2023
DOI: 10.1016/j.talanta.2023.124388
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Nanobody-based magnetic chemiluminescence immunoassay for one-pot detection of ochratoxin A

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Cited by 12 publications
(6 citation statements)
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“…A linear relationship existed between the changed absorbance and logarithm concentration of OTA within the range of 20–500 μg L –1 (Figure c), and the linear equation was fitted as y = −2.98 log­( c OTA /μg L –1 ) + 0.88 ( R 2 = 0.984). The limit of detection (LOD) was estimated to be 4.79 μg L –1 according to the equation LOD = 3 × σ/ S , where σ is the blank standard deviation, and S is the slope of the calibration curve. , Table S3 summarizes the analytical performance of previously reported work on OTA identification. This work is not outstanding in terms of detection limit since riboswitch biosensor analytical methods are just in their infancy. , The aptamer domain sequence of the riboswitch is highly conserved, and the aptamer domain and expression platform domain reporter genes are relatively independent, which means that multiple signal output forms can be achieved by changing the type of reporter gene or various target detection by changing aptamer.…”
Section: Resultsmentioning
confidence: 99%
“…A linear relationship existed between the changed absorbance and logarithm concentration of OTA within the range of 20–500 μg L –1 (Figure c), and the linear equation was fitted as y = −2.98 log­( c OTA /μg L –1 ) + 0.88 ( R 2 = 0.984). The limit of detection (LOD) was estimated to be 4.79 μg L –1 according to the equation LOD = 3 × σ/ S , where σ is the blank standard deviation, and S is the slope of the calibration curve. , Table S3 summarizes the analytical performance of previously reported work on OTA identification. This work is not outstanding in terms of detection limit since riboswitch biosensor analytical methods are just in their infancy. , The aptamer domain sequence of the riboswitch is highly conserved, and the aptamer domain and expression platform domain reporter genes are relatively independent, which means that multiple signal output forms can be achieved by changing the type of reporter gene or various target detection by changing aptamer.…”
Section: Resultsmentioning
confidence: 99%
“…Kloeckera apiculata strains 3187, 3188, 3189, 3197, 3198, and 3200 can eliminate between 25 and 40% of OTA (0.006 µg/mL) over 20 days [292]. In addition, Zou et al [151] demonstrated that an employed UV-mutated Aspergillus niger (FS-UV-21) exhibited an impressive OTA degradation efficiency up to 89.4% under specific conditions, resulting in a substantial reduction of thein OTA cytotoxic effects of treated food. Finally, Fiori et al [293], tested the capacity of viable and nonviable yeast strains to adsorb OTA, demonstrating that strains of Candida friedrichii, C. intermedia, Lachancea thermotolerans, and Cyberlindnera jadinii within an 8-day period exhibited OTA adsorption percentages of 70, 73, 75%, and no significant adsorption, respectively, whether vital, and 72, 74, 84, and 82% after autoclaving, respectively.…”
Section: Microorganisms and Enzymesmentioning
confidence: 99%
“…Among the Ab fragments, Nbs with the smallest antigen‐binding domain have demonstrated superior properties than natural Abs for the fabrication of immunosensors. This is benefited from their variety of fascinating characteristics which includes minimal size (a cylindrical shape with ∼2.5 nm in diameter and 4 nm in height), enhanced tolerance to extreme temperature or pH levels, higher loading density on the carriers, easier incorporation of additional functionality, and preparation of multivalent nanobodies (Zuo, Wang et al., 2023). Another leading advantage of Nbs is their higher tolerance to organic solvents, facilitating their applications in the determination of mycotoxins extracted or eluted with organic solvents.…”
Section: Recognition Elements (Ab and Aptamer) In Preparing Mycotoxin...mentioning
confidence: 99%