2010
DOI: 10.1007/s11947-010-0397-2
|View full text |Cite
|
Sign up to set email alerts
|

Detection of Deoxynivalenol Using Fluorescence Excitation–Emission Matrix

Abstract: Deoxynivalenol (DON) is an acutely toxic mycotoxin produced in wheat and other cereal grains when exposed to fungi such as Fusarium spp. In this study, DON aqueous samples at seven concentration levels were examined using the excitation-emission matrix (EEM). EEM is a graph composed of an excitation wavelength axis, an emission wavelength axis, and a fluorescence intensity axis. It is acquired by measuring the fluorescence intensity of a sample at consecutive excitation and emission wavelengths. The EEM of DON… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
12
0
1

Year Published

2011
2011
2020
2020

Publication Types

Select...
9

Relationship

3
6

Authors

Journals

citations
Cited by 34 publications
(13 citation statements)
references
References 14 publications
0
12
0
1
Order By: Relevance
“…First, data whose excitation wavelength was longer than that of the emission wavelength was removed, since fluorescence is defined as light emission with longer wavelengths than the excitation light. Next, the first-, second-and third-order scattered lights, which occurred at wavelengths where the emission wavelength was equal to, twice, and three times the excitation wavelength, respectively (Fujita et al, 2010), were removed. Finally, the wavelength conditions where excitation wavelengths were shorter than 230 nm or longer than 500 nm were removed, as there was significant noise that would increase the estimation error.…”
Section: Pls Model For Prediction Of Maturation Indices Three Partialmentioning
confidence: 99%
“…First, data whose excitation wavelength was longer than that of the emission wavelength was removed, since fluorescence is defined as light emission with longer wavelengths than the excitation light. Next, the first-, second-and third-order scattered lights, which occurred at wavelengths where the emission wavelength was equal to, twice, and three times the excitation wavelength, respectively (Fujita et al, 2010), were removed. Finally, the wavelength conditions where excitation wavelengths were shorter than 230 nm or longer than 500 nm were removed, as there was significant noise that would increase the estimation error.…”
Section: Pls Model For Prediction Of Maturation Indices Three Partialmentioning
confidence: 99%
“…On the other hand, fluorescence fingerprint (FF), also known as excitation-emission matrix (EEM), is a series of fluorescence emission spectra acquired at consecutive excitation wavelengths (Tsuta et al, 2007;Fujita et al, 2010). The pattern of an FF diagram is unique for each constituent, like a fingerprint, making it possible to identify a particular sub- and were not fluorescence.…”
Section: Methodsmentioning
confidence: 99%
“…Preprocessing of FF data FF data were preprocessed for statistical analysis on the basis of previous studies (Fujita et al, 2010;Shibata et al, 2011). Fluorescence is an emission with a longer wavelength than excitation (Karoui and Blecker 2011).…”
Section: Ffs Of Aflatoxin Solutionsmentioning
confidence: 99%
“…Measurement using an excitation /fluorescence matrix that is obtained by scanning continuously both the excitation wavelength and fluores-cent wavelength and by measuring the fluorescence intensity has been attempted [10]. Sugiyama, who gave a name "fluorescent fingerprint" to this excitation emission matrix, conducted determination of the production area of mango, simultaneous quantitative determination of mycotoxin, and estimation of the mixing ratio of buckwheat and flour by fluorescent fingerprints created using excitation wavelengths of 200-340 nm and an analysis method using partial least squares regression analysis, demonstrating that fluorescent fingerprints can be applied to food/crops containing various ingredients [11].…”
Section: Ultra Violet (Uv)mentioning
confidence: 99%