Placenta and Reproductive Medicine,
Journal Year:
2024,
Volume and Issue:
3
Published: Aug. 6, 2024
Objectives:
The
objective
of
this
review
was
to
summarize
currently
developed
advanced
drug
delivery
systems
that
can
be
used
for
pregnancy
related
disorders
along
with
their
advantages
and
clinical
relevance.
Methods:
This
process
a
defined
search
strategy
indexed
publications
from
databases
like
Google
scholar,
PubMed,
Embase,
Medline,
Scopus
UTMB
library
2000
2020
included
methods
assess
the
quality
evidence
retrieved.
Results:
Pregnancy
is
unique
physiological
condition
where
some
drugs
will
lifesaving
mother,
but
they
toxic
fetal
tissue.
It
mandatory
research
on
novel
systems.
Although
there
substantial
quantity
has
been
carried
out
maternal
-placental-fetal
uptake,
transfer,
toxicity,
therapeutic
evaluations
in
remain
infancy.
Conclusions:
In
review,
we
highlighted
considerations
placenta
summarized
recent
work
as
well
potential
applications
reality.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 9, 2025
Lipid
nanoparticles
(LNPs)
with
highly
efficient
and
specific
extrahepatic
targeting
abilities
are
promising
in
gene
delivery,
the
lipopeptides
(LPs)
excellent
designability
functionality
expected
to
empower
construction
of
functional
LNPs.
This
study
aims
develop
ionizable
components
that
accurately
match
different
lipid
systems
through
modular
design
LPs.
Based
on
this,
a
lipopeptide-based
organ-specific
(POST)
LNP
screening
strategy
is
constructed,
which
lysine-histidine-based
(KH-LPs)
designed
as
components.
The
optimal
KH-LP
screened
vitro
shows
siRNA/mRNA
transfecting
ability
various
hard-to-transfect
cell
lines.
Compared
classic
LNPs,
POST
LNPs
vivo
achieve
even
higher
(or
at
least
comparable)
efficiency
specificity
delivering
mRNA
siRNA
lung,
liver,
spleen,
respectively.
structure-activity
relationship
(SAR)
proves
regulation
LP
structures
can
provide
for
systems,
demonstrating
potential
this
developing
selective
open
up
more
possibilities
therapy.
Journal of Biomedical Science,
Journal Year:
2025,
Volume and Issue:
32(1)
Published: Feb. 19, 2025
Abstract
The
epidermal
growth
factor
receptor
(EGFR)
is
a
protein
embedded
in
the
outer
membrane
of
epithelial
and
mesenchymal
cells,
bone
blood
immune
heart
glia
stem
neural
cells.
It
belongs
to
ErbB
family,
which
includes
three
other
related
proteins:
HER2/ErbB2/c-neu,
HER3/ErbB3,
HER4/ErbB4.
EGFR
binds
seven
known
signaling
molecules,
including
(EGF)
transforming
factor-alpha
(TGF-α).
This
binding
triggers
formation
pairs
(dimers),
self-phosphorylation
EGFR,
activation
several
pathways
within
cell.
These
influence
various
cellular
processes
like
proliferation,
differentiation,
migration,
survival.
plays
critical
role
both
development
tissue
homeostasis,
repair
adult
organ
regeneration.
Altered
expression
linked
disruption
homeostasis
diseases,
among
cancer.
review
focuses
on
how
contributes
different
organs
placenta,
gut,
liver,
bone,
skin,
brain,
T
cell
regulation,
pancreas,
kidneys,
mammary
glands
lungs
along
with
their
associated
pathologies.
involvement
organ-specific
branching
morphogenesis
process
also
discussed.
level
activity
its
impact
vary
across
organs.
Factors
as
affinity
ligands,
recycling
or
degradation
processes,
transactivation
by
proteins
environmental
factors
(such
heat
stress
smoking)
play
regulating
activity.
Understanding
EGFR’s
regulatory
mechanisms
holds
promise
for
developing
targeted
therapeutic
strategies.
Human Gene Therapy,
Journal Year:
2024,
Volume and Issue:
35(17-18), P. 617 - 627
Published: Aug. 14, 2024
Lipid
nanoparticles
(LNPs)
are
the
most
clinically
advanced
drug
delivery
system
for
nucleic
acid
therapeutics,
exemplified
by
success
of
COVID-19
mRNA
vaccines.
However,
their
clinical
use
is
currently
limited
to
hepatic
diseases
and
vaccines
due
tendency
accumulate
in
liver
upon
intravenous
administration.
To
fully
leverage
potential,
it
essential
understand
address
tropism,
while
also
developing
strategies
enhance
tissues
beyond
liver.
Ensuring
that
these
therapeutics
reach
target
cells
avoiding
off-target
both
efficacy
safety.
There
three
potential
targeting
strategies-passive,
active,
endogenous-which
can
be
used
individually
or
combination
nonhepatic
tissues.
In
this
review,
we
delve
into
recent
advancements
LNP
engineering
delivering
Nano Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 17, 2024
Systemic
delivery
of
large
nucleic
acids,
such
as
mRNA,
to
the
brain
remains
challenging
in
part
due
blood-brain
barrier
(BBB)
and
tendency
vehicles
accumulate
liver.
Here,
we
design
a
peptide-functionalized
lipid
nanoparticle
(LNP)
platform
for
targeted
mRNA
brain.
