Detection Of Aflatoxin B1 Research Articles

Development of a Sensitive Cysteine-Modified Au-NPs–Graphene Nanoribbons Nanocomposite Disposable Biosensor for Aflatoxin B1 Detection in Food samples

Development of a Sensitive Cysteine-Modified Au-NPs–Graphene Nanoribbons Nanocomposite Disposable Biosensor for Aflatoxin B1 Detection in Food samples

Highly Sensitive One-Pot Isothermal Assay Combining Rolling Circle Amplification and CRISPR/Cas12a for Aflatoxin B1 Detection.

Occurrences of mycotoxins in cereals are widespread throughout the world. However, the lack of efficient and ultrasensitive tests has largely impeded the identification of these substances in actual samples. Herein, a novel one-pot isothermal assay that integrates rolling-circle amplification (RCA) and CRISPR/Cas12a to detect aflatoxin B1 (AFB1) is reported. Upon addition of AFB1 to the magnetic bead functionalized with a duplex of the AFB1 aptamer and its complementary DNA (cDNA), the specific recognition of AFB1 by the aptamer causes the release of cDNA to activate the RCA reaction. Subsequently, the RCA amplicon initiates both trans-cleavage and cis-cleavage activities of the endonuclease Cas12a. The synergistic coupling of RCA and CRISPR/Cas12a enables exponential amplification of cDNA, which further promotes CRISPR/Cas12a to nonspecifically cleave the single-stranded DNA reporters with enhanced detection signals. Remarkably, the CRISPR/Cas12a-assisted one-pot isothermal assay can not only achieve ultrasensitive quantitative detection through fluorescence detection, but also achieve visual detection through a lateral flow strip, which improves accessibility to mycotoxin detection in resource-limited regions. The limit of detection was 0.016 and 0.408 ng/mL, respectively. The proposed assay successfully applies in real samples with satisfactory recoveries from 90 to 114%. This study presents a powerful and versatile method for reliable and ultrasensitive detection of mycotoxins in various applications.

Electrochemistry–glucosemeter–smartphone integrated multi-mode biosensor for accurate detection of aflatoxin B1

BackgroundAflatoxin B1 (AFB1) is a widely distributed toxic contaminant in food and poses a serious threat to public health. Therefore, an accurate, simple, cost-effective and on-site assay method is needed for sensitive detection of AFB1. Aptamer shows great potential in the construction of biosensor due to its high specificity and affinity. Multimodal biosensor based on aptamer is highly suitable for the analysis of AFB1 under complex conditions. And the detection results in different modes can be verified with each other, which greatly improves the accuracy of AFB1 detection. ResultsHerein, accurate detection of AFB1 was achieved through the development of a multi-mode biosensor integrating electrochemistry, glucosemeter and smartphone-based colorimetric quantification. Streptavidin-Cu3(PO4)2 hybrid nanoflowers (SA-Cu3(PO4)2 HNFs) were synthesised and then conjugated with biotinylated invertase as a signal probe. The electrochemical signal was achieved via intrinsic redox activity. Simultaneously, sucrose could be converted to glucose by the action of invertase, which can cause changes in the glucosemeter signal as well as in the colour of urine glucose test strips. The glucosemeter could complete the signal response in 7 s, and the urine glucose test strips could complete the colour development in 30 s. The detection range of AFB1 by this system in electrochemical mode is 0.001–100 ng/mL, and in glucosemeter mode and smartphone mode is 0.01–50 ng/mL. The limits of detection were 0.49 pg/mL in electrochemistry mode, 5.4 pg/mL in glucosemeter mode and 3.7 pg/mL in smartphone mode. SignificanceThe successful construction of this multi-mode biosensor demonstrates the advantages of multifunctional nanomaterials and mobile technology. Rapid and accurate detection of AFB1 is achieved through the integration of electrochemistry, glucosemeter and smartphone-based colorimetric quantification. And this biosensor provides a novel detection platform that combines sensitivity, accuracy, affordability and portability for rapid on-site food safety screening.

Detection of AFB1 by Immunochromatographic Test Strips Based on Double-Probe Signal Amplification with Nanobody and Biotin-Streptavidin System.

