Methodological support of control of the content of n-nitrozodiphenylamine in food meat and meat/plant products

Мұқаба

Дәйексөз келтіру

Толық мәтін

Аннотация

The methodical methods used in the practice of the development and application of methods for the determination of chemical compounds in food products for practical instrumental studies used in conducting laboratory studies of food safety are considered. An algorithm for the development of a chromatography-mass spectrometric technique for the determination of one of the group of highly toxic, carcinogenic N-nitrosamines (N-nitrosodimethylamine, N-nitrosomethylethylamine, N-nitrosodiethylamine, N-nitrosopyrrolidineamin, N-nitrosomorpholinamine, N-nitrosodipropylamine, N- nitrosopiperidinamine N-nitrosoperidineamine and N-nitrosodiphenylamine in homogenized canned meat and meat products (canned meat) is supposed. The algorithm included experimental development of chromium parameters of chromatography-mass spectrometric determination of an analyte, the selection of optimum conditions of sample preparation of samples of canned meat to minimize the influence of the matrix: the transesterification reaction of fatty acids, organic solvent extraction, solid phase extraction, study of extraction completeness by means of the method “introduced – found”, establishment of metrological characteristics of the process of the measurement. The high sensitivity and selectivity of the chromatography-mass spectrometric determination of N-nitrosodiphenylamine in canned meat samples with a lower limit of 0.0002 mg/kg and a maximum error of not more than 23% was achieved owing to the use of a set of methodical techniques — the selection of optimal chromatographic analysis conditions: capillary column series HP-FFAP 50m • 0,320 mm • 0,50 μm, temperature programming of the column: initial temperature of 50ºС, the temperature rise up to 120ºС at a speed of 8 °C/min; from 120° to 185 °C at a rate of 12 °C min and from 185 ° to 240 °C at a rate of 25 °C/min with exposition at a final temperature of 5 minutes; mode of operation of the mass spectrometric detector: selective ion monitoring (SIM) for three characteristic ions of the analyzed compound of 167, 168, 169 m/z. Using the reaction of transesterification of fatty acids contained in canned meat, potassium methylate, removal of the formed esters from samples of canned meat with an organic solvent (hexane), concentration of N-nitrosodiphenylamine in the aqueous layer on cartridges of an automatic solid-phase extraction system provides the extraction of N-nitrosodiphenylamine from the test samples by 99.94%. In the process of approbation of the chromatography-mass spectrometric method, the content of N-nitrosodiphenylamine in the concentration range 0.030 ± 0.011 ÷ 3.89 ± 0.83 mg/kg was found in samples of homogenized canned food meat and meat products (canned meat) from various manufacturers. The highest concentration of N-nitrosodiphenylamine C = 3.89 ± 0.83 mg/kg was found in the sample of canned meat «beef + chicken».

Авторлар туралы

Tatyana Nurislamova

Federal Scientific Center for Medical and Preventive Health Risk Management Technologies

Хат алмасуға жауапты Автор.
Email: nurtat@fcrisk.ru

MD, PhD, DSci., Deputy Head of the Department of Chemical and Analytical Research Methods of the Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, Perm, 614015, Russian Federation. 

e-mail: nurtat@fcrisk.ru

Ресей

T. Ulanova

Federal Scientific Center for Medical and Preventive Health Risk Management Technologies

Email: noemail@neicon.ru
Ресей

N. Popova

Federal Scientific Center for Medical and Preventive Health Risk Management Technologies

Email: noemail@neicon.ru
Ресей

O. Maltseva

Federal Scientific Center for Medical and Preventive Health Risk Management Technologies

Email: noemail@neicon.ru
Ресей

Әдебиет тізімі

  1. SanPiN 2.3.2.1078-01. Hygienic requirements for quality and safety of food raw materials and food products. Moscow; 2002 (in Russian)
  2. Technical regulations of the Customs Union of the Customs Union of Customs Union 021/2011 «On food safety». (in Russian)
  3. Sannino A., Bolzoni L. GC/CI-MS/MS method for the identification and quantification of volatile N-Nitrosamines in meat products. Food Chem. 2013; 141(4): 3925-30.
  4. Yuan Y., Meng W., Yutian M., Fang C., Xiaosong H. Determination of Eight Volatile Nitrosamines in Meat Products by Ultrasonic Solvent Extraction and Gas Chromatography-Mass Spectrometry Method. Int. J. Food Prop. 2015; 18(6): 1181-90.
  5. Herrmann S.S., Duedahl-Olesen L., Granby K. Simultaneous determination of volatile and non-volatile nitrosamines in processed meat products by liquid chromatography tandem mass spectrometry using atmospheric pressure chemical ionisation and electrospray ionization. J. Chromatogr. A. 2014; 1330: 20-9.
  6. Herrmann S.S., Duedahl-Olesen L., Christensen T., Olesen P.T., Granby K. Dietary exposure to volatile and non-volatile N-nitrosamines from processed meat products in Denmark. Food Chem. Toxicol. 2015; 80: 137-43.
  7. Al-Kaseem M., Al-Assaf Z., Karabeet F. Determination of Seven Volatile N-Nitrosamines in Fast Food. Pharmacol. Pharm. 2014; (5): 195-203.
  8. Malysheva A.G., Rakhmanin Yu.A. Physico-chemical Researches and Methods for Control over Substances in Environmental Health [Fiziko-khimicheskie issledovaniya i metody kontrolya veshchestv v gigiene okruzhayushchey sredy]. St. Petersburg; 2012. (in Russian)
  9. GOST R 8.563-2009 State system for ensuring the uniformity of measurements (ICG). Methods (methods) of measurements. Moscow; 2010. (in Russian)
  10. RMG 61-2010. State system for ensuring the uniformity of measurements. Indicators of accuracy, accuracy, precision of quantitative chemical analysis techniques. Methods of evaluation. Moscow; 2012. (in Russian)
  11. GOST R ISO 5725-1-6-2002. Accuracy (accuracy and precision) of measurement methods and results. Moscow; 2002. (in Russian)
  12. Korenman Ya.I., Kuchmenko T.A. Approaches for food products analyses. Development of mass-sensitive sensors. Rossiyskiy khimicheskiy zhurnal. 2002; 46(4): 34-42. (in Russian)
  13. Yaroshenko D.V., Kartsova L.A. Matrix effect and methods for its elimination in bioanalytical methods using chromatography-mass spectrometry. Zhurnal analiticheskoy khimii. 2014; 69(4): 351-8. (in Russian)
  14. Krupina N.A., Gushchenko A.V., Pashovkina R.N., Krasnova R.R., Kaletina N.I. Use of solid-phase extraction in the study of benzodiazepine derivatives in biological objects on the example of phenazepam. In: Materials of the VI All-Russian Congress of Forensic Medicine [Materialy VI Vserossiyskogo S”ezda sudebnykh medikov]. Moscow-Tyumen’; 2005. (in Russian)
  15. Lebedev A.T. Mass Spectrometry in Organic Chemistry [Mass-spektrometriya v organicheskoy khimii]. Moscow: BINOM. Laboratoriya znaniy; 2003. (in Russian)

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML

© Nurislamova T.V., Ulanova T.S., Popova N.A., Maltseva O.A., 2024



СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ПИ № ФС 77 - 37884 от 02.10.2009.