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Antibiotics and antibacterials, including sulfonamides, are components of the veterinary armamentarium used to prevent and treat diseases in seafood. However, the accumulation of veterinary drug residues in seafood can cause food safety concerns. This study aimed to verify the quantitative analytical method for sulfonamides, trimethoprim, ormetoprim, and dapsone in seafood and to apply it to fish and shrimp distributed in Korean market. In the present study, three types of matrices (shrimp, flatfish, and eels) were used to detect drugs (n = 25) (sulfonamides (n = 21), trimethoprim, ormetoprim, dapsone, and monoacetyldapsone). Matrices were extracted with acetonitrile and mixed with 2 g of magnesium sulfate and 1 g of sodium acetate. After agitation, supernatants were mixed with 300 mg of C18 and centrifuged again. Then the supernatant was evaporated, dissolved in 50% methanol, and filtered through a PTFE filter. Extracts (5 µl) were then injected into the liquid chromatography-tandem mass spectrometry system. The method was validated in terms of limit of detection, limit of quantitation, decision limit, decision capability, matrix effects, intra/inter-day accuracies, precisions, and stabilities and the method was applied to fish and shrimp sold in the Korean market. The validation results were found to be satisfactory. As a result of applying the validated method to fish and shrimp samples purchased from the Korean market, sulfacetamide, sulfadimethoxine, sulfamethoxazole, and sulfanilamide were detected in shrimp samples. The devised method for analysing antibiotics in seafood samples enables antibiotic detection in fish samples distributed in the global market and should aid the adoption of preventative measures. [ABSTRACT FROM AUTHOR]

OVER 60,000 tons of veterinary antibiotics are used globally annually, with an anticipated increase to 67% by 2030. Florfenicol is a veterinary drug its residues enter the environment through fertilizer (manure) application and waste water in agricultural areas, potentially leading to plant toxicity. In the current study, the veterinary antibiotic florfenicol was tested in two ways: first, in Petri dishes during cultivation, and second, by adding the antibiotic to the soil using germination trays. Various antibiotic concentrations were applied (0.005%, 0.01%, 0.02%, and 0.04% v/v, ml/L). Results from the first experiment exhibited significant decrease in germination rates after 8 days it reached to 18.00, and in shoot, root length to 1.26, 0.92 cm, and fresh,dry seedling weights to 0.47,0.28 mg, with increased concentration compared to the control group. The second experiment demonstrated significant differences in germination rates after 8 days, along with changes in shoot and root length, fresh and dry seedling weights, and leaf count, with most traits decreasing as concentrations increased except for root length, which notably decreased at the 0.04% concentration, it record 4.86 cm. Changes in root structure, including the disappearance of fibrous roots and reduction in root system length, were observed. Germination rates after 4 days showed no significant difference in either experiment. The findings suggest that florfenicol concentrations in the first experiment affected the germination and growth of yellow corn (Zea mays L) plants, starting from the lowest concentration of 0.005%. In the second experiment, using organic-rich soil mitigated the toxic effects of florfenicol at low concentrations, except for the highest concentration of 0.04%. Florfenicol did not cause damage to chloroplasts, as the seedlings recovered their usual appearance. [ABSTRACT FROM AUTHOR]

Drug residues that contaminate food and water represent a serious concern for human health. The major concerns regard the possible irrational use of these contaminants, since this might increase the amplitude of exposure. Multiple sources contribute to the overall exposure to contaminants, including agriculture, domestic use, personal, public and veterinary healthcare, increasing the possible origin of contamination. In this review, we focus on crop pesticides and veterinary drug residues because of their extensive use in modern agriculture and farming, which ensures food production and security for the ever-growing population around the world. We discuss crop pesticides and veterinary drug residues with respect to their worldwide distribution and impacts, with special attention on their harmful effects on human reproduction and embryo development, as well as their link to epigenetic alterations, leading to intergenerational and transgenerational diseases. Among the contaminants, the most commonly implicated in causing such disorders are organophosphates, glyphosate and antibiotics, with tetracyclines being the most frequently reported. This review highlights the importance of finding new management strategies for pesticides and veterinary drugs. Moreover, due to the still limited knowledge on inter- and transgenerational effects of these contaminants, we underlie the need to strengthen research in this field, so as to better clarify the specific effects of each contaminant and their long-term impact. [ABSTRACT FROM AUTHOR]

Tulathromycin (TUL) is a widely used veterinary antibiotic for treating bovine and porcine respiratory infections. Consuming animal-derived food contaminated with this medication may jeopardize human health. This work adopted the first portable potentiometric platform for direct TUL sensing in pharmaceutical and food products. The sensor employed a plasticized PVC membrane on a glassy carbon electrode doped with calix[6]arene and multi-walled carbon nanotubes (MWCNT) in a single solid contact layer for selective binding and signal stability. Characterization via scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) confirmed the material's integrity. The MWCNT-based sensor produced a stable Nernstian response (1.0 × 10−7 to 1.0 × 10−3 M) and a limit of detection (LOD) of 9.76 × 10–8 M with instantaneous response (8 ± 2 s). IUPAC validation revealed high selectivity for TUL against interfering ions, minimal drift (0.6 mV/h), and functionality over a broad pH range (2.0–7.0), allowing direct application to dosage form, spiked milk, and liver samples. Eco-Scale, AGREE, and Whiteness assessment proved the method's ecological sustainability, economic viability, and practical feasibility, surpassing traditional approaches. [ABSTRACT FROM AUTHOR]

Detecting and removing pesticide and veterinary drug residues in agricultural products are important for ensuring food safety. Current methods for detecting pesticide residues are mainly relied on sophisticated instruments, which require long detection time and skilled operators, limiting their accessibility. Metal-Organic Frameworks (MOFs) are a hybrid material composed of metal ions/clusters and organic ligands. MOFs possess multiple functions such as adsorption enrichment, catalytic degradation, and fluorescent and electrochemical signal generation. Therefore, MOFs have great potential in rapidly detecting and removing pesticide and veterinary drug residues. This review introduces functionalities of MOFs: Enrichment and removal, catalytic degradation, fluorescence sensing, and electrochemical sensing, and then summarizes their applications for rapid detecting and removing pesticide and veterinary drug residues. Additionally, this article comprehensively analyzes the advantages and disadvantages about combining RGB analysis and portable monitoring devices with MOFs. Also, the challenges of applying MOFs to detecting and removing pesticide and veterinary drug residue are discussed. Overall, this paper provides a reference for developing techniques to rapidly detect and remove containments in agricultural products. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Livestock and poultry meat consumption play an important role in the dietary structure of Chinese residents. However, the extent of residues of veterinary drugs and heavy metal contamination in livestock and poultry meat and their by-products within Hunan province is not extensively studied. This survey aimed to fill this gap by assessing the presence of 76 veterinary drug residues in Hunan province. Additionally, heavy metals in pork and pig liver were also assessed. The obtained findings suggest that residues of veterinary drugs are still present in livestock and poultry meat, as well as their by-products, within Hunan province. However, the contamination of heavy metals remained within the food safety limits. These results underscore the significance of establishing more refined criteria for assessing human exposure, taking into account factors such as consumption patterns, product varieties and chemical compounds of interest. [ABSTRACT FROM AUTHOR]

