Literature DB >> 20619994

Differential heat stability of amphenicols characterized by structural degradation, mass spectrometry and antimicrobial activity.

Catherine A Franje1, Shao-Kuang Chang, Ching-Lin Shyu, Jennifer L Davis, Yan-Wen Lee, Ren-Jye Lee, Chao-Chin Chang, Chi-Chung Chou.   

Abstract

Heat stability of amphenicols and the relationship between structural degradation and antimicrobial activity after heating has not been well investigated. Florfenicol (FF), thiamphenicol (TAP), and chloramphenicol (CAP) were heated at 100 degrees C in water, salt water, soybean sauce and chicken meat for up to 2h. Degradation and antimicrobial activity of the compounds was evaluated using capillary electrophoresis (CE) with UV-DAD spectrometry, minimum inhibitory concentration (MIC) assay, and gas chromatography with electron impact ionization mass spectrometry (GC-EI-MS). Heat stability of amphenicols in matrices was ranked as water> or =salt water>soybean sauce>meat, suggesting that heat degradation of amphenicols was accelerated in soybean sauce and was not protected in meat. Heat stability by drug and matrices was ranked as FF>TAP=CAP in water, FF=TAP>CAP in salt water, TAP> or =FF=CAP in soybean sauce, and TAP> or =FF=CAP in meat, indicating differential heat stability of amphenicols among the 3 drugs and in different matrices. In accordance with the less than 20% degradation, the MIC against Escherichia coli and Staphylococcus aureus did not change after 2h heating in water. A 5-min heating of amphenicols in water by microwave oven generated comparable percentage degradation to boiling in water bath for 30 min to 1h. Both CE and GC-MS analysis showed that heating of FF produced TAP but not FF amine as one of its breakdown products. In conclusion, despite close similarity in structure; amphenicols exhibited differential behavior toward heating degradation in solutions and protein matrices. Although higher degradations of amphenicols were observed in soybean sauce and meat, heating treatment may generate product with antimicrobial activity (FF to TAP), therefore, heating of amphenicol residues in food cannot always be assumed safe. Copyright (c) 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20619994     DOI: 10.1016/j.jpba.2010.06.013

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  9 in total

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Review 5.  Reducing Veterinary Drug Residues in Animal Products: A Review.

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6.  The Food Anti-Microbials β-Phenylethylamine (-HCl) and Ethyl Acetoacetate Do Not Change during the Heating Process.

Authors:  Shelley M Horne; Angel Ugrinov; Birgit M Prüβ
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7.  Florfenicol As a Modulator Enhancing Antimicrobial Activity: Example Using Combination with Thiamphenicol against Pasteurella multocida.

Authors:  Chia-Fong Wei; Jui-Hung Shien; Shao-Kuang Chang; Chi-Chung Chou
Journal:  Front Microbiol       Date:  2016-03-30       Impact factor: 5.640

8.  The degradation mechanism of toxic atractyloside in herbal medicines by decoction.

Authors:  Liang-Yu Chen; Anren Hu; Chih-Jui Chang
Journal:  Molecules       Date:  2013-02-05       Impact factor: 4.411

9.  Biodegradation of Tetracycline Antibiotics by the Yeast Strain Cutaneotrichosporon dermatis M503.

Authors:  Hao Tan; Delong Kong; Qingyun Ma; Qingqing Li; Yiqing Zhou; Xu Jiang; Zhiye Wang; Rebecca E Parales; Zhiyong Ruan
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  9 in total

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