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FOOD CHEMISTRY · 2021 · IF 7.514

Comparison of two fluorescence quantitative immunochromatographic assays for the detection of amantadine in chicken muscle

Yantong Pan,Zhaopeng Wang,Changfei Duan,Leina Dou,Kai Wen,Zhanhui Wang,Xuezhi Yu,Jianzhong Shen

The two sensitive fluorescence quantitative immunochromatographic assays (FQICAs), background fluorescence quenching immunochromatographic assay (bFQICA) and time-resolved fluorescent immunochromatographic assay (TRFICA), play an important role increasingly in rapid detection technology for food safety. Amantadine (AMD), used extensively in virus infections in livestock and poultry, has been prohibited due to hazard concerns over public human health. Therefore, AMD was used as a model molecule in the FQICAs establishment and comparison based on the same bioreagents. The outstanding performance in technical parameters of the two FQICAs indicated that they could provide rapid, precise, reliable technical support for large-scale on-site screening for AMD detection. What’s more, the systematic and comprehensive comparison of the two FQICAs would give useful suggestions for scientists and users in monitoring the harmful compounds.

研究领域: 食品安全检测 · 免疫学 · 分析化学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2021 ·Vol. 11 ·期 36 ·22005-22013 · IF 3.361

Development of a fluorescent immunochromatographic assay based on quantum dots for the detection of fleroxacin

Qingbao Yang,Yanhua Qi,Jingming Zhou,Yumei Chen,Chao Liang,Zhanxiang Liu,Xiaoli Zhang,Aiping Wang

Fleroxacin (FLE) is a broad-spectrum fluoroquinolone antibiotic widely used in animal husbandry, veterinary medicine and aquaculture. Eating animal-derived foods with FLE residues can cause allergies, poisoning or drug resistance. The water-soluble QDs (CdSe/ZnS) and anti-FLE monoclonal antibody (mAb) were used to prepare a fluorescent probe by the method of N-(3-dimethylaminopropyl)-N′-ethylcarbodimide hydrochloride (EDC) activation. The fluorescent probe was characterized by dynamic light scattering (DLS). The better bioactivity and stability of the fluorescent probe was obtained under the pH value of 8.0, the molecule molar ratio of EDC (1 : 2000) and anti-FLE monoclonal antibodies (1 : 10). The control line (C line) and test line (T line) of a nitrocellulose (NC) filter membrane were sprayed with SPA (0.05 mg mL−1) and FLE-OVA (1.4 mg mL−1) solutions with optimal concentration, respectively. A novel method of fluorescent immunochromatographic assay based on quantum dots (QDs-ICA) in this work exhibited good accuracy, reproductivity and excellent specificity under the optimal experimental conditions. Compared with the traditional method for the visual detection of FLE, the developed QDs-ICA can successfully determine FLE residues in pork meat with a better cut-off value of 2.5 ng mL−1. The QDs-ICA could be adapted for the rapid preliminary detection of FLE residues in pork meat for the first time.

CAS / MDL: 25952-53-8
研究领域: 生物化学 · 兽医学 · 食品安全
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JOURNAL OF HAZARDOUS MATERIALS · 2020 · IF 9.038

Development of a fast and ultrasensitive black phosphorus-based colorimetric/photothermal dual-readout immunochromatography for determination of norfloxacin in tap water and river water

Shuyue Ren,Qiaofeng Li,Jingyi Wang,Bingyan Fan,Jialei Bai,Yuan Peng,Shuang Li,Dianpeng Han,Jin Wu,Jiang Wang,Kang Qin,Zunquan Zhao,Baoan Ning,Tie Han,Huanying Zhou,Zhixian Gao

