Downloads provided by UsageCounts
Analytical method was developed for the estimation of Canagliflozin drug substance by liquid chromatography. The chromatographic separation was achieved on C18 column (Inertsil ODS 3V 150*4.6, 5um) at ambient temperature .the separation achieved employing a mobile phase consists of 0.1%v/v Formic acid in water: Methanol (10:90). The flow rate was 1.0 ml/ minute and ultra violet detector at 220nm. The average retention time for Canagliflozin found to be 2.4 min the proposed method was validated for selectivity, precision, linearity and accuracy. All validation parameters were within the acceptable range. The assay methods were found to be linear from 100-300μg/ml for Canagliflozin.
Canagliflozin, Isocratic, HPLC, C18, Formic acid, methanol and validation.
Canagliflozin, Isocratic, HPLC, C18, Formic acid, methanol and validation.
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
| views | 9 | |
| downloads | 12 |

Views provided by UsageCounts
Downloads provided by UsageCounts