DEVELOPMENT OF UV SPECTROSCOPIC METHOD FOR THE DETERMINATION OF GUAIFENESIN IN BULK AND FORMULATION
Journal Title: Int J of Pharm Res & Analy - Year 2015, Vol 5, Issue 2
Abstract
The present research work discusses the development of UV Spectroscopic method for the estimation of Guaifenesin. Simple, specific, accurate and cost effective spectroscopic method has been developed for the estimation of Guaifenesin in bulk as well as formulation. The optimum conditions for the analysis of the drug were established. The maximum wavelength (λmax) was found to be 240nm. The validation was performed as per ICH guidelines for linearity, accuracy, precision, LOD and LOQ. The method shows high sensitivity with linearity in the range of 1-9 μg/ml and shows a linear relationship between the absorbance and concentration with coefficient of correlation 0.9992. The regression of curve was Y = 0.054 + 0.030. The precision of method was found to be good. The percentage recovery was found to be 99.57 ± 0.38. The optimized showed good reproducibility and recovery with RSD < 2%. The proposed method will be suitable for analysis of Guaifenesin in bulk as well as pharmaceutical formulations in quality control purpose. It is thus concluded that the proposed method is new, simple, cost effective, safe, accurate, precise and environmental friendly.
Authors and Affiliations
PUSHPALATHA E , Tejaswini P , Najboon bi M , Vineesha S , Madhuna MD , Anil Kumar T , Raju M
DEVELOPMENT AND VALIDATION OF NEW RP-HPLC METHOD FOR PACLITAXEL IN BULK AND ITS PHARMACEUTICAL DOSAGE FORM
A simple, precise, rapid and accurate reverse phase HPLC method has been developed for the determination of Paclitaxel in bulk and its pharmaceutical dosage form. An enable C18G, 250mm, X4.6mm i.d, 5μm particle siz...
SPECTROPHOTOMETRIC ESTIMATION OF CEFPROZIL IN BULK DRUG AND PHARMACEUTICAL FORMULATIONS
Two simple, accurate, rapid and sensitive spectrophotometric methods (A and B) have been developed for estimation of cefprozil in bulk drug and pharmaceutical formulations. The methods A and B were based on oxidati...
RECENT APPROCHES FOR IMPURITY PROFILING IN PHARMACEUTICAL FORMULATIONS
In the pharmaceutical world, an impurity is considered as any other organic material, besides the drug substance, or ingredients, arise out of synthesis or unwanted chemicals that remains with API’s. The impurity m...
AN OVERVIEW OF ELECTRON PROBE MICROANALYSIS
Electron Probe Microanalysis (EPMA) is an analytical technique that is used to establish the composition of small areas on specimens. It’s one of the several particle-beam techniques These analytical technique has...
RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF METFORMIN AND SITAGLIPTIN IN TABLET DOSAGE FORMS
A new simple and precise reverse phase high performance liquid chromatographic method has been developed andsubsequently validated for the simultaneous estimation of Metformin and Sitagliptin in combination. The chromato...