We
utilize
click
chemistry
functionalize
LNPs
with
peptides
that
target
receptors
overexpressed
on
endothelial
cells
neurons,
namely
RVG29,
T7,
AP2,
mApoE
peptides.
evaluate
effect
LNP
targeting
neuronal
cell
transfection
vitro,
investigating
factors
serum
protein
adsorption,
intracellular
trafficking,
transcytosis,
exosome
secretion.
Finally,
show
peptide
functionalization
enhances
mouse
reduces
hepatic
after
systemic
administration.
Specifically,
RVG29
improved
vivo,
establishing
its
potential
nonviral
delivering
Journal of Controlled Release,
Journal Year:
2024,
Volume and Issue:
376, P. 678 - 700
Published: Oct. 28, 2024
There
is
a
clinical
need
to
develop
lipid
nanoparticles
(LNPs)
deliver
congenital
therapies
the
fetus
during
pregnancy.
The
aim
of
these
restore
normal
fetal
development
and
prevent
irreversible
conditions
after
birth.
As
first
step,
LNPs
be
optimized
for
transplacental
transport,
safety
on
placental
barrier
organs
transfection
efficiency.
We
developed
characterized
library
varying
compositions
used
machine
learning
(ML)
models
delineate
determinants
LNP
size
zeta
potential.
Utilizing
different
in
vitro
with
help
Random
Forest
algorithm,
we
could
identify
top
features
driving
percentage
transport
kinetics
at
24
h,
out
total
18
input
represented
by
41
formulations
48
experiments.
further
evaluated
safety,
cell
uptake,
efficiency
trophoblasts
lung
fibroblasts.
To
ensure
integrity
following
screened
using
high-throughput
integrated
transport-transfection
model.
Finally,
assessed
toxicity
tracheal
occlusion
explant
showed
little
no
cells.
Immunoglobin
G
(IgG)
orientation
surface
LNPs,
PEGylated
lipids,
ionizable
lipids
had
significant
effects
transport.
algorithm
identified
kinetics.
Zeta
potential
emerged
features.
Building
ML
model
results,
new
optimize
leading
622
%
increase
h
versus
control
formulation.
induce
preferential
siRNA
lung,
cationic
lipid-to-siRNA
ratio.
Studying
an
fibroblasts
strong
correlation
between
transfection.
appeared
safe
ex
vivo
lungs
as
indicated
insignificant
changes
apoptosis
(Caspase-3)
proliferation
(Ki67)
markers.
In
conclusion,
have
formulation
that
safe,
high
Our
research
findings
represent
important
step
toward
establishing
effectiveness
gene
delivery
organs.
Kachestvennaya Klinicheskaya Praktika = Good Clinical Practice,
Journal Year:
2025,
Volume and Issue:
4, P. 35 - 45
Published: Jan. 17, 2025
Relevance
.
Pharmacotherapy
during
pregnancy
is
associated
with
great
risks
for
the
fetus
in
case
of
therapy
non-obstetric
diseases
mother,
addition,
issues
improving
effectiveness
treatment
placental
pathology,
thrombophilic
conditions,
and
other
complications
remain
a
priority.
Recently,
possibilities
using
nanomaterials
medicine
have
been
actively
studied,
including
purpose
modifying
delivery
or
distribution
medicines.
Objective
The
aim
was
to
conduct
structured
analysis
published
literature
on
use
therapeutic
purposes
pregnancy.
Methods
publications
PubMed,
Cyberleninka,
eLIBRARY
databases
keywords
“Nanoparticles”
“Pregnancy”
carried
out,
exception
mentioning
nanoparticles
context
environmental
pollutants,
as
well
diagnostic
methods.
Results
Information
provided
nature
that
developed
studied
prospect
An
overview
areas
clinical
application
such
materials
provided,
available
evidence
their
safety.
Conclusion
Therapeutic
systems
containing
drugs
various
good
potential
order
ensure
targeted
drug
delivery,
modification
bio-distribution
increase
efficacy
reduce
toxicity
drugs.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
The
mRNA-lipid
nanoparticles
(mRNA@LNPs)
offer
a
novel
opportunity
to
treat
targets
previously
considered
undruggable.
Although
antibody
conjugation
is
crucial
for
enhancing
the
specificity,
delivery
efficiency,
and
minimizing
toxicity
of
mRNA
therapeutics,
current
chemical
methods
are
complex
produce
heterogeneous
particles
with
misoriented
antibodies.
In
this
work,
we
introduce
chemical-free
approach
functionalize
mRNA@LNPs
antibodies,
mimicking
protein
corona
formation
targeted
delivery.
By
fusing
apolipoprotein
Fc
domain
targeting
antibody,
enabled
spontaneously
display
on
surface
without
altering
existing
LNP
process
or
employing
techniques.
We
demonstrated
precise
expression
using
trastuzumab-bound
mRNA@LNPs,
facilitating
specific
in
HER2-positive
cancer
cells.
was
efficiently
delivered
tumor
site
after
intravenous
administration.
While
control
LNPs
lacking
antibodies
caused
acute
liver
toxicity,
trastuzumab-displayed
showed
no
systemic
toxicity.
tumor-specific
p53
suppressor
led
complete
regression
Thus,
fusion
enables
straightforward
scalable
production
antibody-functionalized
offering
significant
therapeutic
potential
gene
therapy.