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We want to analyze Aspirin in aqueous dissolution media. Spectrophotometric method is used in original procedure (USP, BP), but we need more sensitive method because the composition of API in our tablets is lower. Aspirin is unstable in aqueous media and partially degrades to salicylic acid. So we found 2 peaks in chromatogram: Aspirin and Salicylic acid. We could calculate the peak of Salicylic acid but we couldn’t on Aspirin peak because the reference standard of Aspirin will be hydrolyzed too in the same media.
Aspirin in non-aqueous solvent was injected and the peak shape was different with Aspirin in dissolution media.
Should Aspirin be degraded completely to form Salicylic acid? Then from the calculation of Salicylic acid concentration we could get concentration of Aspirin using MW ratio. Is it OK?
Regards,
SYX
