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Mycotoxins are natural contaminants whose presence in food- and feedstuffs cannot be completely avoided. Since several mycotoxins have been associated with and implicated in human and animal diseases there is a need to establish maximum levels, guidelines or action levels for them in some kinds of commodities. International and government authorities in many countries have been investing in mycotoxins research and initiating administrative actions for elaboration of legislation and implementing regulatory measures for the control of mycotoxins. Codex Alimentarius Commission is established international legislation on food and feed. In European Union specific limits and regulations for mycotoxins and other contaminants are constructed under the general Codex standards and based on proposal from European Commission. The legal basis for European Commission became available with the framework Council Regulation (EEC) No 315/93. In this paper, legislation regarding maximum levels for certain mycotoxins in food- and feedstuffs in European Community and other countries were reviewed and discussed.
Between 2003 and 2012, 1413 samples of kidneys, liver, and muscles from swine, cattle, sheep, horses, chickens, turkeys, geese, ducks, and fish were examined for the presence of ochratoxin A. The examination was performed in the framework of "The National Residue Control Programme for Chemical, Biological, and Drug Residue in Animal Tissues and in the Food of Animal Origin". The mycotoxin was determined by liquid chromatography with fluorescence detection after immunoaffinity column clean up. The limit of quantification was 0.2 µg/kg. Ochratoxin A was found only in swine kidney samples (n = 1092). It was detected in 28.8% of the kidney samples at the concentrations from 0.2 to 29.2 µg/kg. The most of the samples (25.5%) contained OTA at the concentration ranging from 0.2 to 5 µg/kg, which is below the provisional action level for OTA in kidneys, established in Poland at the concentration of 5 µg/kg. Furthermore, 24 (2.2%) samples had mycotoxin concentrations between 5 and 10 µg/kg and 13(1.2%) samples above 10 µg/kg.
Przedstawiono wyniki badań zawartości azotanów i azotynów w zbiorczym mleku surowym, serach twarogowych i serach twardych dojrzewających z obszaru całej Polski. Do oznaczeń stosowano metodę opartą na reakcji Griessa, po uprzedniej redukcji azotanów do azotynów za pomocą aktywnego kadmu metalicznego. Stwierdzone stężenia azotanów i azotynów nie budzą poważniejszych zastrzeżeń toksykologicznych.
A total number of 208 samples of mixed feeds for poultry, swine, cattle and sheep, and 36 samples of concentrates were received in 1991 from feed mills located over the territory of Poland. In collected samples concentrations of aflatoxins B₁, B₂, G₁, G₂, ochratoxins A and B, sterigmatocystin and zearalenone were analysed. The presence of ochratoxin A (OA) was confirmed in above 9% of the mixed feeds in the range of 2.5—120 µg/kg. The lowest percentage of samples contaminated with mycotoxins was found in poultry mixed feeds and the highest one in swine mixed feeds. Neither presence of aflatoxins, nor sterigmatocystin or zearalenone was detected in the samples of mixed feeds. Whereas in concentrates aflatoxin B₁ and ochratoxin A were found in 5.5% of samples (mean 40 µg/kg) and 13,8% of samples (mean 198 µg/kg) respectively. Zearalenon was detected only in the one sample of examined concentrates in concentration 1600 µg/kg.
A multiresidue method for determination and quantification of Fusarium mycotoxins: deoxynivalenol, zearalenone, T-2 toxin, HT-2 toxin, and metabolite of Aspergillus and Penicillium species - ochratoxin A in feeds was described. The method was based on the simultaneous extraction of selected mycotoxins from matrix, followed by liquid chromatography coupled with tandem mass spectrometry using a hybrid triple quadmpole - linear ion trap mass spectrometer with the multiple reaction monitoring in both positive- and negative-ion modes. The method was validated in accordance with the Commision Decision 2002/657/EC requirements. The mean recoveries of mycotoxins from spiked feed samples ranged from 74.6% to 113.9%, whereas limit of detection and quantification ranged from 0.72 to 12.4 µg/kg and 1.86 to 31.7 µg/kg, respectively.