Pesticides and veterinary drugs are widely employed to support food production. Assessing potential risks associated with the dietary consumption of pesticide and veterinary drug residues is, however, essential. Potential risks depend on the toxicity degree of the analyzed residue and population exposure levels. Human populations are exposed to numerous chemical substances through different pathways with varying exposure times, leading to increased health risks when compared to exposure to individual chemicals. Cumulative exposure assessments usually assess combined exposures to multiple chemicals through multiple exposure pathways. In this sense, this comprehensive review aims to provide insights into cumulative dietary pesticide and veterinary drug residue exposures. The main methodologies, strategies, and legislation employed by international agencies to this end are discussed. A review concerning articles that apply existing methodologies and approaches, as well as the challenges in this context faced by Brazil is also presented. As this is a critical issue not only for Brazilian public health but also for the global community, regulatory agencies should prioritize formulating regulations that incorporate exposure assessments regarding the simultaneous presence of residues and contaminants in foodstuffs. [ABSTRACT FROM AUTHOR]

Flunixin (usually formulated as flunixin meglumine (FLN)), a common non-steroidal anti-inflammatory drug (NSAID) given to cattle, raises human health concerns when it is present in milk. Maximum residue limit (MRL) of 10 µg/kg has been set by Food Safety and Standards Authority of India (FSSAI) for FLN residues in milk. Attenuated Total Reflectance- Fourier-Transform Mid-Infrared (FT-MIR) spectroscopy in conjunction with multivariate techniques was applied to detect the presence of FLN residues in milk. Samples of FLN, pure milk as well as milk samples spiked with FLN at concentrations (1, 5, 10, 20 and 50 µg/kg) below and above the MRL were analysed. ATR-FTIR measurements were conducted in the 4000 –400 cm− 1 wavenumber range, and the wavenumber regions (2942 − 2838, 1748 − 1734 and 1149 –1012 cm− 1) were selected based on the maximum variability in the intensity of peaks and chemometrics techniques such as Principal Component Regression (PCR), Partial Least Square Regression (PLSR), Principal Component Analysis (PCA) and Soft Independent Modeling of Class Analogy (SIMCA) were applied. The study concluded that the presence of parent drug- FLN residues in milk even at 1 µg/kg level (below MRL prescribed by regulatory bodies) can be detected using ATR-FT-MIR coupled with chemometrics. [ABSTRACT FROM AUTHOR]

Background The presence of veterinary drug residues in food-producing animals and animal products is regulated through the enforcement of maximum residue limits (MRLs). To answer the need of the food sector to monitor these substances in a wide range of food commodities, stakeholders at AOAC INTERNATIONAL identified the need for a reliable confirmatory screening method. Such a qualitative approach is required for compliance checking and to support product release in manufacturing. Objective Data were collected from five independent laboratories that applied the First Action Official Method   2020.04 to demonstrate adequate performance under reproducibility conditions. The probability of detection (POD) was calculated in blank test samples and test samples spiked at the screening target concentration (STC) level, with the objective to achieve PODs ≤10% and ≥90%, respectively. Additionally, the effectiveness of the screening method was evaluated by participating in 92 proficiency tests. Methods Four streams were optimized to screen for 152 veterinary drug residues by LC–MS/MS in a wide variety of food commodities including milk-based ingredients and related products (e.g. milk fractions, infant formula, infant cereals, and baby foods), meat- and fish-based ingredients and related products (fresh, powdered, cooked, infant cereals, and baby foods), and other ingredients based on eggs, animal fat, and animal byproducts. The four streams covered 105 antibiotic residues, anti-inflammatory and antiparasitic agents (stream A), 23 beta-lactams (stream B), 14 aminoglycosides (stream C), and 10 tetracyclines (Stream D). Results The multilaboratory validation led to PODs at the STC ≥94% and PODs in the blank ≤9%. Further application of the multilaboratory validated method to 92 proficiency tests provided more than 99% satisfactory submitted results (n  = 784). Conclusion The interlaboratory reproducibility determined for this method met the acceptance criteria defined in AOAC Standard Method Performance Requirement (SMPR®) 2018.010. Highlights AOAC has approved the method for Final Action status. [ABSTRACT FROM AUTHOR]

Milk, as a widely consumed nutrient‐rich food, is crucial for bone health, growth, and overall nutrition. The persistent application of veterinary drugs for controlling diseases and heightening milk yield has imparted substantial repercussions on human health and environmental ecosystems. Due to the high demand, fresh consumption, complex composition of milk, and the potential adverse impacts of drug residues, advanced greener analytical methods are necessitated. Among them, functional materials‐based analytical methods attract wide concerns. The magnetic molecularly imprinted polymers (MMIPs), as a kind of typical functional material, possess excellent greenification characteristics and potencies, and they are easily integrated into various detection technologies, which have offered green approaches toward analytes such as veterinary drugs in milk. Despite their increasing applications and great potential, MMIPs' use in dairy matrices remains underexplored, especially regarding ecological sustainability. This work reviews recent advances in MMIPs' synthesis and application as efficient sorbents for veterinary drug extraction in milk followed by chromatographic analysis. The uniqueness and effectiveness of MMIPs in real milk samples are evaluated, current limitations are addressed, and greenification opportunities are proposed. MMIPs show promise in revolutionizing green analytical procedures for veterinary drug detection, aligning with the environmental goals of modern food production systems. [ABSTRACT FROM AUTHOR]

