Optimization of an extraction procedure for the simultaneous quantification of riboflavin, nicotinamide and nicotinic acid in anchovies (Engraulis enrasicolus) by high-performance liquid chromatography-tandem mass spectrometry
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作者:
Caprioli, Giovanni
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Univ Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, ItalyUniv Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, Italy
Caprioli, Giovanni
[1
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Sagratini, Gianni
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Univ Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, ItalyUniv Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, Italy
Sagratini, Gianni
[1
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Vittori, Sauro
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Univ Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, ItalyUniv Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, Italy
Vittori, Sauro
[1
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Torregiani, Elisabetta
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Univ Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, ItalyUniv Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, Italy
Torregiani, Elisabetta
[1
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[1] Univ Camerino, Sch Pharm, Via St Agostino 1, I-62032 Camerino, Italy
A new analytical method that uses high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed for the first time for the analysis of vitamins B2 (riboflavin) and B3 (nicotinamide and nicotinic acid) in anchovies. Samples were extracted using four different extraction procedures: acidic hydrolysis (method 1), acidic hydrolysis plus peptide precipitation (method 2), acidic plus enzymatic hydrolysis (method 3) and enzymatic hydrolysis (method 4), and method 1 was found to be very good in terms of recoveries and quantitative results. From an analytical point of view, the separation of three analytes was achieved using a Kinetex Hilic analytical column (100 mm x 4.6 mm i.d.) with isocratic elution in a very short time (2.5 min or chromatography run). The recovery percentages (for method 1) obtained by spiking the matrices at 2.5 and 20 mg kg(-1) with a standard mixture of the three analytes were in the range 96.2-105.3%; the correlation coefficients (R-2) were always higher than 0.9996, and limits of quantification (LOQs) for all compounds were in the range 1-5 mu g kg(-1). Once validated, method 1 was applied to the analysis of 28 anchovy samples, both fresh and canned ones.
机构:
Univ Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, TurkeyUniv Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, Turkey
Ersoy, Beyza
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Oezeren, Akif
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Univ Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, TurkeyUniv Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, Turkey
机构:
Univ Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, TurkeyUniv Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, Turkey
Ersoy, Beyza
;
Oezeren, Akif
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Univ Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, TurkeyUniv Mustafa Kemal, Fac Fisheries, Dept Fishing & Fish Proc Technol, TR-31200 Antakya, Turkey