Rapid
protein
detection
is
crucial
for
medical
diagnosis,
clinical
trials,
and
drug
development
but
often
faces
challenges
in
balancing
sensitivity
with
multiplex
detection,
low
reagent
consumption,
a
short
time.
In
this
work,
we
developed
an
automated
sensitive
electroosmotic
digital
optofluidics
(e-DOF)
platform
rapid
label-free
biomarker
quantification
microliter
blood
samples.
The
hyperspectral
computation
reveals
nanoscale
morphology
changes
caused
by
target
capture,
eliminating
multifarious
enzyme-linked
labeling.
Electroosmosis-driven
molecular
circulation
accelerates
the
immuno-hybridization,
enhancing
(with
limit
of
0.21
nM)
reducing
time
to
15
min,
compared
2–3
h
traditional
immunosorbent
assay.
hepatitis
A
E
IgM
17
samples,
results
were
completely
consistent
trial
outcomes.
This
e-DOF
system
presents
automated,
rapid,
highlighting
potential
applications
diagnosis
immunoassay
research.
Lab on a Chip,
Год журнала:
2024,
Номер
24(5), С. 1441 - 1493
Опубликована: Янв. 1, 2024
This
review
explores
emerging
microfluidic-based
technologies
incorporating
innovative
assay
strategies
for
infectious
disease
diagnostics.
Our
classification
scheme
is
based
on
the
human
body
systems
or
pathogen
transmission
modes.
Chemosensors,
Год журнала:
2025,
Номер
13(1), С. 11 - 11
Опубликована: Янв. 8, 2025
Dual-
or
multi-template
molecularly
imprinted
polymers
have
been
an
attractive
research
field
for
many
years
as
they
allow
simultaneous
detection
of
more
than
one
target
with
high
selectivity
and
sensitivity
by
creating
template-specific
recognition
sites
multiple
targets
on
the
same
functional
monomer.
Dual/multi-template
molecular
imprinting
techniques
applied
to
identify,
extract,
detect
targets,
from
heavy
metal
ions
viruses,
different
methods,
such
high-performance
liquid
chromatography
(HPLC),
chromatography–mass
spectrometry
(LC-MS),
piezoelectric,
optical,
electrochemical
methods.
This
article
focuses
sensors
based
dual/multi-template
detecting
a
wide
range
Furthermore,
this
work
highlights
use
these
point-of-care
applications,
their
commercialization
integration
microfluidic
systems.
Abstract
The
focus
on
precise
medicine
enhances
the
need
for
timely
diagnosis
and
frequent
monitoring
of
chronic
diseases.
Moreover,
recent
pandemic
severe
acute
respiratory
syndrome
coronavirus
2
poses
a
great
demand
rapid
detection
surveillance
viral
infections.
protein
biomarkers
antigens
in
saliva
allows
identification
diseases
or
disease
changes
scenarios
where
when
test
response
at
point
care
is
mandated.
While
traditional
methods
testing
fail
to
provide
desired
fast
results,
electrochemical
biosensors
based
nanomaterials
hold
perfect
characteristics
point‐of‐care
settings.
advances
sensors
salivary
are
critically
reviewed
this
work,
with
emphasis
role
boost
biosensor
analytical
performance
increase
reliability
human
samples.
Furthermore,
work
identifies
critical
factors
further
modernization
nanomaterial‐based
sensors,
envisaging
development
implementation
next‐generation
sample‐in‐answer‐out
systems.
ACS Nano,
Год журнала:
2023,
Номер
17(13), С. 12052 - 12071
Опубликована: Июнь 27, 2023
Extracellular
vesicles
(EVs)
are
continually
released
from
cancer
cells
into
biofluids,
carrying
actionable
molecular
fingerprints
of
the
underlying
disease
with
considerable
diagnostic
and
therapeutic
potential.
The
scarcity,
heterogeneity
intrinsic
complexity
tumor
EVs
present
a
major
technological
challenge
in
real-time
monitoring
complex
cancers
such
as
glioblastoma
(GBM).
Surface-enhanced
Raman
spectroscopy
(SERS)
outputs
label-free
spectroscopic
fingerprint
for
EV
profiling.
However,
it
has
not
been
exploited
to
detect
known
biomarkers
at
single
level.
We
developed
multiplex
fluidic
device
embedded
arrayed
nanocavity
microchips
(MoSERS
microchip)
that
achieves
97%
confinement
minute
amount
fluid
(<10
μL)
enables
profiling
SERS.
arrays
combine
two
featuring
characteristics:
(1)
An
MoS2
monolayer
isolation
nanoconfinement
due
physical
interaction
(Coulomb
van
der
Waals)
between
edge
sites
lipid
bilayer;
(2)
A
layered
plasmonic
cavity
sufficient
electromagnetic
field
enhancement
inside
cavities
obtain
level
signal
resolution
stratifying
alterations.
used
GBM
paradigm
demonstrate
potential
SERS
approach.
