The New Developments of Adulteration Detection for Honey. Dr. Jinzhong Xu Jiangsu Sinography Testing CO., LTD.

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The New Developments of Adulteration Detection for Honey Dr. Jinzhong Xu Jiangsu Sinography Testing CO., LTD.

Content 1. The current development of honey adulteration 2. Overview of honey adulteration detection techenologies 3. The new method for honey adulteration detection after 21.

1. The current development of honey adulteration Honey is the natural sweet substance, produced by bees from nectar and honey dew of plants or from secretions of living parts of plants or excretions of plant-sucking insects on the living parts of plants. The mainly ingredients of honey are carbohydrates such as fructose, glucose, sucrose, and the other sugar. Apart from these, honey also contains vitamins, minerals, amino acids and bio-enzymes.

Raw materials added into pure honey Initial stage: water, sucrose, maltose, starch, and so on Development stage: high fructose corn syrup(hfcs), corn syrup, sugarcane syrup, and so on Advanced stage: Beet sugar syrup, rice syrup. And these syrup can pass the different test.

2. Overview of honey adulteration detection techenologies before 211 2.1 Identified by sensory evaluation 2.2 Identified by physical and chemical indexes such as HMF, L-proline 2.3 Identified by TLC method 2.4 Identified by EA-IRMS method 2.5 Identified by LC-IRMS method 2.6 Identified by foreign enzyme method (BFF)

2.1 Identified by sensory evaluation Conventional method Identified by experienced experts according to the color, odor, taste, viscosity of honey Disadvantage: different people have different opinion

2.2 Identified by physical and chemical indexes Including water content, the composition of sugar, amylase activities, HMF content, L-proline content, and so on The quality of honey could be controled by detecting these insexes

2.3 Identified by TLC method Test acoording to GB/T 18932.2 oligosaccharide in sample was enrichment by charcoal column and seperated by thin layer chromatography on silicon gel plate. This method could be used to detect honey adulterated with HFCS. However, qualified HFCS has been presented in market!

2.4 Identified by EA-IRMS method As the carbon isotope of C3 and C4 plants in photosynthetic cycles are different, the 13 C/ 12 C ratios of C3 and C4 plants fall in the range of -28~-23 and -15~-9, respectively. As bees mainly produce honey from C3 plants, honey samples having δ 13 C less negative than -23.5 could be suspicious. EA-IRMS method could be used to detect honey adulterated with syrup product from C4 plants Disadvantage: This method can't be used to detect honey adulterated with syrup product from C3 plants!!!

2.5 Identified by LC-IRMS method Coupling an isotope ratio mass spectrometer to a liquid chromatography The fructose, glucose, di- and tri-saccharides were separated by LC and tested by IRMS.

The limits for Δδ 13 C values of pure honey Δδ 13 C ( ) P - H (differences between protein and honey δ 13 C values): 1. Δδ 13 C ( ) fru-glu (differences between fructose and glucose δ 13 C values): ±1. Δδ 13 C ( ) max. (maximum difference between all measured δ 13 C values): ± 2.1

2.6 Identified by foreign enzyme method (BFF) BFF was used to transfer the beet sucrose to fructose and glucose (1:1) The composition of the product is very close to the component of pure honey, therefore, it is very difficult to detect the adulteration with the product This method was developed for the determination of beta-fructofuranosidase activity in honey. to verify the adulteration of honey.

3. The New Methods for Honey Adulteration Detection 3.1 SM-R method for rice syrup (211) 3.2 SM-B method for beet syrup (212) 3.3 TMR methdo for rice syrup (212) 3.3 oligosaccharide method (212)

3.1 SM-R method This is a new and typical marker which was found to be presented in rice syrup and unable to be detected in pure honey This method could be used to detect the adulteration of honey with rice surup by the LC-MS/MS

Rice syrup RT:. - 9. SM: 3G 5.55 8 Relative Abundance 6 4 2.43 1.22 1.9 2.28 3.9 3.44 4.23 4.46 5.35 5.69 5.91 6.35 7.26 8. 8.97 5.54 Relative Abundance 8 6 4 2.95 1.18 1.68 2.24 2.65 3.35 5.7 7.23 3.96 4.61 5.2 5.84 7.26 8.53 1 2 3 4 5 6 7 8 Time (min) Fig.1 Chromatogram of rice syrup with rice syrup marker (SM-R)

Pure honey RT:. - 9. SM: 3G Relative Abundance 8 6 4 2 6.22 5.51 6.14 6.29 5.44 4.6 4.42 5.27 6.33 3.96 7.17 7.2.6.74 1.28 1.68 2.42 3.28 3.43 7.25 8.56 Relative Abundance 8 6 4 2 3.96 4.91 5.45 5.66 5.87 6.3 7.2 6.3.6.69 1.39 1.66 2.2 2.91 3.49 3.92 6.53 7.28 8.1 8.8 1 2 3 4 5 6 7 8 Time (min) Fig.2 Chromatogram of pure honey

3.2 SM-B method This is a typical marker in beet syrup. This method could be used to detect the adulteration of honey with rice surup by the LC-MS/MS

