Method for determining glucose, fructose and saccharose in tobacco essence perfume
A technology for tobacco flavor and glucose, applied in the field of tobacco, can solve the problems of low detection sensitivity, large baseline fluctuation, large chromatographic column, etc., and achieve the effects of good repeatability, low detection limit, repeatability and reproducibility
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Embodiment 1
[0025] Reagents and materials
[0026] Sucrose and D(-)-fructose, D-(+)-anhydroglucose (≥99.5%, HPLC), Sigma-Aldrich;
[0027] Acetonitrile (≥99.9%, GC), MERCK company;
[0028] Sodium hydroxide, Pure Chemical Analysis Co., Ltd., Belgium;
[0029] Milli-Q grade water, prepared by Milliore Element A10, unless otherwise specified, the water used in the experiment is Milli-Q grade water;
[0030] Tobacco essence, tobacco flavor.
[0031] instrument
[0032] 1200HPLC from Agilent, USA, equipped with G1378B degasser, G1311A quaternary pump, G1329A autosampler, G1316A column thermostat and G1362A differential refractive index detector;
[0033] American Millipore Company Milli-Q Element A10 pure water machine.
[0034] experimental method
[0035] 1. Chromatographic conditions Metacarb Pb PLUS chromatographic column (300mm × 7.8mm) of Varian Company, Metacarb 87P pre-column core. Injection volume: 20μL; flow rate: 0.4mL / min; pump stop time: 63min; column oven: 80°C; temperatu...
Embodiment 2
[0077] Embodiment 2, linearity, correlation coefficient, detection limit of the method of the present invention
[0078] Quantification by external standard method. With the concentration (μg / mL) as the abscissa x and the peak area as the ordinate y, a linear regression was performed to obtain the linear regression equation and correlation coefficient. The results show that the linearity of the method of the present invention is good, and the correlation coefficients are all greater than 0.9999 (see Table 6). With a signal-to-noise ratio (S / N) of 3, the detection limit was determined by serially diluting low-concentration standard solutions. The detection limit of the method is lower than 1.8 μg / mL, and the sensitivity is good.
[0079] Table 6 Linear equation, correlation coefficient, detection limit of standard curve
[0080]
Embodiment 3
[0081] Embodiment 3, method repeatability test of the present invention
[0082] According to the processing method described in 3 in Example 1, sample A was carried out 8 parallel measurements in 1 day to obtain the intraday precision of the method; the sample was measured 6 times in 8 days to obtain the interday precision of the method. The intra-day and inter-day precision results are expressed as RSD%, and the results are shown in Table 7 and Table 8, respectively. The intraday precision of fructose, glucose and sucrose was less than 1.2%, and the interday precision was less than 3.0%. The repeatability of the method was good.
[0083] The intraday precision test results of the method in Table 7
[0084]
[0085] The day-to-day precision test results of the method in Table 8
[0086]
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