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NEW VALIDATED METHOD DEVELOPMENT FOR THE ESTIMATION OF SULFAMETHOXAZOLE AND TRIMETHOPRIM IN BULK FORM BY VISIBLE SPECTROSCOPY

By: Gajjela, Swetha.
Contributor(s): Kusuma, Praveen Kumar.
Publisher: M P Innovare Academic Sciences Pvt Ltd 2018Edition: Vol.10(12).Description: 50-57p.Subject(s): PHARMACEUTICSOnline resources: Click here In: International journal of pharmacy and pharmaceutical scienceSummary: Objective: To develop three novel , sensitive, simple validated visible spectrophotometric methods for the quantitative estimation of sulfamethoxazole (SMZ) and trimethoprim (TMP) in bulk form . Method s: Methods were based on coupling the d iazotized aromatic primary amino group of the studied drugs with o- phenylenediamine (OPD ) in an acidic medium . The first two methods have been proposed for estimation of SMZ and rest for TMP . The resulting products were m easured by spectrophotometric (m ethod I, II and III) tools. The methods we re validated as per ICH guidelines . Result s: In method I, the absorbance was measured at 482 and 457 nm with linearity ranges of 4.0 -40.0 and 5.0 -45.0 μg /ml for SMZ . On the other hand, method III was devoted to estimate TMP spectrophotometrically at 457 nm with linearity range of 5 - 30 μg /ml . The r 2 Conclusio n: The study concludes that visible spectrophotometric validation method s can be very efficien t and economically promising technique for the quantitative analysis of S MZ and TMP in bulk form . The statistical analysis of data indicates that the developed methods were reproducible and specific. It was found that there is a good agreement between the obtained results and those obtained by the reported method s; moreover they can be used for the routine estimations of SMZ and TMP in bulk form
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Objective:
To
develop
three
novel
, sensitive, simple
validated
visible
spectrophotometric methods
for
the quantitative estimation
of
sulfamethoxazole
(SMZ)
and
trimethoprim
(TMP)
in bulk form
.
Method
s:
Methods were based on coupling the d
iazotized
aromatic
primary amino group of the studied drugs with
o-
phenylenediamine
(OPD
) in
an acidic medium
. The first two methods have been proposed for estimation of SMZ
and rest
for
TMP
. The resulting products were m
easured by
spectrophotometric (m
ethod I, II
and
III) tools.
The methods we
re validated as per ICH guidelines
.
Result
s:
In
method
I, the absorbance was measured at 482 and
457 nm with linearity ranges of 4.0
-40.0 and 5.0
-45.0 μg
/ml
for
SMZ
. On the other
hand, method III was
devoted to estimate
TMP
spectrophotometrically
at 457 nm with
linearity range of 5
-
30 μg
/ml
. The
r
2
Conclusio
n:
The study concludes that
visible
spectrophotometric validation method
s can be very efficien
t and economically promising technique
for
the quantitative
analysis of S
MZ
and
TMP
in bulk form
. The statistical analysis of data indicates that the
developed methods were
reproducible
and specific.
It was found that there is a good agreement between the obtained results and those obtained by the reported method
s;
moreover
they
can be
used for
the routine estimations of
SMZ and TMP
in bulk form

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