| Literature DB >> 29743461 |
Yuzo Nishizaki1, Naoko Sato-Masumoto1, Akihito Nakanishi2, Yushi Hashizume2, Mahamadou Tandia2, Taichi Yamazaki3, Miho Kuroe3, Masahiko Numata3, Toshihide Ihara3, Naoki Sugimoto1, Kyoko Sato1.
Abstract
We designed an off-line combination of HPLC/photodiode array detector (PDA) and 1H-quantitative NMR (1H-qNMR) to estimate the relative molar sensitivity (RMS) of an analyte to a reference standard. The RMS is calculated as follows: a mixture of the analyte and the reference is analyzed using 1H-qNMR and HPLC/PDA. The response ratio of the analyte and the reference obtained by HPLC/PDA is then corrected using the molar ratio obtained by 1H-qNMR. We selected methylparaben (MPB), which is a certified reference material, as the reference standard and hesperidin (Hes) and monoglucosylhesperidin (MGHes) as analytes, and the RMSs of Hes283 nm/MPB255 nm and MGHes283 nm/MPB255 nm were determined as 1.25 and 1.32, respectively. We determined the contents of Hes and MGHes in processed foods by the conventional absolute calibration method and by the internal standard method employing the RMS values with respect to MPB. The differences between the values obtained with the two methods were less than 2.0% for Hes and 3.5% for MGHes.Entities:
Keywords: 1H-qNMR; HPLC HPLC/PDA; hesperidin; methylparaben; monoglucosylhesperidin; relative molar sensitivity
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Year: 2018 PMID: 29743461 DOI: 10.3358/shokueishi.59.1
Source DB: PubMed Journal: Shokuhin Eiseigaku Zasshi ISSN: 0015-6426 Impact factor: 0.464