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Problem! Retention time increase by time in Codeine analysis

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

5 posts Page 1 of 1
Hi everyone, this is my problem. I analyze Codeine with buffer prepare as following: 1.6g Sodium butansulfonat in 780ml Water and make up to volume with CH3OH then adjust pH 2.8 with HCl 2M. My mobile phase consists of 100% buffer and it is isocratic. The flow rate is 1.5ml/min, one injection lasts 25 minutes.
The RT of Codeine is always around 5-6 minute at first but after a few injections ( 3 or four) it will increase a bit (0.2 - 0.3 minute). After more than 15 injections, the RT from my first injection and my 15th injection is extremely different ( the RT of first injection is 5 and the 15th is 5.5). That make RSD of RT isn't good whereas the area after 15 injection is the same.
I also have thought that give the column more time for equilibration so I inject 15 injection before my real analysis but the RT still inceases as the above mentioned way above.
What can I do to stop the RT increase? Please help me. Thanks!
Hi everyone, this is my problem. I analyze Codeine with buffer prepare as following: 1.6g Sodium butansulfonat in 780ml Water and make up to volume with CH3OH then adjust pH 2.8 with HCl 2M. My mobile phase consists of 100% buffer and it is isocratic. The flow rate is 1.5ml/min, one injection lasts 25 minutes.
The RT of Codeine is always around 5-6 minute at first but after a few injections ( 3 or four) it will increase a bit (0.2 - 0.3 minute). After more than 15 injections, the RT from my first injection and my 15th injection is extremely different ( the RT of first injection is 5 and the 15th is 5.5). That make RSD of RT isn't good whereas the area after 15 injection is the same.
I also have thought that give the column more time for equilibration so I inject 15 injection before my real analysis but the RT still inceases as the above mentioned way above.
What can I do to stop the RT increase? Please help me. Thanks!
This is possibly because of using ion-pair agent in your mobile phase. Longer chain sulfonate salts (hexane, heptane etc) may decrease this equibration time (it also changes your RT)
prepare higher concentration buffer (5 times higher) and flash your column with it, then switch to your regular method
Vlad Orlovsky
HELIX Chromatography
My opinions might be bias, but I have about 1000 examples to support them. Check our website for new science and applications
www.helixchrom.com
Thanks for your reply. I have tried using Sodium hexan instead of Sodium Butan. The RT seem to be stable but longer and I aslo got a poor, broaden peak shape. Is there some ways to resovle these problems?

To increase the concentration of buffer I thought it is very hard to do because the IP reagent quite expensive. But thanks anyway, I will try if I have a chance.
May be one day you can consider mixed-mode chromatography where ion-pairing reagent is attached to the surface:

http://www.sielc.com/Compound-Codeine.html and retention time is controlled by amount of ACN and amount of ions in the mobile phase. You don't need to equilibrate your column with ion-pairing reagent, you don't need to dedicate column for analysis with ion-pairing reagents and you life will be much easier.
Vlad Orlovsky
HELIX Chromatography
My opinions might be bias, but I have about 1000 examples to support them. Check our website for new science and applications
www.helixchrom.com
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