HPTLC Method Development and Validation of Cefpodoxime Proxetil and Ofloxacin in Bulk and Combined Tablet Dosage form

Order of Publishing in Issue: 
Volume :10
Issue :1
January, 2016
Page No: 
Deepshikha Patle
Faculty of Pharmaceutical Sciences, PCTE Group of Institutes, Ludhiana, Punjab, India-141004

The aim of the study is to develop and validate a simple, precise and rapid high performance thin layer chromatographic (HPTLC) method for Cefpodoxime Proxetil and Ofloxacin in bulk and combined tablet dosage form. Chromatographic separation was accomplished by using precoated silica gel 60F254 TLC plate (20cm x10cm) with 250μm thickness with mobile phase Chloroform in ratio methanol (9:1 v/v). Detection was performed at isobestic point 255 nm for both drugs. The retesion factor of Cefpodoxime Proxetil and Ofloxacin were found to be 0.63 and 0.25, respectively. The reliability of the method was assessed by evaluation of linearity range (500-3000 ng/spot for both Cefpodoxime proxetil and ofloxacin respectively. Accuracy (99.56 % for Cefpodoxime Proxetil and 99.33% for Ofloxacin), and specificity, in compliance with ICH guidelines.

Cefpodoxime proxetil, Ofloxacin, High performance thin layer chromatography (HPTLC), method development, validation.
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