Green Processing and Synthesis,
Journal Year:
2024,
Volume and Issue:
13(1)
Published: Jan. 1, 2024
Abstract
Breast
cancer
affects
millions
of
women
worldwide.
This
study
explores
the
potential
combining
pentoxifylline
(PTX)
and
simvastatin
(SIM)
as
a
treatment
for
breast
cancer.
We
aimed
to
develop
six
sustainability
tools
using
green
white
metrics
evaluate
environmental
impact
reversed-phase
high-performance
liquid
chromatography
(RP-HPLC)
methods
analyzing
separating
PTX
SIM
in
their
pure
forms.
The
include
analytical
GREEnness,
procedure
index,
Complexgreen
greenness
metric
sample
preparation,
blue
applicability
grade
RGB
12
algorithm.
For
separation,
we
used
Novapack
C8
column
(15
×
0.46
cm,
5
µm)
at
25°C.
injection
volume
was
5.0
µL,
wavelength
set
210
nm,
total
runtime
min.
identified
optimal
chromatographic
conditions
efficiently
Box–Behnken
design
with
minimal
trials.
investigated
effects
three
factors
on
retention
time
resolution:
acetonitrile
ratio,
pH,
flow
rate.
overlay
plots
60:40
ratio
(v/v)
bi-distilled
water
forecast
most
effective
mobile
phase.
calibration
curves
showed
correlation
value
over
0.999
within
range
5–60
µg·mL
−1
.
recovery
rates
ranged
from
99.9%
100.2%,
indicating
high
accuracy.
Our
RP-HPLC
technique
proves
be
reliable
efficient
simultaneous
estimation
multiple
anticancer
drugs.
evaluated
this
approach
metrics,
recommended
method
has
been
thoroughly
validated
according
International
Council
Harmonisation
guidelines,
making
it
highly
new
formulations.
Green Chemistry Letters and Reviews,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: Jan. 7, 2024
A
study
on
green
analytical
chemistry
aims
to
develop
eco-friendly
alternatives
hazardous
substances
and
minimize
waste
generation.
The
thoroughly
examined
various
tools
determine
their
greenness.
newly
validated
RP-UPLC
method
was
then
employed
quantitatively
detect
Triamcinolone
Acetonide
(TRA)
in
a
creamy
pharmaceutical
formulation
using
UPLC
BEH
C18
(50
×
2.1
mm,
1.7μm)
column
for
analysis,
with
detection
wavelength
set
at
240
nm.
Box-Behnken
design
developed
efficiently
the
optimal
chromatographic
conditions
while
minimizing
required
trials.
effectively
assessed
impact
of
three
independent
variables
responses,
including
retention
time,
tailing
factor,
theoretical
plates.
ethanol
ratio,
pH
levels,
flow
rate
were
meticulously
tested
optimize
experimental
conditions.
utilization
desirability
overlay
plots,
along
mobile
phase
purified
water
volumetric
ratio
30:70
adjustment
5.0.
Calibration
curves
constructed
assess
linearity
TRA
within
concentration
range
2.5-50
µg/mL,
yielding
correlation
coefficients
(r
=
0.9999).
accuracy
through
recovery
studies
acceptable
99.6-101.2%.
specificity
has
been
by
conducting
forced
degradation
per
ICH
guidelines.
Reviews in Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
43(1)
Published: Jan. 1, 2024
Abstract
A
green
analytical
chemistry
study
attempts
to
generate
environmentally
friendly
alternatives
dangerous
compounds
while
reducing
waste
output.
The
thoroughly
analyzed
eight
tools
determine
their
greenness.
Given
its
importance
in
treating
hallucinations
and
delusions
produced
by
Parkinson’s
disease
psychosis,
it
is
critical
have
a
reliable
precise
method
for
identifying
pimavanserin
(PVS)
both
pure
form
pharmaceutical
formulations.
current
used
straightforward
approach
forced
degradation
experiments
establish
novel
reversed-phase
high-performance
liquid
chromatography
evaluating
stability.
was
executed
on
the
Agilent
Zorbax
Eclipse
Plus
C18
column
(100
×
4.6
mm,
3.5
μm
particle
size)
with
ultraviolet
detection
at
226
nm.
Box–Behnken
design
ultimate
solution
optimal
chromatographic
conditions
timely
efficient
manner,
minimal
trials
required.
investigated
impact
of
three
factors:
acetonitrile
ratio,
oven
temperature,
flow
rate
various
responses,
namely,
retention
time,
tailing
factor,
theoretical
plates.
Desirability
overlay
plots
were
utilized
forecast
best
mobile
phase
containing
buffer
solution:
acetonitrile:
tetrahydrofuran
ratio
(65:
20:
15,
v/v/v),
which
proved
highly
effective
experiments.
Linearity
conducted
PVS
3–50
µg·mL
−1
range
an
R
2
coefficient
determination
0.9997.
had
quantification
limits
1.1
,
respectively,
indicating
significant
correlation
between
variables
studied.
PVS’s
recovery
percentage
determined
be
101.30%.
We
also
Six
Sigma
lean
technique
ensure
precision
productivity.
tested
acid,
base,
oxidative
hydrolysis,
photodegradation,
heat,
as
per
International
Council
Harmonisation
guidelines.
highest
obtained
from
hydrolysis
thermal
degradation.