Aflatoxin B1 (AFB1) is highly toxic and difficult to prevent. It is mainly produced by fungi and exists in plants and animals and is classified by the World Health Organization as a class I carcinogen, posing a serious threat to human and animal health. Therefore, it is important to establish an efficient, sensitive, and on-site detection method for AFB1 to protect human health. The immunochromatographic test strip method is simple, sensitive, and can achieve real-time detection. However, traditional immunochromatographic test strips have low sensitivity due to their relatively weak optical properties. In this study, Nb-G8 was biotinylated using a chemical method. Two sizes of gold nanoflowers (AuNFs) were prepared and combined with biotinylated G8 and streptavidin to form two types of probes. These probes were sprayed on gold standard pads and expanded pads, respectively, to enhance the signals through the high affinity interaction between streptavidin and biotin. Under the optimal experimental conditions, the half maximal inhibitory concentration (IC50) of this method was 5.0 ng/mL and the limit of detection (IC10) was 0.03 ng/mL, which increased the sensitivity of the test strip by four-fold compared with that of the traditional biotinylated nanoantibody immunochromatography test strip and had a wider detection range. In conclusion, the use of a high-affinity amplification signal between biotin and streptavidin is a valuable method for the detection of aflatoxin.

MNPs-aptazymes-PtNPs molecular motor biosensor mediated by circular cleavage reactions for the ultrasensitive detection of aflatoxin B1 in real samples

As a significant food safety risk factor linked to cancer, liver diseases, and kidney diseases, aflatoxin B1 (AFB1) necessitates rapid and ultrasensitive detection to mitigate its associated high morbidity and mortality rates. In this study, we developed an advanced biosensor for AFB1 detection by optimizing magnetic nanoparticles (MNPs), platinum nanoparticles (PtNPs), and aptazymes. The resulting MNPs-aptazymes-PtNPs molecular motor biosensor demonstrates promising capabilities for AFB1 detection. Initially, the specific binding between AFB1 and a split aptamer pair facilitates the conversion of intermolecular hybridization of DNAzyme strands into intramolecular hybridization on the MNPs surface. Then the catalytic strands of DNAzyme cleave substrate strands, resulting in PtNPs-containing fragments being released from the MNPs surface and enabling the molecular motor’s movement. The extensive cleavage of substrate strands by the long catalytic strands and the stepwise movement on MNPs surface are driven by the target-specific binding of AFB1. With high peroxidase-mimicking activity, the released PtNPs enable AFB1 detection after short incubation period. The MNPs-aptazymes-PtNPs molecular motor exhibits a sensitivity of 98.95 % and a specificity of 100 %, with a minimum detectable concentration of 300 fg/mL. This thermostabilized, cyclic, and enzyme-free nanomachine demonstrates broad applicability for the detection of various aflatoxins due to its target-empowered, sequence-independent mechanism, possesses excellent guarantee and supervision for enormous Ganoderma products in Shandong province, China.

Aptamer-Conjugated Covalent-Organic Framework Nanochannels for Selective and Sensitive Detection of Aflatoxin B1.

Sensitive and selective detection of trace aflatoxin B1 (AFB1) in foods is of great importance to guarantee food safety and quality but still challenging because of its trace amount and the interference from the complex food matrix. Here, we report the integration of aptamer (Apt) and an ordered 2D covalent organic framework (COF) to solid-state anodic aluminum oxide (AAO) nanochannels (Apt/COF/AAO) for selective and sensitive detection of trace AFB1. The high specificity of Apt for AFB1 led to a selective change in the surface charge of Apt/COF/AAO and in turn the current change of the nanochannel, permitting the selective and sensitive determination of trace AFB1 in complex food samples. The developed nanofluidic sensor gave a wide linear range (1-500 pg mL-1), low detection limit (0.11 pg mL-1), and good precision (relative standard deviation of 1.5% for 11 replicate determinations of 100 pg mL-1). In addition, the developed sensor was successfully used for the detection of AFB1 in food samples with the recovery of 86.9%-102.5%. The coupling of Apt-conjugated 2D COF with an AAO nanochannel provides a promising way for sensitive and selective determination of food contaminants in complex samples.

