4.7 Article

Visual-afterglow dual-mode immunochromatographic strip for 17β-estradiol detection in milk

期刊

TALANTA
卷 232, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2021.122427

关键词

Afterglow; Dual-mode; Immunochromatographic strip; Estradiol; Milk

资金

  1. National Natural Science Foundation of China [21876066]
  2. National First-Class Discipline Program of Food Science and Technology [JUFSTR20180301]
  3. Science and Technology Project of Jiangsu Market Supervision Administration [KJ204131]
  4. Hebei Medical Science Research Project [20212039, 20211856]

向作者/读者索取更多资源

Continuous intake of 17 beta-estradiol (E2) residue from animal-derived food can pose health risks to consumers, making rapid and sensitive E2 detection essential. A dual-mode ICS strategy was developed for this purpose, with an afterglow detection mode achieving a limit of detection of 0.5 ng/mL, twenty times more sensitive than the visual mode. This strategy has been successfully applied to detect estradiol in milk and validated by HPLC-FLD.
The continuous intake of 17 beta-estradiol (E2) residue from animal-derived food may pose a threat to the health of consumers, so the rapid screen and detection of E2 is very necessary. Although visual immunochromatographic strip (ICS) has played a great role in food safety control such as the screen of many food contaminants, it cannot meet the requirements for E2 detection due to the insufficient sensitivity of traditional visual ICS and the low concentration range of estrogen in food. Here, we developed a dual-mode ICS strategy to achieve rapid and highly sensitive detection of E2. Based on the visual detection mode of a competitive ICS, the afterglow detection mode working in fluorescence resonance energy transfer mechanism was introduced by using the afterglow particles (APs) as energy donor and gold nanoparticles (AuNPs) as energy acceptor. In this method, large APs of micron size with superior afterglow were applied as the test zone-fixed fluorescence signal source, thus the contradiction between migration and afterglow characteristics was skillfully resolved. In addition, a 6 W UV lamp was used as the light source to excite APs, and a smartphone was used to capture an image of 0.5 s after the UV light was turned off to effectively remove the autofluorescence from the strips and improve the signal-to-noise ratio. The limit of detection of this afterglow mode was 0.5 ng/mL, twenty times more sensitive than that of visual mode (10 ng/mL). The strategy has been successfully applied to the detection of estradiol in milk and verified by HPLC-FLD.

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