A rapid and ultrasensitive method for colourimetric/photothermal dual-readout detection was developed using an 808 nm NIR laser and a thermal imaging app on mobile phone. Norfloxacin was used as a model contaminant to demonstrate this universal rapid detection method. It is innovatively, to use the advanced two-dimensional material black phosphorus as a colourimetric/photothermal reagent for the first time. The samples were added to the strip, and the analytes were selectively captured on the conjugate pad by monoclonal antibody-modified magnetic/upconversion nanocomposites . The samples flowed through the strips by capillary action until reaching the control line, where immune complex formation occurred due to the presence of secondary antibody. The added black phosphorus could be captured by the the antigens which were directly exposed to the test line and a brown band could be observed by naked eye. Upon illumination by NIR light for 1 min, the real-time temperature is obtained for quantitative analysis through the thermal imaging performed by mobile phone camera. This method can achieve the detection of norfloxacin in water samples within 20 min, and the detection limits of colorimetric and photothermal readout can reach 45 pg mL −1 . Compared with conventional strips, this method provided an increased sensitivity by about two orders of magnitude, with a integrated portable laser and a mobile phone. It is a valuable method for rapid detection and can be applied to other environmental contaminants as well.

研究领域: 环境科学 · 分析化学 · 纳米技术
✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2020 · IF 4.192

Developing a Simple Immunochromatography Assay for Clenbuterol with Sensitivity by One-Step Staining

Han Zhang,Lulu Wang,Xiaolin Yao,Zonghan Wang,Leina Dou,Lihong Su,Man Zhao,Jing Sun,Daohong Zhang,Jianlong Wang

An innovative lateral flow competition immunoassay (LFCIA) for detecting clenbuterol (CL) was developed by employing the advantages of the coomassie brilliant blue (CBB) staining method. An antibody stained by CBB was used both as a recognition reagent and as a chromogenic probe, enabling the simple but sensitive LFCIA of CL. The CBB-based LFCIA exhibited sensitivity for CL with a detection limit of 2 ng mL–1. Furthermore, this strategy was preliminarily verified by screening for CL in milk, pork tenderloin, and swine liver with recoveries ranging from 81 to 102%. Compared with conventional LFCIAs, the use of CBB as a signal label not only avoided the complicated material synthesis and surface modification process but also simplified the cross-linking with antibodies, meanwhile reducing the steric hindrance and increasing the possibility of immune recognition reactions, which was propitious for the effective utilization of antibodies. Taking advantages of the simplicity, rapidity, and cost-effectiveness, the CBB-based LFCIA may have potential for on-demand monitoring of general harmful small molecules by changing the kind of the staining antibody.

研究领域: 分析化学 · 食品安全 · 生物技术
✓ 已验证 DOI PubMed 高影响因子
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LWT-FOOD SCIENCE AND TECHNOLOGY · 2024 · IF 6

Immunochromatographic method based on PCN-222 with dual-signal output for the rapid and sensitive detection of furazolidone metabolites in animal-derived food

Siyao Zhong,Haizhi Huang,Xiaoyao Wang,Xiaoping Yu,Xuping Shentu

The residues of furazolidone and its metabolites (3-amino-2-oxazolidinone [AOZ]) in food would have adverse effects on humans. Herein, a colorimetric and fluorescent dual-signal output immunochromatographic method with a zirconium-based porphyrin metal-organic framework (PCN-222) as the signal label was developed for the detection of 3-[(4-carboxyphenyl) monomethyl] amino-2-oxazolidinone (CPAOZ), a derivative of furazolidone metabolite. PCN-222 was synthesized using the solvothermal method, and the material was characterized via scanning electron microscopy, Fourier-transform-infrared spectroscopy, and powder X-ray diffraction, which proved the successful synthesis of PCN-222. Synthesized PCN-222, as a nanotag, was bound to antibodies to prepare PCN-222-mAbs with dual optical properties. Under the optimized conditions, PCN-222- lateral flow assay (LFA) exhibited a great linear relationship in the range of 0.25–100 ng/mL. The visual limit detection of CPAOZ using colorimetric and fluorescent signals were 1.0 ng/mL and 0.5 ng/mL, respectively, and the sensitivity was 5- and 10-fold higher than that of the colloidal gold-based LFA method. In addition, PCN-222-LFA was successfully applied to the detection of CPAOZ in shrimp, chicken and milk samples achieving satisfactory recoveries from 92.34% to 117.44%. This study provides an alternative, convenient and sensitive method for the rapid detection of veterinary drug residues.

