The
prevalence
and
lack
of
good
solutions
for
cow's
milk
allergy
(CMA)
in
young
children
are
leading
to
public
concern
increasing
socioeconomic
problems.
This
requires
new
preventive
approaches.
In
this
thesis,
we
investigated
the
potential
an
oral
formulation
–
based
on
poly(lactic
acid-co-glycolic
acid)
(PLGA)
nanoparticles
(NP)
selected
peptides
from
whey
proteins
CpG-Oligodeoxynucleotides
CMA
prevention,
using
both
vitro
vivo
studies.
vitro,
showed,
through
Förster
Resonance
Energy
Transfer
(FRET)
imaging
living
cells,
that
PLGA
NP
protected
encapsulated
up
6
hours
simulated
gastric
fluid
extended
their
residence
time
isolated
mouse
dendritic
cells
96
hours.
demonstrates
hypothesis
improved
stability
peptide
cargo
gastrointestinal
lumen
retention
intestinal
DC
upon
internalization.
vivo,
showed
pretreatment
with
two
PLGA-NP-encapsulated
peptides,
prior
allergic
sensitization
whey,
mice
acute
skin
reactions
intradermal
exposure
whey.
addition,
have
shown
protection
is
dose-related
may
be
associated
whey-specific
systemic
silencing
ex
whey-stimulated
TNF-α
release
by
splenocytes.
Intriguingly,
superior
tolerogenic
effect
orally
administered
co-loaded
T-cell
epitopes
containing
a
CpG
adjuvant
as
compared
separately
counterpart.
combination
prevented
rise
specific
IgE
antibody
levels
serum
whey-induced
reactions,
beneficial
immunomodulatory
immune
cells.
Finally,
allergy-associated
effects
empty,
or
CpG-containing
were
evaluated
derived
human
monocytes.
immature
moDCs
primed
CpG-ODN
loaded
also
effectively
increased
ratios
Treg/Th2
Th1/Th2.
finding
supports
co-encapsulated
facilitates
inhibition
Th2
immunity
vivo.
conclusion,
our
findings
substantiate
translational
which
future
development
effective
safe
strategies
early
life
prevention
(i.e.,
supplementing
hydrolyzed
formula
infants
at
risk).
besides
BLG-peptides
motives,
include
bacterial
DNA
strains,
can
increase
efficacy
formulations
tolerance
induction.
strategy
further
developed
modality
treat
cow’s
example
adjunct
treatment
allergen
immunotherapy.
Advanced Functional Materials,
Journal Year:
2022,
Volume and Issue:
33(7)
Published: Dec. 7, 2022
Abstract
Stimuli‐responsive
peptides
and
proteins
are
an
exciting
class
of
smart
biomaterials
for
various
applications
have
received
significant
attention
over
the
past
decades.
A
wide
variety
stimuli
such
as
temperature,
pH,
ions,
enzymes,
magnetic
field,
redox,
etc.,
explored.
This
article
provides
a
review
five
intensively
studied
types
stimuli‐responsive
proteins,
their
design
principles
applications,
including
temperature‐,
pH‐,
light‐,
metal
ion‐,
enzyme‐responsive
with
emphasis
on
key
concepts
switch
function.
Moreover,
typical
examples
discussed
to
provide
better
understanding
concept
underlying
methodology.
will
facilitate
inspire
future
innovation
toward
new
peptide‐
protein‐based
materials
diverse
applications.
ACS Nano,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 17, 2024
The
simultaneous
detection
of
proteins
and
microRNA
(miRNA)
at
the
single
extracellular
vesicle
(EV)
level
shows
great
promise
for
precise
disease
profiling,
owing
to
heterogeneity
scarcity
tumor-derived
EVs.
However,
a
highly
reliable
method
multiple-target
analysis
EVs
remains
be
developed.
In
this
study,
digital
dual
CRISPR-Cas-powered
Single
EV
Evaluation
(ddSEE)
system
was
proposed
enable
concurrent
surface
protein
inner
miRNA
single-molecule
level.
By
optimizing
reaction
conditions
CRISPR-Cas12a
CRISPR-Cas13a,
detected
by
Cas12a
using
antibody-DNA
conjugates
transfer
signal
DNA,
while
analyzed
Cas13a
through
EV-liposome
fusion.
A
microfluidic
chip
containing
188,000
microwells
used
convert
CRISPR-Cas
into
assay
format
absolute
quantification
miRNA/protein-positive
without
bias
fluorescence
imaging,
which
can
detect
as
few
214
EVs/μL.
Finally,
total
31
blood
samples,
21
from
breast
cancer
patients
10
healthy
donors,
were
collected
tested,
achieving
diagnostic
accuracy
92%
in
distinguishing
with
donors.
With
its
quantification,
ease
use,
multiplexed
capability,
ddSEE
demonstrates
potential
both
research
clinical
applications.
Biosensors,
Journal Year:
2021,
Volume and Issue:
11(12), P. 505 - 505
Published: Dec. 9, 2021
Fluorescence
labelling
is
often
used
for
tracking
nanoparticles,
providing
a
convenient
assay
monitoring
nanoparticle
drug
delivery.
