Stumped by HPLC
Posted: Fri Jan 24, 2014 9:56 pm
Hello all,
I have a problem and I am feeling extremely stupid, because I cannot solve it.
Background: boss decides I am to perform an HPLC analysis. Fine, have never run Agilent software or instrument. Whatever, figured this out, ran my sample.......now what?
I am supposed to calculate the % of the analyte in the sample. I am also to calculate the % recovery for the spike sample I prepared.
Never have done these before and I have NO formula. And the only procedure I have is an AOAC method. I am also using 2 older sample runs (just what the analyst wrote up, not the actual files). Both analysts are no longer here and they are both different. *head, desk*
Sample: filtered into HPLC vial
Spike: 10mL of filtered sample + 910uL of a 10mg/ml standard, diluted to 50mL. 550uL of this solution was then diluted to 1 mL and injected. (no idea why I did this, it is what a prior analyst did)
Results:
Sample peak area: 6400
Spike peak area: 950
????????
how did that happen? and yes, I did check vial placement and my sequence table to ensure I did not switch the vials. I think I need to add a dilution factor to the formula....
Any info I am missing to calculate the amount of analyte or % recovery of the spike?
Help appreciated greatly. And please keep it simple, as I do not run HPLC ever and have little to no background.
Thanks!
I have a problem and I am feeling extremely stupid, because I cannot solve it.
Background: boss decides I am to perform an HPLC analysis. Fine, have never run Agilent software or instrument. Whatever, figured this out, ran my sample.......now what?
I am supposed to calculate the % of the analyte in the sample. I am also to calculate the % recovery for the spike sample I prepared.
Never have done these before and I have NO formula. And the only procedure I have is an AOAC method. I am also using 2 older sample runs (just what the analyst wrote up, not the actual files). Both analysts are no longer here and they are both different. *head, desk*
Sample: filtered into HPLC vial
Spike: 10mL of filtered sample + 910uL of a 10mg/ml standard, diluted to 50mL. 550uL of this solution was then diluted to 1 mL and injected. (no idea why I did this, it is what a prior analyst did)
Results:
Sample peak area: 6400
Spike peak area: 950
????????
how did that happen? and yes, I did check vial placement and my sequence table to ensure I did not switch the vials. I think I need to add a dilution factor to the formula....
Any info I am missing to calculate the amount of analyte or % recovery of the spike?
Help appreciated greatly. And please keep it simple, as I do not run HPLC ever and have little to no background.
Thanks!