DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS DETERMINATION OF METHOCARBAMOL AND DICLOFENAC SODIUM IN INJECTION DOSAGE FORM
Nikita P. Patel* and Madhuri Hinge
ABSTRACT
A simple, precise and accurate liquid chromatographic method was
developed for simultaneous determination of methocarbamol and
diclofenac sodium in injection dosage form. The chromatography was
carried on BDS Hypersil C18 (250 mm x 4.6 mm, 5μm) column and
with Mobile phase Composition of Phosphate buffer: Methanol (30:70
v/v), pH 4.5 with Orthophosphoric acid at a Flow rate of 1ml/min and
detection was carried out at 281 nm. RP-HPLC method was found to
be linear over the range of 3-9 μg/ml for Diclofenac sodium and 18-54
μg/ml for Methocarbamol. Retention time of Diclofenac sodium and
Methocarbamol was found to be 4.2501 and 6.7832 respectively.
Correlation Co- efficient of Diclofenac sodium and Methocarbamol
was found to be 0.9968 and 0.9945 respectively. The method has been
validated for Linearity, Precision, Accuracy, LOD, LOQ and System
suitability according to ICH Q2 (R1) guideline.
Keywords: Methocarbamol, Diclofenac sodium, RP-HPLC.
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