Skip to main content
Log in

Determination of 8α-hydroxymutilin as a Marker Residue for Tiamulin in Swine Tissue by Liquid Chromatography-Tandem Mass Spectrometry

  • Published:
Food Analytical Methods Aims and scope Submit manuscript

Abstract

Tiamulin is a semi-synthetic derivative of the natural antibiotic pleuromutilin and is widely used as a veterinary drug for swine. Herein, we report the development of a sensitive and reliable method for determining 8α-hydroxymutilin as a marker residue for tiamulin in swine tissue using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The method consists of sample extraction with acetone, defatting by acetonitrile/hexane partitioning, hydrolysis of the tiamulin metabolites to 8α-hydroxymutilin under alkaline conditions, liquid-liquid extraction with ethyl acetate, cleanup using a primary secondary amine cartridge, and LC-MS/MS analysis. The developed method was validated for 8α-hydroxymutilin in swine muscle, fat, and liver at two levels, namely 0.01 mg/kg and the maximum residue limits established in Japan (i.e., 0.1 mg/kg for swine muscle and fat, and 0.6 mg/kg for liver). The trueness ranged from 82 to 89%, and the relative standard deviations ranged from 1 to 3%. No chromatographic interference was observed near the retention time of 8α-hydroxymutilin, and matrix effects were negligible for all matrices, suggesting that the cleanup protocol was effective. The calibration curve was linear in the 0.005–0.5 μg/mL range, with a coefficient of determination greater than 0.997. The developed method enabled accurate quantification using solvent-based calibration without compensating for matrix effects and losses during sample preparation. The limit of detection of the method was 0.0005 mg/kg for each matrix. The developed method is suitable for regulatory-purpose analysis of 8α-hydroxymutilin as a marker residue for tiamulin as defined by the European Union and several other countries.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

Download references

Funding

This study was supported by the Ministry of Health, Labour and Welfare of Japan (grant number 19KA1002).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Shizuka Saito-Shida.

Ethics declarations

Conflict of Interest

Shizuka Saito-Shida declares no conflict of interest. Nao Kashiwabara declares no conflict of interest. Satoru Nemoto declares no conflict of interest. Hiroshi Akiyama declares no conflict of interest.

Ethical Approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Informed Consent

Not applicable.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

ESM 1

(DOCX 121 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Saito-Shida, S., Kashiwabara, N., Nemoto, S. et al. Determination of 8α-hydroxymutilin as a Marker Residue for Tiamulin in Swine Tissue by Liquid Chromatography-Tandem Mass Spectrometry. Food Anal. Methods 14, 845–855 (2021). https://doi.org/10.1007/s12161-020-01950-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12161-020-01950-w

Keywords

Navigation