Abstract

Nontargeted analysis can be used for the rapid screening and confirmatory analysis of veterinary drugs and their metabolites, which are important for the comprehensive safety evaluation of animal-derived foods. Here, a novel nontargeted screening approach based on liquid chromatography coupled with electrospray ionization–high-resolution mass spectrometry (LC/ESI–HR-MS) was developed to determine erythromycin, clarithromycin, and their metabolites in chicken liver microsomes. Erythromycin and clarithromycin were incubated in vitro in the presence of NADPH for 60 min to generate metabolites in chicken liver microsomes. After the incubation, the supernatant was extracted using ultrasonic shaking, orbital shaking, and centrifugation before analysis using LC/ESI-HR-MS in positive ion mode on an Agilent Eclipse Plus C18 column (100 mm × 2.1 mm; i.d. 3.5 µm) with 0.1 percent formic acid-water and acetonitrile as the mobile phases for gradient elution at 0.4 mL/min. The results show that erythromycin can produce N-desmethyl-erythromycin A in chicken liver microsomes, but clarithromycin cannot produce N-desmethyl-clarithromycin in chicken liver microsomes. The N-desmethyl-erythromycin A and N-desmethyl-clarithromycin were tentatively identified in chicken liver microsomes using the established quick analytic method, which will provide a theoretical foundation for future research on pharmacokinetics and drug elimination in poultry.

Highlights

  • Erythromycin (ERY) and clarithromycin (CLA) are macrolide antibiotics (MACs) with broad-spectrum antibacterial activity and have effects on both Gram-positive and Gramnegative bacteria

  • Chicken liver microsomes contain human isoenzymes of CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP450 3A4 (CYP3A4), which were evaluated by PRIMACYT GmbH (Schwerin, FRG, Germany)

  • This study verified whether ERY and CLA produced N-desmethyl-erythromycin A and N-desmethyl-clarithromycin in chicken liver microsomes

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Summary

Introduction

Erythromycin (ERY) and clarithromycin (CLA) are macrolide antibiotics (MACs) with broad-spectrum antibacterial activity and have effects on both Gram-positive and Gramnegative bacteria. The antibacterial mechanism of ERY and CLA involves irreversible binding to the 50S subunit of the bacterial ribosome and selective inhibition of protein synthesis by blocking transpeptidation and mRNA displacement, which is the same as the antibacterial mechanism of chloramphenicol [1,2]. MACs are mainly used to treat diseases caused by aerobic Gram-positive and Gram-negative cocci, anaerobic bacteria, Legionella, Mycoplasma, and Chlamydia. Soluble erythromycin thiocyanate powder has been used as a veterinary medicine to treat chickens artificially infected with chronic respiratory diseases [3]. The toxicity of this type of antibiotic is low, unreasonable or excessive use can lead to contamination of animal-derived food and an increase in resistant strains that pose risks to humans. MACs and their metabolites will damage human health once swallowed and accumulated to a sufficient concentration in the body [4,5,6]

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