研究领域: 食品安全检测 · 分析化学 · 免疫学
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Food Chemistry-X · 2025 · IF 8.2

Lateral flow immunochromatographic assay for rapid detection of dichlorvos residue in fruits and vegetables

Bao-Zhu Jia,Yan-Yan Liu,Feng-Yan Chen,Phannika Tongchai,Sumed Yadoung,Anurak Wongta,Zhen-Lin Xu,Lin Luo,Surat Hongsibsong

Dichlorvos (DDVP), a widely used yet environmentally hazardous organophosphate pesticide, necessitates rapid field monitoring due to increasing regulatory restrictions. In this study, we firstly present a gold-nanoparticle-based lateral flow immunochromatographic assay (LFIA) employing a highly specific anti-DDVP monoclonal antibody for onsite DDVP detection within 20 min. The optimized LFIA exhibited exceptional analytical performance, with limits of detection spanning 16 μg/kg to 108 μg/kg across six fruit and vegetable matrices—all below the established maximum residue limits in foods. Method validation with spiked fruit and vegetable samples showed recovery rates of 87.3–109.4 % and 89.2–103.3 %, respectively, with coefficients of variation below 8.3 % and 7.9 %, respectively, confirming the accuracy and precision of the assay. Notably, LFIA exhibited good agreement with standard GC–MS/MS analysis when applied to 144 authentic samples, further validating its reliability for real-world applications. This LFIA offers key advantages including portability, cost-effectiveness, and compatibility with regulatory thresholds, making it an ideal alternative to conventional instrumental methods for routine pesticide residue screening in food safety supervision settings.

CAS / MDL: 13453-07-1
研究领域: 食品安全 · 分析化学 · 环境科学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES · 2018 · IF 2.706

Development of an immunochromatographic assay as a screen for detection of total phthalate acid esters in cooking oil

Fan He,Yuanxin Tian,Zhenlin Xu,Lin Luo,Jinyi Yang,Hong Wang,Yuanming Sun,Qingfeng Du,Yudong Shen

Phthalate acid esters (PAEs) contamination raised concerns as a result of migration from food packaging and environmental exposure. Because of the adverse effects of PAE reported in humans, the aim of this study was to examine the ability to screen for the detection these chemicals as an indicator of potential exposure. Too develop a sensitive screening test to determine PAE, a specific polyclonal antibody against phthalic acid (PA), the hydrolysate of PAEs, was used as a marker of total PAEs. This method involved the use of 4-aminophthalic acid (APA) as an immunizing hapten to generate antibody. Subsequently, this antibody conjugated with labeled gold nanoparticles (GNPs) was then used to develop an immunochromatographic assay (ICA) for visually detecting PA. After establishing optimal assay conditions, the ICA strip detected visually PA at 3 μg/ml rapidly in less than 5 min. Further, this assay exhibited reliable specificity for PA with no apparent cross-reactivity with structurally related PAEs. A significant correlation between data obtained with the ICA strip and high-performance liquid chromatography (HPLC) analysis was achieved using cooking oils as model spiked samples. The proposed use of ICA offers an effective tool for rapid on-site screening for total PAEs in cooking oils.

CAS / MDL: 5434-21-9 88-99-3
研究领域: 食品科学 · 免疫学 · 分析化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Analytical Methods · 2014 ·Vol. 7 ·期 2 ·513-520 · IF 1.938

A novel immunochromatographic assay (ICA) based on surface-enhanced Raman scattering for the sensitive and quantitative determination of clenbuterol

Yun Xie,Huafang Chang,Kang Zhao,Jianguo Li,Hong Yang,Liyun Mei,Shouming Xu,Anping Deng

