Following this discovery, a reproducible method was developed and successfully validated for ramipril and ramiprilat. Additional stability tests were performed in the presence of glucuronide and diketopiperazine metabolites of ramipril and ramiprilat to demonstrate the method specificity.
This strategy demonstrated its usefulness by removing co-eluting isobaric interference, and reducing chemical background ions from the mobile phase, while drastically improving S/N.
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