Ultrasensitive aflatoxin B1 detection based on vertical organic electrochemical transistor

Herein, we presented an ultrasensitive Aflatoxin B1 (AFB1) detection platform based on vertical organic electrochemical transistor (vOECT) first time. Chitosan-graphene nanosheets nanocomposites and AFB1 antibodies were modified on commercial electrodes as immunosensors, in series with gate electrodes of vOECT, operated at enhancement mode with ultrahigh transconductance gm 94 mS to amplify current signals. When AFB1 is added, the impedance of the immunosensors increased due to antigen-antibody immune binding, resulting in a potential decrease in reaction cell. Then, the potential decrease leads to an effective gate voltage VGeff increase, contributing to a significant drain-source current IDS decrease as a consequence of ultrahigh gm of vOECT. As a result, the presented vOECT platform exhibited an ultrahigh sensitivity of ∼1 mA/dec, and an ultralow detection limit of 0.01 fg/mL (S/N = 3), superior to all previous reported values. Furthermore, the platform exhibited satisfactory stability and specificity, and was applied to detect AFB1 in corn samples.

Ratiometric electrochemical and impedimetric dual-mode aptasensor based on thionine-functionalized Ti3C2Tx MXene/Pt and Au nanoparticle composites for reliable detection of aflatoxin B1

Rapid and reliable detection of aflatoxin B1 (AFB1) is critical in public health, food safety and environmental control. Herein, a ratiometric electrochemical (EC) and electrochemical impedance spectroscopy (EIS) dual-mode aptasensing platform based on thionine-functionalized Ti3C2Tx MXene/Pt and Au nanoparticle composites (MXene@Thi/PtAuNPs) was constructed for accurate and reliable detection of AFB1. The MXene@Thi/PtAuNPs composites were prepared by a facile and mild approach. The electroactive molecule Thi embedded in MXene could not only inhibit the aggregation of MXene nanosheets, but also act as an internal reference probe to form a ratiometric sensing strategy. The decoration of Pt and Au nanoparticles can further effectively enhance the conductivity and catalytic activity of the composites. The MXene@Thi/PtAuNPs composites were then served as a support to sequentially assemble hairpin DNA (hDNA) and ferrocene-labelled AFB1 aptamer (Fc-Apt) to construct the dual-mode sensor. The developed dual-mode sensor with both ratiometric EC detection (based on IThi/IFc) and EIS detection (based on Ret) can mutually verify the detection results obtained by two modes, offering more accurate and reliable results, which enabled sensitive and reliable AFB1 detection in the concentration range of 10.0 pg mL−1-30.0 ng mL−1 (ratiometric EC mode) and 3.0 pg mL−1-30.0 ng mL−1 (EIS mode), respectively. The sensing platform also demonstrated favorable selectivity, reproducibility and stability, and satisfactory applicability in corn sample, showing great potential in the sensing of mycotoxins in agricultural products.

Mycotoxin Detection through Colorimetric Immunoprobing with Gold Nanoparticle Antibody Conjugates.

Driven by their exceptional optical characteristics, robust chemical stability, and facile bioconjugation, gold nanoparticles (AuNPs) have emerged as a preferred material for detection and biosensing applications in scientific research. This study involves the development of a simple, rapid, and cost-effective colorimetric immuno-sensing probe to detect aflatoxin B1 and zearalenone using AuNP antibody (AuNP-mAb) conjugates. Anti-toxin antibodies were attached to the AuNPs by using the physical adsorption method. The colorimetric immunosensor developed operates on the principle that the optical properties of the AuNP are very sensitive to aggregation, which can be induced by a critical high salt concentration. Although the presence of antibodies on the AuNP surface inhibits the aggregation, these antibodies bind to the toxin with higher affinity, which leads to exposure of the surface of AuNPs and aggregation in a salt environment. The aggregation triggers a noticeable but variable alteration in color from red to purple and blueish gray, as a result of a red shift in the surface plasmon resonance band of the AuNPs. The extent of the shift is dependent on the toxin exposure dose and can be quantified using a calibration curve through UV-Visible-NIR spectroscopy. The limit of detection using this assay was determined to be as low as 0.15 ng/mL for both zearalenone and aflatoxin B1. The specificity of the prepared immunoprobe was analyzed for a particular mycotoxin in the presence of other mycotoxins. The developed immunoprobe was evaluated for real-world applicability using artificially spiked samples. This colorimetric immunoprobe based on localized surface plasmon resonance (LSPR) has a reduced detection limit compared to other immunoassays, a rapid readout, low cost, and facile fabrication.

