Dual Extraction Methods for Nitrofuran Antibiotics Residues; Furaltadone, Furazolidone, and Nitrofurazone from Biotransformation Assay

Zaidah Zainal ariffin
{"title":"Dual Extraction Methods for Nitrofuran Antibiotics Residues; Furaltadone, Furazolidone, and Nitrofurazone from Biotransformation Assay","authors":"Zaidah Zainal ariffin","doi":"10.32802/asmscj.2023.1188","DOIUrl":null,"url":null,"abstract":"This study aims to extract nitrofuran antibiotics residues, furaltadone, furazolidone, nitrofurazone from biotransformation assays by local Aspergillus tamarii KX610719.1. Nitrofuran antibiotics were quantified by using a high-performance liquid chromatography-diode array detector (HPLC-DAD). Liquid-liquid extraction (LLE) and solid phase extraction (SPE) were employed to extract nitrofurans residue for the optimal purification and cleaned up procedures. In this study, a good linearity with the coefficient of determination R² value of 0.9951 – 0.9972 mg/L with the concentration range of 1 to 50 mg/L nitrofuran antibiotics was achieved. The relative standard deviation (RSD) for triplicate nitrofurans assay were less than 10.0 %. The limit of detection (LOD) and limit of quantification (LoQ) of furazolidone, furaltadone and nitrofurazone were found to be in the range of 2.37 – 10.56 mg/L and 7.17 – 31.99 mg/L, respectively. Moreover, the recovery of the nitrofuran antibiotics investigated in biotransformation assays ranged from 70.0 % - 88.0 %. The developed technique was effectively employed to determine nitrofurans residue in biotransformation assays and demonstrated remarkable clean-up capacity.","PeriodicalId":503593,"journal":{"name":"ASM Science Journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ASM Science Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32802/asmscj.2023.1188","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

This study aims to extract nitrofuran antibiotics residues, furaltadone, furazolidone, nitrofurazone from biotransformation assays by local Aspergillus tamarii KX610719.1. Nitrofuran antibiotics were quantified by using a high-performance liquid chromatography-diode array detector (HPLC-DAD). Liquid-liquid extraction (LLE) and solid phase extraction (SPE) were employed to extract nitrofurans residue for the optimal purification and cleaned up procedures. In this study, a good linearity with the coefficient of determination R² value of 0.9951 – 0.9972 mg/L with the concentration range of 1 to 50 mg/L nitrofuran antibiotics was achieved. The relative standard deviation (RSD) for triplicate nitrofurans assay were less than 10.0 %. The limit of detection (LOD) and limit of quantification (LoQ) of furazolidone, furaltadone and nitrofurazone were found to be in the range of 2.37 – 10.56 mg/L and 7.17 – 31.99 mg/L, respectively. Moreover, the recovery of the nitrofuran antibiotics investigated in biotransformation assays ranged from 70.0 % - 88.0 %. The developed technique was effectively employed to determine nitrofurans residue in biotransformation assays and demonstrated remarkable clean-up capacity.
硝基呋喃类抗生素残留的双重萃取方法;生物转化试验中的呋喃他酮、呋喃唑酮和硝基呋喃酮
本研究的目的是提取本地曲霉 KX610719.1 在生物转化实验中残留的硝基呋喃类抗生素、呋喃他酮、呋喃唑酮、硝基呋喃酮。使用高效液相色谱-二极管阵列检测器(HPLC-DAD)对硝基呋喃类抗生素进行定量。采用液液萃取(LLE)和固相萃取(SPE)提取硝基呋喃类药物残留物,以优化纯化和净化程序。在 1 至 50 mg/L 硝基呋喃类抗生素浓度范围内,该方法线性关系良好,测定系数 R² 值为 0.9951 - 0.9972 mg/L。一式三份硝基呋喃类抗生素检测结果的相对标准偏差(RSD)均小于 10.0%。呋喃唑酮、呋喃他酮和硝呋酮的检出限(LOD)和定量限(LoQ)分别为 2.37 - 10.56 mg/L 和 7.17 - 31.99 mg/L。此外,在生物转化试验中调查的硝基呋喃类抗生素的回收率在 70.0 % - 88.0 % 之间。所开发的技术可有效测定生物转化实验中硝基呋喃类药物的残留量,并具有显著的净化能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
文献相关原料
公司名称 产品信息 采购帮参考价格
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信