Diagnostic
biomolecule
quantification
in
healthcare
relies
on
effective
but
centralized
laboratory
testing
procedures.
However,
as
the
need
for
rapidly
grows,
current
process
is
struggling
to
meet
demand.
Rapid
point-of-contact
analysis
devices
are
not
capable
of
non-invasive
small,
dilute
molecules
such
steroid
hormones
saliva.
Current
literature
bioquantification
suffer
from
drawbacks
short
shelf
life,
high
intra-device
variability,
sample
matrix
effects,
material
incompatibilities,
high-cost
fabrication
and
data
collection
that
rely
conditions
processes.
This
body
work
took
our
organic
electrolyte
gated
field
effect
transistor
(OEGFET),
a
novel
biosensor
architecture,
developed
it
into
feasible
platform
real-world
applications.
Iterative
development
through
architecture
prototyping,
optimization
selection
has
solved
key
challenges
scale
biosensors
whilst
adding
functionalities.
Expensive,
specialized
requirements
gradually
replaced
with
wet
lab-based
solution
processing
techniques
facile
manufacturing,
making
cost
effective,
flexible,
suitable
scale-up
manufacturing.
The
OEGFET
improved
electrical
characteristics:
on/off
ratio
(from
140
up
103);
reduced
leakage
currents
90nA
down
5.8nA);
threshold
voltage
4V
0.23V).
Real
world
needs
biosensing
applications
life
3
days
1
month),
translation
dopamine
cortisol
α-synuclein
been
demonstrated
selectivity
broad,
physiologically
relevant
detection
range
(over
1mM–100fM,
limit
10fM)
buffer
solutions
complex
samples
spiked
saliva
supernatant.
Key
additional
functionalities
integration
bespoke
small
footprint
printed
circuit
board
low
power
(<300mW)
thus
removing
reliance
equipment,
integrated
microfluidic
channels
consistent
plate
separation
handling.
resulting
handling
fluidics,
low-power
operation,
simple
method,
broadly
applicable.
Presently,
neurotransmitters,
proteins,
hormones.
During
course
author’s
doctoral
program
was
transformed
potential
rapid,
quantification.
ACS Synthetic Biology,
Journal Year:
2025,
Volume and Issue:
14(1), P. 21 - 40
Published: Jan. 6, 2025
The
field
of
healthcare
diagnostics
is
navigating
complex
challenges
driven
by
evolving
patient
demographics
and
the
rapid
advancement
new
technologies
worldwide.
In
response
to
these
challenges,
biosensors
offer
distinctive
advantages
over
traditional
diagnostic
methods,
such
as
cost-effectiveness,
enhanced
specificity,
adaptability,
making
their
integration
with
point-of-care
(POC)
platforms
more
feasible.
recent
years,
aptasensors
have
significantly
evolved
in
capabilities
through
emerging
microfluidics,
Clustered
Regularly
Interspaced
Short
Palindromic
Repeats
(CRISPR)
systems,
wearable
devices,
machine
learning
(ML),
driving
progress
precision
medicine
global
solutions.
Moreover,
advancements
not
only
improve
accuracy
but
also
hold
potential
revolutionize
early
detection,
reduce
costs,
outcomes,
especially
resource-limited
settings.
This
Account
examines
key
advancements,
focusing
on
how
scientific
breakthroughs,
including
artificial
intelligence
(AI),
improved
sensitivity
precision.
Additionally,
has
enabled
real-time
monitoring
data
analysis,
fostering
advances
personalized
healthcare.
Furthermore,
commercialization
aptasensor
could
increase
availability
clinical
settings
support
use
widespread
solutions
for
health
challenges.
Hence,
this
review
discusses
technological
improvements,
practical
uses,
prospects
while
surrounding
standardization,
validation,
interdisciplinary
collaboration
application.
Finally,
ongoing
efforts
address
are
ensure
that
can
be
effectively
implemented
diverse
systems.
Lab on a Chip,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
review
examines
contributions
of
microfluidic
technology
to
SELEX-based
aptamer
identification,
with
alternative
methods
such
as
in
vivo
-like
SELEX
and
Non-SELEX
for
selecting
aptamers
discussed
critical
steps
over
the
past
decade.
Nanomaterials,
Journal Year:
2024,
Volume and Issue:
14(2), P. 170 - 170
Published: Jan. 12, 2024
Analytical
methods
for
the
early
detection
of
neurodegenerative
biomarker
Parkinson’s
disease
(PD),
α-synuclein,
are
time-consuming
and
invasive,
require
skilled
personnel
sophisticated
expensive
equipment.
Thus,
a
pain-free,
prompt
simple
α-synuclein
biosensor
in
plasma
is
highly
demanded.
In
this
paper,
an
electrochemical
based
on
hierarchical
polyglutamic
acid/ZnO
nanowires
decorated
by
gold
nanoparticles,
assembled
as
nanostars
(NSs),
determination
human
proposed.
ZnO
NSs
were
prepared
chemical
bath
deposition
(CBD)
with
electrodeposited
Au
nanoparticles
(Au
NPs).
Then,
electro-polymerized
glutamic
acid
was
grown
functionalized
anti-α-synuclein.
A
synergistic
enhancement
electrode
sensitivity
observed
when
NPs
embedded
into
NSs.
The
analytical
performance
evaluated
cyclic
voltammetry
(CV)
impedance
spectroscopy
(EIS),
using
Fe(II)(CN)64−/Fe(III)(CN)63−
probe.
charge
transfer
resistance
after
recognition
found
to
be
linear,
concentration
range
0.5
pg·mL−1
10
pg·mL−1,
limit
0.08
good
reproducibility
(5%
variation)
stability
(90%).
also
shown
reliably
discriminate
between
healthy
PD
plasma.
