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用于同时测定含油酸豆角中苯甲酸和山梨酸的高效液相色谱法及非水毛细管电泳法的开发

Development of HPLC and NACE methods for the simultaneous determination of benzoic and sorbic acids in sour snap beans containing oil.

作者信息

Han Po, Jia Zhenmin, Liu Mian, Li Yongbo, Liu Hongxia, Yang Hui, Wang Xie, Ban Fuguo, Zhang Shusheng

机构信息

Chemistry Department, Key Laboratory of Chemical Biology and Organic Chemistry of Henan, Zhengzhou University, Zhengzhou, P R China.

出版信息

Electrophoresis. 2007 Nov;28(22):4114-9. doi: 10.1002/elps.200600146.

Abstract

The practical methods were developed for the simultaneous determination of benzoic acid (BA) and sorbic acid (SA) in sour snap bean samples containing oil. BA and SA in the samples were extracted by ultrasonication with water, followed by cleanup procedures with precipitation for removing the potential proteins and with petroleum ether liquid-liquid extraction for removing the edible oil contained in the samples. The HPLC method was developed using Supelco C18 (250 mm x 4.6 mm id, 5 microm) as column, MeOH-20 mM NH(4)Ac (25:75 v/v) at 1.0 mL/min as the mobile phase and 230 nm as the detection wavelength. The optimal NACE method was established with a running buffer of 20.0 mM NH(4)Ac in 95% MeOH (pH* 10.6), and an applied voltage of -30 kV over a capillary of 50 microm id x 48.5 cm (40 cm to the detector window), which gave a baseline separation of BA and SA, and as well as of the blank matrix within ca. 10 min. Both HPLC and NACE methods gave the relatively lower limits of quantification at about 0.01-0.02 and 0.04-0.05 mg/kg, respectively, whereas the overall recoveries were larger than 85.0%. The proposed methods have been successfully applied to measure 15 real sour bean samples and the content profile of BA and SA in sour bean samples was obtained and evaluated.

摘要

开发了用于同时测定含油酸豆角样品中苯甲酸(BA)和山梨酸(SA)的实用方法。样品中的BA和SA通过用水超声提取,然后进行沉淀净化程序以去除潜在的蛋白质,并用石油醚液 - 液萃取去除样品中所含的食用油。采用Supelco C18(250 mm×4.6 mm内径,5微米)作为色谱柱,以甲醇 - 20 mM NH₄Ac(25:75 v/v),流速1.0 mL/min作为流动相,检测波长为230 nm建立了HPLC方法。建立了最佳的非水毛细管电泳(NACE)方法,运行缓冲液为95%甲醇中的20.0 mM NH₄Ac(pH 10.6),在50微米内径×48.5厘米(至检测窗口40厘米)的毛细管上施加-30 kV的电压,可在约10分钟内实现BA和SA以及空白基质的基线分离。HPLC和NACE方法的定量下限相对较低,分别约为0.01 - 0.02和0.04 - 0.05 mg/kg,而总体回收率大于85.0%。所提出的方法已成功应用于测定15个实际酸豆角样品,并获得和评估了酸豆角样品中BA和SA的含量分布。

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