Improved determination of malonaldehyde by high-performance liquid chromatography with UV detection as 2,3-diaminonaphthalene derivative

被引:3
|
作者
Panseri, Sara [1 ]
Chiesa, Luca Maria [1 ]
Brizzolari, Andrea [2 ]
Santaniello, Enzo [2 ]
Passero, Elena [3 ]
Biondi, Pier Antonio [3 ]
机构
[1] Univ Milan, Dept Vet Sci & Publ Hlth, I-20133 Milan, Italy
[2] Univ Milan, Dept Hlth Sci, I-20142 Milan, Italy
[3] Univ Milan, Dept Hlth Anim Sci & Food Safety, I-20133 Milan, Italy
关键词
Malonaldehyde; HPLC-UV; 2,3-Diaminonaphthalene; Canned mackerel fillet; MACKEREL SCOMBER-SCOMBRUS; GAS-CHROMATOGRAPHY; QUANTITATIVE-DETERMINATION; LIPID-PEROXIDATION; HUMAN PLASMA; MALONDIALDEHYDE; OXIDATION; CHEMISTRY; REAGENT; ASSAY;
D O I
10.1016/j.jchromb.2014.11.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid, specific and simple procedure is proposed for the determination of free malonaldehyde (MA) contained in fish tissue. The method is the optimization of the reaction of MA with 2,3-diaminonaphthalene to afford a naphtodiazepinium ion that present a UV absorption at 311 nm, useful for MA determination by HPLC with UV detection. The reaction proceeds in the presence of 25% acetonitrile at 37 degrees C in 20 min at pH 2 using 2,4-pentanedione as internal standard. The method has been applied to homogenized samples of canned mackerel fillets that were treated with 2,3-diaminonaphthalene in an acidic aqueous:acetonitrile mixture. The produced naphtodiazepinium ion was extracted in acetonitrile by a salting-out homogeneous liquid-liquid extraction. A standard calibration was carried out in the range 0.625-10 nmol/g. The reliability of the procedure is demonstrated by linearity (r(2) = 0.998), limit of detection (0.16 nmol/g), limit of quantification (0.22 nmol/g), repeatibility (RSD 5.57%), and intermediate precision (RSD 8.92%). (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 95
页数:5
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