Journal of Chromatography A,
Journal Year:
2024,
Volume and Issue:
1718, P. 464697 - 464697
Published: Feb. 3, 2024
Quantification
of
proteins
is
still
predominantly
done
by
the
traditional
bottom-up
approach.
Targeting
intact
in
complex
biological
matrices
connected
with
multiple
challenges
during
sample
pretreatment,
separation,
and
detection
step
analytical
workflow.
In
this
work,
we
focused
on
development
an
on-line
hyphenated
capillary
zone
electrophoresis-mass
spectrometry
method
employing
off-line
microscale
solid-phase
extraction
based
hydrophilic
lipophilic
balance
(HLB)
sorbent
as
a
pretreatment
for
analysis
low
molecular
mass
(<20
kDa)
spiked
various
fluids
(human
serum,
plasma,
urine,
saliva).
A
detailed
optimization
process
involved
selection
suitable
surface,
background
electrolyte
(BGE),
comparison
two
in-capillary
preconcentration
methods,
namely
transient
isotachophoresis
(tITP)
dynamic
pH
junction
(DPJ),
to
enhance
sensitivity
method.
Optimum
separation
analytes
was
achieved
using
uncoated
bare
fused
silica
500
mM
formic
acid
(pH
1.96)
+
5%
(v/v)
acetonitrile
BGE.
tITP
utilized
optimum
technique,
achieving
19-
127-fold
increase
signal
intensity
when
200
ammonium
formate
(adjusted
4.00)
leading
BGE
terminating
electrolyte.
Off-line
eluate
treatment
procedures
evaluated
ensure
compatibility
selected
preconcentration,
process.
Achieved
recoveries
were
range
76-100%
12-54%
21-106%
25-98%
saliva
evaporated
reconstituted
solution
achieve
The
validated
across
different
matrices,
offering
good
linearity,
accuracy,
precision,
making
it
proteomic
studies
(e.g.,
therapeutic
drug
monitoring,
biomarker
research)
samples.
Molecules,
Journal Year:
2024,
Volume and Issue:
29(2), P. 380 - 380
Published: Jan. 12, 2024
Non-steroidal
anti-inflammatory
drugs
(NSAIDs)
have
been
recognized
as
a
potentially
serious
threat
to
the
natural
environment.
NSAIDs
are
popular
painkillers,
and
main
pathway
for
them
reach
water
is
via
discharge
from
wastewater
sewage
treatment
plants.
In
order
monitor
contamination
caused
by
these
drugs,
well
their
impact
on
environment,
new
material
based
Silica
Gel
60,
functionalized
with
dendrimeric
copolymer
of
methylamine
1,4-butanediol
diglycidyl
ether
(named
MA-BDDE),
was
prepared.
Initial
physicochemical
characterization
MA-BDDE
carried
out
using
ATR
FT-IR
spectroscopy
solid-state
carbon-13
NMR
spectroscopy.
Its
effectiveness
at
NSAID
extraction
evaluated
application
five
select
in
dispersive
solid-phase
(dSPE):
aspirin,
ketoprofen,
naproxen,
diclofenac
ibuprofen.
This
followed
simultaneous
determination
HPLC-UV/Vis
system
demonstrating
good
sensitivity,
limits
detection
values
within
63-265
ng
mL
Journal of Chromatography A,
Journal Year:
2024,
Volume and Issue:
1718, P. 464697 - 464697
Published: Feb. 3, 2024
Quantification
of
proteins
is
still
predominantly
done
by
the
traditional
bottom-up
approach.
Targeting
intact
in
complex
biological
matrices
connected
with
multiple
challenges
during
sample
pretreatment,
separation,
and
detection
step
analytical
workflow.
In
this
work,
we
focused
on
development
an
on-line
hyphenated
capillary
zone
electrophoresis-mass
spectrometry
method
employing
off-line
microscale
solid-phase
extraction
based
hydrophilic
lipophilic
balance
(HLB)
sorbent
as
a
pretreatment
for
analysis
low
molecular
mass
(<20
kDa)
spiked
various
fluids
(human
serum,
plasma,
urine,
saliva).
A
detailed
optimization
process
involved
selection
suitable
surface,
background
electrolyte
(BGE),
comparison
two
in-capillary
preconcentration
methods,
namely
transient
isotachophoresis
(tITP)
dynamic
pH
junction
(DPJ),
to
enhance
sensitivity
method.
Optimum
separation
analytes
was
achieved
using
uncoated
bare
fused
silica
500
mM
formic
acid
(pH
1.96)
+
5%
(v/v)
acetonitrile
BGE.
tITP
utilized
optimum
technique,
achieving
19-
127-fold
increase
signal
intensity
when
200
ammonium
formate
(adjusted
4.00)
leading
BGE
terminating
electrolyte.
Off-line
eluate
treatment
procedures
evaluated
ensure
compatibility
selected
preconcentration,
process.
Achieved
recoveries
were
range
76-100%
12-54%
21-106%
25-98%
saliva
evaporated
reconstituted
solution
achieve
The
validated
across
different
matrices,
offering
good
linearity,
accuracy,
precision,
making
it
proteomic
studies
(e.g.,
therapeutic
drug
monitoring,
biomarker
research)
samples.