Fresh Dual Presaturation Method for Analyzing H2O-Rich Samples Using Quantitative 1H NMR

A fresh dual presaturation (pre-SAT) method was developed to quantify analytes accurately near the suppressed water signal in 1H NMR spectra obtained from H2O-rich samples. The method includes an extra dummy pre-SAT with a suitable offset for each analyte signal in addition to the water pre-SAT. The residual HOD signal at 4.66 ppm was observed using D2O solutions containing L- phenylalanine (Phe) or L-valine (Val) and an internal standard of 3(trimethylsilyl)-1-propanesulfonic acid -d6 sodium salt (DSS-d6). When the HOD signal was suppressed using the conventional single pre-SAT method, the measured concentration of Phe from the NCH signal at 3.89 ppm decreased by a maximum of 48%, whereas the dual pre-SAT method gave a reduction in the Phe concentration measured from the NCH signal of less than 3%. The proposed dual pre-SAT method achieved accurate quantification of glycine (Gly) and maleic acid (MA) in a 10 vol % D2O/H2O solution. The measured concentrations of Gly of 513.5 +/- 8.9 mg kg-1 and MA of 512.2 +/- 10.3 mg kg-1 corresponded to sample preparation values of Gly of 502.9 +/- 1.7 mg kg-1 and MA of 506.7 +/- 2.9 mg kg-1 (the number after +/- indicates the expanded uncertainty (k = 2)).

Automated summary

A fresh dual pre-SAT method was developed to accurately quantify analytes near the suppressed water signal in 1H NMR spectra from H2O-rich samples. The method includes an extra dummy pre-SAT with a suitable offset for each analyte signal, in addition to the water pre-SAT. The proposed method achieved accurate quantification of glycine and maleic acid in D2O/H2O solutions.