Abstract

To develop a new simple and simultaneous purification method for mycotoxins in feeds and grains, magnetic nanoparticles (MNPs) conjugated with monoclonal antibodies (mAbs) against mycotoxins were used to separate aflatoxin B1 (AFB1), zearalenone (ZEA) and deoxynivalenol (DON). For a single spike of each mycotoxin into the buffer solution (16% MeOH in PBS), mean recoveries were 93.1–95.0% for AFB1 (5–20 ng/mL spiked), 87.2–96.0% for ZEA (125–500 ng/mL spiked) and 75.2–96.9% for DON (250–1,000 ng/mL spiked) by HPLC and ELISA. Recoveries of AFB1 (20 ng/mL) and ZEA (500 ng/mL) simultaneously spiked into the buffer solution were 87.0 and 99.8%, respectively. Recovery rates of AFB1/DON and DON/ZEA spiked simultaneously were 86.2%/76.6% and 92.0%/86.7%, respectively, at concentrations of 20 ng/mL AFB1, 500 ng/mL ZEA, and 1,000 ng/mL DON. Recoveries using the novel mAb–MNP conjugated system in a buffer solution simultaneously spiked with AFB1, ZEA and DON were 82.5, 94.6 and 73.4%, respectively. Recoveries of DON in animal feed were 107.7–132.5% at concentrations of 250–1,000 ng/g spiked in feed. The immunoaffinity chromatography (IAC) clean-up method was compared with the purification method using novel mAb–MNP. After fortification of animal feed with AFB1 (5, 10 and 20 ng/g feed) and ZEA (125, 250 and 500 ng/g feed), AFB1 and ZEA were purified using both the methods. In the case of the novel mAb-MNP conjugated system, mean recoveries for AFB1 were 89.4, 73.1 and 88.3% at concentrations of 5, 10 and 20 ng/g feed, respectively. For ZEA, mean recoveries were 86.7, 85.9 and 79.1% at concentrations of 125, 250 and 500 ng/g, respectively. For IAC purification, recoveries were 42.9–45.1% for AFB1 and 96.8–103.2% for ZEA. In conclusion, the present purification method using monoclonal antibodies conjugated to MNPs can be used for simple and simultaneous purification of mycotoxins from feed and maize.

Highlights

  • Mycotoxins produced by fungi in grains and animal feeds threaten animal and human health

  • magnetic nanoparticles (MNPs) were coupled with monoclonal antibodies (mAbs) against their specific mycotoxins: A­ FB1, ZEA and DON

  • The recovery of each mycotoxin from the spiked buffer solution was confirmed by High-performance liquid chromatography (HPLC) and enzyme-linked immunosorbent assay (ELISA)

Read more

Summary

Introduction

Mycotoxins produced by fungi in grains and animal feeds threaten animal and human health. High-performance liquid chromatography (HPLC) [1], and HPLC—tandem mass spectrometric methods [2] have been used to quantitatively determine toxin concentrations in grains and biological samples, these methods require expensive, time-consuming extraction steps, which require use of hazardous organic solvents. To replace these steps, immunoaffinity chromatography (IAC) combined with antibodies has become a popular method. The present study aimed to develop an advanced multi-purification tool for three mycotoxins in animal feed and grains using mAbs for each mycotoxin and MNPs to facilitate purification by magnetism

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call