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Authors
Affiliations
1 Axis Clinicals Ltd, Hyderabad, Andhra Pradesh, IN
2 Dept. of Pharmaceutical Analysis, Adhiparasakthi College of Pharmacy, Melmaruvathur-603319, Tamilnadu, IN
3 Department of Pharmaceutics, Shri Vishnu College of Pharmacy, Bhimavaram, Andhra Pradesh, IN
4 Department of Pharmacology, Shri Vishnu College of Pharmacy, Bhimavaram, Andhra Pradesh, IN
Source
Asian Journal of Research in Chemistry, Vol 3, No 3 (2010), Pagination: 542-544
Abstract
Two new simple, sensitive, rapid, accurate and precise methods, namely UV spectrophotometric and RP-HPLC methods were developed for the estimation of Levosulpiride in bulk and in tablet formulation. In UV spectrophotometric method, Levosulpiride exhibited maximum absorbance at 291.5 nm with apparent molar absorptivity of 2.6031×103 L mol-1 cm-1 in 0.1 M HCl. Beer’s law was obeyed in the concentration range of 10-50 mg/ml. In RP-HPLC method, the elution was done using a mobile phase consisting of methanol and 25 mM phosphate buffer pH 3.5 (pH adjusted with phosphoric acid, 15:85 v/v) on Shimadzu HPLC C18 (4.6×150 mm) column at a flow rate of 0.8 ml/min with UV detection at 293 nm. An external standard calibration method was employed for quantization. The elution time was 5.08 minutes. Beer’s law was found to be obeyed in the concentration range of 4-24 ×g/ml. The results of proposed methods were validated statistically and by recovery studies. The % RSD values for recovery studies were found to be less than 2% for the both methods. Hence the proposed methods were successfully used to determine the drug content in bulk and in tablet formulation.
Keywords
Levosulpiride, UV Spectrophotometry, RP-HPLC, External Standard Calibration.
