Cristina Ribeiro, M. T. Martins, L. Jank, F. Barreto, R. Hoff, J. Arsand
{"title":"DEVELOPMENT AND VALIDATION OF A SIMPLE AND FAST METHOD FOR SULFONAMIDES, TETRACYCLINES AND MACROLIDES IN HONEY USING LC-MS/MS","authors":"Cristina Ribeiro, M. T. Martins, L. Jank, F. Barreto, R. Hoff, J. Arsand","doi":"10.22456/2527-2616.84248","DOIUrl":null,"url":null,"abstract":"Antibacterial are widely used in veterinary applications for diseases treatment and prophilatic purposes. Inadequate uses of these drugs can lead of undesirable residues in honey for consumption. In Brazil, the legal authorities set a maximum residue limit (MRL) for different compound in honey, ranging from 10 to 20 ng ml-1. The monitoring of antibacterials is a concern, since it constitutes a risk to human health and collaborates with the growth of resistant bacteria. Brazil has the National Residue Control Plan (NRCP) to ensure that the products traded are compliant with the safety and quality criteria required by consumers. The goal of this work was to develop and validate a method suitable to determine sulfonamides, tetracyclines and macrolides in honey, using liquid chromatography tandem mass spectrometry. The main objective was to develop an efficient technique, combining simplicity, speed and low cost, since the method will be employed in routine analysis. Recoveries between 36 to 139% were obtained. Good linearity (r2) above 0.95, considering three different days, for all drugs was achieved in concentrations ranging from 0 to 200% of the MRL. Intraday and inter-day precision with CV% (n=6) lower than 18%, in agreement with specifications were obtained in concentrations ranging from 0.5 to 1.5 MRL, except for erythromycin. Accuracy was between 97 to 108%. Limits of quantitation for macrolides were 2.5 ng g-1and for sulfonamides and tetracyclines were 5 ng g-1. Decision limit (CCα) was evaluated and the results obtained were between 12.9 to 28.1 ng g-1. The detection capability (CCβ) obtained was between 15.8 to 36.3 ng g-1. The proposed method demonstrated to be suitable for this intended purpose and will contribute to antibacterial honey monitoring.","PeriodicalId":11314,"journal":{"name":"Drug Analytical Research","volume":"15 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Analytical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22456/2527-2616.84248","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Antibacterial are widely used in veterinary applications for diseases treatment and prophilatic purposes. Inadequate uses of these drugs can lead of undesirable residues in honey for consumption. In Brazil, the legal authorities set a maximum residue limit (MRL) for different compound in honey, ranging from 10 to 20 ng ml-1. The monitoring of antibacterials is a concern, since it constitutes a risk to human health and collaborates with the growth of resistant bacteria. Brazil has the National Residue Control Plan (NRCP) to ensure that the products traded are compliant with the safety and quality criteria required by consumers. The goal of this work was to develop and validate a method suitable to determine sulfonamides, tetracyclines and macrolides in honey, using liquid chromatography tandem mass spectrometry. The main objective was to develop an efficient technique, combining simplicity, speed and low cost, since the method will be employed in routine analysis. Recoveries between 36 to 139% were obtained. Good linearity (r2) above 0.95, considering three different days, for all drugs was achieved in concentrations ranging from 0 to 200% of the MRL. Intraday and inter-day precision with CV% (n=6) lower than 18%, in agreement with specifications were obtained in concentrations ranging from 0.5 to 1.5 MRL, except for erythromycin. Accuracy was between 97 to 108%. Limits of quantitation for macrolides were 2.5 ng g-1and for sulfonamides and tetracyclines were 5 ng g-1. Decision limit (CCα) was evaluated and the results obtained were between 12.9 to 28.1 ng g-1. The detection capability (CCβ) obtained was between 15.8 to 36.3 ng g-1. The proposed method demonstrated to be suitable for this intended purpose and will contribute to antibacterial honey monitoring.
抗菌药物广泛应用于兽医疾病治疗和生殖目的。这些药物的使用不当会导致蜂蜜中的不良残留物。在巴西,法律当局为蜂蜜中的不同化合物设定了最大残留限量(MRL),范围为10至20 ng ml-1。对抗菌素的监测是一个令人关切的问题,因为它对人类健康构成风险,并与耐药细菌的生长相辅相成。巴西有国家残留控制计划(NRCP),以确保交易的产品符合消费者要求的安全和质量标准。本工作的目的是建立并验证一种适用于测定蜂蜜中磺胺类、四环素类和大环内酯类的液相色谱串联质谱法。主要目标是开发一种高效的技术,结合简单,快速和低成本,因为该方法将用于常规分析。加样回收率为36 ~ 139%。考虑到三个不同的天数,所有药物的浓度在0到200%的MRL范围内均达到良好的线性(r2),高于0.95。除红霉素外,日内日内精密度CV% (n=6)低于18%,符合标准,浓度范围为0.5 ~ 1.5 MRL。准确率在97 - 108%之间。大环内酯类的定量限为2.5 ng g-1,磺胺类和四环素类的定量限为5 ng g-1。评价决策限(CCα),结果在12.9 ~ 28.1 ng g-1之间。所得的检测能力(CCβ)在15.8 ~ 36.3 ng g-1之间。所提出的方法被证明适合于这一预期目的,并将有助于抗菌蜂蜜的监测。