However,
it
difficult
to
be
quantitative,
as
many
factors
affect
the
fluorescence
intensity.
Förster
resonance
energy
transfer
(FRET),
taking
advantage
of
from
donor
fluorophore
an
acceptor
fluorophore,
provides
distance
ruler
probe
NP
This
article
review
different
FRET
approaches
ratiometric
self-assembly
and
formation
their
in
vivo
fate,
integrity
release.
We
anticipate
that
fundamental
understanding
gained
these
studies
will
offer
new
insights
into
design
nanoparticles
with
improved
better-controlled
properties.
Aggregate,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 3, 2024
Abstract
Single‐drug
therapies
or
monotherapies
are
often
inadequate,
particularly
in
the
case
of
life‐threatening
diseases
like
cancer.
Consequently,
combination
emerge
as
an
attractive
strategy.
Cancer
nanomedicines
have
many
benefits
addressing
challenges
faced
by
small
molecule
therapeutic
drugs,
such
low
water
solubility
and
bioavailability,
high
toxicity,
etc.
However,
it
remains
a
significant
challenge
encapsulating
two
drugs
nanoparticle.
To
address
this
issue,
computational
methodologies
employed
to
guide
rational
design
synthesis
dual‐drug‐loaded
polymer
nanoparticles
while
achieving
precise
control
over
drug
loading.
Based
on
sequential
nanoprecipitation
technology,
five
factors
identified
that
affect
formulation
candidates
into
dual‐drug
loaded
nanoparticles,
then
screened
176
formulations
under
different
experimental
conditions.
these
data,
machine
learning
methods
applied
pin
down
key
factors.
The
implementation
methodology
holds
potential
significantly
mitigate
complexities
associated
with
co‐assembly
compounds
nanoparticulate
systems
demonstrates
promising
avenue
for
therapy.
This
approach
provides
new
strategy
enabling
streamlined,
high‐throughput
screening
nanoscale
drug‐loaded
entities.
ACS Applied Nano Materials,
Journal Year:
2024,
Volume and Issue:
7(4), P. 3656 - 3667
Published: Feb. 2, 2024
This
study
investigates
the
uptake
and
retention
of
stable
fluorescent
organosilica
nanoparticles
by
macrophages,
which
play
a
vital
role
in
scavenging
environmental
nanomedicines
within
body.
We
used
rhodamine
6G-loaded
(SiNP-R6G)
synthesized
from
thiol-functionalized
organosilane
precursor.
Our
primary
objective
was
to
establish
quantitative
relationship
between
measurements
nanoparticle
tracking
analysis,
enabling
precise
"counting"
taken
up
macrophages
under
kinetic
measurement
conditions.
demonstrated
concentration-dependent,
saturable
internalization
model
macrophage
(RAW
264.7
cells),
with
maximum
rate
(Vmax)
7.9
×
104
per
hour
cell.
The
estimated
number
concentration
for
half-maximum
approximately
0.8
trillion
milliliter,
significant
portion
(∼80%)
internalized
SiNP-R6G
remained
entrapped
cells
48
h,
indicating
sustained
particle
capacity
macrophages.
data
further
demonstrate
that
occupy
more
than
10%
total
cell
volume,
without
inducing
cytotoxic
effects.
heightened
is
attributed
intracellular
vesicles
capable
accommodating
50
densely
packed,
yet
nonaggregated,
single
vesicle.
In
summary,
our
underscores
effective
development
methodology
cellular
providing
valuable
insights
into
kinetics
capabilities
nanoparticle-based
drug
delivery.
Journal of Nanobiotechnology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Dec. 19, 2024
Radiotherapy
(RT)
is
a
primary
clinical
approach
for
cancer
treatment,
but
its
efficacy
often
hindered
by
various
challenges,
especially
radiation
resistance,
which
greatly
compromises
the
therapeutic
effectiveness
of
RT.
Mitochondria,
central
to
cellular
energy
metabolism
and
regulation
cell
death,
play
critical
role
in
mechanisms
radioresistance.
In
this
context,
cuproptosis,
novel
copper-induced
mitochondria-respiratory-dependent
death
pathway,
offers
promising
avenue
radiosensitization.
study,
an
innovative
theranostic
nanoplatform
was
designed
induce
cuproptosis
synergy
with
low-dose
therapy
(LDRT,
i.e.,
0.5–2
Gy)
treatment
situ
hepatocellular
carcinoma
(HCC).
This
aims
reverse
hypoxic
tumor
microenvironment,
promoting
shift
from
glycolysis
oxidative
phosphorylation
(OXPHOS),
thereby
enhancing
sensitivity
cuproptosis.
Concurrently,
Fenton-like
reaction
ensures
sustained
supply
copper
depletion
glutathione
(GSH),
inducing
disrupting
mitochondrial
function,
interrupting
supply.
strategy
effectively
overcomes
radioresistance
enhances
against
tumors.
conclusion,
study
elucidates
intricate
interactions
among
hypoxia
reversal,
metabolic
reprogramming,
radiosensitization,
particularly
context
treating
carcinoma,
providing
paradigm
radiotherapy.