A rapid and online microvolume flow-through dialysis probe designed for sample preparation in the analysis of veterinary drug residues is introduced. This study addresses the need for efficient and green sample preparation methods that reduce chemical waste and reagent use. The dialysis probe integrates with liquid chromatography and mass spectrometry (LC-MS) systems, facilitating automated, high-throughput analysis. The dialysis method utilizes minimal reagent volumes per sample, significantly reducing the generation of solvent waste compared to traditional sample preparation techniques. Several veterinary drugs were spiked into tissue homogenates and analyzed to validate the probe's efficacy. A diagnostic sensitivity of >97% and specificity of >95% were obtained for this performance evaluation. The results demonstrated the effective removal of cellular debris and particulates, ensuring sample integrity and preventing instrument clogging. The automated dialysis probe yielded recovery rates between 27 and 77% for multiple analytes, confirming its potential to streamline veterinary drug residue analysis, while adhering to green chemistry principles. The approach highlights substantial improvements in both environmental impact and operational efficiency, presenting a viable alternative to conventional sample preparation methods in regulatory and research applications. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Soil is one of the main destinations for pesticides and veterinary drugs used in agriculture and animal production. The negative consequences of the accumulation of these compounds in the environment make it important to monitor these compounds in the soil. In this study, we compared different extraction procedures using solvent shaking, ultrasound, or QuEChERS, and their combinations, for the simultaneous determination of 75 pesticide and seven veterinary drug residues in agricultural soil by ultra-high performance liquid chromatography coupled to serial mass spectrometry (UHPLC–MS/MS). The method using QuEChERS combined with shaking showed the best results for soil using the addition of water, followed by extraction with acetonitrile acidified with acetic acid and shaking in a shaker. For partitioning, anhydrous magnesium sulfate and anhydrous sodium acetate were used. The extract was centrifuged, filtered, and diluted (1:4, v/v) in water for determination by UHPLC–MS/MS. Method validation showed adequate accuracy and precision results, with recoveries between 70 and 120% and RSD ≤ 20% for the vast majority of the compounds evaluated at the spike levels of 10, 25, 50, and 100 μg kg−1. The method limits of detection (LOD) and quantification (LOQ) ranged from 3.0 to 7.5 μg kg−1 and from 10 to 25 μg kg−1, respectively. The method was applied to different agricultural soil samples and proved to be efficient for routine analysis. [ABSTRACT FROM AUTHOR]

Veterinary medications are necessary for both contemporary animal husbandry and food production, but their residues can linger in foods obtained from animals and pose a dangerous human risk. In this review, we aim to highlight the sources, occurrence, human exposure pathways, and human health effects of drug residues in food-animal products. Following the usage of veterinary medications, pharmacologically active compounds known as drug residues can be found in food, the environment, or animals. They can cause major health concerns to people, including antibiotic resistance development, the development of cancer, teratogenic effects, hypersensitivity, and disruption of normal intestinal flora. Drug residues in animal products can originate from variety of sources, including water or food contamination, extra-label drug use, and ignoring drug withdrawal periods. This review also examines how humans can be exposed to drug residues through drinking water, food, air, and dust, and discusses various analytical techniques for identifying these residues in food. Furthermore, we suggest some potential solutions to prevent or reduce drug residues in animal products and human exposure pathways, such as implementing withdrawal periods, monitoring programs, education campaigns, and new technologies that are crucial for safeguarding public health. This review underscores the urgency of addressing veterinary drug residues as a significant and emerging public health threat, calling for collaborative efforts from researchers, policymakers, and industry stakeholders to develop sustainable solutions that ensure the safety of the global food supply chain. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The application of veterinary drugs has brought great economic benefits, but its unreasonable application has also caused a series of safety problems. The study aimed to establish methods that will provide accurate quantitative information for the monitoring of veterinary drug residues in animal‐derived foods. Selecting nine veterinary drugs in four categories, the study combined quick, easy, cheap, effective, rugged, and safe technology with high‐performance liquid chromatography (HPLC) to detect multiple veterinary drugs in animal foods simultaneously. The study established two rapid, efficient, and accurate HPLC‐diode array detection methods to achieve the simultaneous detection of nitroimidazoles and β‐adrenergic agonists, and the simultaneous detection of benzimidazoles and diethylstilbestrol. The limit of detection of the former was 1.36–2.05 μg/kg and the latter 0.42–0.72 μg/kg. Then the two methods were used to detect veterinary drug residues in 297 animal foods from 10 categories to investigate the drug residues. For the seven banned drugs, the detection rates ranged from 1.35% to 7.41%. And for the two restricted drugs, the over‐standard rates were 4.38% and 0.00%. [ABSTRACT FROM AUTHOR]

β-Lactam is one of the widely used veterinary drugs, but simultaneous analytical methods for β-lactam on various animal foods have not been established. In this study, we aimed to detect 34 β-lactam antibiotics simultaneously in livestock samples (beef, pork, chicken, egg, and milk) by liquid chromatography-tandem mass spectrometry (LC–MS/MS). Samples were extracted using phosphate buffer/acetonitrile or water/acetonitrile and then cleaned with 150 mg of C18 and 900 mg of MgSO4. The method showed acceptable recovery and repeatability of 66.1–119% and 1.5–26%, respectively. The method was employed to monitor 127 real samples from the domestic market to confirm its applicability, and no β-lactam residues were detected. It was also applied to other matrices (eel, flat fish, and shrimp) and showed acceptable recovery (62.1–120%) and repeatability (1.0–28%). The method is expected to improve the efficiency of monitoring veterinary drug residues in domestic livestock products and fishery foods. [ABSTRACT FROM AUTHOR]

Objective: In this study, a one-step purification method combined with liquid chromatography tandem mass spectrometry (LC-MS/MS) was established for the simultaneous detection of 54 veterinary drug residues belongs to 13 classes of ya-fish (Schizothorax prenati). Methods: 8 mL of 0.2% formic acid-acetonitrile:water solution (90:10, V/V) was added to 2.0 g sample and extracted by ultrasonication in an ice-water bath and cleaned up in one step by LPAS. The determination was performed on a C18 column with a gradient elution of methanol-0.1% formic acid-5 mmol/L ammonium acetate solution, dynamic multiple reaction monitoring (dMRM), positive/negative ionization mode, and quantitative LC-MS/MS by internal standard method. By adding 54 veterinary drugs, the extraction method, extraction volume, salt addition, liquid phase and mass spectrometry conditions were optimized, and the method performance (matrix effect, detection limit, quantification limit, accuracy and precision) were verified. Results: The linear relationships between the 54 drugs and their concentrations were good within the range of 0.1~50 μg/L, coefficient of determination (R2) ≥0.992. The limits of detection (LODs) were between 0.03~2.5 μg/kg and the limits of quantification (LOQs) were 0.1~8.3 μg/kg. The average recoveries of the 54 drugs at low (5~10 μg/kg), medium (10~20 μg/kg) and the high level (50 μg/kg) ranged from 70.45% to 118.1%, with relative standard deviations (RSD) between 0.01% and 9.9%. This method was applied to detect the drug in 50 samples of cultured ya-fish, and drugs were detected in seven of them. Enrofloxacin and danofloxacin were each detected twice, and sulfamethoxazole was detected four times, all at levels below the limit of quantification. Conclusion: The method was simple to operate, one-step purification, and had low limits, high sensitivity, good accuracy and precision, which met the technical requirements of multi-veterinary drug residue detection, and can provide technical support for the rapid and efficient detection of various veterinary drug residues in large quantities of ya-fish.

