Exploiting automatic on-line renewable molecularly imprinted solid-phase extraction in lab-on-valve format as front end to liquid chromatography: application to the determination of riboflavin in foodstuffs

被引:29
作者
Oliveira, Hugo M. [1 ]
Segundo, Marcela A. [1 ]
Lima, Jose L. F. C. [1 ]
Miro, Manuel [2 ]
Cerda, Victor [2 ]
机构
[1] Univ Porto, REQUIMTE, Serv Quim Fis, Fac Farm, P-4099030 Oporto, Portugal
[2] Univ Balearic Isl, Dept Chem, Fac Sci, Palma De Mallorca 07122, Illes Balears, Spain
关键词
Solid-phase extraction; Molecularly imprinted polymer; Flow analysis; Lab-on-valve; Riboflavin; Foodstuff; WATER-SOLUBLE VITAMINS; BEAD-INJECTION; TRACE LEVELS; CAPILLARY-ELECTROPHORESIS; FLUORESCENCE DETECTION; MASS-SPECTROMETRY; SAMPLE TREATMENT; POLYMERS; MILK; PRECONCENTRATION;
D O I
10.1007/s00216-010-3522-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the present work, it is proposed, for the first time, an on-line automatic renewable molecularly imprinted solid-phase extraction (MISPE) protocol for sample preparation prior to liquid chromatographic analysis. The automatic microscale procedure was based on the bead injection (BI) concept under the lab-on-valve (LOV) format, using a multisyringe burette as propulsion unit for handling solutions and suspensions. A high precision on handling the suspensions containing irregularly shaped molecularly imprinted polymer (MIP) particles was attained, enabling the use of commercial MIP as renewable sorbent. The features of the proposed BI-LOV manifold also allowed a strict control of the different steps within the extraction protocol, which are essential for promoting selective interactions in the cavities of the MIP. By using this on-line method, it was possible to extract and quantify riboflavin from different foodstuff samples in the range between 0.450 and 5.00 mg L-1 after processing 1,000 mu L of sample (infant milk, pig liver extract, and energy drink) without any prior treatment. For milk samples, LOD and LOQ values were 0.05 and 0.17 mg L-1, respectively. The method was successfully applied to the analysis of two certified reference materials (NIST 1846 and BCR 487) with high precision (RSD<5.5%). Considering the downscale and simplification of the sample preparation protocol and the simultaneous performance of extraction and chromatographic assays, a cost-effective and enhanced throughput (six determinations per hour) methodology for determination of riboflavin in foodstuff samples is deployed here.
引用
收藏
页码:77 / 86
页数:10
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