Review Article

Potentially Harmful Maillard Reaction Products in Food and Herb Medicines

Table 2

Analysis of Maillard reaction productions in Chinese herbal medicine materials and food.

MRPsMaterialsDetection methodsColumnMobile phaseWL/MWLinear responseRecovery/RSD (%)Refs

Arg-FruKorean red ginsengHPAEC-PADCarboPac PA1 column400 mM NaOH : H2O = 90 : 10, isocratic elutionr2 = 0.9999,
0.05–20 g/mL
0.020 μg/mL, 2.20 μg/mL (n = 5)Joo et al. [23]
Arg-Fru-GlcKorean red ginsengHPAEC-PADCarboPac PA1 column400 mM NaOH : H2O = 90 : 10, isocratic elutionr2 = 0.9998,
0.05–20 g/mL
0.1 μg/mL, 1.98 μg/mL (n = 5)Joo et al. [23]
Arg-FruPanax quinquefoliusLC-DADVenusil AA column0.05 M CH3COONa(CH3CN : H2O = 4 : 1), gradient elute254 nmY = 492377X-3193.4 (r = 0.9997)Gao et al. [24]
Arg-FruPanax quinquefoliusLC-MSVenusil AA column0.03 M CH3COONH4-(CH3CN : H2O = 4), gradient elute337 [M + H]Gao et al. [24]
Arg-Fru-GlcPanax quinquefoliusLC-DADVenusil AA column0.05 M CH3COONa(CH3CN : H2O = 4 : 1), gradient elute254 nmY = 336229X-2894.4 (r = 0.9993)Gao F F, [24]
Arg-Fru-GlcPanax quinquefoliusLC-MSVenusil AA column0.03 M CH3COONH4-(CH3CN : H2O = 4 : 1), gradient elute449 [M + H]Gao et al.[24]
Arg-Fru-GlcRed ginsengUPLC-MSAgilent eclipse C18 columnCH3CN: 0.3% CH3COOH = 60 : 40, isocratic elution497 (M)Du et al. [25]
5-HMFMaltLC-DADKromasil C18 columnCH3OH : H2O = 10 : 90, isocratic elution285 nmr2 = 0.998, 0–0.505 mg/mLR = 95.40%, RSD = 2.07%Zhou et al. [26]
5-HMFAngelica sinensisLC-DADDiamonsil C18 columnCH3CN : H2O = 5 : 95, isocratic elution286 nmY = 7800.4X-2.4701, 0.01572–0.1572 μgR = 97.75%, RSD = 1.17% (n = 6)Qian et al. [27]
5-DDMFAngelica sinensisLC-DADDiamonsil C18 columnCH3CN : H2O = 5 : 95, isocratic elution286 nmQian [27]
MaltolRed ginsengLC-DADZorbax SB-C18 column0.1% HCOOH : CH3CN, gradient elute276 nmA = 413425C-165763 (r2 = 0.9998), 1.54–15.44 μg/mLR = 99.98%, RSD = 0.63% (n = 6)Pang et al. [28]
FuranmethanolRed ginsengGC-MSHP-5 ms columnIon source temperature at 230°C98 (M)Lee et al. [29]
MaltolRed ginsengIon source temperature at 230°C126 (M)Lee et al. [29]
MaltolGC-MS126 (M)2.64Ferreira et al. [30]
MaltolFIA-CLKMnO4–C21H38ClN(hexadecylpyridinium chloride)system0.5–4.0 mg L−1RSD = 2.9% (n = 50)Alonso et al. [31]
MaltolGrape wineLC-PDASol-gel GCE0.03 M ammonia buffer solution-ep (μA-1/2) = 0.117 + 27.4 C (r = 0.9990), 0.005–0. 5 mmol/LR = 98%–100%, RSD = 3%Peng et al. [32]
MaltolGrape wineLC-DADODS C18 columnCH3OH : H2O = 60 : 40
isocratic elution
274.5 nmS = -0.37 + 14.34 C,(r = 0.9965)Peng et al. [32]
5-HMFPolygonatumLC-DADHC C18 columnCH3OH : H2O = 15 : 85
isocratic elution
284 nmY = 27206168X (r = 0.9999), 0–0.10535 μgR = 100.64%, RSD = 2.32% (n = 5)Yang et al. [33]
5-HMFLigustrum lucidumLC-DADKromasil C18 columnCH3CN : H2O = 7 : 93, isocratic elution278 nmY = 227.61X-3.4742 (R = 0.9997) 0.2475–2.475 μgR = 98.87%, RSD = 1.22%Hou et al. [34]
5-HMFCortex Moutan RadicisLC-DADLichrospher 5-C18 columnCH3OH-0.5% C2HF3O2(TFA), gradient eluteY = 84935346.664X-23602.910 (r = 0.999), 0.01084–0.3468 μgR = 95.76%, RSD = 1.13%Rui et al. [35]
5-HMFCibot rhizomeTLCSilica gel GF254C6H12(cyclohexane) : C4H8O2(ethylacetate):CH3COCH(acetone) = 3 : 3 : 1 as the developing agentVanillin sulphuric acid reagentJia et al. [36]
5-HMFRehmannia rootLC-DADZorbax SB-C18 columnCH3OH : 0.01 M H3PO4 = 70 : 30
isocratic elution
284 nm0.44–2.18 μg (r = 0.9999)R = 99.0%, RSD = 0.8% (n = 6)Qin et al. [37]
5-HMFCornus officinalisGC-MSHP-5 MS 5% PhenylMethl siloxane126 (M)Ding et al. [38]
AcrylamideRadix AsparagiLC-SPDDiamonsil C18 columnCH3CN :1 g/L CH3COOH = 20 : 80
isocratic elution
238 nm0.015–4.5 g/mLR = 106.6 ± 6.6%, RSD = 1.59% (n = 5)Shi et al. [19]