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Rapid Simultaneous Determination of Sumatriptan Succinate and Naproxen Sodium in Combined Tablets by Validated Ultra Performance Liquid Chromatographic Method
A stability- indicating ultra perfomance liquid chromatography (UPLC) method was developed for the simultaneous determination of sumatriptan succinate and Naproxen sodium in pharmaceutical dosage…
A Validated stability indicating LC method of assay and related substances for Finasteride
The present paper describes the development of a st ability indicating reverse phase liquid Chromatography (RPLC) method for Finasteride in the presence of its impurities and degradation products…
Development and validation of stability indicating method for the quantitative determination of Raloxifene hydrochloride and its related impurities using UPLC
The present paper describes the development of a simple, economic and time efficient stability indicating UPLC method for Raloxifene hydrochloride (RLH) in the presence of its impurities and…
RP-UPLC method development and validation for the simultaneous estimation of ibuprofen and famotidine in pharmaceutical dosage form
A stability-indicating LC method developed for the simultaneous determination of Ibuprofen and Famotidine in pharmaceutical dosage forms was validated for accuracy, precision, and linearity and was also found to be stability indicating.
Analysis of duloxetine hydrochloride and its related compounds in pharmaceutical dosage forms and in vitro dissolution studies by stability indicating UPLC.
- D. D. Rao, S. Sait, A. M. Reddy, D. Chakole, Y. R. Reddy, K. Mukkanti
- ChemistryJournal of chromatographic science
- 1 November 2010
A reproducible gradient reversed-phase ultra-performance liquid chromatographic method is developed for quantitative determination of duloxetine hydrochloride in pharmaceutical dosage forms and is validated for linearity, specificity, accuracy, precision, ruggedness, and robustness.
A Validated Rapid Stability-Indicating Method for the Determination of Related Substances in Vardenafil Hydrochloride by Ultra-Performance Liquid Chromatography
A novel, sensitive, stability indicating RP-LC method has been developed for the quantitative determination of Varde- nafil and its related impurities in both bulk drugs and Pharmaceutical dosage…
Rapid determination of amlodipine besylate and valsartan in pharmaceutical preparations by stability-indicating ultra performance liquid chromatography
A stability- indicating UPLC method was developed for the simultaneous quantitative determination of amlodipine besylate and valsartan in pharmaceutical dosage forms in the presence of degradation…
Rapid simultaneous determination of aspirin and esomeprozole magnesium in combined tablets by validated ultra performance liquid chromatographic method
A stabilityindicating ultra Performance liquid ch romatography (UPLC) method has been developed and v li ated for the simultaneous determination of Aspirin and E someprozole Magnesium in…