3.75-fold
higher
than
that
pure
powder,
respectively.
Additionally,
in
vitro
studies
showed
gelatin-based
had
initial
rate.
SEM
PS
analyses
confirmed
this
smaller
more
uniform
particles
PVPK30
HP-β-CD
Therefore,
successful
preparations
improved
rates,
which
may
have
potential
drug
delivery
systems.
Language: Английский
Harnessing Natural Inhibitors of Protein Synthesis for Cancer Therapy: A Comprehensive Review
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
209, P. 107449 - 107449
Published: Oct. 4, 2024
Cancer
treatment
remains
a
formidable
challenge
in
modern
medicine,
necessitating
nuanced
understanding
of
its
molecular
underpinnings
and
the
identification
novel
therapeutic
modalities.
Among
intricate
web
cellular
pathways
implicated
oncogenesis,
protein
synthesis
has
emerged
as
fundamental
process
warranting
meticulous
investigation.
This
review
elucidates
multifaceted
role
tumor
initiation
progression,
highlighting
potential
targeting
key
nodes
within
these
viable
strategies.
Natural
products
have
long
served
source
bioactive
compounds
with
owing
to
their
structural
diversity
evolutionary
honing.
Within
this
framework,
we
provide
thorough
examination
natural
inhibitors
promising
candidates
for
cancer
therapy,
drawing
upon
recent
advancements
mechanistic
insights.
By
synthesizing
current
evidence
elucidating
challenges
opportunities,
aims
galvanize
further
research
into
development
product-based
anticancer
therapeutics,
thereby
advancing
clinical
armamentarium
against
malignancies.
Language: Английский
Development and In Vitro characterization of Azadirachta Indica Gum grafted polyacrylamide Based pH‐Sensitive Hydrogels to improve the Bioavailability of Lansoprazole
Chemistry & Biodiversity,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 15, 2024
Abstract
The
present
study
intended
to
develop
a
pH‐responsive
hydrogel
based
on
Neem
gum
(Ng)
improve
Lansoprazole
(LSP)
oral
bioavailability.
Azadirachta
Indica
seed
extract
was
used
obtain
Ng.
formulations
(F1–F9)
were
prepared
using
different
Ng
ratios,
Acrylamide
(AAm),
and
methylene‐bis‐acrylamide
(MBA).
formulated
hydrogels
characterized
through
FTIR,
thermal
analysis,
swelling
ratio,
SEM,
sol‐gel
In‐Vitro
drug
release,
cytotoxicity
analysis.
extracted
produce
powder
containing
21.5
%
Prepared
showed
maximum
at
pH
7.4,
whereas
the
an
acidic
insignificant.
LSP‐loaded
demonstrated
regulated
release
of
LSP
for
up
24
h
indicated
Super
Case
II
transport
mechanism.
During
cytotoxic
evaluation,
delivery
system
minimal
towards
normal
cells,
while
percent
carried
out
longer
duration
(up
96
h).
revealed
indica
gum‐based
as
promising
technique
precisely
delivering
LSP.
Language: Английский