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基于腙的配体用于微固相萃取-高效液相色谱法测定橙汁中的生物胺。

Hydrazone-based ligands for micro-solid phase extraction-high performance liquid chromatographic determination of biogenic amines in orange juice.

机构信息

Department of Chemistry, King Fahd University of Petroleum and Minerals, KFUPM Box 1059, Dhahran, Saudi Arabia.

出版信息

J Chromatogr A. 2011 Jul 15;1218(28):4332-9. doi: 10.1016/j.chroma.2011.04.073. Epub 2011 May 6.

DOI:10.1016/j.chroma.2011.04.073
PMID:21621782
Abstract

Eight hydrazone-based ligands were synthesized, trapped in a silica sol-gel matrix, and were subsequently used in the micro-solid phase extraction (μ-SPE) of biogenic amines (BAs). The BAs investigated were tryptamine, phenylethylamine, putrescine, histamine, tyramine and spermidine. Prior to the extraction, dansyl chloride was added to the samples which were heated to 70°C for 10 min. The samples were extracted with μ-SPE, after which analytes were desorbed using acetonitrile via ultrasonication. The extracts were analysed by high performance liquid chromatography (HPLC) with ultraviolet detection. Of the eight ligands investigated as sorbents, benzophenone 2,4-dinitrophenylhydrazone was found to be the most promising. The enhanced π-π interaction between the analytes and the ligand facilitated the adsorption process. Under the most suitable extraction conditions, the method demonstrated good linearity with correlation coefficient of more than 0.985 over a concentration range of 1-50 μg L(-1). Satisfactory repeatability with relative standard deviations of 7.43-11.30% (n=3) were obtained. Detection limits ranged from 3.8 to 31.3 ng L(-1). The μ-SPE method exhibited lower recoveries (71.5-87.4%) when compared to the solid phase extraction technique (79.7-95.0%), but enrichment factors of 94-460 were obtained. The proposed μ-SPE-HPLC method was applied to the determination of BAs in orange juice purchased from local supermarkets, with satisfactory results. The orange juices were characterized by the presence of relatively high levels of putrescine (range, 550-2210 μg L(-1)) but tryptamine and phenylethylamine were not detected in any of the tested samples.

摘要

合成了 8 种腙基配体,将其包埋在硅胶溶胶-凝胶基质中,随后用于生物胺(BAs)的微固相萃取(μ-SPE)。所研究的 BAs 包括色胺、苯乙胺、腐胺、组胺、酪胺和亚精胺。在萃取之前,向样品中加入丹磺酰氯,然后将样品加热至 70°C 10 min。通过超声处理用 μ-SPE 萃取样品,然后用乙腈解吸分析物。采用高效液相色谱(HPLC)法,紫外检测对提取物进行分析。在所研究的 8 种配体作为吸附剂中,二苯甲酮-2,4-二硝基苯腙被认为是最有前途的。分析物与配体之间增强的π-π相互作用促进了吸附过程。在最适宜的萃取条件下,该方法在 1-50μg L(-1)浓度范围内表现出良好的线性,相关系数大于 0.985。通过 3 次重复实验获得了 7.43-11.30%(n=3)的相对标准偏差,表明具有良好的重现性。检测限范围为 3.8-31.3ng L(-1)。与固相萃取技术(79.7-95.0%)相比,μ-SPE 方法的回收率(71.5-87.4%)较低,但获得了 94-460 的富集因子。该方法已应用于当地超市购买的橙汁中 BAs 的测定,结果令人满意。橙汁的特点是腐胺含量相对较高(范围为 550-2210μg L(-1)),但在所有测试样品中均未检测到色胺和苯乙胺。

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