2023
DOI: 10.1002/bab.2447
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Highly sensitive colorimetric aptasensor for 17β‐estradiol detection in milk based on the repetitive‐loop aptamer

Abstract: Trace of 17β‐estradiol (E2) contamination in food has been a concern for its negative impacts on human health, leading to the need for an E2‐monitoring system. This work reported a new simple, sensitive, and colorimetric E2 detection based on the designed repetitive‐loop aptamer and gold nanoparticles (AuNPs). The designed aptamers (L2–L5) exhibited a higher binding capability to E2 than the original truncated aptamer (L1). Although L3–L5 aptamers exhibited the highest binding capability, only L3‐aptasensor de… Show more

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Cited by 8 publications
(6 citation statements)
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“…The long-length aptamer exhibits a strong absorption on the surface of AuNPs, resulting in more stable dispersion of AuNPs and lower capability of the aptasensor to detect paraquat at low concentration. 30 Based on the C LOD values, the R3- and R4-aptasensors are 2.14 and 1.59 times more sensitive than the R1-aptasensor ( C LOD = 2.76 nM), respectively (Fig. 7(D)).…”
Section: Resultsmentioning
confidence: 97%
See 1 more Smart Citation
“…The long-length aptamer exhibits a strong absorption on the surface of AuNPs, resulting in more stable dispersion of AuNPs and lower capability of the aptasensor to detect paraquat at low concentration. 30 Based on the C LOD values, the R3- and R4-aptasensors are 2.14 and 1.59 times more sensitive than the R1-aptasensor ( C LOD = 2.76 nM), respectively (Fig. 7(D)).…”
Section: Resultsmentioning
confidence: 97%
“…The optimized pH was dened as the pH value that yielded the maximum absorbance ratio between A 650 and A 525 . Additionally, the optimization of temperature was determined by incubating AuNPs (7 nM) and aptamer (25 nM) at different temperatures (20,25,30,35, and 40 °C) for 30 min. Then, paraquat (50 nM) was added and incubated for an additional 30 min.…”
Section: Optimization For Experimental Conditionsmentioning
confidence: 99%
“…This operation effectively increased the compatibility between the aptamer and E2 as well as the performance of the sensor. In Pakawat Kongpreecha team’s work ( Kongpreecha et al, 2023 ), the E2 aptamer was required to wrap gold nanoparticles. Therefore, the original E2 aptamer (original E2 aptamer 22-mer (5′-GCC​GTT​TGG​GCC​CAA​GTT​CGG​C-3′)) structure was removed, and two to five loops were repeatedly added to determine which structure was most effective for E2 recognition.…”
Section: Various Biosensors For Detecting E2mentioning
confidence: 99%
“…(B) Remove and repeat the E2 aptamer structure. Reprinted with permission from Kongpreecha et al (2023) . (C) Split E2 aptamer.…”
Section: Various Biosensors For Detecting E2mentioning
confidence: 99%
“…27,28 Accordingly, developing efficient and sensitive methods for the monitoring of E2 levels is of great significance. So far, many different techniques have been established for the determination of E2, such as gas chromatography/ liquid chromatography-mass spectrometry (GC/LC-MS), 29,30 enzyme-linked immunosorbent assay (ELISA), 31,32 colorimetry, [33][34][35] fluorescence, [36][37][38][39] electrochemistry, [40][41][42][43][44][45][46] and surface-enhanced Raman spectroscopy. 47,48 Nevertheless, these methods might suffer from the high cost of devices, the need for high levels of technical skill, low sensitivity, cumbersome operation processes and the need for sample pretreatment.…”
Section: Introductionmentioning
confidence: 99%