Beet syrup E:\213\213-8\SMB\8-28\std5 8/28/213 6:21:7 PM RT:. - 11.1 SM: 3G 95 9 N m E [ 1 1 G 85 8 75 RT: 5.73 AA: 5286 SN: 95549 7 65 6 Relative Abundance 55 5 45 4 35 3 25 2 15 1 5..5 1. 1.5 2. 2.5 3. 3.5 4. 4.5 5. 5.5 6. 6.5 7. 7.5 8. 8.5 9. 9.5 1. 1.5 11. Time (min) Fig.3 Chromatogram of beet syrup with beet syrup maker (SM-B)

Pure honey E:\213\213-8\SMB\8-28\JSST13-H81255 8/28/213 9:2:25 PM RT:. - 11.1 SM: 3G 95 9 N m S [ J 85 8 75 7 65 6 Relative Abundance 55 5 45 4 35 3 25 2 15 1 5 RT: 4.57 AA: 329 SN: 167 RT: 5.28 RT: 5.64 AA: 66 AA: 735 SN: 265 SN: 336..5 1. 1.5 2. 2.5 3. 3.5 4. 4.5 5. 5.5 6. 6.5 7. 7.5 8. 8.5 9. 9.5 1. 1.5 11 Time (min) RT: 6.5 AA: 443 SN: 69 RT: 6.47 AA: 353 SN: 47 RT: 7.24 AA: 151 SN: 27 RT: 7.54 AA: 369 SN: 6 RT: 8.17 AA: 448 SN: 69 RT: 8.88 AA: 498 SN: 173 RT: 9.67 AA: 456 SN: 251 Fig.4 Chromatogram of pure honey

3.3 TMR method The method was proposed by the Intertek in 212. The method detect the Arsenic in the honey to confirm the adulteration. The positive limit is 15ppb.

3.4 oligosaccharide method Improvement for the TLC method for oligosaccharide analysis. The method can indentify the oligosaccharide from the syrup and honeydew honey.

Syrup sample E:\213\...\8-27\JSST13-H81144 8/27/213 5:18:5 PM RT:. - 6.5 5 RT: 4.31 AA: 111841 SN: 58156 NL: 2.3E4 m/z= 526.5-527.5 F: + c ESI SRM ms2 851.3 [365.415-365.425, 527.418-527.428, 689.295-689.35, 851.295-851.35] MS Genesis JSST13-H81144 5 RT: 4.4 AA: 91792 SN: 4851 NL: 1.96E4 m/z= 688.8-689.8 F: + c ESI SRM ms2 113.5 [689.295-689.35, 851.295-851.35, 113.495-113.55] MS Genesis JSST13-H81144 5 RT: 4.46 AA: 57149 SN: 27561 NL: 1.9E4 m/z= 688.8-689.8 F: + c ESI SRM ms2 1175.5 [689.295-689.35, 851.295-851.35, 113.495-113.55] MS Genesis JSST13-H81144..5 1. 1.5 2. 2.5 3. 3.5 4. 4.5 5. 5.5 6. Time (min) JSST13-H81144 #924 RT: 4.44 AV: 1 NL: 1.6E4 F: + c ESI SRM ms2 1175.5 [689.295-689.35, 851.295-851.35, 113.495-113.55] 689.3 9 8 7 Relative Abundance 6 5 4 113.5 3 2 851.3 1 689.296 689.298 689.3 689.32 689.34 m/z 851.296 851.298 851.3 851.32 851.34 m/z 113.496 113.498 113.5 113.52 113.54 m/z

Pure honey E:\213\...\8-27\JSST13-H81122 8/27/213 4:56:51 PM RT:. - 6.5 5 RT: 4.25 AA: 142444 SN: 59566 NL: 1.52E5 m/z= 526.5-527.5 F: + c ESI SRM ms2 851.3 [365.415-365.425, 527.418-527.428, 689.295-689.35, 851.295-851.35] MS Genesis JSST13-H81122 5 RT: 4.38 AA: 138544 SN: 44267 NL: 2.15E4 m/z= 688.8-689.8 F: + c ESI SRM ms2 113.5 [689.295-689.35, 851.295-851.35, 113.495-113.55] MS Genesis JSST13-H81122 RT: 4.46 AA: 21696 SN: 9917 RT: 4.7 5 AA: 2414 SN: 1316..5 1. 1.5 2. 2.5 3. 3.5 4. 4.5 5. 5.5 6. Time (min) JSST13-H81122 #928 RT: 4.46 AV: 1 NL: 2.27E4 F: + c ESI SRM ms2 1175.5 [689.295-689.35, 851.295-851.35, 113.495-113.55] 113.5 NL: 4.28E3 m/z= 688.8-689.8 F: + c ESI SRM ms2 1175.5 [689.295-689.35, 851.295-851.35, 113.495-113.55] MS Genesis JSST13-H81122 9 8 7 Relative Abundance 6 5 4 3 2 689.3 1 851.3 689.296 689.298 689.3 689.32 689.34 m/z 851.296 851.298 851.3 851.32 851.34 m/z 113.496 113.498 113.5 113.52 113.54 m/z

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