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一测多评法同时测定烟草及烟草制品中8种多酚类化合物OA

Simultaneous determination of eight polyphenols in tobacco and tobacco products by quantitative analysis of multi-components via single marker

中文摘要英文摘要

为实现烟草及烟草制品中多酚类化合物的快速测定和质量评价,建立了一测多评法同时测定新绿原酸、东莨菪苷、绿原酸、隐绿原酸、咖啡酸、莨菪亭、芸香苷、山奈酚-3-O-芸香糖苷等8种多酚类化合物.采用高效液相色谱-二极管阵列(HPLC-DAD)分段检测技术,以甲醇、水和乙酸为流动相,采用梯度洗脱方式,流速1.0 mL/min,柱温30℃,在C18色谱柱上分离8种多酚类化合物.以绿原酸为内参物,建立其他7种多酚类化合物的相对校正因子,分别采用外标法和一测多评法(多点校正法、斜率校正法和单点校正法)测定烟草及烟草制品中8种成分的质量分数.结果表明:①在优化条件下,8种多酚类化合物在各自线性范围内线性关系良好,相关系数R2>0.999 9,检出限和定量限分别为0.01~0.15和0.02~0.48 mg/L,加标回收率为92.00%~102.38%,相对标准偏差为1.56%~4.10%.②以绿原酸为内参物,斜率校正法计算相对校正因子具有良好的耐用性和重现性(RSD<3.00%).斜率校正法所获结果与外标法的一致性最佳,平均相对偏差均不大于3.21%.③该方法操作简便、准确,适用于烟草及烟草制品中8种多酚类化合物的批量测定和质量评价.

In order to achieve rapid determination of polyphenols in tobacco and tobacco products for quality assessment,a quantitative multi-component analysis by single marker(QAMS)was proposed to simultaneously determine 8 polyphenols including neochlorogenic acid,scopolamine,chlorogenic acid,cryptochlorogenic acid,caffeic acid,scopoletin,rutin and kaempferol 3-O-rutinoside.The analysis was performed using high-performance liquid chromatography with diode array detection(HPLC-DAD)for a segmented detection program.Separation of the 8 polyphenols was achieved on a C18 column using a mobile phase consisting of methanol,water and acetic acid under a gradient elution mode.The flow rate was set at 1.0 mL/min,and the column temperature was maintained at 30℃.Using chlorogenic acid as the internal reference,the relative correction factors for the other 7 polyphenols were calculated.The mass fractions of the 8 polyphenols in tobacco and tobacco products were determined using both the external standard method and the QAMS method(calibrated via multi-point,slope,and single-point methods).The results showed that:1)Under the optimized conditions,the 8 polyphenols exhibited good linear relationships within their concentration ranges(R2>0.999 9),and the limits of detection(LODs)and quantification(LOQs)were 0.01‒0.15 and 0.02-0.48 mg/L.The spiked recoveries ranged from 92.00%to 102.38%with relative standard deviations(RSDs)of 1.56%-4.10%.2)Using chlorogenic acid as the internal reference,the relative correction factors calculated by the slope correction method demonstrated good durability and reproducibility(RSDs<3.00%).Furthermore,the slope correction method achieved the highest consistency with the external standard method,yielding an average relative deviation no more than 3.21%.3)The established method is simple,accurate and suitable for the batch determination and quality evaluation of the 8 polyphenols in tobacco and tobacco products.

汤晓东;苏燕;蒋佳磊;陈晓水;夏骏;斯文;潘力;李霞;朱书秀

浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024浙江中烟工业有限责任公司技术中心,杭州市西湖区转塘镇科海路118号 310024

轻工纺织

烟草烟草制品多酚类化合物一测多评法高效液相色谱分段检测

TobaccoTobacco productPolyphenolsQuantitative analysis of multi-components by single markerHigh-performance liquid chromatographySegmented detection

《烟草科技》 2026 (6)

13-22,10

浙江中烟工业有限责任公司科技项目"烟草主要化学成分的近红外定量分析模型拓展研究"(ZJZY2022B011).

10.16135/j.issn1002-0861.2025.0771

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