Simultaneous Determination and Validation of Paracetamol and Codeine Phosphate in Pharmaceutical Preparation by Rp-hplc
نویسندگان
چکیده
An accurate, simple, reproducible and sensitive method for the determination of Paracetamol and Codeine phosphate was developed and validated. Paracetamol and Codeine were separated by HPLC using a LiChrospher® RP-18 column and isocratic elution with a flow rate of 1.0 ml/min. Mixture of Acetonitile with Buffer solution (pH=2.5) (15:85) was used as mobile phase. The detection was at 210 nm wavelength. The proposed method was validated for linearity, accuracy, precision, limit of detection and limit of quantification. The linear range of determination for Paracetamol and Codeine phosphate were 100-1000μg/ml and 6-60 μg/ml, respectively. The percentage recovery of Paracetamol and Codeine phosphate were obtained form range of 99.88-100.2% and 99.33-100.3% respectively. The developed method is suitable for routine quality control analysis of titled drugs in combination of tablet formulation.
منابع مشابه
Simultaneous RP-HPLC and UV Spectroscopic Method Development and Validation for Estimation of Ibandronate Sodium in Bulk and Pharmaceutical Dosage Form
The present study describes a simple, accurate, precise and cost effective UV-Vis Spectroscopic and RP-HPLC method for the estimation of Ibandronate sodium (IBN). The determination of Ibandronate sodium (IBN) was performed by both UV and RP-HPLC method using 215 nm as the determination wavelength. The drug was dissolved in NaOH solution (0.1N NaOH) for estimation in UV and in distilled water fo...
متن کاملSimultaneous Determination of Chlorpheniramine Maleate, Phenylephrine Hydrochloride, Paracetamol and Caffeine in Pharmaceutical Preparation by Rp-hplc
A reversed-phase High-Performance Liquid-Chromatography (RP-HPLC) method was successfully developed for the simultaneous determination of quaternary mixture consisting of chlorpheniramine maleate (CPM), phenylephrine hydrochloride (PE), paracetamol (PCM) and caffeine in pharmaceutical preparation. The method was found to be simple, sensitive and rapid. The separation of the drugs was carried ou...
متن کاملA stability-Indicating HPLC Method for Simultaneous Determination of Creatine Phosphate Sodium and its Related Substances in Pharmaceutical Formulation
The objective of the study was to develop a simple, specific and stability-indicating HPLC method for the simultaneous determination of creatine phosphate sodium (CPS) and its related substances in pharmaceutical formulation. Separation of creatine phosphate sodium from its major process impurities and degradation products was achieved on a Hypersil BDS C18 column (250 × 4.6 mm, 5 μm) with an a...
متن کاملA stability-Indicating HPLC Method for Simultaneous Determination of Creatine Phosphate Sodium and its Related Substances in Pharmaceutical Formulation
The objective of the study was to develop a simple, specific and stability-indicating HPLC method for the simultaneous determination of creatine phosphate sodium (CPS) and its related substances in pharmaceutical formulation. Separation of creatine phosphate sodium from its major process impurities and degradation products was achieved on a Hypersil BDS C18 column (250 × 4.6 mm, 5 μm) with an a...
متن کاملOptimization and validation of RP-HPLC method for the estimation of meloxicam and paracetamol with its genotoxic impurity (p-amino phenol) in bulk and pharmaceutical drug product using PDA detector
A simple, accurate, precise, reproducible RP-HPLC method has been developed for simultaneous estimation of meloxicam and paracetamol with its genotoxic impurity (p-amino phenol) in bulk and combined dosage form (tablet). The method was validated in compliance with ICH guidelines[1-2]. The LC separation was achieved on Lichrospher RP-18e (250X4.6mm), 5μm column at 285 nm in isocratic mode using ...
متن کامل