MoSERS
multiplexing
parallel
acquisition
glioma
variants
(EGFRvIII
oncogenic
mutation
MGMT
expression)
cells.
detection
limit
1.23%
was
found
these
key
wild-type
population.
When
interfaced
convolutional
neural
network
(CNN),
improved
accuracy
(87%)
which
mutations
were
detected
12
patient
blood
samples,
on
par
clinical
pathology
tests.
Thus,
demonstrates
stratification
patients
using
circulating
EVs.
Acta Pharmaceutica Sinica B,
Год журнала:
2023,
Номер
13(7), С. 2877 - 2896
Опубликована: Фев. 24, 2023
The
ongoing
coronavirus
disease
2019
(COVID-19)
pandemic
has
boosted
the
development
of
antiviral
research.
Microfluidic
technologies
offer
powerful
platforms
for
diagnosis
and
drug
discovery
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
discovery.
In
this
review,
we
introduce
structure
SARS-CoV-2
basic
knowledge
microfluidic
design.
We
discuss
application
devices
in
based
on
detecting
viral
nucleic
acid,
antibodies,
antigens.
highlight
contribution
lab-on-a-chip
to
manufacturing
point-of-care
equipment
accurate,
sensitive,
low-cost,
user-friendly
virus-detection
devices.
then
investigate
efforts
organ-on-a-chip
lipid
nanoparticles
(LNPs)
synthesizing
chips
screening
mRNA
vaccine
preparation.
contribute
research
provide
tools
future
outbreaks.
ACS Applied Materials & Interfaces,
Год журнала:
2024,
Номер
16(21), С. 27714 - 27727
Опубликована: Май 8, 2024
Rapid
and
accurate
quantification
of
metabolites
in
different
bodily
fluids
is
crucial
for
a
precise
health
evaluation.
However,
conventional
metabolite
sensing
methods,
confined
to
centralized
laboratory
settings,
suffer
from
time-consuming
processes,
complex
procedures,
costly
instrumentation.
Introducing
the
MXene/nitrogen-doped
electrochemically
exfoliated
graphene
(MXene@N-EEG)
nanocomposite
as
novel
biosensing
platform
this
work
addresses
challenges
associated
with
leveraging
concept
molecularly
imprinted
polymers
(MIP)
enables
highly
sensitive,
specific,
reliable
detection
metabolites.
To
validate
our
technology,
we
utilize
agmatine
significant
biologically
active
metabolite.
The
MIP
biosensor
incorporates
electrodeposited
Prussian
blue
nanoparticles
redox
probe,
facilitating
direct
electrical
signaling
binding
polymeric
matrix.
MXene@N-EEG
nanocomposite,
excellent
metal
conductivity
large
electroactive
specific
surface
area,
effectively
stabilizes
nanoparticles.
Furthermore,
increasing
content
agmatine-imprinted
cavities
on
electrode
enhances
sensitivity
biosensor.
Evaluation
designed
buffer
solution
plasma
samples
reveals
wide
linear
concentration
range
1.0
nM–100.0
μM
(R2
=
0.9934)
limit
0.1
nM.
Notably,
developed
microfluidic
offers
low
cost,
rapid
response
time
target
molecule
(10
min
sample
incubation),
good
recovery
results
detecting
samples,
acceptable
autonomous
performance
on-chip
detection.
Moreover,
its
high
reliability
position
MIP-based
promising
candidate
miniaturized
devices
potential
scalable
production
point-of-care
applications.
Abstract
The
last
pandemic
exposed
critical
gaps
in
monitoring
and
mitigating
the
spread
of
viral
respiratory
infections
at
point‐of‐need.
A
cost‐effective
multiplexed
fluidic
device
(NFluidEX),
as
a
home‐test
kit
analogous
to
glucometer,
that
uses
saliva
blood
for
parallel
quantitative
detection
infection
body's
immune
response
an
automated
manner
within
11
min
is
proposed.
technology
integrates
versatile
biomimetic
receptor
based
on
molecularly
imprinted
polymers
core–shell
structure
with
nano
gold
electrodes,
fluidic‐impedimetric
readout,
built‐in
collection/preparation,
smartphone‐enabled
data
acquisition
interpretation.
NFluidEX
validated
Influenza
H1N1
SARS‐CoV‐2
(original
strain
variants
concern),
achieves
low
limit
proteins
anti‐receptor
binding
domain
(RBD)
Immunoglobulin
G
(IgG)
M
(IgM),
respectively.
It
demonstrated
nanoprotrusions
electrodes
are
essential
fine
templating
antibodies
spike
during
molecular
imprinting,
differentiation
IgG
IgM
whole
blood.
In
clinical
setting,
100%
sensitivity
specificity
by
testing
44
COVID‐positive
25
COVID‐negative
samples
par
real‐time
polymerase
chain
reaction
(
p
<
0.001,
95%
confidence)
enzyme‐linked
immunosorbent
assay.