These
results
suggest
that
proposed
provides
rapid,
quantitative
high-sensitivity
result
content
plasma,
represents
feasible
tool
capable
accelerating
non-invasive
identification
disease.
Micromachines,
Journal Year:
2024,
Volume and Issue:
15(2), P. 273 - 273
Published: Feb. 15, 2024
Parkinson’s
Disease
(PD)
is
a
debilitating
neurodegenerative
disease,
causing
loss
of
motor
function
and,
in
some
instances,
cognitive
decline
and
dementia
those
affected.
The
quality
life
can
be
improved,
disease
progression
delayed
through
early
interventions.
However,
current
methods
confirming
PD
diagnosis
are
extremely
invasive.
This
prevents
their
use
as
screening
tool
for
the
onset
stages
PD.
We
propose
surface
imprinted
polymer
(SIP)
electroimpedance
spectroscopy
(EIS)
biosensor
detecting
α-Synuclein
(αSyn)
its
aggregates,
biomarker
that
appears
saliva
blood
during
blood-brain
barrier
degrades.
stamp
fabricated
by
low-temperature
melt
stamping
polycaprolactone
(PCL)
on
interdigitated
EIS
electrodes.
result
low-cost,
small-footprint
highly
suitable
non-invasive
monitoring
biomarker.
sensors
were
tested
with
αSyn
dilutions
deionized
water
constant
ionic
concentration
matrix
solutions
decreasing
concentrations
to
remove
background
effects
concentration.
device
response
confirmed
specificity
these
devices
target
protein
monomeric
αSyn.
sensor
limit
detection
was
measured
5
pg/L,
linear
range
pg/L–5
µg/L.
covers
physiological
makes
this
promising
method
quantifying
monomers
patients
future.
SIP
regenerated,
reused
demonstrate
capability
repeat
sensing
potential
continuous
Biosensors,
Journal Year:
2025,
Volume and Issue:
15(3), P. 151 - 151
Published: Feb. 28, 2025
Neurodegenerative
diseases,
such
as
Parkinson’s
disease
(PD)
and
Alzheimer’s
(AD),
represent
a
growing
global
health
challenge
with
overlapping
biomarkers.
Key
biomarkers,
including
α-synucleins,
amyloid-β,
Tau
proteins,
are
critical
for
accurate
detection
but
often
assessed
using
conventional
methods
like
enzyme-linked
immunosorbent
assay
(ELISA)
polymerase
chain
reaction
(PCR),
which
invasive,
costly,
time-intensive.
Electrochemical
biosensors
have
emerged
promising
tools
biomarker
due
to
their
high
sensitivity,
rapid
response,
potential
miniaturization.
The
integration
of
nanomaterials
has
further
enhanced
performance,
improving
specificity,
practical
application.
To
this
end,
review
provides
comprehensive
overview
recent
advances
in
electrochemical
detecting
neurodegenerative
highlighting
strengths,
limitations,
future
opportunities.
By
addressing
the
challenges
early
diagnosis,
work
aims
stimulate
interdisciplinary
innovation
improve
clinical
outcomes
patients.
Biosensors,
Journal Year:
2025,
Volume and Issue:
15(4), P. 228 - 228
Published: April 3, 2025
Surface-imprinted
polymers
(SIPs)
represent
an
exciting
and
cost-effective
alternative
to
antibodies
for
electrochemical
impedance
spectroscopy
(EIS)-based
biosensing.
They
can
be
produced
using
simple
printing
techniques
have
shown
high
efficacy
in
detecting
large
biomolecules
microorganisms.
Stamp
imprinting,
a
novel
SIP
method,
creates
the
target
analyte’s
imprint
soft
lithography
mask
of
analyte
matrix,
thereby
reducing
material
complexities
eliminating
need
cross-linking,
which
makes
process
more
scalable
than
conventional
SIPs.
In
this
work,
we
demonstrate
stamp-imprinted
EIS
biosensor
biocompatible
polymer,
polycaprolactone
(PCL),
quantifying
amyloid
beta-42
(Aβ-42),
small
peptide
involved
pathophysiology
Alzheimer’s
disease.
The
evaluated
SIP-EIS
biosensors
showed
detection
limit
close
10
fg/mL,
range
covering
physiologically
relevant
concentration
blood
serum
(from
fg/mL
μg/mL).
device
sensitivity,
is
found
comparable
antibody-based
devices,
demonstrates
potential
as
diagnostic
approaches.
We
also
evaluate
viability
analyzing
these
proteins
complex
media,
notably
presence
albumin
proteins,
cause
biofouling
non-specific
interactions.
combination
selectivity,
ease
fabrication
particularly
suited
portable
point-of-care
applications.
Biosensors,
Journal Year:
2025,
Volume and Issue:
15(5), P. 280 - 280
Published: April 29, 2025
Parkinson’s
disease
(PD),
a
neurodegenerative
disorder
marked
by
the
progressive
loss
of
dopaminergic
neurons
in
substantia
nigra,
imposes
substantial
economic
burdens,
including
both
direct
and
indirect
costs.
The
medical
community
currently
lacks
definitive
cure
for
disease,
early
detection
is
crucial
timely
intervention
management.
As
innovative
diagnostic
tools,
biosensors
have
shown
great
potential
detecting
PD
at
its
stages.
This
review
comprehensively
summarizes
recent
advances
PD,
with
particular
focus
on
two
key
biomarkers:
dopamine
(DA)
α-synuclein
(α-syn).
Furthermore,
it
illustrates
variety
nanotechnology-based
biosensors,
optical,
electrochemical,
transistor
detailing
their
underlying
principles,
advantages,
limitations,
applications
detection.
Moreover,
explores
challenges
prospects
advancing
diagnosis.