by
parya_m » Fri Feb 01, 2013 6:01 pm
Please check out the websites from Waters, Phenomenex, Agilent etc. where you will find tons of applications. Just a little google will help you.
If you face problems with reproducibility of a method you found we will be happy to give you as much as possible support.
thank you so much for your kind reply, I check out above websites, there is an application method in phenomenex website, but they don't explain anything about sample preparation.
I found this method and be setting it up on my column :
Column: c18 150x4.6mm
Detection: 205nm
Mobile Phase: Buffer/ ACN (80:20)
Buffer: H3PO4 20 mmol
pH= 2.1 (adjusted by KOH 1M)
Temp.=50
sample preparation: 1 to 2 of serum and Acetonitile/H3PO4 0.1 M (1000:1) then vortexed for 1 min and centrifuged
at 9700 rpm for 5 min. The organic (upper) layer was diluted to half by water.
I have been struggling to separate carbamazepin and phenytoin appropriately, peaks are very close and broad
what I really can do to obtain sharp and specific peaks and decrease their retention time?