Graphene coated optical microfiber for aflatoxin B1 detection

We proposed a graphene coated microfiber-based sensor for enhancing Aflatoxin B1 detection at room temperature. The heat-and-pull technique was used to fabricate the microfiber while the graphene layer was coated using a drop-casting technique. Aflatoxin samples are used as a sensor sensing area soaking solution, whereby the prepared graphene-coated microfiber was used as a sensor probe. The sensing is based on the modulation of transmission intensity and wavelength shift induced by the alteration of concentration of aflatoxin B1 from 0 ppm to 10 ppm. There is an increase in sensitivity from 0.129 dBm/ppm to 0.187 dBm/ppm and an increase in resolution from 0.17 ppm to 0.037 ppm by coating graphene on the microfiber sensor. For the graphene coated microfiber-based sensor, the wavelength shift from 1525.37 nm to 1525.19 nm was obtained when the aflatoxin B1 concentration was increased from 0 to 10 ppm. It reveals a sensitivity of 0.018 nm/ppm with a linearity of more than 90 %. This finding shows that the proposed sensor can be used to detect various concentration of Aflatoxin sample with the ability to offer real time measurement.

A highly sensitive Photothermal Immunochromatographic test strip for detection of aflatoxin B1 based on CoS@TA Nanospheres

A novel photothermal immunochromatographic test strip (PITS) with tannic acid (TA) modified cobalt sulfide (CoS) nanospheres (CoS@TA) as immuno-probe element was developed for the detection of aflatoxin B1 (AFB1). CoS nanospheres (CoS NPs) with excellent photothermal conversion efficiency (η = 47.5 %) was synthesized and skillfully chelated with TA to improve its dispersion, biocompatibility, and chromatographic properties. After modification, the CoS@TA coupled with monoclonal antibody (mAb) against AFB1 (CoS@TA-mAb) by simple physical adsorption. The CoS@TA based PITS achieved highly sensitive detection of AFB1 with the limit of detection in photothermal signal (photothermal-LOD) of 0.00503 μg/L, which was 19.88-fold higher than the LOD in visual signal (visual-LOD, 0.1 μg/L). The application of TA in the modification of CoS provided ideas to improve the properties of functional nanomaterials such as dispersion and biocompatibility, and the application of CoS@TA in PITS construction laid a methodological foundation for further improving the detection sensitivity of trace targets.

A disposable microfluidic aptasensor for one-step and real-time detection of sub-femtomolar-level aflatoxin B1 in food

Aflatoxin B1 (AFB1) is a highly toxic substance found in food, necessitating rapid and sensitive detection methods. Combining interfacial capacitive sensing with AC electrothermal (ACET) enrichment, an aptasensor based on a PCB electrode array is developed for real-time detection of trace AFB1. Owing to the sensitive solid–liquid capacitance with a pF-level resolution, AFB1 detection at sub-femtomolar level is achieved. The induced ACET flows enrich AFB1 molecules towards the electrode surface during capacitance measurement, enabling a one-step detection containing target enrichment, with an overall time of 20 s without any extra concentrating devices or processes. This sensor has a low detection limit of 620 aM, a selectivity of 2262:1 against interferences, and a wide semi-log linear range from 1 fM to 10 pM. It is with a cost below 1 US dollar for disposable detection and a convenient operation for on-site application. The detection of AFB1 in three types of quality control samples demonstrates a good feasibility for food safety inspection.

A disposable paper-based electrochemical biosensor for detection of aflatoxin B1 based on a structure-switching aptamer

Aflatoxin B1 (AFB1) is a highly toxic mycotoxin that readily contaminates major food crops. This study presents a novel ratiometric electrochemical paper-based aptasensor for AFB1 detection that utilizes a structure-switching aptamer. The sensor detects AFB1 by folding the DNA aptamer, reducing the electron transfer efficiency between the methylene blue (MB) molecules attached to the DNA and the electrode surface. An inner reference element modified with ferrocene (Fc) is co-assembled on the electrode surface of the paper-based biosensor to enhance the accuracy of AFB1 detection. In the presence of target AFB1, a folded target–aptamer complex is formed, distancing the MB molecules from the electrode and generating a low current signal in a differential pulse voltammetry mode. The ratio of oxidation currents for MB and Fc serves as the metric for monitoring AFB1 levels. The detection range spans from 20.0 to 1000.0 ng mL−1, with a limit of detection of 7.6 ng mL−1. The paper-based aptasensor exhibits excellent specificity and stability. Additionally, its high reliability and applicability are validated by the strong correlation observed between the sensor results and the results obtained using UPLC−MS/MS analysis of real samples. This study offers a low-cost, readily available approach for portable detection of foodborne hazards.

