Analytical method development and validation of Anagliptin by RP-HPLC

pharmacy (Quality Assurance)

Analysis is important in every product but it is vital in medicines as it involves life. The assurance of quality is achieved through analysis of the drug product. Now a days, the antidiabetic drugs are very much useful in single therapies, rather than the use of multiple drug formulation because of multiple action side effects. Aanagliptin is a life saving molecules for the treatment of Type II Diabetes. Quantification of drug molecule is important task for routine analysis of API in its finished product analysis. Literature survey exposed very few analytical procedure for routine analysis of Anagliptin. Therefore, in present research an attempt was made to develop and validate, simple, precise and economic method for routine analysis of Anagliptin in bulk and tablet dosage form. It was competed that method would be consistent for quantification of Anagliptin throughout its lifecycle.

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