Search Results - "Kumar, Y. Ravindra"
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LC-MS/MS and NMR characterization of forced degradation products of mirabegron
Published in Journal of liquid chromatography & related technologies (25-02-2016)“…A rapid, precise, and reliable liquid chromatography tandem mass spectrometry (LC-MS/MS) method has been developed for the characterization of stressed…”
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A validated chiral HPLC method for the enantiomeric separation of tolterodine tartarate
Published in Journal of pharmaceutical and biomedical analysis (03-09-2004)“…An isocratic chiral HPLC method was developed for the separation of tolterodine tartarate enantiomers. The mobile phase consists of n-hexane and isopropyl…”
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Structural identification and characterization of impurities in moxifloxacin
Published in Journal of pharmaceutical and biomedical analysis (10-03-2004)“…In the synthesis of Moxifloxacin four prominent impurities were detected in HPLC analysis. These impurities were detected in gradient HPLC method. They were…”
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Isolation, synthesis and characterization of impurities in Celecoxib a cox-2 inhibitor
Published in Journal of pharmaceutical and biomedical analysis (29-06-2004)“…During the impurity profile of Celecoxib, four polar impurities (impurity I, II, III and IV) and one non-polar impurity (impurity V) with respect to Celecoxib…”
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Application of LC–MS/MS for the identification of a polar impurity in mosapride, a gastroprokinetic drug
Published in Journal of pharmaceutical and biomedical analysis (01-06-2003)“…In the impurity profile of mosapride a polar impurity (0.1%) was detected in HPLC with respect to mosapride. Based on the mass spectral data obtained by…”
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Impurity profile study of loratadine
Published in Journal of pharmaceutical and biomedical analysis (24-04-2003)“…Three unknown impurities in loratadine bulk drug at levels below 0.1% (ranging from 0.05 to 0.1%) were detected by a simple isocratic reversed-phase high…”
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DEVELOPMENT AND VALIDATION OF A STABILITY INDICATING UPLC METHOD, IDENTIFICATION, AND CHARACTERIZATION OF THREE DEGRADANT IMPURITIES IN PHARMACEUTICAL DOSAGE FORM OF RABEPRAZOLE SODIUM
Published in Journal of liquid chromatography & related technologies (01-06-2013)“…A simple, sensitive, and reproducible ultra performance liquid chromatography (UPLC) coupled with a photodiode array detector method was developed for the…”
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Validated chiral LC Method for the Enantiomeric Separation of Galantamine
Published in Chromatographia (01-02-2008)“…A rapid isocratic chiral HPLC method has been developed for the separation of R-galantamine from S-galantamine. Good resolution viz. Rs > 3 between R- and S-…”
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Structural studies on the impurities of troglitazone
Published in Journal of pharmaceutical and biomedical analysis (26-02-2003)“…The impurity profile study of troglitazone has been carried out primarily by (liquid chromatography–mass spectrometry) LC–MS. Four process-related impurities…”
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Stability Indicating HPLC Method Development and Validation of Rivaroxaban Impurities and Identification Forced Degradation Products by LC-MS/MS
Published in Biomedical chromatography (13-06-2022)“…Aim of the study was to develop a single sensitive and robust analytical method which can separate enantiomers, degradants, potential and process related…”
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LC-MS/MS and NMR Characterization of Key Impurities in Linagliptin and Pramipexole
Published in Journal of liquid chromatography & related technologies (26-11-2015)“…A sensitive, rugged, and robust LC-MS/MS and NMR analysis has been developed for the identification and characterization of key impurities of Linagliptin and…”
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