2020
DOI: 10.1007/s00604-020-4192-0
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Aptamer and gold nanorod–based fumonisin B1 assay using both fluorometry and SERS

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Cited by 44 publications
(28 citation statements)
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“…So far, two aptamers composed by 96 and 80 nucleotides, have been reported through SELEX and utilized in different biosensing approaches [148,149], all the aptamer-based sensors are chronologically described in Table 5, while the binding and functionalization conditions are illustrated in Table 6. From the 31 aptasensors found in the literature, 24 utilized the 96 nt aptamer [148], one method applied a shortened version (60 nt) from this first sequence [159], one platform included the second 80 nt aptamer [156], two biosensors manipulated a condensed version (40 nt) of the second main aptamer [164,167], and three references did not specify their single-stranded (ss) DNA sequence [175,177,198]. The schematic representation of each type of aptasensor assay is illustrated in Fig 6a a for the biosensors involving the initial 96 nt aptamer, and in Fig 6b for the application of the subsequent and not specified aptamers.…”
Section: Other Methodsmentioning
confidence: 99%
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“…So far, two aptamers composed by 96 and 80 nucleotides, have been reported through SELEX and utilized in different biosensing approaches [148,149], all the aptamer-based sensors are chronologically described in Table 5, while the binding and functionalization conditions are illustrated in Table 6. From the 31 aptasensors found in the literature, 24 utilized the 96 nt aptamer [148], one method applied a shortened version (60 nt) from this first sequence [159], one platform included the second 80 nt aptamer [156], two biosensors manipulated a condensed version (40 nt) of the second main aptamer [164,167], and three references did not specify their single-stranded (ss) DNA sequence [175,177,198]. The schematic representation of each type of aptasensor assay is illustrated in Fig 6a a for the biosensors involving the initial 96 nt aptamer, and in Fig 6b for the application of the subsequent and not specified aptamers.…”
Section: Other Methodsmentioning
confidence: 99%
“…Three studies published by the same research group did not specify the aptamers sequence for the detection of FB1. The first approach relied on the hybridization of Cy5.5-aptamer and its cDNA on gold nanorods, with a further measurement of their SERS (LOD: 0.0003 µg/L) and fluorescent (LOD:0.0005 µg/L) signals under the presence of the target mycotoxin [175]. The second work, which so far is the most sensitive aptasensor for FB1, was reported with a LOD of 0.000003 µg/L.…”
Section: Not Specified Sequences and Alternative Methodsmentioning
confidence: 99%
“…and inorganic nanomaterials (graphene, [34][35][36] boron nitride, [37][38][39] semiconductor, [40][41][42] etc.). The metal substrates have been shaped into spheres, [43,44] rods, [45][46][47] stars, [48][49][50][51] internal nanogaps, [52,53] and so on. As a permutation and combination of the former two terms, gold nanostar is more adopted one on account of the following reasons: Gold has the advantages of chemical inertness, shape and size controllability, and good biocompatibility.…”
Section: Design Of Responsive Sers Probesmentioning
confidence: 99%
“…On the other hand, the lack of highly affinitive, specific, and reliable aptamers for other mycotoxins becomes a major hindrance to expanding the scope of targets. A new study made breakthrough on this aspect by developing a SERS and fluorescence dual detection of FB 1 (D. He et al., 2020). In a more recent work, they applied a similar strategy for simultaneous detection of ZEN, OTA, and FB 1 by constructing an AuNP–upconversion nanoparticle (UCNP)–AuNP trimer (Z. Wu et al., 2020).…”
Section: Sers Detection With Specific Recognitionmentioning
confidence: 99%