Bad integration: Example [Bioanalytics]

posted by sagark – India, 2010-07-31 14:57 (4989 d 16:05 ago) – Posting: # 5705
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Dear members,

Thank you very much for your detailed explanations. Aspects for integration are much clear for me.

Dear HS, in the example you mentioned, can we say that the method was not properly developed. Ideally one would have expected a method which separates the RT of the two enantiomers by a consideration time to minimise overlapping. You said the first peak was not integrated at all. Does that mean the separation was achieved but not quantification of the first peak isomer was achieved? Please guide

Sagar

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