On-cartridge derivatisation using matrix solid phase dispersion for the determination of cyclamate in foods

被引:8
作者
Li, Jianjun [1 ,2 ]
Liu, Yun [3 ]
Liu, Qianping [2 ]
Hui, Junfeng [1 ]
Liu, Yangzi [2 ]
机构
[1] Northwest Univ Xian, Minist Educ, Key Lab Synthet & Nat Funct Mol Chem, Xian 710069, Peoples R China
[2] Natl Engn Res Ctr Miniaturized Detect Syst, Xian 710069, Peoples R China
[3] Shaanxi Normal Univ, Coll Food Engn & Nutr Sci, Xian 710062, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Matrix solid phase dispersion; Cyclamate; High performance liquid chromatography; Derivatisation; 2-chlorocyclohexanone; PERFORMANCE LIQUID-CHROMATOGRAPHY; INJECTION SPECTROPHOTOMETRIC DETERMINATION; SINGLE-LABORATORY VALIDATION; TANDEM MASS-SPECTROMETRY; CALORIE SOFT DRINKS; ARTIFICIAL SWEETENERS; CAPILLARY-ELECTROPHORESIS; NONNUTRITIVE SWEETENERS; BEVERAGES; EXTRACTION;
D O I
10.1016/j.aca.2017.04.032
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel method for determination of sodium cyclamate in foods was developed. In this method, a syringe was loaded with the homogeneous mixture of the sample, KMnO4 powder and silica dispersant and used as a matrix solid phase dispersion (MSPD) reactor. As the reactor was infiltrated with small amounts of concentrated HCl, cyclamate was converted to 2-chlorocyclohexanone quickly and effectively within 5 min and determined by HPLC on a reversed-phase column using UV detection at a wavelength of 310 nm. Comparing with the traditional derivatisation in solution, the better clean-up was provided using on-cartridge derivatisation of MSPD, and much time, labor, and expense were saved. The results showed good linearity ( r(2) = 0.9998) over the concentration range of 1-500 mg/L. The limit of detection (LOD) and limits of quantification (LOQ) of the cyclamate were 0.3 mg/L and 1 mg/L respectively. The recoveries ranged from 91.6% to 101.3% with the relative standard deviations ( RSDs) in the range of 2.5% -4.3%. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 53
页数:8
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