Validated UV Method Development for the Simultaneous Estimation of Rabeprazole sodium and Cinitapride in Tablets
Journal Title: International Journal of Pharmacy and Analytical Research - Year 2014, Vol 3, Issue 1
Abstract
Current research attempts to develop simple, cost effective, and time saving, validated UV spectrophotometric method for the simultaneous estimation of Rabeprazole (RPZ) and Cinitapride (CTP) in tablet formulations by simultaneous equation method. The sampling wavelengths for RPZ and CTP are 284.5 nm and 267 nm respectively. Assay results showed 10.008 mg of RPZ and 2.974 mg of CTP were found in the tablet dosage form. The method was validated as per ICH guidelines. Linearity was obtained in the concentration range of 3-8 μg/mL for RPZ and 2-7 μg/mL for CTP. The %RSD for intraday and interday variations of RPZ was found to be 0.183±0.002 and 0.317±0.001 respectively. An intraday and interday variation of CTP was found to be 0.194±0.002 and 0.298±0.001 respectively. In both cases values were within the acceptance limit of < 2%. The mean percent recovery for RPZ and CTP were found to be 98.57 % and 99.43 % respectively, within the acceptance limit of 98% to 102%. From the high recovery values (> 98%) it can be inferred that the method is free from the interference of excipients used in the formulation. Based on the results obtained the proposed method can be regarded as simple, accurate, precise, reliable and cost effective which can be employed for routine quality control of RPZ and CTP in combined tablet dosage forms.
Authors and Affiliations
Shanta Kumari Adiki
Synthesis and Pharmacological evaluation of new Benzoxozole Derivatives
Benzoxazoles1 are usually prepared by heating 2-Aminophenol with formic acids in the presence of Boric acid under reflux. Condensation of these two substances under milder conditions. Being a heterocyclic compound, benzo...
RP-HPLC Method Development and Validation for the Simultaneous estimation of Simvastatin and Ezetimibe in Tablet Dosage Form
A simple reversed-phase high-performance liquid chromatographic (RP-HPLC) method has been developed and validated for simultaneous determination of Simvastatin and Ezetimibe in pharmaceutical tablet dosage form. Chromato...
Synthesis, Characterization and Biological evaluation of substituted Pyrazole derivatives
The work presented in this article consists of synthesis, characterization and biological evaluation of substituted pyrazole derivatives. Pyrazole derivatives have been shown to have wide variety of pharmacological activ...
Development and Validation of RP-HPLC method for the simultaneous estimation of Miglitol and Metformin Hcl in Pharmaceutical formulations
A simple, accurate, precise and rapid reversed-phase high performance liquid chromatographic (RP-HPLC) method has been developed and subsequently validated for the simultaneous estimation of Miglitol (MG) and Metformin H...
Formulation of mebeverine hydrochloride MR pellets in capsules and comparative characterization against colofac MR capsules
The aim and objective of the present study is to develop Mebeverine Hydrochloride MR pellets in the form of capsule. Pellets with coating for Modified Release have a lower risk of dose dumping than coated tablets. Modifi...