In this study, we present a novel immunochromatographic assay (ICA) based on surface-enhanced Raman scattering (SERS) for the sensitive and quantitative determination of clenbuterol in urine samples. The principle of this new ICA is similar to that based on colloidal gold particles, but using AuMBA@Ag–Ab [e.g. the polyclonal antibody of clenbuterol labelled Au@Ag core–shell nanoparticles (NPs) sandwiched with a Raman reporter (4-mercaptobenzoic acid, MBA)] as a probe. The clenbuterol in solution and the clenbuterol–ovalbumin conjugate previously coated on the test line of the ICA strip competed for limited antibody binding sites on the probe. The specific Raman scattering intensity of MBA on the test line was measured for the quantitative detection of clenbuterol. This proposed assay was completed within 15 min. The IC50 and limit of detection (LOD) values of the assay for clenbuterol were found to be 0.02 ng mL−1 and 0.24 pg mL−1, respectively. The relative standard deviations (RSD) of the signal obtained from 10 points along the middle part of the test line were within 4.3–8.7%. There was no cross-reactivity (CR) of the assay with ractopamine or phenylethanolamine A, and only 19% CR with salbutamol. The recoveries of clenbuterol from spiked swine urine samples were in the range of 93.8–112.4% with RSD values in range of 5.2–11.5% (n = 9). The proposed SERS-based ICA was demonstrated to be a rapid, simple and ultrasensitive analytical method for detecting clenbuterol in urine samples and could also be applied for the determination of other target analytes in different matrices.

CAS / MDL: 1074-36-8
研究领域: 分析化学 · 食品安全
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ANALYST · 2024 · IF 3.6

Fluorescent microsphere-based strip for sensitive and quantitative detection of etomidate and metomidate

Qingqing Liu,Aihua Qu,Chuanlai Xu,Xinxin Xu,Liqiang Liu,Hua Kuang

In this research, we used a novel hapten to generate a sensitive monoclonal antibody (mAb) 2C3 that targeted etomidate (ET) and metomidate (MT). We used this mAb to establish a lateral-flow immunoassay (LFIA) that incorporated fluorescent microsphere sensors, enabling both the qualitative and quantitative detection of ET and MT within 10 min. Analysis indicated that the visual colorimetric values for ET and MT in water samples were 0.3 µg/kg, respectively, with quantitative detection ranges of 0.08 to 1.31 µg/kg and 0.08 to 2.21 µg/kg, respectively. The visual colorimetric values for ET and MT in urine samples were 0.3 to 1 µg/kg, with quantitative detection ranges of 0.12 to 3.13 µg/kg and 0.09 to 2.98, respectively. The visual colorimetric values for ET and MT in serum samples were 3 µg/kg, with quantitative detection ranges of 0.15 to 21.2 µg/kg and 0.08 to 13.8 µg/kg, respectively. Recovery tests and detection were conducted in water, urine and serum samples, validating the reliability of this method in real clinical samples. Collectively, our novel LFIA provides a promising option for rapid on-site detection of ET and MT.

CAS / MDL: 25952-53-8 6066-82-6
研究领域: 医学检测 · 免疫学 · 分析化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Food Bioscience · 2025 · IF 5.9

Colloidal gold-based lateral flow immunoassay for detecting cyclosulfamuron residues in cereal samples

Lu Zeng,Huan Lv,Xiangrui Li,Wenjia Yang,Wencan Luo,Linghong Kong,Qiujin Zhu

Cyclosulfamuron (CS) is a widely used sulfonylurea herbicide in plant cultivation and food production, and poses significant threats to ecological balance and food safety. To address this concern, we designed a novel CS hapten using computer-simulated semi-antigens. A monoclonal antibody (mAb) exhibiting high specificity and affinity was generated, with an affinity constant of 1.049×10 9 L/mol and a semi-inhibitory concentration (IC 50 ) of 4.94 ng/mL. Leveraging this anti-CS mAb, we constructed a rapid, visually detectable, quantitative lateral flow immunoassay (LFIA) to detect CS in cereals. Under the optimal conditions, the cut-off values were determined to be 100 μg/kg for brown rice and corn samples and 50 μg/kg for rice samples. The corresponding limits of detection values (LODs) were found to be 1.93 μg/kg in brown rice, 2.18 μg/kg in corn and 1.93 μg/kg in rice, respectively. The recovery rates ranged from 96.2% to 104.8% with coefficients of variation ranging from 3.5% to 6.4%, showing good agreement with the results obtained by liquid chromatography–tandem mass spectrometry (LC–MS/MS). The proposed assay demonstrated robust analytical performance, with significant application potential for rapid, on-site detection.

