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Poor recovery of neat standards vs. extracted controls GCMS

Discussions about GC-MS, LC-MS, LC-FTIR, and other "coupled" analytical techniques.

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Does anyone have any insight as to why we would be getting poor/no recovery of a neat opiate standard (TMS derivatives) on GCMS compared to when we extract a positive blood control spiked with the same standard? Both are the same concentration. Does the presence of the matrix really make a difference? We are using Agilent Ultra Inert deactivated liners, splitless, single taper, with glass wool. It seems like we should be getting higher recovery for the neat standard.
Add additional derivatizing agent to both, and re-inject. If the standard has a little more water in it, might be using up all the derivatization chemical.
Thank you - this is good advice. I also just noticed that the standard and control are dried down at different temperatures in the Turbovap prior to derivatization, so we are looking into that as well.
3 posts Page 1 of 1

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