Benchtop NMR spectroscopy for quantitative determination of milk fat and qualitative determination of lactose: From calibration curve to deep learning

被引:0
|
作者
Belmonte-Sanchez, Jose Raul [1 ]
Romero-Gonzalez, Roberto [1 ]
Orosa, Manuel Angel Martinez [2 ]
Morata, Maria Calvo [2 ]
Frenich, Antonia Garrido [1 ]
机构
[1] Univ Almeria, Dept Chem & Phys, Analyt Chem Area, Res Ctr Agr Food Biotechnol CIAIMBITAL, Agrifood Campus Int Excellence ceiA3, E-04120 Almeria, Spain
[2] Tentamus Lab Control SLU, Edificio Rozas 23,Ctra Coruna,Km 23-200, E-28290 Madrid, Spain
关键词
Milk fat quantification; Benchtop NMR spectroscopy; Machine learning; Artificial neural networks; Partial least squares regression; RESONANCE; QUANTIFICATION; OPTIMIZATION;
D O I
10.1016/j.lwt.2024.117000
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
This study compares three different methodologies for the quantification of the fat content of ultra-high temperature (UHT) milk using benchtop proton nuclear magnetic resonance (1H NMR) spectroscopy, a flagship of green, accessible, and state-of-the-art technology suitable for modern laboratory environments. The evaluated approaches included traditional calibration curve and machine learning algorithms, with emphasis on partial least squares regression (PLS-R) and artificial neural networks (ANN), to estimate the fat content in skimmed, semi-skimmed and whole milk. Among these, ANN provided the most accurate results for all types of milk, particularly in skimmed milk, with a relative standard deviation (RSD) of 14.9% and an accuracy of -7.3%. The calibration curve showed higher variability, with an RSD of 34.1% and trueness of 25.3% for skimmed milk. PLSR improved accuracy in relation to the calibration curve approach, reducing RSD to 18.9% and trueness to -17.7%. The developed method has been successfully applied to determine the fat content in 51 samples of UHT milk purchased in different Spanish supermarkets, providing adequate results for each of the three categories considered, including goat's milk, sheep's milk, and milk coffee. Furthermore, the application of machine learning has proven its validity by successfully distinguishing between lactose and lactose-free UHT milk.
引用
收藏
页数:8
相关论文
共 30 条
  • [21] Quantitative 1H NMR Spectroscopy Method for Determination of Anthraquinone Derivatives in Extracts from Rubia tinctorum L. Roots and Rhizomes
    Vasil'ev, Vasilii
    Sheremeta, Anzhelika
    Ivlev, Vasilii
    Goriainov, Sergey
    Hajjar, Fadi
    Esparza, Cesar
    Platonov, Evgeniy
    Khromov, Arkadiy
    Kolesnov, Alexandr
    Romashchenko, Victoria
    Kalabin, Gennady
    SCIENTIA PHARMACEUTICA, 2024, 92 (02)
  • [22] Quantitative Γ-HCNCH:: determination of the glycosidic torsion angle χ in RNA oligonucleotides from the analysis of CH dipolar cross-correlated relaxation by solution NMR spectroscopy
    Rinnenthal, Joerg
    Richter, Christian
    Ferner, Jan
    Duchardt, Elke
    Schwalbe, Harald
    JOURNAL OF BIOMOLECULAR NMR, 2007, 39 (01) : 17 - 29
  • [23] Quantitative Γ-HCNCH: determination of the glycosidic torsion angle χ in RNA oligonucleotides from the analysis of CH dipolar cross-correlated relaxation by solution NMR spectroscopy
    Jörg Rinnenthal
    Christian Richter
    Jan Ferner
    Elke Duchardt
    Harald Schwalbe
    Journal of Biomolecular NMR, 2007, 39 : 17 - 29
  • [24] Qualitative and quantitative 1H NMR spectroscopy for determination of divalent metal cation concentration in model salt solutions, food supplements, and pharmaceutical products by using EDTA as chelating agent
    Hafer, Elina
    Holzgrabe, Ulrike
    Kraus, Katharina
    Adams, Kristie
    Hook, James M.
    Diehl, Bernd
    MAGNETIC RESONANCE IN CHEMISTRY, 2020, 58 (07) : 653 - 665
  • [25] Identification and quantitative determination of eudesmane-type acids from the essential oil of Dittrichia viscosa sp viscosa using 13C-NMR spectroscopy
    Blanc, MC
    Bradesi, P
    Casanova, J
    PHYTOCHEMICAL ANALYSIS, 2005, 16 (03) : 150 - 154
  • [26] Structural determination of 3β-stearyloxy-urs-12-ene from Maytenus salicifolia by 1D and 2D NMR and quantitative 13C NMR spectroscopy
    Miranda, RRS
    Silva, GDF
    Duarte, LP
    Fortes, ICP
    Vieira, SA
    MAGNETIC RESONANCE IN CHEMISTRY, 2006, 44 (02) : 127 - 131
  • [27] NMR-SPECTROSCOPY IN STRUCTURAL ISOTOPE ANALYSIS - COMPOSITE METHOD FOR QUANTITATIVE FRAGMENTAL DETERMINATION OF H-2 LABELS FROM SETS OF H-1-NMR, H-2-NMR, AND C-13-NMR SPECTRA
    DEVYATKO, HG
    KALABIN, GA
    LIPOVICH, VG
    GLUKHIKH, VI
    JOURNAL OF ANALYTICAL CHEMISTRY OF THE USSR, 1977, 32 (11): : 1755 - 1764
  • [29] Structural determination of novel lacto-N-decaose and its monofucosylated analogue from human milk by electrospray tandem mass spectrometry and 1H NMR spectroscopy
    Chai, WG
    Piskarev, VE
    Zhang, YB
    Lawson, AM
    Kogelberg, H
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2005, 434 (01) : 116 - 127
  • [30] STUDIES ON CONSTITUENTS OF CAPSICUM .3. QUANTITATIVE-DETERMINATION OF OLEFINIC AND SATURATED COMPONENTS BY NMR AND OF TRANS-COMPONENTS BY IR SPECTROSCOPY IN A CAPSAICINOID MIXTURE FROM NATURAL SOURCE
    MULLERSTOCK, A
    JOSHI, RK
    BUCHI, J
    HELVETICA CHIMICA ACTA, 1973, 56 (02) : 799 - 803