纪鹏飞,张 强,宋俊男,王希平,孙令超,王 芳.分光光度法检测葡萄酒中花青素方法可行性分析[J].食品安全质量检测学报,2020,11(23):8977-8982
分光光度法检测葡萄酒中花青素方法可行性分析
Feasibility analysis for the determination of anthocyanin in wine by spectrophotometry
投稿时间:2020-07-21  修订日期:2020-11-13
DOI:
中文关键词:  分光光度法  葡萄酒  花青素
英文关键词:spectrophotometry  wine  anthocyanin
基金项目:
作者单位
纪鹏飞 青岛科创质量检测有限公司 
张 强 青岛市计量技术研究院 
宋俊男 青岛科创质量检测有限公司 
王希平 青岛科创质量检测有限公司 
孙令超 青岛斯坦德检测股份有限公司 
王 芳 青岛科创质量检测有限公司 
AuthorInstitution
JI Peng-Fei Qingdao Sci-tech Innovation Quality Testing Co., Ltd 
ZHANG Qiang Qingdao Institute of Measurement and Technology 
SONG Jun-Nan Qingdao Sci-tech Innovation Quality Testing Co., Ltd 
WANG Xi-Ping Qingdao Sci-tech Innovation Quality Testing Co., Ltd 
SUN Ling-Chao Qingdao Standard Testing Co., Ltd 
WANG Fang Qingdao Sci-tech Innovation Quality Testing Co., Ltd 
摘要点击次数: 608
全文下载次数: 310
中文摘要:
      目的 分析分光光度法检测葡萄酒中花青素方法的可行性, 并对方法进行优化。方法 通过分析标准品和样品的全波长扫描图, 确定分光光度法的最佳检测波长; 通过检测不同储存时间时标准品吸光值, 分析标准品稳定性, 确定标准品储备液最佳使用时间; 通过检测加标回收率、检出限、定量限等参数, 同时与液相色谱法的数据作对比, 分析该方法的稳定性和准确性。结果 最佳检测波长为518 nm; 标准品母液在2 d内吸光值比较稳定; 线性范围为1~20 μg/mL时, r2为0.9998, 检出限为0.188 mg/100 mL, 定量限为0.625 mg/ 100 mL。加标水平为4、8、12 mg/100 mL时, 加标回收率为102.3%~106.5%。分光光度法检测葡萄酒样品中花青素含量为(6.58±0.38) mg/100 mL, 液相色谱法检测样品中总花青素含量为(6.84±0.021) mg/100 mL。结论 分光光度法适合用于葡萄酒中花青素含量的检测, 方法准确性较好。
英文摘要:
      Objective To analyze the feasibility of spectrophotometric determination of anthocyanins in wine and optimize the method. Methods The best detection wavelength of spectrophotometry was optimized by analyzing the scanning diagram of the standard sample with full wavelength. By detecting the absorbance value of the standard at different storage time, the stability of the standard was analyzed, and the optimal storage time of the standard reserve liquid was analyzed. By detecting standard recovery, detection limit and quantitative limit, and comparing with the data of liquid chromatography, the stability and accuracy of the method were analyzed. Results The best detection wavelength was 518 nm. The absorbance of standard solution was stable within 2 d. When the linear range was 1?20 μg/mL, r2 was 0.9998, the limit of detection was 0.188 mg/100 mL, and the limit of quantification was 0.625 mg/100 mL. The recoveries were 102.3%?106.5% when the spiked levels were 4, 8 and 12 mg/100 mL. The content of anthocyanin in wine samples was (6.58±0.38) mg/100 mL by spectrophotometry and (6.84±0.021) mg/100 mL by liquid chromatography. Conclusion Spectrophotometry is suitable for the determination of anthocyanin content in wine with high accuracy.
查看全文  查看/发表评论  下载PDF阅读器