A comparative study of aptasensor vs. immunosensor for ultrasensitive detection of aflatoxin B1 using Ag-pSi SERS substrate

Numerous SERS based platforms have been designed to address the emerging need for detecting fungal metabolite contamination in foodstuffs, and specifically the Group 1 carcinogen aflatoxin B1. Herein, 4-aminothiophenol modified silver-coated porous silicon was used as the SERS substrate. Two ratiometric responses were individually assessed upon direct target capture using specific aptamers or antibodies. Under optimized physical features, elevated enhancement factor, wide dynamic range, low detection limits and pronounced recycling capabilities were achieved (7.39 × 107, 0.2–200 ppb, 0.0085 and 0.0110 ppb, 7 and 1 regeneration cycles without impairing the performances for aptasensor and immunosensor, respectively). The accuracy and anti-interference responses in several intricate matrices (maize, peanut, wheat, oats and rice) were compared to a routine HPLC method with equivalent recoveries. Overall, the comparative assessment revealed preferable features of reusability, durability and accuracy of the aptasensor over the immunosensor. Furthermore, the results demonstrate the substantial potential of the proposed SERS substrate for diverse on-site analytical applications using simple and portable monitoring instrumentation.

Competitive aptamer assay for aflatoxin B1 detection using CRISPR/Cas12a as a signal amplifier

Competitive aptamer assay for aflatoxin B1 detection using CRISPR/Cas12a as a signal amplifier

Laser-induced CdS/TiO2/graphene dual photoanodes for ratiometric self-powered photoelectrochemical sensor: an innovative approach for aflatoxin B1 detection.

A ratiometric self-powered photoelectrochemical sensor based on laser direct writing technology was constructed to address the problem that the conventional single-signal detection mode was susceptible to the influence of instrumentation and environmental factors, which interfered with the detection results. Laser-induced CdS/TiO2/Graphene was prepared as dual photoanodes (PA1 and PA2), which were controlled by multiplexed switches to form a photocatalytic fuel cell with Pt cathode. By modifying the aptamer of aflatoxin B1 (AFB1) on the photoanode surface, the target was specifically captured to the electrode surface to form a biological complex, which increased the steric hindrance and affected the electron transfer, thus reducing the output signal of the sensor. Targets with different concentrations were incubated on the surface of PA1, and targets with fixed concentrations were incubated on the surface of PA2. Under the control of the multiplex switch, the output signals of the two photoanodes were recorded, and the ratio of these two signals was used as the basis for the quantitative detection of AFB1. The sensor output was linearly increasing with the logarithm of AFB1 concentration from 1.0 to 150ngmL-1 and the detection limit was 0.0974ngmL-1. Additionally, this method had good stability, fast response, and good selectivity to real samples, providing an effective method for food safety monitoring.

DNA tetrahedral scaffold based one-step ratiometric electrochemical detection of aflatoxin B1 in tobacco samples

To effectively monitor Aflatoxin B1 (AFB1) in tobacco samples, a ratiometric electrochemical biosensor based on DNA tetrahedral scaffold (DTS) and AuNPs/chitosan (CS) modified electrode has been successfully fabricated. The ultra-thin AuNPs not only present a larger specific sensing surface, but also can graft more DTS onto the surface of the electrode. The DTS is directly grated with two strands of AFB1 aptamer, which leading to a facile one-step detection of AFB1. In the presence of AFB1, the current of methylene blue (MB) keeps stable, while the current of ferrocene (Fc) decreases since the target takes away the Fc-labeled aptamer from the electrode surface. The fabricated biosensor can monitor AFB1 in the linear range of 0.01–1000 pg·mL−1 with the detection limit of (LOD) 2.6 fg·mL−1. More importantly, the biosensor performs well in the detection of AFB1 in tobacco samples with the LOD of 2.86 fg·mL−1. The developed ratiometric electrochemical biosensor displays high selectivity, good stability and high potential in tobacco sample’s AFB1 detection.