The purpose of the experiment was to study the feasibility of fox carcass as meat and bone meal and evaluate the safety of fox meat and bone meal. Three healthy blue foxes (39 in total) weighing about 15 kg were randomly selected from 13 fox breeding areas in China. Fox carcass (including viscera and toe claws) was made into meat and bone meal by grinding, high-pressure hydrolysis, degreasing, drying, and crushing. Routine nutrients, heavy metals, veterinary drug residues, and canine distemper virus were determined, respectively, and the safety was evaluated. The results showed that the content of crude protein in meat and bone meal was between 55% and 67%, which meets the requirements of crude protein in the first-class index of Bone Meal and Meat and Bone Meal for Feed. The concentrations of lead, arsenic, mercury, cadmium, and chromium meet the requirements of the national standard for the hygiene and safety standards of meat and bone meal. Sulfamethazine, sulfamethoxazole, sulfamethoxazine, sulfadiazine, penicillin, oxytetracycline, and gentamicin meet the standard requirements of maximum residue limits of veterinary drugs in food. The results showed that fox meat and bone meal was rich in nutritional value, and its hygiene and safety indexes met the raw material standard of protein feed. [ABSTRACT FROM AUTHOR]

Brazil plays an important role in ensuring its position on the international market by assuring high food safety standards for its products, and all products should meet the requirements for residues from veterinary drugs and contaminants in animal products. Statutory monitoring provides insights into the compliance of the Brazilian industry regarding these legal requirements. The objective of this study was to provide insight into the safety of Brazilian animal products by reporting the occurrence of residues from veterinary drugs and contaminants according to an analysis of an 11-year report published by the Brazilian Ministry of Agriculture, Livestock and Food Supply (MAPA). Between 2010 and 2021, 166,647 samples from animal-derived products were analyzed in Brazil, and 624 of those samples were non-compliant (0.37%) exceeding maximum residue limits (>MRLs) or showed the presence of prohibited substances. The most common types of substances found in the non-compliant samples were heavy metals, parasiticides, and antimicrobials, accounting for 82% of all documents from the MAPA. Among Brazilian products, the challenge related to occurrence of substances varied across the food supply chain, with highest incidence rates observed in the fish chain, followed by eggs, milk, equids, sheep/goat, honey, bovine, swine, and broilers chains in decreasing order. Considering the type of substance, heavy metals were found to be more prevalent in fish products, mainly arsenic in wild fish. The prevalence of contaminants and heavy metals decreased, while that of veterinary drugs increased in Brazilian products from 2010 to 2021. From these results, it can be concluded that the number of accidental incidents including those associated with environmental contaminants decreased over the last decade, opposed to those involving human adversaries and deliberate illegal actions, such as the abuse of veterinary drugs, increased. Future monitoring plans need to take this paradigm shift into account. [ABSTRACT FROM AUTHOR]

The safety issue of animal food has received widespread public attention due to increased reports of problematic foods. Once veterinary drugs are overused or abused in the process of animal husbandry, drug residues will bring serious harm to human health. Common residue detection methods have the disadvantages of high cost, slow speed and low efficiency, which usually requires professional personnel to operate, and the traditional physical and chemical methods can't meet the needs of food quality testing. As a result, the research and development of rapid and efficient detection methods for veterinary drug residues is necessary. In recent years, surface-enhanced Raman spectroscopy (SERS) has been widely used in many fields such as authenticity identification, illegal additives detection, agricultural and veterinary residues, etc, and has a broader development prospect in the field of food testing due to its advantages of fast detection and nondestructive. SERS is different from other detection methods in that it can rapidly identify target analytes through signal amplification and highly sensitive fingerprint spectroscopy for qualitative or semi-quantitative analysis. This paper mainly introduces the research and application of Raman spectroscopy and SERS in the detection of veterinary drug residues in foods of animal origin, focusing on the advantages of SERS, the pre-treatment of food samples, and the related research on the detection of a variety of veterinary drugs by SERS combined with other techniques, and proposing the challenges faced by SERS in practical monitoring. [ABSTRACT FROM AUTHOR]

Objective To understand the detection of four prohibited veterinary drugs of fresh and live freshwater fish sold in Guangzhou by analyzing the test data from risk monitoring and supervision sampling, so as to provide reference basis for food safety supervision. Methods Through the Guangzhou Food Safety Risk Monitoring system and the Food Safety Supervision and Inspection Public Information report of Guangzhou Market Administration, the test results of fresh water fish samples col-lected from supermarkets, markets, and online e-commerce in Guangzhou from 2017 to 2021 were obtained. The detection of nitrofuran drugs, chloramphenicol, sodium pentachloro phenate, and malachite green drugs were analyzed. Results The total detection rate of banned veterinary drugs in risk monitoring samples was 35.3% (84/238), and that in supervised sampling samples was 3.10% (118/3 806). The banned veterinary drugs with high detection rates of the two data sources were different. The risk monitoring rates of chloramphenicol and sodium pentachloro phenate were 17.23% (41/238) and 17.23% (41/238), respectively, and that of malachite green was 2.18% (83/3 806). The drug detection rate of the samples collected by risk monitoring in the network e-commerce link was Al.50% (19/40), which was the highest among all sampling links. The results of the two data sources showed that the detection rate of banned veterinary drugs in the wholesale market was high: 47.37% (18/38) and 4.13% (5/121), respectively. Conclusion The results of data analysis from the two sources complement each other and jointly reveal the problem of banned veterinary drug residues in fresh freshwater fish sold in Guangzhou from 2017 to 2021. It is suggested that the relevant departments pay more attention to the illegal use of chloramphenicol, sodium pentachloro phenate, and malachite green drugs. [ABSTRACT FROM AUTHOR]

Antimicrobial resistance (AMR) as one of the world's most pressing public health problems needs immediate attention, because it has the ability to affect the human healthcare, agriculture, and veterinary industries. Despite warnings about overuse and their implications, antimicrobials are overprescribed worldwide for humans and animals, which leads to the promotion of resistant microorganisms such as bacteria. Food is a medium for exposure to or transfer of residues of the drugs and can contribute to the burden of the pharmaceuticals associated with development of AMR. Studying on residues of veterinary drugs in foods is essential in the fight against AMR. Herein, we introduce a new method for visualizing the residues of a veterinary drug in animal matrices using radionuclides, called "Depletion Imaging". Amoxicillin was chosen to be the first antimicrobial for this study. The drug was labeled with [62Zn/65Zn] ZnCl2. Radiolabelled amoxicillin and non-labeled amoxicillin were administrated to rainbow trout fish simultaneously. To enable visualization of the remaining residues of amoxicillin in fish, In-vivo positron emission tomography (PET) imaging was done at different intervals from 30 min to 21 days after administration. Evaluation of the amount of radiolabelled amoxicillin in fish was done using a high purity germanium (HPGe) nuclear detector, and enzyme linked immunosorbent assay (ELISA) technique was used for the non-labeled drug. In this study, a comprehensive method for in-house production of zinc radioisotopes was also included. The results showed that depletion imaging and biodistribution study based on gamma spectroscopy of radionuclides in tissues, is a precise method for accurate understanding of the drug's distribution, metabolic and excretory profile. [ABSTRACT FROM AUTHOR]