The aim of this study was to investigate the presence of ochratoxin A (OTA) in the tissues and organs of wild game. The surveys were carried out between November 2011 and March 2014. The samples were taken from 584 animals: 315 from wild boars (Sus scrofa), 157 from roe deer (Capreolus capreolus) and 112 from deer (Cervus elaphus); a total of 2329 samples, including 584 kidney samples, 584 liver samples, 579 muscle tissue samples and 582 digestive tract content samples. The samples were collected from wild game hunted in four industrial regions of Poland: the Upper Silesian Industrial District, the Turoszów Brown Coal Basin, the Bełchatów Brown Coal Basin, the Legnica-Głogów Copper District, and in the agricultural region of the Lakeland of Warmia-Masuria. The concentration of OTA was determined using a method based on immunoaffinity column clean-up followed by high performance liquid chromatography with fluorescence detection (HPLC-FLD). The detection limit and the quantification limit were 0.2 and 0.3 µg/kg, respectively. The presence of OTA was detected in 103 samples from wild boars; in 64 samples of kidney, 19 samples of liver, 13 samples of muscle tissue and 7 samples of digestive tract content. Furthermore, OTA was found at low concentrations – from 0.3 to 1.3 µg/kg – in 3 and 2 samples of kidney collected from roe deer and deer, respectively. In contrast, up to about 19% of positive kidney samples from wild boars had higher concentrations of mycotoxin than the action level established in Poland (5 µg/kg); the highest content was 39.6 µg/kg, a mean concentration – 0.69 µg/kg and 95-percentile was 2.7 µg/kg. The content of OTA in liver samples ranged from 0.3 to 26 µg/kg, while in muscle tissue samples from 0.3 to 4 µg/kg. In 22 cases OTA was found in samples of kidney, liver and tissue muscle taken from the same animal. In digestive tract content, OTA was detected at concentrations from 0.3 to 283.3 µg/kg (71.4% of these samples were obtained from the Lakeland of Warmia-Masuria). The results of this study suggest that wild boars are more exposed to OTA than roe deer, deer and even pigs. The organs of wild boars can be contaminated with high concentrations of OTA. This may cause nephropathy in animals and the possibility of toxin carry-over to the food chain.
Przedstawiono ocenę przydatności testu immunoenzymatycznego Ridascreen® Af- latoxin B, do oznaczania zawartości aflatoksyny B, w paszach. Wartość testu oceniono przeprowadzając równolegle analizy porównawcze badanych pasz zalecaną metodą chromatografii cieczowej. Przeprowadzona ocena statystyczna uzyskanych wyników świadczy o istotnej zgodności między obu metodami.
The procedure for the determination of T-2 and HT-2 toxins in feedstuffs has been developed. The test portion was extracted with methanol-water (80:20, v/v) after adding sodium chloride and cleaned-up through immunoaffinity column. Mycotoxins were quantified by a high-performance liquid chromatography coupled with fluorescence detector (λex=381 nm, λem=470 nm) after pre-column derivatisation, which was achieved with 4-dimethylaminopyridine and 1-anthroyl cyanide solutions. The method was validated according to the Commission Regulation (EC) No 401/2006. Average recoveries for the compounds ranged from 94.0% to 106.5% for T-2 toxin and from 80.3% to 102.9% for HT-2 toxin. The limits of detection and quantification for T-2 and HT-2 toxins were 6 and 15 µg kg⁻¹, respectively.
A case of acute poisoning of nine horses accidentally fed Polfamix R-1 designated for cattle was described. Polfamix R-1, vitamin-mineral supplement contains 3.25 g of monensin per 1 kg. Each horse was fed about 200 g of the supplement (approx. 650 mg of monensin per 1 horse). After the Polfamix administration, two horses died suddenly and three other sick animals were observed for 7-10 days. Clinical signs of poisoning were characterized by motor and cardio-vascular disturbances. Residues of monensin were found in the kidney, heart and in the content of the two horses which died within 2 days after consuming monensin. The levels of the drug were 690 and 580 mcg per 1 kg in the kidneys of two horses and in the content of the stomachs - 440 and 360 mcg/kg, respectively. Only some traces of monensin were noted in the hearts. However, no presence of monensin was found in the samples of the three horses which died after a week.
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