“…requiring only a sample extraction step before use; 2. simplicity of procedure with single step, e.g., only adding test solution to the sample pad on the strip; 3. rapid on-site detection within a few minutes (5-15 min); 4. concentration levels of target analytes can be observed directly with the naked eyes; 5. user-friendly format no need for skill personnel; 6. less interference due to chromatographic separation; and 7. low cost Because of these advantages, lateral flow strip assay has become one of the commercial and widely-used immunoassays for rapid determination of mycotoxins, such as ochratoxin A (Lai et al, 2009;Liu, Tsao, Wang, & Yu, 2008;Wang, Liu, Xu, Zhang, & Wang, 2007;Cho et al, 2005), deoxynivalenol (Kolosova, De Saeger, Sibanda, Verheijen, & Van Peteghem, 2007;Xu et al, 2010;Kolosova et al, 2008), T-2 Toxin (Molinelli et al, 2008), zearalenone (Kolosova, De Saeger, Sibanda, Verheijen, & Van Peteghem, 2007), fumonisin B1 (Wang, Quan, Lee, & Kennedy, 2006), aflatoxins (Sun, Zhao, Tang, Zhou, & Chu, 2005;Sheibani, Tabrizchi, & Ghaziaskar, 2008) and so on. The visual detection limit (VDL), defined as the minimum concentration producing the color on the test line significantly different or weaker to that on the test line of negative control strip without aflatoxin (Li, Wei, Yang, Li, & Deng, 2009;Zhou et al, 2009), was used to express the sensitivity of the lateral flow strip assay. The visual detection limit of published conventional lateral flow strip assay for aflatoxins are summaried in Table 2.…”