A disposable electrochemical sensor based on silver nanoparticle-embedded cellulose hydrogel composites was developed for sensitive detection of sulfamethoxazole residues in meat samples. Scanning electron microscopy confirmed the porous structure of the cellulose matrix anchored with 20–50 nm silver nanoparticles (AgNPs). Fourier transform infrared spectroscopy and X-ray diffraction verified that the metallic AgNPs coordinated with the amorphous cellulose chains. At an optimum 0.5% loading, the nanocomposite sensor showed a peak-to-peak separation of 150 mV, diffusion-controlled charge transfer kinetics, and an electron transfer coefficient of 0.6 using a ferro/ferricyanide redox probe. Square-wave voltammetry was applied for sensing sulfamethoxazole based on its two-electron oxidation peak at 0.72 V vs. Ag/AgCl in Britton–Robinson buffer of pH 7.0. A linear detection range of 0.1–100 μM sulfamethoxazole was obtained with a sensitivity of 0.752 μA/μM and limit of detection of 0.04 μM. Successful recovery between 86 and 92% and less than 6% RSD was achieved from spiked meat samples. The key benefits of the proposed disposable sensor include facile fabrication, an antifouling surface, and a reliable quantification ability, meeting regulatory limits. This research demonstrates the potential of novel cellulose–silver nanocomposite materials towards developing rapid, low-cost electroanalytical devices for decentralized on-site screening of veterinary drug residues to ensure food safety. [ABSTRACT FROM AUTHOR]

Food is vital to the people, and safety comes first in food. Food safety is crucial to people's livelihood, economic development, and social stability. It represents people's aspiration for a better life and grabs great public attention. In recent years, while China has achieved significant progress in food safety, the situation remains severe, with incidents such as excessive residues of agricultural and veterinary drugs, as well as illegal addition of toxic and harmful substances. As an important technical support for ensuring food safety, food safety inspection and testing institutions also exhibit a mixed bag of performance. Problems such as inadequate personnel management, improper use of facilities and equipment, weak legal awareness resulting in issuance of false reports have frequently occurred, seriously disrupting the normal order of the inspection and testing market and affecting the authority and accuracy of food safety testing. Based on the capacity verification of inspection and testing organizations in Zhejiang Province in recent years, this paper studies the typical problems faced by food inspection and testing institutions in terms of management level and testing capabilities, analyzes the root causes in depth, and proposes specific strategies from three aspects: Strengthening the main responsibility of inspection and testing institutions, combining regulatory departments with supervision and guidance, and enhancing industry self-discipline, aiming to continuously improve their inspection and testing capabilities, promote the high-quality development of food inspection and testing institutions, and effectively ensure the safety of every bite of food. [ABSTRACT FROM AUTHOR]

Sheep's milk is a significant source of nucleotide monophosphates (NMPs) but can also contain undesirable residues from veterinary drugs, posing a potential human health risk. This study introduces a novel application of two-dimensional liquid chromatography (2D-LC), in heart-cutting mode, for the simultaneous determination of nucleotides and veterinary drug residues in sheep's milk. 2D-LC allows for the separation of these compounds in a single chromatographic run despite their differing physicochemical properties. The proposed method separates six veterinary drug residues and five NMPs in a single injection. The compounds were separated using a C18 reversed-phase column in the first dimension and a Primesep SB analytical column in the second dimension. The method performance was evaluated in terms of linearity range, detection and quantification limits, matrix effects, precision, and accuracy. The results demonstrated good linearity and sensitivity, with quantification limits allowing for the quantification of veterinary drugs at the maximum residue level and nucleotides at typical levels found in milk samples. The method has been successfully applied to the analysis of sheep's milk samples acquired from local supermarkets, with recoveries within a range of 70–119% and 82–117% for veterinary residues and NMPs, respectively. [ABSTRACT FROM AUTHOR]

Dexamethasone is approved for cattle in Canada for several conditions, but no withdrawal times are currently provided on the approved labels. Recently, the list of Maximum Residues Limits for Veterinary Drugs in Foods in Canada was amended to include dexamethasone. The objectives of this study were to determine the residue depletion profile of dexamethasone after an extra‐label dosage regimen in milk of healthy lactating dairy cattle (n = 18) and in edible tissues of healthy beef cattle (n = 16) and to suggest withdrawal intervals. Dexamethasone was administered intramuscularly at 0.05 mg/kg daily for 3 days. Milk samples were collected prior to treatment and every 12 h up to 96 h post‐dose. Muscle, liver, kidney, and peri‐renal fat tissues were collected from beef cattle at 3, 7, 11, or 15 days post‐dose. Dexamethasone analysis was performed by liquid chromatography/mass spectrophotometry. Dexamethasone residues were detected in milk samples up to 36 h. Muscle and fat had no detectable dexamethasone residues while kidney and liver had detectable residues only on day 3 post‐dose. A withdrawal interval of 48 h for milk in Canadian dairy cattle and 7 days for meat in Canadian beef cattle are suggested for the dexamethasone treatment regimen most commonly requested to CgFARAD™. [ABSTRACT FROM AUTHOR]

[Objective]To establish a method for the simultaneous determination of 33 kinds of veterinary drug residues in mutton by ultra high performance liquid chromatography-tandem mass spectrometry. [Method] The sample was extracted with 90% acetonitrile water ( containing 2. 0% formic acid), purified by Oasis Prime HLB, concentrated, and diluted with mobile phase. Then separated by Waters ACQUITY UPLC HSS T3 column(2. 1 mm×100 mm,1. 8 μm),using 0. 1% formic acid and acetonitrile as mobile phase. Under electrospray ionization source, switching between positive and negative ion modes, in Multiple Reaction Monitoring ( MRM) mode, utilizing the isotope internal standard method for quantification by combining retention time and characteristic ion information. [Result] The linear relationship of the 33 kinds of veterinary drugs was good in the concentration range of 0. 5 - 40. 0 ng / mL( r > 0. 99),and the lowest detection concentration was 0. 08 - 0. 10 ng / mL. Adding standard recovery rates was 83. 7%-115. 0%,the RSD was 0. 58%-11. 49%. [Conclusion]The method has the simple processing,high sensitivty and good reproducibility,and is suitable for the quantitative detection of 33 kinds of veterinary drug residues in mutton. [ABSTRACT FROM AUTHOR]

A combination of sample screening and subsequent confirmatory detection of contaminants represents an optimal strategy for routine analysis in implementing food safety monitoring programs. We propose ultra-high-performance liquid chromatography coupled with high-resolution mass spectrometry for the multicomponent determination of a wide range of veterinary drugs and their metabolite residues with minimal sample preparation. Isotopic dilution was employed to mitigate matrix effects. The procedure proposed in this study enables the simultaneous identification and assessment of residual levels of 214 veterinary drugs at limits of detection of 0.1–10.0 ng/g with a significantly shortened analysis time (40–50 min) and reduced cost. [ABSTRACT FROM AUTHOR]

