Determination of Ochratoxin A contamination in grapes, processed grape products and animal-derived products using ultra-performance liquid chromatography-tandem mass spectroscopy system
Abstract:We developed a sensitive and rapid analytical method to determine the level of Ochratoxin A contamination in grapes, processed grape products and in foods of animal origin (a total of 11 different food matrices). A pretreatment that followed a “quick, easy, cheap, effective, rugged, and safe” protocol was optimized to extract Ochratoxin A from the matrices, and the extracted Ochratoxin A was then detected with the use of a highly sensitive ultra-performance liquid chromatography-tandem mass spectrometry system… Show more
“…Real Sample Analysis. Ultraperformance liquid chromatography (UPLC) was used to compare both standard OTA solutions and spiked-beer samples, obtained from a local store, using conditions as reported by Wei et al 25 Beer samples were degassed with argon gas before being directly applied to either the aptasensor electrode or UPLC analysis. Testing was performed by spiking OTA into beer at concentrations of 1, 10, and 100 ng mL −1 .…”
Ochratoxin A (OTA)a mycotoxin produced by Aspergillus and Penicillium fungiis a carcinogen and common trace contaminant in agricultural and processed food products. As consumption is detrimental to human and animal health, regular product monitoring is vital, and highly sensitive and portable OTA sensors are necessary in many circumstances. Herein, we report an ultrasensitive, electroanalytical aptasensor for precise determination of OTA at trace levels. The sensor leverages a DNA aptamer to capture OTA and silver metallization as a signal enhancer. Exonuclease I is used to digest unbound aptamers, engendering excellent background signal suppression and sensitivity enhancements. Efficient optimization of assay conditions is achieved using central composite design (CCD), allowing rapid evaluation of both the electrode and square wave voltammetry parameter space. The sensor exhibits excellent analytical performance, with a concentration limit of detection of 0.7 pg mL −1 , a limit of quantitation of 2.48 pg mL −1 , and a linear dynamic range (R 2 = 0.968) of over 6 orders of magnitude (between 1 pg mL −1 and 0.1 μg mL −1 ). Direct comparison with ultraperformance liquid chromatography (UPLC) indicates excellent analytical performance for standard solutions (R 2 = 0.995) and spiked beer samples (R 2 = 0.993), with almost quantitative recovery and less than 5% relative standard deviation (RSD).
“…Real Sample Analysis. Ultraperformance liquid chromatography (UPLC) was used to compare both standard OTA solutions and spiked-beer samples, obtained from a local store, using conditions as reported by Wei et al 25 Beer samples were degassed with argon gas before being directly applied to either the aptasensor electrode or UPLC analysis. Testing was performed by spiking OTA into beer at concentrations of 1, 10, and 100 ng mL −1 .…”
Ochratoxin A (OTA)a mycotoxin produced by Aspergillus and Penicillium fungiis a carcinogen and common trace contaminant in agricultural and processed food products. As consumption is detrimental to human and animal health, regular product monitoring is vital, and highly sensitive and portable OTA sensors are necessary in many circumstances. Herein, we report an ultrasensitive, electroanalytical aptasensor for precise determination of OTA at trace levels. The sensor leverages a DNA aptamer to capture OTA and silver metallization as a signal enhancer. Exonuclease I is used to digest unbound aptamers, engendering excellent background signal suppression and sensitivity enhancements. Efficient optimization of assay conditions is achieved using central composite design (CCD), allowing rapid evaluation of both the electrode and square wave voltammetry parameter space. The sensor exhibits excellent analytical performance, with a concentration limit of detection of 0.7 pg mL −1 , a limit of quantitation of 2.48 pg mL −1 , and a linear dynamic range (R 2 = 0.968) of over 6 orders of magnitude (between 1 pg mL −1 and 0.1 μg mL −1 ). Direct comparison with ultraperformance liquid chromatography (UPLC) indicates excellent analytical performance for standard solutions (R 2 = 0.995) and spiked beer samples (R 2 = 0.993), with almost quantitative recovery and less than 5% relative standard deviation (RSD).
“…In Poland, 26.7% (16/66) of grape beverages tested positive for OTA at the highest value of 0.7 µg/kg [ 26 ]. Wei et al analyzed 41 grape juices and found that all of the samples were exposed to OTA, the incidence of positives was 100% and the OTA concentration of six grape juice samples was between 0.1 and 0.2 μg/kg [ 27 ]. In Iran, it was found that the OTA level of 39 out of 70 samples (55.7%) was higher than 2 µg/L, and the upper bound mean was 2.6 μg/L [ 28 ].…”
Section: Occurrence Contamination and Toxicity Of Mycotoxinsmentioning
Mycotoxins are secondary metabolites produced by pathogenic fungi that colonize fruits and vegetables either during harvesting or during storage. Mycotoxin contamination in fruits and vegetables has been a major problem worldwide, which poses a serious threat to human and animal health through the food chain. This review systematically describes the major mycotoxigenic fungi and the produced mycotoxins in fruits and vegetables, analyzes recent mycotoxin detection technologies including chromatography coupled with detector (i.e., mass, ultraviolet, fluorescence, etc.) technology, electrochemical biosensors technology and immunological techniques, as well as summarizes the degradation and detoxification technologies of mycotoxins in fruits and vegetables, including physical, chemical and biological methods. The future prospect is also proposed to provide an overview and suggestions for future mycotoxin research directions.
“…Ochratoxin A (OTA) is a secondary fungal metabolite produced by filamentous fungal strains, viz., Aspergillus and Penicillium species. OTA possess severe health risks if ingested including nephrotoxicity and hepatotoxicity, and it is a potential carcinogen (Akdeniz et al, 2013;Wei et al, 2018). The European Union set OTA maximum accepted levels in grape products as juice, nectar, and wine not to exceed 2 µg/kg (Commission, 2005).…”
Section: Aspergillus and Penicillium Toxinsmentioning
confidence: 99%
“…The European Union set OTA maximum accepted levels in grape products as juice, nectar, and wine not to exceed 2 µg/kg (Commission, 2005). Different analytical procedures have been developed for the detection of these toxins in grapes, wine, juice, and other food products (Wei et al, 2018). Patulin is a toxic metabolite produced by Aspergillus and Penicillium with possible human hazards being carcinogenic and to be monitored in fruit juices including that of grape (Cho et al, 2010;Rahimi & Rezapoor Jeiran, 2015).…”
Section: Aspergillus and Penicillium Toxinsmentioning
Red and purple grape juices (GJs) have long been consumed worldwide for their unique taste and nutritive value. Moreover, grape is postulated to play an important role in the improvement of cardiovascular risk factors owing to its rich polyphenol content. Little is known regarding GJ’s holistic chemistry and functionality as compared to those of other fruit juices. This review aims to compile the state-of-the art chemistry of colored grape juices and in context to its analysis and nutritional values. Further, a review of potential contaminants to be introduced during manufacturing and other factors that influence juice quality and or health effects are presented to help maximize GJ’s quality. A comparison between analytical methods for juice QC establishment is presented employing hyphenated platforms versus direct spectroscopic techniques. The enrichment of the colored skin with a myriad of phenolics poses it as a functional beverage compared to that of skinless juice.
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