Polydopamine-coated magnetic Spirulina nanocomposite for efficient magnetic dispersive solid-phase extraction of aflatoxins in pistachio.

An efficient adsorbent was synthesized and used in magnetic dispersive solid phase extraction (MDSPE) of aflatoxins B1, B2, G1, and G2 at trace levels in pistachio prior to analysis by HPLC equipped with a fluorescence detector. Spirulina (Sp) algae was first magnetized, followed by surface modification with dopamine (Dp). The adsorbent was characterized using FT-IR, XRD, FE-SEM, EDX, VSM, and BET analyses. The effects of different analytical parameters on the extraction performance were evaluated. Under optimal conditions, good limits of detection (LODs) and quantifications (LOQs) were achieved in the ranges of 0.02-0.07 and 0.06-0.21 ng g-1, respectively. The RSDs were 5.9, 6.3, 5.6, and 7.3% for AFB1, G1, B2, and G2, respectively. The proposed method was successfully used to determine AFs in pistachio samples and acceptable recoveries in the range of 72-95% were obtained.

Synthesised magnetic nano-zeolite as a mycotoxins binder to reduce the toxicity of aflatoxins, zearalenone, ochratoxin A, and deoxynivalenol in barley.

Agricultural commodities, particularly cereals can be contaminated with mycotoxins during the pre- and post-harvest stage. The main goal of this study was to evaluate the efficacy of magnetic zeolite nanocomposite (MZNC) as an adsorbent for the reduction of mycotoxins in barley flour. The MZNC is synthesised using an eco-friendly and efficient procedure and characterised by zeta potential, field emission scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The adsorbent amount that affects the adsorption capacity was optimised. Low amounts of the nanocomposite removed >99% of aflatoxins, 50% of ochratoxin A, 22% of zearalenone, and 1.8% of the deoxynivalenol from the contaminated sample and adsorption by MZNC was better than the natural zeolite; this phenomenon is related to the wide surface of nanocomposites. Results provide new insights into possible future research that could overcome the challenges of using nanotechnology to eliminate mycotoxins from agricultural products. It can be hoped that the presence of cheap and eco-friendly mycotoxin binders such as the MZNC that is synthesised and utilised in this research will help to produce secure food and feed products.

Extraction of Sulfathiazole from Urine Samples Using Biosynthesized Magnetic Nanoparticles.

The application of Pd/Fe3O4 nanoparticles (NPs) for the adsorption of sulfathiazole (STZ) from urine samples prior to high performance liquid chromatography-ultraviolet detection was studied. Pd/Fe3O4 NPs were synthesized using plant extract. Possible impact parameters in the extraction process such as magnetic adsorbents amount, extraction time, sample pH, and desorption conditions were investigated and optimized. Under the optimum conditions, the detection and quantification limits were 10 and 30 ng mL-1, respectively. The relative standard deviation for five measurements of 100 ng mL-1 of STZ was 5.8 %. The proposed method was used for the analysis of different urine samples, and acceptable recoveries in the range of 87.6 - 101.3% were obtained. These results indicated that biosynthesized Pd/Fe3O4 NPs can be used as an efficient adsorbent for extraction of sulfathiazole from urine samples.

Simultaneous Chloramphenicol and Florfenicol Determination by A Validated DLLME-HPLC-UV Method in Pasteurized Milk.

The antibiotic residues in milk are a well-known serious problem and pose several health hazards to consumers. We have described a simple, rapid, and inexpensive DLLME-HPLC/UV technique for the extraction of chloramphenicol and florfenicol residues in milk samples. Under the optimum conditions, linearity of the method was observed over the range 0.02-0.85 µg/L with correlation coefficients > 0.999. The proposed method has been found to have a good limit of detection (signal to noise ratio = 3) for chloramphenicol (12.5 µg/Kg) and florfenicol (12.2 µg/Kg), and precision with relative standard deviation values under 15% (RSD, n = 3). Good recoveries (69.1-79.4%) were obtained for the extraction of the target analytes in milk samples. This simple and economic method has been applied for analyses of 15 real milk samples. Among all samples only one of them was contaminated to florfenicol; 62.4 µg/Kg and contamination to chloramphenicol was not detected.

A validated dispersive liquid-liquid microextraction method for extraction of ochratoxin A from raisin samples.

A method based on dispersive liquid-liquid microextraction (DLLME) was developed for the quantitative extraction of Ochratoxin A (OTA) from raisin samples. The influence of various parameters on the recovery of OTA such as type and volume of DLLME extractant, centrifuging and sonication time, also volume of deionized water was investigated. Recovery values under the optimum conditions were between 68.6 and 85.2 %, the inner and intra-day precision expressed as relative standard deviation (RSD%, n = 3), were less than 15 % at spiking levels of 2.5-30 µg kg(-1). Linearity was studied from 0.5 to 30 µg L(-1), and the limits of detection (LOD) and quantification (LOQ) were 0.7 and 2.0 µg kg(-1), respectively. Real samples were analyzed by DLLME method and compared with confirmative immunoaffinity Column Chromatography (IAC) clean-up. Low cost, simplicity of operation, speed and minimum consumption of organic solvent were the main advantages of proposed method. The mean contamination of samples was 0.88 µg kg(-1) that was lower than European Legal Limit.

Extraction and Determination of Cyproheptadine in Human Urine by DLLME-HPLC Method.

Novel dispersive liquid-liquid microextraction (DLLME), coupled with high performance liquid chromatography with photodiode array detection (HPLC-DAD) has been applied for the extraction and determination of cyproheptadine (CPH), an antihistamine, in human urine samples. In this method, 0.6 mL of acetonitrile (disperser solvent) containing 30 µL of carbon tetrachloride (extraction solvent) was rapidly injected by a syringe into 5 mL urine sample. After centrifugation, the sedimented phase containing enriched analyte was dissolved in acetonitrile and an aliquot of this solution injected into the HPLC system for analysis. Development of DLLME procedure includes optimization of some important parameters such as kind and volume of extraction and disperser solvent, pH and salt addition. The proposed method has good linearity in the range of 0.02-4.5 µg mL(-1) and low detection limit (13.1 ng mL(-1)). The repeatability of the method, expressed as relative standard deviation was 4.9% (n = 3). This method has also been applied to the analysis of real urine samples with satisfactory relative recoveries in the range of 91.6-101.0%.