Although filtration is one of the most common steps in sample preparation for chemical analysis, filter membrane materials can leach contaminants and/or retain some analytes in the filtered solutions. In multiclass, multiresidue analysis of veterinary drugs, it is challenging to find one type of filter membrane that does not retain at least some of the analytes before injection in ultrahigh‐performance liquid chromatography‐tandem mass spectrometry (UHPLC‐MS/MS). In this study, different filter membranes were tested for use in UHPLC‐MS/MS analysis of 183 diverse drugs in bovine muscle, kidney, and liver tissues. Membranes evaluated consisted of polytetrafluoroethylene (PTFE), polyvinylidene difluoride (PVDF), polyethersulfone, nylon, and regenerated cellulose. Drug classes represented among the analytes included β‐agonists, β‐lactams, anthelmintics, macrolides, tetracyclines, sulfonamides, tranquilizers, (fluoro)quinolones, anti‐inflammatories, nitroimidazoles, coccidiostats, phenicols, and others. Although the presence of a matrix helped reduce the binding of analytes on surface active sites, all of the filter types partially retained at least some of the drugs in the final extracts. In testing by flow‐injection analysis, all of the membrane filters were also observed to leach interfering components. Ultimately, filtration was avoided altogether in the final sample preparation approach known as the quick, easy, cheap, effective, rugged, safe, efficient, and robust (QuEChERSER) mega‐method, and ultracentrifugation was chosen as an alternative. [ABSTRACT FROM AUTHOR]

A freeze-dried bovine muscle–certified reference material (CRM), known as BOTS-1 (DOI: https://doi.org/10.4224/crm.2018.bots-1), containing incurred residues of commonly used veterinary drugs was produced and certified for the mass fraction of eight veterinary drug residues. Value assignment was carried out using liquid chromatography tandem mass spectrometry (LC–MS/MS) methods in conjunction with isotope dilution and standard addition approaches involving stable isotope internal standards. Data from the National Research Council of Canada (NRC), Canadian Food Inspection Agency (CFIA), United States Department of Agriculture (USDA), and the Federal Office of Consumer Protection and Food Safety in Germany (BVL) were used for value assignment. Results for two drug residues were also obtained through an international inter-laboratory comparison CCQM-K141/P178 organized under the auspices of the International Bureau of Weights and Measures (BIPM). Quantitative NMR (1H-qNMR) was used to characterize primary standards of all veterinary drugs certified. The certified mass fractions of the veterinary drug residues were 490 ± 100 µg/kg for chlorpromazine, 44 ± 4.4 µg/kg for ciprofloxacin, 3.3 ± 1.4 µg/kg for clenbuterol, 9.5 ± 0.8 µg/kg for dexamethasone, 57 ± 4.8 µg/kg for enrofloxacin, 3.0 ± 0.4 µg/kg for meloxicam, 12.4 ± 1.2 µg/kg for ractopamine, and 2290 ± 120 µg/kg for sulfadiazine with expanded uncertainties quoted (95% confidence) which include the effects due to between-bottle inhomogeneity, instability during long-term storage and transportation, and characterization. [ABSTRACT FROM AUTHOR]

This study introduces a cost‐effective, automated ultra‐high‐performance liquid chromatography–tandem mass spectrometry method for the detection of 14 β‐agonists in pork using a novel solid‐phase microextraction probe composed of polyacrylonitrile and molecularly imprinted polymer. Integrated into an automated extraction device, the probe optimizes extraction prior to analysis while reducing expenses and time compared to traditional solid‐phase extraction procedures. The method validation followed the Chinese National Standard (GB/T 27404‐2008) and examined limits of detection, limits of quantification, matrix effects, linearity, intraday, and interday precision. Average recovery rates ranged from 71.6% to 82.2%, with relative standard deviations less than 15%. Limits of detection and limits of quantification ranged from 0.09 to 0.39 and 0.27 to 0.99 μg/kg, respectively. The new method identified positive samples more accurately than the current National Standard GB/T 31658.22‐2022 and demonstrated its potential for routine assessment and regulatory compliance in the detection of β‐agonists in pork. [ABSTRACT FROM AUTHOR]

Background An LC-MS/MS method was developed for determination and confirmation of tilmicosin in bovine, swine, chicken, and turkey tissues (liver, kidney, muscle, and skin/fat) and bovine milk. Objective The method was subjected to single-laboratory validation to establish method performance parameters. Method Animal tissues and bovine milk were fortified at four concentrations ranging from 0.5 times the lowest maximum residue limit (MRL) or tolerance to 2 times the highest MRL or tolerance considering the Codex and EU MRLs and the US tolerances in the various tissues and milk studied. Incurred tissues were analyzed to verify the precision of the method. Results The data demonstrated linearity of matrix-matched calibration curves using a weighted (1/×) regression. Recoveries varied from 83.3 to 107.1%. Repeatability precision (RSDr) ranged from 0.465 to 13.4% and intermediate precision (RSDi) ranged from 2.24 to 14.7% in fortified tissue. Repeatability of the method was verified in incurred tissues, ranging from 3.41 to 16.0%. The limits of detection and quantitation of the method are presented and vary by matrix. One confirmatory transition ion was examined across all matrixes and met US and EU criteria for mass spectrometry confirmation. The method was shown to be robust when small changes in method parameters were made, and stability of the analyte in fortified tissues, extracts, standard solutions, and matrix-matched standards was estimated. Conclusions The data satisfy the requirements of the AOAC Stakeholder Panel for Veterinary Drug Residue Methods for single-laboratory validation studies and the U.S. Food and Drug Administration Center for Veterinary Medicine Guidance for Industry #208 (VICH GL49). Highlights The LC-MS/MS method was demonstrated to be suitable for determination and confirmation of tilmicosin residues in bovine, swine, chicken, and turkey tissues and bovine milk based on Codex and EU MRLs and US tolerances. [ABSTRACT FROM AUTHOR]

From farm to plate, food meets various challenges and pollution. Food detection is essential to ensure food safety. Although detection techniques have obtained great development, the accuracy, sensitivity and operating conditions still have room for improvement. Composed of dielectric media with different refractive indices to form a periodic structure, an optical material named photonic crystal (PC) can offer a breakthrough. Owing to the periodic structure, Bragg diffraction happens with optical waves propagating in a PC and photonic band gap (PBG), a characteristic parameter of the PC, will form. The properties of PBG are widely used in the field of detection. Combined with the techniques of biology, immunology, optics and fluorescence etc., PCs can play the role of specific, efficient, sensitive and convenient sensors in food detection. At present, PCs have been successfully applied to analyze hazardous substances in food, such as microorganisms, biotoxins, veterinary drug residues, pesticide residues, excessive additives, illegal additives, environmental pollutants and heavy metal composition. This article introduces PCs about the fabrication methods, principles and techniques applied in detection and research progress in food detection. [ABSTRACT FROM AUTHOR]

