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A portable Mid-Infrared spectroscopy-based approach was developed for the non-destructive and rapid (∼1 min) detection of aflatoxins in Aspergillus -infected peanuts, effectively addressing the challenges in screening biological samples. In this study, a total of 274 kernels were inoculated with Aspergillus flavus ( A. flavus , NRRL 3357 and AF13) strains of fungus. Spectral data of inoculated peanut kernels were collected by a field-deployable FT-IR system, and further analyzed by chemometrics. Reference results of aflatoxins levels in inoculated peanuts were determined by uHPLC-MS/MS analysis. Interestingly, aflatoxin M 1 was detected in A. flavus -infected peanut kernels, which was confirmed by its fragmentation pattern. Supervised classification algorithms, developed by OPLS-DA (orthogonal partial least squares discriminant analysis) and SIMCA (Soft independent modeling of class analogies) both achieved high sensitivity (94.7%) in identifying fungal contamination with aflatoxin levels exceeding 3 ppb. In addition, the regression algorithm, developed by PLSR (partial least squares regression), showed a strong regression correlation (Rpre=0.85) and excellent residual predictive deviation (RPD=6.2) for quantifying total aflatoxins level in individual kernels. The integration of this FT-IR system with advanced predictive algorithms provided a rapid, user-friendly, and non-invasive solution for detecting A. flavus -infected peanuts with aflatoxins and quantifying aflatoxin levels. This proposed method would offer the feasibility of doing routine, in-plant aflatoxin screening "on the go," offering a cost-effective and scalable alternative to labor-intensive wet chemistry methods (e.g., uHPLC-MS/MS). This study would also inspire further innovation in non-destructive and high-throughput screening technologies for food safety applications. • A portable FT-IR method was developed to detect aflatoxins in infected peanuts. • Challenges in non-destructively screening biological samples can be addressed. • Aflatoxin M1 was detected in A. flavus -infected peanut kernels. • Both detection and quantification of toxic metabolites, aflatoxins were evaluated. • Portable alternative method to traditional testing for in-situ assessment.
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Yao et al. (2024) studied this question.
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