Detection of Multiple Antibiotic Residues in Turkish Pine and Blossom Honeys Using LC–MS/MS Method

Author:

Gün Ramazan12ORCID,Dursun İnan23,Arıcı Buket2,Saraç Yasemin4

Affiliation:

1. Department of Nutrition and Dietetics Faculty of Health Sciences Bingöl University Bingöl 12000 Turkey

2. Central Laboratory Application and Research Center Bingöl University Bingöl 12000 Turkey

3. Department of Beekeeping Vocational School of Food Agriculture and Livestock 12000 Bingöl University Bingöl Turkey

4. Sem Laboratuar Cihazlari Pazarlama San. ve Tic. Inc. R&D Center Istanbul 34746 Turkey

Abstract

AbstractDue to the high demand for honey, beekeepers often feed the bees with antibiotics to protect honeybees against illnesses; the determination of veterinary drugs and their residues in bee products especially in honey is gaining importance. In this study, commercially available 15 different brands, a total of 22 honey (14 blossoms and 8 pines) samples obtained from 5 chain supermarkets in the city of Bingöl and Diyarbakır, Turkey were analysed for 29 antibiotic residues. These antibiotics belong to 10 different categories, including tetracyclines, aminoglycosides, macrolides, sulfonamides, fluoroquinolones, benzimidazoles, anthelmintic, amphenicols, quinolines, and oxazolidines. For the qualitative and quantitative determination of the antibiotics, a triple quadrupole liquid chromatography‐tandem mass spectrometry (LC‐MS/MS) was used. A total of 10 out of 22 honey (8 blossom, 57.14 % and 2 pine, 25 %) samples were found to be positive for antibiotics. Among the tested antibiotics, tetracycline, dihydrostreptomycin, streptomycin, erythromycin, and sulfadimidine were detected in the honey samples. Dihydrostreptomycin and sulfadimidine were detected in 6 samples, erythromycin was determined in 4 samples, streptomycin was found in 2 samples, and lastly, tetracycline was detected only in one sample. The highest and the lowest concentrations of antibiotics detected in the samples were dihydrostreptomycin and erythromycin found at the amount of 992.58 μg/kg and 0.77 μg/kg respectively. The proposed method was validated with a limit of quantification (LOQ) and limit of detection (LOD) ranging between 0.42 and 3.22 μg /kg and 0.13–0.97 μg /kg respectively. Good linearities were also achieved ranging between R2=0.987 and 0.999.

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

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