Honey is regarded as natural and healthy. However, a variety of contaminants could be present in the areas of production. The study aimed to identify the top hazard categories in Rapid Alert System for Food and Feed (RASFF) notifications for honey from 2002 to 2022, taking into account the notification year and type, country of origin, notifying country, risk decision, and actions taken. All RASFF notifications were processed in Pivot tables using Microsoft Excel. Out of 388 notifications for honey in the last 21 years 309 (79.64%) concerned the unauthorized residues of veterinary medicinal products hazard category, followed by adulteration/fraud (5.15%), foreign bodies (2.83%), pesticide residues (2.58%), and poor or insufficient controls (2.58%). China was the most frequently notified country of origin (25.77%), followed by Turkey (6.44%), Ukraine (6.19%), Argentina (6.19%), and Bulgaria (5.67%). Germany was the most frequently notifying country (16.49%), followed by the UK (16.24%), Spain (13.40%), Italy (10.82%), and Belgium (7.99%). Among all notifications, 22.68% were alerted and 12.37% were border rejected. The notification frequency (%) and mean concentration ± standard deviation (SD) (μg/kg) of the most frequently reported contaminants in the honey were as follows: chloramphenicol (25.26%, 172.10 ± 827.92 μg/kg), followed by streptomycin (12.11%, 104.94 ± 209.44 μg/kg), sulfathiazole (9.54%, 52.31 ± 52.62 μg/kg), tylosin (4.90%, 9.03 ± 11.23 μg/kg), and sulfadimidine (4.64%, 254.99 ± 587.00 μg/kg), respectively, due to their application by beekeepers to control infectious diseases of bees. Strict restrictions must be put in place to reduce the risk posed by these contaminants in honey. [ABSTRACT FROM AUTHOR]

The problem of veterinary drug residues in food of animal origin is of great importance in developing countries. The concerns are mostly related to food safety and the development of antibiotic-resistant pathogens. This study was carried out during the hot dry season (March) between 2016 - 2018 to detect antibiotic presence in beef, chevon and pork sold for human consumption in abattoirs in Benue state. Thirty-nine samples each of 100-150g of kidney, liver and muscle were collected from cattle, goats and pigs making a total of 351 samples from abattoirs across the three geopolitical zones of Benue state. The samples were screened for multidrug residues using the modified agar gel diffusion method. A total of 144 were positive out of which 40.3% (58/144) were beef, while 29.2% (42/144) and 30.5% (44/144) were chevon and pork respectively. From the results of this study, it could be inferred that the meat consumed within Benue State contains residues of antibiotics possibly because of non-adherence to the withdrawal period by farmers and lack of knowledge of its consequences on the consumers. [ABSTRACT FROM AUTHOR]

Tailless amphibians belonging to the order Batrachia are a significant component of human consumption. However, there is limited literature on the consumption of these amphibians by humans. Therefore, the present work aimed to examine the presence of drug residues in edible Batrachia, and compare them with other aquatic products. We assessed 22 veterinary drug residues, including 12 sulfonamides (SAs) and ten quinolones (QNs), in various aquatic products, including edible Batrachia. To provide a comparative analysis, we referenced literature from China between 2005 and 2020 regarding SAs and QNs detected in aquatic products. Additionally, we calculated the food safety index (IFS) of antibiotics, and conducted a health risk assessment. The findings revealed that the detection rate, average residual amount, and over-standard rate of antibiotics in edible Batrachia were higher than most other aquatic products. Furthermore, the systematic cluster analysis demonstrated that edible Batrachia could serve as a potential sentinel animal, distinguishing them from several other aquatic products. The total IFS of all residues obtained from different aquatic products in the present work was less than 1, thus indicating their safety in terms of public health. Nevertheless, it is essential to conduct detailed investigations into the maximum residues of certain antibiotics in specific aquatic products that exceed the safety limits to understand their impact on human health. [ABSTRACT FROM AUTHOR]

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Food safety has emerged as a significant concern for global public health and sustainable development. The development of analytical tools capable of rapidly, conveniently, and sensitively detecting food safety hazards is imperative. Over the past few decades, personal glucose meters (PGMs), characterized by their rapid response, low cost, and high degree of commercialization, have served as portable signal output devices extensively utilized in the construction of biosensors. This paper provides a comprehensive overview of the mechanism underlying the construction of PGM-based biosensors, which consists of three fundamental components: recognition, signal transduction, and signal output. It also detailedly enumerates available recognition and signal transduction elements, and their modes of integration. Then, a multitude of instances is examined to present the latest advancements in the application of PGMs in food safety detection, including targets such as pathogenic bacteria, mycotoxins, agricultural and veterinary drug residues, heavy metal ions, and illegal additives. Finally, the challenges and prospects of PGM-based biosensors are highlighted, aiming to offer valuable references for the iterative refinement of detection techniques and provide a comprehensive framework and inspiration for further investigations. [ABSTRACT FROM AUTHOR]

ObjectiveTo provide a scientific basis for the risk assessment of the dietary exposure of local characteristic dairy products and veterinary drug residues in dairy products in Inner Mongolia and the formulation and revision of local food safety standards， the current situation regarding this matter was studied.MethodsA total of 951 samples of seven types of local characteristic dairy products and dairy-containing products in Inner Mongolia were collected in 12 league cities， including milk skins， milk tea powder， and chewable milk products. Among them， 370 samples were in bulk and 581 samples were in standardized packaging. The samples were analyzed for quinolones， tetracyclines， macrolides， and β-sulfonamides.ResultsThe detection rate of veterinary drug residues was 0.83%-3.62% in five types of local characteristic dairy products， including milk skin， milk tea powder， chew， chula， and milk-containing solid molding products. The detected veterinary drugs were naphthyric acid， norfloxacin， pefloxacin， sulfamethoxazole， sulfamethoxazole， sulfamethoxazole， and tylosin， with the detection rate ranging from 0.11% to 1.37%. According to the statistical test， there was no statistical difference between the detection rate of veterinary drug residues in bulk samples and that of veterinary drug residues in stereotyped packaging samples （χ2=0.484， P>0.05）.ConclusionAlthough the overall qualification rate of tetracycline， sulfonamide， and macrolide residues in local characteristic dairy products in Inner Mongolia is relatively high （>99%）， there are still cases of veterinary drug detection. It is recommended that relevant departments further strengthen the promotion and supervision of veterinary drug use.

Rapid detection technology developed rapidly due to its simple operation and ability to quickly detect test results. This paper reviews the types and negative effects of veterinary drug residues commonly found in poultry tissues and eggs. The pros and cons of various rapid detection techniques are compared from the point of view of their practical application. The future development trends and application values of detection techniques (e.g., enzyme-linked immunosorbent assay, colloidal gold immunochromatography, biochip technology, chemiluminescent immunoassay, biosensor, and surface-enhanced Raman spectroscopy) in poultry tissues and eggs are discussed. Finally, the development of new functional materials (e.g., nucleic acid aptamers, affinity bodies, and genetically engineered antibodies) is proposed to improve the sensitivity and accuracy of rapid detection technology through the fusion of modern network technology with various detection technologies. The goal is to improve the applications and effects of rapid detection technology in poultry food safety management and to provide new ideas for the evaluation, detection, and supervision of veterinary drug residues.

