Abstract
Aflatoxins have posed serious threat to food safety and human health. Therefore, it is important to detect aflatoxins in samples rapidly and accurately. In this review, various technologies to detect aflatoxins in food are discussed, including conventional ones such as thin-layer chromatography (TLC), high performance liquid chromatography (HPLC), enzyme linked immunosorbent assay (ELISA), colloidal gold immunochromatographic assay (GICA), radioimmunoassay (RIA), fluorescence spectroscopy (FS), as well as emerging ones (e.g., biosensors, molecular imprinting technology, surface plasmon resonance). Critical challenges of these technologies include high cost, complex processing procedures and long processing time, low stability, low repeatability, low accuracy, poor portability, and so on. Critical discussion is provided on the trade-off relationship between detection speed and detection accuracy, as well as the application scenario and sustainability of different technologies. Especially, the prospect of combining different technologies is discussed. Future research is necessary to develop more convenient, more accurate, faster, and cost-effective technologies to detect aflatoxins.
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All data generated or analysed during this study are included in this published article.
Abbreviations
- ADC:
-
Analogue-digital-converter
- AFB1 :
-
Aflatoxin B1
- AFB2 :
-
Aflatoxin B2
- AFG1 :
-
Aflatoxin G1
- AFG2 :
-
Aflatoxin G2
- AFM1 :
-
Aflatoxin M1
- AFM2 :
-
Aflatoxin M2
- AFP1 :
-
Aflatoxin P1
- AFQ1 :
-
Aflatoxin Q1
- AuNPs:
-
Gold nanoparticles
- AuNRs:
-
Gold nanorods
- BSA:
-
Bovine albumin
- CM:
-
Chemical enhancement
- CMO:
-
Carboxymethoxylamine hemihydrochloride
- CTAB:
-
Cetyltrimethylammonium bromide
- dcFLISA:
-
Direct competitive fluorescence-linked immunosorbent assay
- ELISA:
-
Enzyme linked immunosorbent assay
- EM:
-
Electromagnetic enhancement
- FA:
-
Fluorescence anisotropy
- FLD:
-
Fluorescence detector
- FS:
-
Fluorescence spectroscopy
- GICA:
-
Colloidal gold immunochromatographic assay
- HLB:
-
Hydrophilic-lipophilic balance
- HPLC:
-
High performance liquid chromatography
- ICA:
-
Immunochromatographic assay
- KLH:
-
Keyhole limpet
- LED:
-
Light emitting diode
- LFIA:
-
Lateral flow immunoassay
- LLE:
-
Liquid-liquid extraction
- LOD:
-
Limit of detection
- LTP:
-
Low temperature partitioning
- MIPs:
-
Molecularly imprinted polymers
- MIT:
-
Molecular imprinting technology
- MRLs:
-
Maximum residue levels
- MOF:
-
Metal-organic framework
- MOFLISA:
-
MOF-linked immunosorbent assay
- OA:
-
Operational amplifier integrated circuit
- OVA:
-
Ovalbumin
- PBS:
-
Phosphate-buffered saline
- PBST:
-
Phosphate-buffered saline with Tween 20
- PRiME:
-
Process, robustness, improvements, matrix effects, ease of use
- QCM:
-
Quartz crystal microbalance
- QDs:
-
Quantum dots
- RIA:
-
Radioimmunoassay
- RSD:
-
Relative standard deviation
- SERS:
-
Surface-enhanced Raman scattering
- SPR:
-
Surface plasmon resonance
- TFA:
-
Trifluoroacetic acid
- TLC:
-
Thin-layer chromatography
- TMB:
-
Tetramethylbenzidine
- TMR:
-
Tetramethylrhodamine
- UHPLC-MS/MS:
-
Ultra-high performance liquid chromatography-tandem mass spectrometry
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This work was supported by the Beijing Municipal Commission of Education (grant no. PXM2019_014213_000007) and School Level Cultivation Fund of Beijing Technology and Business University for Distinguished and Excellent Young Scholars (grant no. BTBUYP2020).
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Shenqi Liu: Methodology, Investigation, Writing - Original Draft; Shanxue Jiang: Conceptualization, Methodology, Writing - Original Draft, Writing - Reviewing and Editing; Zhiliang Yao: Supervision, Funding acquisition, Writing - Reviewing and Editing; Minhua Liu: Supervision, Writing - Reviewing and Editing
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Liu, S., Jiang, S., Yao, Z. et al. Aflatoxin detection technologies: recent advances and future prospects. Environ Sci Pollut Res 30, 79627–79653 (2023). https://doi.org/10.1007/s11356-023-28110-x
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DOI: https://doi.org/10.1007/s11356-023-28110-x