Small,
Journal Year:
2023,
Volume and Issue:
19(37)
Published: April 28, 2023
The
treatment
of
human
immunodeficiency
virus
(HIV)
infection
is
notoriously
difficult
due
to
the
ability
this
remain
latent
in
host's
CD4+
T
cells.
Histone
deacetylases
(HDACs)
interfere
with
DNA
transcription
HIV-infected
hosts,
resulting
viral
latency.
Therefore,
HDAC
inhibitors
can
be
used
activate
latently
infected
cells,
after
which
eliminated
through
a
shock-and-kill
strategy.
Here,
drug
delivery
system
developed
effectively
deliver
Given
that
efficacy
reduced
under
hypoxic
conditions,
oxygen-containing
nanosomes
are
as
carriers.
Oxygen-containing
improve
efficiency
chemotherapy
by
delivering
essential
oxygen
Additionally,
their
phospholipid
bilayer
structure
makes
them
uniquely
well-suited
for
delivery.
In
study,
novel
taking
advantage
carriers
these
nanosomes,
incorporating
multi-drug
strategy
consisting
and
PKA
activators,
introducing
CXCR4
binding
peptides
specifically
target
Oxygen
enhanced
targeting
capability
introduction
peptide
mitigate
toxicity
slow
down
release.
observed
changes
expression
p24,
capsid
protein
HIV,
indirectly
confirm
proposed
induce
transcriptional
reactivation
HIV
Abstract
Messenger
RNA
(mRNA)
holds
great
potential
in
developing
immunotherapy,
protein
replacement,
and
genome
editing.
In
general,
mRNA
does
not
have
the
risk
of
being
incorporated
into
host
need
to
enter
nucleus
for
transfection,
it
can
be
expressed
even
nondividing
cells.
Therefore,
mRNA‐based
therapeutics
provide
a
promising
strategy
clinical
treatment.
However,
efficient
safe
delivery
remains
crucial
constraint
application
therapeutics.
Although
stability
tolerability
enhanced
by
directly
retouching
structure,
there
is
still
an
urgent
improve
mRNA.
Recently,
significant
progress
has
been
made
nanobiotechnology,
providing
tools
nanocarriers.
Nano‐drug
system
used
loading,
protecting,
releasing
biological
microenvironment
stimulate
translation
develop
effective
intervention
strategies.
present
review,
we
summarized
concept
emerging
nanomaterials
latest
enhancing
function
mRNA,
primarily
focusing
on
role
exosomes
delivery.
Moreover,
outlined
its
applications
so
far.
Finally,
key
obstacles
nanocarriers
are
emphasized,
strategies
overcome
these
proposed.
Collectively,
nano‐design
materials
exert
functions
specific
applications,
new
perception
next‐generation
nanomaterials,
thus
revolution
technology.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(4), P. 3375 - 3375
Published: Feb. 8, 2023
Gene
therapy
has
attracted
much
attention
because
of
its
unique
mechanism
action,
non-toxicity,
and
good
tolerance,
which
can
kill
cancer
cells
without
damaging
healthy
tissues.
siRNA-based
gene
downregulate,
enhance,
or
correct
expression
by
introducing
some
nucleic
acid
into
patient
Routine
treatment
hemophilia
requires
frequent
intravenous
injections
missing
clotting
protein.
The
high
cost
combined
causes
most
patients
to
lack
the
best
resources.
siRNA
potential
lasting
even
curing
diseases.
Compared
with
traditional
surgery
chemotherapy,
fewer
side
effects
less
damage
normal
cells.
available
therapies
for
degenerative
diseases
only
alleviate
symptoms
patients,
while
drugs
upregulate
expression,
modify
epigenetic
changes,
stop
disease.
In
addition,
also
plays
an
important
role
in
cardiovascular
diseases,
gastrointestinal
hepatitis
B.
However,
free
is
easily
degraded
nuclease
a
short
half-life
blood.
Research
found
that
be
delivered
specific
through
appropriate
vector
selection
design
improve
therapeutic
effect.
application
viral
vectors
limited
their
immunogenicity
low
capacity,
non-viral
are
widely
used
immunogenicity,
production
cost,
safety.
This
paper
reviews
common
recent
years
introduces
advantages
disadvantages,
as
well
latest
examples.
ACS Applied Bio Materials,
Journal Year:
2024,
Volume and Issue:
7(4), P. 2175 - 2185
Published: March 13, 2024
Lung
cancer
and
Mycobacterium
avium
complex
infection
are
lung
diseases
associated
with
high
incidence
mortality
rates.
Most
conventional
anticancer
drugs
antibiotics
have
certain
limitations,
including
drug
resistance
rates
adverse
effects.
Herein,
we
aimed
to
synthesize
mannose
surface-modified
solid
lipid
nanoparticles
(SLNs)
loaded
curcumin
(Man-CUR
SLN)
for
the
effective
treatment
of
disease.
The
synthesized
Man-CUR
SLNs
were
analyzed
using
various
instrumental
techniques
structural
physicochemical
characterization.
Loading
into
improved
encapsulation
efficiency
release
capacity,
as
demonstrated
by
high-performance
liquid
chromatography
analysis.
Furthermore,
characterized
effect
A549
cell
line.
Cells
treated
SLN
exhibited
an
increased
cellular
uptake
cytotoxicity.
Moreover,
free
CUR
could
more
effectively
reduce
migration
than
SLNs.
Similarly,
elicited
a
stronger
apoptosis-inducing
that
SLNs,
reverse
transcription-quantitative
PCR
Finally,
examined
antibacterial
effects
against
intracellulare
(M.i.)
M.i.-infected
macrophages,
revealing
exerted
strongest
effect.
