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- Posts: 2
- Joined: Thu Oct 22, 2009 10:41 pm
I have a HPLC separation of enantiomers - not quite baseline resolved but pretty darn good. Certainly good enough to drop a line and get a good and reproducible isomeric ratio results. The "active" component is the second peak and is usually ~3:1 over the first peak. Forced degradation studies show its stability indicating (both peaks). We use this method to assay and we combine the peak areas of the two peaks for this analysis. So we use the same method for assay and isomeric ratio. All is well and the method works great.
I'm transferring this to someone who says thay require a tailing factor of < 1.25. (!!) . So I have a double peak - peak shape looks good on the front end of the first peak and the tail end of the second peak. But theres enough overlap to make it difficult to do the measurement at 5% peak height. But the peak shapes look really good. I'm forced to do manual calculations becasue I don't have access to sys suit software. But the eventual testing lab will.
Assuming that we have done everything we can to separate the two peaks, any ideas on how to demonstrate adequate peak tailing fot two non-resolved well shaped peaks? Will software take care of this?
Thanks!