Reproducible, Accurate, and Sensitive Food Toxin On-Site Detection with Carbon Nanotube Transistor Biosensors.

Field-effect transistor (FET) biosensors based on nanomaterials are promising in the areas of food safety and early disease diagnosis due to their ultrahigh sensitivity and rapid response. However, most academically developed FET biosensors lack real-world reproducibility and comprehensive methodological validation to meet the standards of regulatory bodies. Here, highly uniform and well-packaged semiconducting carbon nanotube (CNT) FET biosensor chips were developed and assessed for the plug-and-play sensing for the rapid and highly sensitive detection of aflatoxin B1 (AFB1) in real food samples to meet international standards. In order to meet the requirements for reproducibility and stability, a scalable residual-free passivation and packaging process was developed for CNT FET biosensors. Portable detection systems were then constructed for on-site detection. The resulting packaged chips were functionalized with nucleic aptamers to enable highly selective detection of AFB1 in food samples with a detection limit (LOD) of 0.55 fg/mL (standard) for AFB1 and cross-reactivity coefficients to interferences as low as 1.8 × 10-7 in simulated solutions. Utilizing the portable detection system, on-site real food detection was achieved with a rapid response time less than 60 s, and LOD of 0.25 pg/kg (standard) in complex corn sample matrices. Single-blind tests demonstrated the ability of the chips to detect AFB1-positive food with 100% accuracy, using a set of 30 peanut samples. Validation experiments confirmed that the detection range, stability, and repeatability met international standards. This study showcased the accuracy, reliability, and potential practical applications of CNT FET biosensor chips in areas such as food safety and rapid biomedical testing.

A silicon-based functional self-assembled aptasensor for the detection of aflatoxin B1 by SERS sensing.

One of the most harmful contaminants found in corn and its products is aflatoxin B1 (AFB1) and thus developing reliable detection methods is of great significance to consumers and the food industry. In this research, AuMBA@Ag nanoparticles (NPs) and AgNPs deposited on a silicon wafer (Si@AgNPs) were functionalized with an aptamer and its complementary strand, respectively, and self-assembled into a SERS aptasensor, which generated strong SERS signals. AFB1 bound to the aptamer prior to the complementary chain, causing AuMBA@Ag NPs to detach from Si@AgNPs. The complex dissociated, leading to a decrease in signal intensity from the solid-phase substrate. Under optimal conditions, the linear detection range was 0.05-20.0 ng mL-1, and the detection limit was 0.039 ng mL-1. Notably, the aptasensor demonstrated a recovery rate between 92.77% and 110.13% when utilized for the detection of AFB1 in corn flour and oil, indicating its good potential for detecting AFB1 in real sample matrices. In conclusion, a quantitative and reliable specific SERS detection system for AFB1 was developed in this study with significant applicability to food safety.

DNA template triggered copper nanoparticles generation coupled with hybridization chain reaction amplification for simultaneous detection of three mycotoxins in food samples

The co-occurrence of various mycotoxins in food, resulting from fungal infections, can lead to increased toxicity and enhanced harm through synergistic effects. In this work, a fluorescent assay was developed for simultaneous detection of zearalenone (ZEN), ochratoxin A (OTA) and aflatoxin B1 (AFB1) to address the issue of multiple mycotoxins co-contamination. Specific DNA hairpin-based aptamers were employed to recognize the mycotoxins and form a double-stranded DNA structure. Exonuclease III was introduced for the DNA cleavage, releasing single-stranded DNA triggers that could activate the assembling of DNA quadrilateral template. Copper nanoparticles were generated on the frame of DNA quadruplex template and produced fluorescent detection signals, while two hybridization chain reactions occurring on the different branches of the template and provided two additional detection signals. Inadequately reacted DNA chains were efficiently adsorbed and eliminated by Fe3O4@graphene oxide through magnetic separation. The limits of detection and linear ranges for ZEN, AFB1 and OTA were determined as 0.008 ng/mL, 0.003 ng/mL, 0.006 ng/mL and 0.010–100.000 ng/mL, 0.010–100.000 ng/mL, 0.010–50.000 ng/mL, respectively. Moreover, successful verification for real samples yielded recoveries from 99.2% to 102.7%, with a relative standard deviation of <5.23%. Artificially prepared toxic fungus infected samples were also analyzed. This method has demonstrated practical implications for the monitoring of food contaminants.