研究领域: 食品安全 · 分析化学 · 免疫学
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RSC Advances · 2015 ·Vol. 5 ·期 96 ·78833-78840 · IF 3.84

A sensitivity-enhanced heterologous immunochromatographic assay based on a monoclonal antibody for the rapid detection of histamine in saury samples

Lin Luo,Jin-Yi Yang,Zhi-Li Xiao,Dao-Ping Zeng,Yong-Jun Li,Yu-Dong Shen,Yuan-Ming Sun,Hong-Tao Lei,Hong Wang,Zhen-Lin Xu

Histamine (HA) is an essential test item for fishery samples. However, the fast and effective determination of HA is difficult due to its simple structure and small molecular size. In this study, a sensitive and specific monoclonal antibody against p-nitrobenzoylated histamine (NPHA), which can be easily obtained from the reaction of HA and p-nitrobenzoic acid N-hydroxysuccinimide ester (PNBA-OSu) under mild conditions, was generated for the first time. Based on this mAb, an immunochromato-graphic assay strip (ICA strip) using a colloidal gold nano particles-antibody (GNPs) probe for rapid detection of HA in saury samples was established. After screening the coating antigens and optimization of analytical parameters, a heterologous coating based ICA strip exhibited the most excellent detection ability with a visual detection limit (VDL) of 6.0 mg kg−1 in qualitative experiments and a detection limit (by a strip reader) of 1.0 mg kg−1 in semi-quantitative experiments for saury samples, with no cross-reactivity with HA analogs. Good correlation between the ICA strip with liquid chromatography-tandem mass spectrometry was achieved for spiked and naturally contaminated saury samples. Overall, this method is suitable for screening of HA residue for large scale fish samples in a quick, simple and low-cost manner.

研究领域: 分析化学 · 食品安全 · 免疫学 · 分子诊断 · 兽药残留检测
✓ 已验证 DOI 高影响因子
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JOURNAL OF HAZARDOUS MATERIALS · 2021 · IF 10.588

Rational hapten design to produce high-quality antibodies against carbamate pesticides and development of immunochromatographic assays for simultaneous pesticide screening

Zi-Jian Chen,Hui-Ling Wu,Zhi-Li Xiao,Hui-Jun Fu,Yu-Dong Shen,Lin Luo,Hong Wang,Hong-Tao Lei,Surat Hongsibsong,Zhen-Lin Xu

Carbamate pesticides (CPs) are the most used pesticides in agricultural production and pest control. In this study, carbofuran , isoprocarb and carbaryl were employed as models, and a general hapten strategy based on carbamate moiety recognition was proposed. Molecular modeling of the three-dimensional (3D) structure and surface electrostatic potential of the CPs indicated that the amide group formed by conjugation significantly influenced recognition by antibodies. The proposed strategy was used to obtain three sensitive and specific monoclonal antibodies (mAbs) with IC 50 values of 1.4 ng/mL, 8.4 ng/mL and 13.8 ng/mL for carbofuran, isoprocarb and carbaryl, respectively. Negligible cross-reactivity (%) with analogs was observed, except for fenobucarb (84.6%) for isoprocarb. The obtained antibodies were used to develop an immunochromatographic assay (ICA) to simultaneously and quantitatively detect the three CPs. A strip reader was used to determine the limits of quantitation (LOQs) as 0.05 ng/mL (carbofuran), 31.3 ng/mL (isoprocarb) and 31.3 ng/mL (carbaryl). The recoveries of cucumber and Chinese cabbage samples ranged from 76% to 111%, with CVs from 1.3% to 10.6%, indicating good potential for the rapid simultaneous detection of multiple pesticide residues in a large batch of samples.

研究领域: 农业科学 · 免疫学
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