Enhancing Sensitivity in the Hyphenation of High-Performance Liquid Chromatography to Benchtop Nuclear Magnetic Resonance Spectroscopy at Isocratic and Onflow Conditions

The onflow hyphenation of high-performance liquid chromatography (HPLC) in adsorption mode with a benchtop <sup>1</sup>H nuclear magnetic resonance (NMR) spectrometer is described for the first time. Protonated solvents and isocratic conditions are used. The sensitivity was increased by choosing suitable NMR acquisition parameter as well as optimizing injection parameters and postacquisition data processing methods. With optimized conditions, the limit of detection (LOD) and the limit of quantification (LOQ) were LOD = 0.010 g L<sup>-1</sup> and LOQ = 0.031 g L<sup>-1</sup> for the methoxy <sup>1</sup>H of methyl paraben at 4.07 ppm, LOD = 0.038 g L<sup>-1</sup> and LOQ = 0.134 g L<sup>-1</sup> for the aromatic <sup>1</sup>H of pentyl paraben between 7.00 and 8.50 ppm. These are expressed in injection concentration and are comparable to existing HPLC hyphenation with high-field NMR spectrometers. The analysis of a 2 g L<sup>-1</sup> paraben mixture, far below the legal limits for usage in cosmetics, illustrates the applicability of the method. Taking advantage of the spectral resolution, chromatographically overlapping peaks are resolved using analyte-specific NMR elution traces. A methodology is detailed to facilitate the transfer of the optimized method to other (analyte) systems.

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Publication Details

Journal
The Journal of Physical Chemistry B
Published
2024-09-20
DOI
https://doi.org/10.1021/acs.jpcb.4c03509
Citations
2
Primary Topic
NMR spectroscopy and applications
Type
article
Field-Weighted Citation Impact
1.32

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article

Enhancing Sensitivity in the Hyphenation of High-Performance Liquid Chromatography to Benchtop Nuclear Magnetic Resonance Spectroscopy at Isocratic and Onflow Conditions

Markus Matz, Carlo Botha, Marianne Gaborieau, Michael Pollard et al.
2 citations
The Journal of Physical Chemistry B
NMR spectroscopy and applications
1.32
article

Enhancing Sensitivity in the Hyphenation of High-Performance Liquid Chromatography to Benchtop Nuclear Magnetic Resonance Spectroscopy at Isocratic and Onflow Conditions

Markus Matz, Carlo Botha, Marianne Gaborieau, Michael Pollard, Manfred Wilhelm, Johanna Tratz
article en
2 citations

Abstract

The onflow hyphenation of high-performance liquid chromatography (HPLC) in adsorption mode with a benchtop <sup>1</sup>H nuclear magnetic resonance (NMR) spectrometer is described for the first time. Protonated solvents and isocratic conditions are used. The sensitivity was increased by choosing suitable NMR acquisition parameter as well as optimizing injection parameters and postacquisition data processing methods. With optimized conditions, the limit of detection (LOD) and the limit of quantification (LOQ) were LOD = 0.010 g L<sup>-1</sup> and LOQ = 0.031 g L<sup>-1</sup> for the methoxy <sup>1</sup>H of methyl paraben at 4.07 ppm, LOD = 0.038 g L<sup>-1</sup> and LOQ = 0.134 g L<sup>-1</sup> for the aromatic <sup>1</sup>H of pentyl paraben between 7.00 and 8.50 ppm. These are expressed in injection concentration and are comparable to existing HPLC hyphenation with high-field NMR spectrometers. The analysis of a 2 g L<sup>-1</sup> paraben mixture, far below the legal limits for usage in cosmetics, illustrates the applicability of the method. Taking advantage of the spectral resolution, chromatographically overlapping peaks are resolved using analyte-specific NMR elution traces. A methodology is detailed to facilitate the transfer of the optimized method to other (analyte) systems.

The Journal of Physical Chemistry BVol. 128(39)
Karlsruhe Institute of Technology (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 11%
NMR spectroscopy and applications
1.32
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Enhancing Sensitivity in the Hyphenation of High-Performance Liquid Chromatography to Benchtop Nuclear Magnetic Resonance Spectroscopy at Isocratic and Onflow Conditions — Markus Matz, Carlo Botha, et al. · The Journal of Physical Chemistry B (2024) | TGRS Research Map | TGRS