Peaks in established HPLC assay now not resolving
Posted: Fri Nov 18, 2011 2:28 am
Hi all,
So I have an established assay for separation of paracetamol, paracetamol sulphate (PS) and paracetamol glucuronide (PG) using UV-HPLC (IS=3-acetamidophenol). Mobile phase is 0.1M KH2PO4: 1.5% isopropanol, 0.1% THF - pH 3.7. Column is a 60mm 3um rocket column, flow rate 2mL/min, oven 35 C.
Until resently para had an RT of ~3.1 min and PS was 2.7 min however now they are coleuting at 2.9. I have no idea what the problem is. I have remade the standards, altered the flow rate, made up several batches of MP etc so it's none of the obvious (to me anyway). The only thing I can think of is that the pH meter might be off - is this likely to make that big a difference?
Any suggestions would be fantastic!
Thanks.
Merrin
So I have an established assay for separation of paracetamol, paracetamol sulphate (PS) and paracetamol glucuronide (PG) using UV-HPLC (IS=3-acetamidophenol). Mobile phase is 0.1M KH2PO4: 1.5% isopropanol, 0.1% THF - pH 3.7. Column is a 60mm 3um rocket column, flow rate 2mL/min, oven 35 C.
Until resently para had an RT of ~3.1 min and PS was 2.7 min however now they are coleuting at 2.9. I have no idea what the problem is. I have remade the standards, altered the flow rate, made up several batches of MP etc so it's none of the obvious (to me anyway). The only thing I can think of is that the pH meter might be off - is this likely to make that big a difference?
Any suggestions would be fantastic!
Thanks.
Merrin