Collectively,
these
findings
indicate
mannose-receptor-targeted
delivery
be
in
treating
diseases.
Accordingly,
this
system
can
used
target
variety
cancers
immune
cells.
International Journal of Nanomedicine,
Journal Year:
2025,
Volume and Issue:
Volume 20, P. 25 - 52
Published: Jan. 1, 2025
Abstract:
The
effective
clinical
translation
of
messenger
RNA
(mRNA),
small
interfering
(siRNA),
and
microRNA
(miRNA)
for
therapeutic
purposes
hinges
on
the
development
efficient
delivery
systems.
Key
challenges
include
their
susceptibility
to
degradation,
limited
cellular
uptake,
inefficient
intracellular
release.
Polymeric
drug
conjugates
(PDCs)
offer
a
promising
solution,
combining
benefits
polymeric
carriers
agents
targeted
treatment.
This
comprehensive
review
explores
nucleic
acid
therapeutics,
focusing
conjugates.
It
investigates
how
these
address
obstacles,
enhance
systemic
circulation,
reduce
immunogenicity,
provide
controlled
release,
improving
safety
profiles.
delves
into
conjugation
strategies,
preparation
methods,
various
classes
PDCs,
as
well
strategic
design,
highlighting
role
in
delivery.
Applications
PDCs
treating
diseases
such
cancer,
immune
disorders,
fibrosis
are
also
discussed.
Despite
significant
advancements,
adoption
persist.
concludes
with
insights
future
directions
this
transformative
technology,
underscoring
potential
advance
acid-based
therapies
combat
infectious
significantly.
Keywords:
polymer
conjugates,
Plants,
Journal Year:
2025,
Volume and Issue:
14(6), P. 977 - 977
Published: March 20, 2025
RNA
interference
(RNAi)
has
emerged
as
a
potent
mechanism
for
combating
pathogenic
fungi
and
oomycetes
over
the
past
decades.
It
offers
promising
gene-silencing
approach
by
targeting
crucial
genes
involved
in
diseases
caused
economically
scientifically
significant
fungal
pathogens,
such
Botrytis
cinerea
Fusarium
species.
Simultaneously,
nano-agro-products
have
gained
attention
alternatives
to
traditional
fungicides
plant
protection
strategies.
However,
instability
of
naked
molecules
outside
cellular
environment
presents
challenge,
they
degrade
rapidly,
limiting
their
efficacy
prolonged
disease
control.
Concerns
regarding
toxicity
protective
nanoparticles
non-target
organisms
also
arisen.
Integrating
RNAi
with
nano-agro-products,
particularly
nanocarriers,
form
RNA-nano
complexes
demonstrated
potential,
providing
enhanced
stability,
reduced
toxicity,
extended
This
review
explores
mechanisms
complexes-mediated
protection,
addressing
stability
nano-toxicity
issues
while
examining
prospects
complex
research
pathogen
management.
Molecules and Cells,
Journal Year:
2023,
Volume and Issue:
46(1), P. 41 - 47
Published: Jan. 1, 2023
The
rapid
development
of
mRNA
vaccines
has
contributed
to
the
management
current
coronavirus
disease
2019
(COVID-19)
pandemic,
suggesting
that
this
technology
may
be
used
manage
future
outbreaks
infectious
diseases.
Because
antigens
targeted
by
can
easily
altered
simply
changing
sequence
present
in
coding
region
structures,
it
is
more
appropriate
develop
vaccines,
especially
during
rapidly
developing
In
addition
allowing
development,
have
great
potential
inducing
successful
antigen-specific
immunity
expressing
target
cells
and
simultaneously
triggering
immune
responses.
Indeed,
two
COVID-19
approved
U.S.
Food
Drug
Administration
shown
significant
efficacy
preventing
infections.
ability
mRNAs
produce
proteins
are
defective
specific
diseases
enabled
options
treat
intractable
Clinical
applications
vaccines/therapeutics
require
strategies
safely
deliver
RNA
molecules
into
cells.
review
summarizes
knowledge
about
vaccines/
therapeutics,
their
clinical
applications,
delivery
strategies.
Nanoscale Advances,
Journal Year:
2023,
Volume and Issue:
5(7), P. 1853 - 1869
Published: Jan. 1, 2023
This
review
article
demonstrated
nucleic
acid-based
therapeutics
and
lipid
nanoparticle
type
as
a
carrier
of
acid
for
further
applications
LNPs
flexible
carriers
in
immuno-therapeutics
anti-cancer
reagents.
Small,
Journal Year:
2023,
Volume and Issue:
19(46)
Published: July 20, 2023
Abstract
mRNA
therapy
has
shown
great
potential
in
infectious
disease
vaccines,
cancer
immunotherapy,
protein
replacement
therapy,
gene
editing,
and
other
fields
due
to
its
central
role
all
life
processes.
However,
is
challenging
pass
through
the
cell
membrane
significant
negative
charges
degradation
from
RNase,
so
key
efficient
packaging
delivery
of
it
with
appropriate
vectors.
Presently
researchers
have
developed
various
vectors
such
as
viruses
liposomes,
but
these
conventional
are
now
difficult
meet
growing
requirement
like
safety,
efficiency,
targeting,
many
novel
unique
advantages
emerged
recently.
This
review
mainly
introduces
two
categories
vectors:
biomacromolecules
inorganic
nanoparticles,
well
methods
control
administration
based
on
controlled‐release
non‐invasive
administration.
These
strategies
high
biocompatibility,
versatility,
intelligence,
targeting.
paper
analyzes
challenges
faced
by
field
depth,
discusses
how
use
characteristics
administrations
solve
problems.