4.7 Article

Direct Use of a Saliva-Collected Cotton Swab in Lateral Flow Immunoassay for the Detection of Cotinine

期刊

BIOSENSORS-BASEL
卷 12, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/bios12040214

关键词

lateral flow immunoassay; on-site salivary test; cotinine detection; point of care; smoking test; saliva test

资金

  1. National Research Foundation of Korea (NRF) - Korean government (MSIT) [NRF-2021R1A2B5B03001417]
  2. BioNano Health-Guard Research Center - Ministry of Science, ICT & Future Planning (MSIP) of Korea as Global Frontier Project [H-GUARD_NRF-2019M3A6B2060097]

向作者/读者索取更多资源

In this study, a modified paper-based lateral flow immunoassay (LFIA) called gap-LFIA was developed for the direct detection of saliva collected using cotton swabs. The method reduced interference and improved signals, allowing for the direct use of whole saliva without additional steps. Compared to traditional methods, the gap-LFIA showed less deviation in results and enabled clearer distinction between smokers and non-smokers.
The detection of salivary cotinine is useful for convenient smoking tests in spite of the high background effect of saliva. For precise results, the conventional salivary cotinine analysis for smoking detection requires complex pretreatment processes. Hence, in this study, we developed a modified paper-based lateral flow immunoassay (LFIA), termed gap-LFIA, for the direct application of saliva collected using cotton swabs for on-site detection. The gap-LFIA was constructed by modifying a conventional LFIA sensor, where the sample pad was divided to have a 3 mm gap. A saliva-collected cotton swab was inserted into the gap, and then, a buffer solution was added to the outer sample pad to dilute the saliva automatically. The gap-LFIA reduced the interference in salivary samples and showed improved signals, allowing for using the whole saliva directly without additional steps. Further, the deviation of results using a strip was less than that when the saliva was not diluted in a conventional cotinine kit, and it helped to distinguish between smokers and non-smokers more clearly in 15 min. This method of automatic dilution may apply to various clinical samples, including blood and serum, for direct application in future detections.

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