Peak area selection

[goldforest12345]

Hi all,

Which selection (a or b) in the following figure is right? Or do you have other options?


Thank for your time,
Lam

[Peter Apps]

Take your pick - by eye the relative difference between the two areas will be less than 2%. If that makes a practical difference then you need to get the peaks separated or find a selective wavelength.

As long as you do it the same way every time AND as long as the small peak in front of your analyte always stays about the same size your results will still be repeatable.

Peter

[goldforest12345]

Take your pick - by eye the relative difference between the two areas will be less than 2%. If that makes a practical difference then you need to get the peaks separated or find a selective wavelength.

As long as you do it the same way every time AND as long as the small peak in front of your analyte always stays about the same size your results will still be repeatable.

Peter

Thank you for your reply, Peter. But in several cases the difference between two areas may reach 20%. Please refer to the pic posted below.
I wonder that which peak area selection method is more acceptable without separating the small peak in front of my analyte.

[Peter Apps]

If the interference peak varies by that much then you have to go with A, but you really need to improve the chomatography - you have lots of space either side of these two peaks to shift them into.

Peter

[danko]

In my opinion, B in the first example and A in the second.
I think this is a great example/argument for the the above

Best Regards

[Fernando]

Hi goldforest12345

I'll try a gradient elution run to separate the first peak (impurity?, decomposition?) and then try to run isocratically. The integration criteria is correct .

Best regards.

Fernando

[Kreall]

This is how the intergation of the peak should look like. I think only couple of chromatographic programs can do this.



If you have trouble with not separeted peaks you can always make a baseline and use peak height instead of peak area.

Kreall

[Peter Apps]

I disagree I'm afraid. The reconstructed peak shape assumes that both peaks have an ideal shape, and is still vulnerable to changes in the size of the interfering peak. And if the target peak is riding on the tail of an interference than there is no way of knowing where the baseleine should be set.

Peter

[Consumer Products Guy]

Here's my take:

You've got partial separation, so small changes may significantly help resolve the two peaks and make your question moot. And don't throw USP crap or "validated procedure", any robustness studies - if done correctly - document that small changes are acceptable.

If mine, first thing I would do is run at 10C lower temperature, and 10C higher temperature. The resolution will either be better, worse, or the same. If one temperature is better, explore that, and go from there. If both higher and lower do not help, then time to tweak a different parameter.

I recently did similar to separate two chelating agents that practically coeluted using our 20-year-old procedure; in that case, going to smaller particle size and increasing column temperature from 30C to 50C gave me baseline resolution.

[tom jupille]

Neither one is any better than guesswork. The only way to get an accurate result is to do a better job with the separation.

There's an illuminating couple of sentences in Dyson's book on integration:

“. . . errors arising from peak overlap are introduced by the algorithms of perpendicular and tangent separation and cannot be eliminated by anything but better chromatography. Integrators are able to generate a highly precise and totally inaccurate set of results for all the foregoing examples.”

Dyson, Chromatographic Integration Methods, 2nd ed. , pg 67; RSC Monographs (1998) (emphasis added)

[goldforest12345]

Thank you guys so much for your precious comments!
Lam