The aim of this study was to detect the presence of antibiotic residues in foods of animal origin, including 42 pieces of chicken gizzard and 46 pieces of bovine kidney and 102 chicken eggs belonging to various brands. These samples were gathered from December 2020 to April 2021 in the Aegean province of Turkey. A sensitive, simple, rapid, experimentally convenient and cost effective RP-LC method with high recovery output was developed. The method was thoroughly validated for the optimized parameters and produced satisfactory results. The analysis of bovine offal by the developed RP-LC method showed the presence of oxytetracycline, tetracycline, and chlortetracycline residues in 14 (30.43%) kidney samples. Chlortetracycline was detected in 7 (16.67%) chicken gizzard samples. In addition, the analysis of chicken eggs revealed the presence of oxytetracycline and tetracycline residues in nine egg samples (8.82%). Since, the amount of antibiotic residues in these samples was below the detection limit, quantification could not be carried out. Only one (0.98%) of the 102 egg samples exceeded the MRL (267.1 mg/kg) for oxytetracycline concentration. According to the study's overall findings, it is recommended that tetracycline antibiotics should be regularly checked in a variety of foods made from animals because they were found in 32 out of 190 analysed samples. Tetracycline residues may pose dangers to human health, so it's important to conduct further research and more information should be given for both producers and consumers.

Abstract In this study, an analysis method was established for the quantification of residues of halquinol and its metabolites in livestock and fishery products using liquid chromatography–tandem mass spectrometry (LC–MS/MS). We selected beef, pork (muscle and fat), chicken, egg, milk, flat fish, eel, and shrimp as target samples for validation of the method owing to them being typical livestock and fishery products. Validation of the developed analysis method was performed using liquid chromatography–tandem mass spectrometry (LC–MS/MS) at three concentration levels (0.5, 1, and 2 × the maximum residue limits) following the Codex Alimentarius (CODEX) guidelines (CAC/GL 71–2009). For all samples, correlation coefficients (R2) exceeded 0.99, recoveries ranged between 75.59 and 119.36%, and coefficients of variation (CV) ranged between 1.39 and 28.66%, thus satisfying CODEX guidelines. In addition, inter-laboratory validation was conducted, and the resulting recoveries and CVs satisfied the CODEX guidelines; LOQ was established as 10 μg kg–1 for pig muscle and 5 μg kg–1 for the other samples. Therefore, the analysis method developed in this study can accurately and precisely screen for and quantify halquinol and its metabolites in livestock and fishery products.

The aim of this study was to analyze and evaluate the safety performance of processing meat and bone meal from Ussuri raccoon dogs carcasses. Samples were obtained from 17 major raccoon dog breeding areas in China to explore the feasibility of processing meat and bone meal from raccoon car‐ casses, to provide a theoretical basis for the effective utilization of raccoon dog by-products after slaugh‐ ter, and to provide data support for the enrichment of animal protein feed sources in China. A total of 51 healthy Ursuline raccoon dogs were randomly selected from 17 raccoon farms in each region. Each rac‐ coon dog carcass weighing about 9 kg was taken as a test sample (including internal organs and toe claws), and raccoon dog meat and bone meal was made by grinding, high-pressure hydrolysis, degreasing, drying and crushing, and its nutritive value analysis safety evaluation was made. The results showed that the crude protein, crude ash, moisture, calcium and total phosphorus contents of raccoon dogs meat and bone meal met the requirements of the national standard for meat and bone meal, and the crude protein contents of raccoon dogs meat and bone meal from Hengshui, Weifang and Qingdao were as high as 67.29%, 66.14% and 73.5%, re‐ spectively, which met the first level index of Bone Meal, Meat and Bone Meal for Feedstuffs. The con‐tent of lead, arsenic, mercury, cadmium and chromium heavy metal elements meet the requirements of the national standard for meat and bone meal health and safety standards. Sulfadimethoxine, sulfamethoxa‐ zole, sulfamonomethoxine, sulfadiazine, penicillin, oxytetracycline and gentamicin meet the requirements of the standard for maximum residue limits of veterinary drugs in food. The carcass of raccoon dogs after slaughtering and skin removal is made into meat and bone meal according to the meat and bone meal pro‐ cessing procedure, which is rich in nutritional value, and the health and safety indexes meet the standard of protein feed materials, and can be used as an alternative high-quality protein feed material. [ABSTRACT FROM AUTHOR]

Microwave‐assisted extraction (MAE) is an important technique in analytical chemistry. It offers several advantages over traditional extraction methods, such as improved extraction efficiency, shorter extraction times, reduced solvent consumption, and enhanced analyte recovery. Using microwaves, heat is directly applied to the sample, leading to rapid and efficient extraction of target compounds by enhancing the solubility and diffusion of the target compounds, thus requiring lower solvent volume. Therefore, MAE can be considered a more environmentally friendly and cost‐effective option facilitating the transition toward greener and more sustainable analytical chemistry workflows. This contribution systematically reviews the application of MAE to a selection of target compounds/compounds classes of relevance for food quality and safety assessment. As inclusion criteria, MAE active temperature control and molecularly‐resolved characterization of the extracts were considered. Contents include a brief introduction of the principles of operation, available systems characteristics, and key parameters influencing extraction efficiency and selectivity. The application section covers functional food components (e.g., phenols, diterpenes, and carotenoids), lipids, contaminants (e.g., polycyclic aromatic hydrocarbons and mineral oil hydrocarbons), pesticides, veterinary drug residues, and a selection of process contaminants and xenobiotics of relevance for food safety. [ABSTRACT FROM AUTHOR]

The research progress in matrix purification combined with liquid chromatography-mass spectrometry (LC-MS) method as well as their applications in determination of veterinary drugs in animal-derived foods was reviewed. Among various matrix purification methods, liquid liquid extraction (LLE), dispersed liquid liquid microextraction (DLLME), solid phase extraction (SPE), solid phase microextraction (SPME), dispersed solid phase extraction (DSPE), and magnetic solid phase extraction (MSPE) are mostly widely used in different animal derived foods such as meat, eggs, milk, and their products. However, there are still some limitations, such as weak matrix selectivity of LLE, limited applicability of DLLME, moderate purification efficiency DPSE, poor reproducibility of SPME, and time-consuming operation of SPE. In the future, the detection technology of veterinary drugs in various animal-derived foods could be further studied in terms of establishing simultaneous purification methods for various kinds of veterinary drugs, developing novel and efficient matrix-based purification materials, and enhancing convenience and automation in matrix purification process to meet the urgent needs in screening of multi-residues of veterinary drugs in animal-derived foods. [ABSTRACT FROM AUTHOR]