Detection of aflatoxin M1 in milk using spectroscopy and multivariate analyses

Pranita Jaiswal1, Shyam Narayan Jha1, Jaspreet Kaur1

  • 1Agricultural Structures and Environmental Control Division, Central Institute of Postharvest Engineering & Technology, Ludhiana 141004, India.

Food Chemistry
|September 5, 2017
PubMed

Insights

Aflatoxin M1 (AFM1) in milk can be rapidly detected and quantified using attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy and chemometrics. This method accurately identifies even low levels of AFM1, ensuring milk safety.

Area of Science:

  • Analytical Chemistry
  • Food Safety
  • Spectroscopy

Background:

  • Aflatoxin M1 (AFM1) is a carcinogenic mycotoxin found in milk from cows consuming contaminated feed.
  • Accurate and rapid detection of AFM1 is crucial for ensuring milk product safety and preventing public health risks.

Purpose of the Study:

  • To investigate the feasibility of using attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy combined with chemometrics for AFM1 detection in milk.
  • To develop a rapid and reliable method for quantifying AFM1 levels in bovine milk.

Main Methods:

  • Bovine milk samples were spiked with varying concentrations of AFM1 (0-0.1 μg/l).
  • Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectra were acquired for all samples.
  • Chemometric techniques, including Principal Component Analysis (PCA), SIMCA classification, and Partial Least Square (PLS) regression, were applied for data analysis.

Main Results:

  • ATR-FTIR spectra showed significant differences between pure and AFM1-spiked milk samples, particularly in the 1800-650 cm⁻¹ and 3689-3499 cm⁻¹ regions.
  • PCA demonstrated clear sample clustering (p≤0.05), indicating distinct spectral profiles based on AFM1 presence.
  • SIMCA models achieved >86% classification accuracy and successfully detected AFM1 at concentrations as low as 0.02 μg/l (p≤0.05).
  • PLS regression provided high prediction accuracy for AFM1 quantification (R²=0.99 for calibration, R²=0.98 for validation) in the 1800-650 cm⁻¹ range.

Conclusions:

  • ATR-FTIR spectroscopy coupled with chemometrics offers a feasible and effective approach for the rapid detection and quantification of AFM1 in milk.
  • The developed method demonstrates high sensitivity and accuracy, suitable for routine milk quality control and safety monitoring.