Team:TU Darmstadt/Protocols/GC-MS/Results

Sample preparation

We used two methods for our TPA analytics. Therefore we used standard sample preparation protocol:

Purge and Trap

• OP-1 add. 20 µl in 10 ml Water
• OP-2 add. 20 µl in 10 ml Water
• OP-K add. 20 µl in 10 ml Water

TPA short

• OP-1 add. 1ml in vial
• OP-2 add. 1ml in vial
• OP-K add. 1ml in vial

Results

TPA Short ATS

OP2

The first sample we measured was OP-2. Simultaneously, it was the proof of principal that our method worked. Here we present the corresponding SCAN, SIM of our sample:

Here we measured a biological sample hence we got a lot of peaks in the SCAN (first window). Surprisingly, in the SIM we got a huge peak at 7 minutes RT. We checked the mass spectrum out of the SCAN (third window) and obtained nearly the same fragmentation pattern we measured in the reference. Due to this, we compared the quality of our spectrum:

Here we can see that our spectrum is nearly identical to the reference spectrum of the TPA-methylester.

This screen-shot shows our SCAN and SIM (zoomed in). Due to the quantification, we need a peak with an sophisticated shape. Fortunately, the peak is perfect for the integration. After the integration we obtained a peak area of 43113.

Notably,  we are now able to quantify and qualify TPA out of biological sample via GC-MS!

OP1

The second sample is OP1.

Here you can see the mass spectrum of our molecule as well as the SIM and the SCAN. Hence we are able to reproduce the results from our method (look at the peak at 7 RT)

Here we illustrate the mass spectra of TPA with the corresponding reference spectrum.

KO