ACS Omega,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 20, 2025
Modern
society
is
increasingly
reliant
on
sustainable
solutions.
We
suggest
a
creative
study
that
meets
the
standards
of
sustainability
in
analytical
chemistry.
The
objective
to
promote
eco-friendly
methods
for
concurrently
detecting
Gatifloxacin
(GAT)
and
benzalkonium
chloride
(BEN)
ocular
Using
sustained
mobile
phase
flow
rate
0.8
mL/min-1
acidic
water:
10%
1-butanol
water
(40:60,
v/v),
GAT
was
retained
2.242
min
at
287
nm,
followed
by
BEN
homologues
215
nm
next
2.982
4.201
min.
This
process
simple,
quick,
precise.
method
demonstrated
peak
symmetry,
low
processing
times,
good
resolution,
correlation
values
0.999.
For
GAT,
linearity
ranged
from
0.001
0.023
mgmL-1,
while
BEN,
it
0.003
0.060
mgmL-1
HPLC
system,
UV
range
0.005-0.03
all
drugs.
A
unique
feature
this
integration
multiple
assessment
tools,
such
as
AGREE,
AGREEprep,
ComplexGAPI,
ESA,
BAGI,
NEMI
pictograms,
providing
an
exhaustive
appraisal
methods'
environmental
impact
enhancing
robustness
findings.
In
addition,
cost-effective
alternatives
were
explored
using
solvent
complementary
spectrophotometric
procedures
mean
centering
ratio
spectra
(MCR).
Each
technique
showed
respectable
accuracy
precision
(RSD
≤
2%)
high
r2
>
0.9990.
proposed
methodologies
provide
inexpensive,
conventional
approaches,
promoting
less
harmful
future
quality
control
moving
chemistry
closer
more
methods.
Biomedical Chromatography,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 14, 2024
Abstract
The
efficacious
treatment
of
muscle
and
joint
pain
relies
heavily
on
etofenamate
(ETO)
benzyl
nicotinate
(BN),
which
possess
robust
anti‐inflammatory
pain‐relieving
properties
when
paired
with
methylparaben
(MP)
or
alcohol
(BA).
In
this
study,
we
have
established
validated
innovative
RP‐UPLC
methods
for
assessing
ETO
BN
in
the
presence
MP
BA
their
dosage
forms,
employing
eight
green
tools
to
evaluate
eco‐friendliness
effectiveness.
Reversed
phase‐ultra‐performance
liquid
chromatography
(RP‐UPLC)
technique
employs
a
flow
rate
0.3
mL/min
Waters
Acquity
UPLC
BEH
Column
(C18,
1.7
μm,
100
mm
×
2.1
mm),
detection
at
254
nm
using
photo
diode
array
(PDA)
detector
mobile
phase
0.05
M
KH
2
PO
4
buffer,
acetonitrile,
methanol
(50:15:35,
v/v/v)
adjusted
pH
6.0
0.2%
triethylamine.
For
ETO,
BN,
MP,
BA,
calibration
curves
were
linear
ranged
from
0.005
1.0,
0.001
0.2,
0.002
0.08,
0.0001
0.1
mg/mL,
respectively.
correlation
value
was
0.9999,
accuracy
findings
98.81%
100.56%.
Consequently,
methodology
has
been
successfully
implemented
assay
testing
pharmaceuticals
demonstrating
high
selectivity
these
approaches.
present
study
presents
Blue
Applicability
Grade
Index
(BAGI),
an
approach
that
complements
metrics
practical
white
analytical
chemistry.
According
International
Council
Harmonisation
(ICH)
criteria,
procedures
effectively
validated.
ACS Omega,
Journal Year:
2024,
Volume and Issue:
9(45), P. 45011 - 45024
Published: Nov. 1, 2024
Clinical
trials
revealed
that
pioglitazone
(PGZ)
and
dapagliflozin
(DGZ)
not
only
maintain
normal
blood
glucose
levels
but
also
reduce
complications
of
diabetes
mellitus.
To
meet
the
demand
for
simultaneous
measurement
these
drugs
in
fixed
combinations,
an
optimized
green
UPLC
method
is
required.
The
present
study
utilized
Design
Experiments
(DoE)
software
to
optimize
analytical
parameters
drug
analysis.
was
validated
its
linearity,
accuracy,
precision.
Furthermore,
content
estimated
different
pharmaceutical
dosage
forms.
Finally,
Analytical
Greenness
(AGREE)
assess
environmental
sustainability
method.
Drugs
were
successfully
separated
using
conditions
on
C18
Acquity
BEH
column
(2.1
mm
×
100
mm,
1.7
μm)
at
a
temperature
45
°C.
mobile
phase
consisted
ethanol
9
mM
ammonium
formate
buffer
(43.7:56.3),
with
elution
carried
out
flow
rate
0.246
mL/min.
showed
excellent
linearity
(R2
>
0.999),
accuracy
(92.45–109.25%),
good
precision
(RSD
<
6.27%)
both
drugs.
In
addition,
able
determine
within
marketed
form
accurately.
developed
prioritized
eco-friendliness
by
solvents
minimize
negative
impact
environment.
provides
reliable
accurate
approach
estimate
PGZ
DGZ
treatment
combination.
It
promotes
sustainable
lab
practices
paves
way
methods
new
dose
combinations.