Advertisement

lc-ms s-adenosylhomocysteine and s-adenosylmethionine

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

2 posts Page 1 of 1
Hi,

I am interested in LC-MS detection of SAH and SAM in brain tissue at nmolar levels. I am following a paper where this is achieved using phenylboronic acid SPE cartridges for extraction followed with LC using a 2 x 100 Waters Symmetry shield column with water, methanol, 0.02% acetic acid as solvents. SAM and SAH elute at about ~ 0.5% methanol. In this paper SAH and SAM are detected down to nM levels (20 uL injection of 5 nM solution) and the calibration curve is linear up to ~800 nM. Flow into the source is split four-fold.

I am using a TSS uplc column, 2.0 x 100 mm, and similar solvents and gradients. SAM peak looks broad but symmetrically tailing. SAH peak is terribly broad. Sensitivity is very bad.

I switched to an old 1 x 150 mm column and noticed that the SAH peak was better but still terrible.

Any suggestions with this analysis is greatly appreciated.

Thanks,
Mona
Hi,

I am interested in LC-MS detection of SAH and SAM in brain tissue at nmolar levels. I am following a paper where this is achieved using phenylboronic acid SPE cartridges for extraction followed with LC using a 2 x 100 Waters Symmetry shield column with water, methanol, 0.02% acetic acid as solvents. SAM and SAH elute at about ~ 0.5% methanol. In this paper SAH and SAM are detected down to nM levels (20 uL injection of 5 nM solution) and the calibration curve is linear up to ~800 nM. Flow into the source is split four-fold.

I am using a TSS uplc column, 2.0 x 100 mm, and similar solvents and gradients. SAM peak looks broad but symmetrically tailing. SAH peak is terribly broad. Sensitivity is very bad.

I switched to an old 1 x 150 mm column and noticed that the SAH peak was better but still terrible.

Any suggestions with this analysis is greatly appreciated.

Thanks,
Mona

Just wanted to mention that my analyses are working quite well now. Three things helped: switching from TSS column to a Symmetry BEH, adding some TFA to the sample, modifying source conditions (a lot hotter) on the ESI source. Thanks to those who read the post.
2 posts Page 1 of 1

Who is online

In total there are 39 users online :: 0 registered, 0 hidden and 39 guests (based on users active over the past 5 minutes)
Most users ever online was 5108 on Wed Nov 05, 2025 8:51 pm

Users browsing this forum: No registered users and 39 guests

Latest Blog Posts from Separation Science

Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.

Subscribe to our eNewsletter with daily, weekly or monthly updates: Food & Beverage, Environmental, (Bio)Pharmaceutical, Bioclinical, Liquid Chromatography, Gas Chromatography and Mass Spectrometry.

Liquid Chromatography

Gas Chromatography

Mass Spectrometry