Tong Jia-Qi, Zhu Gu-Huan, Lan Hang-Zhen, Shi Hong-Lan, Zhu Xiao-Yan, Sun Yao
Ningbo Customs Technology Center, Ningbo 315000, China.
Ningbo Joysun Product Testing Service Company, Ningbo 315000, China.
Se Pu. 2024 Nov;42(11):1077-1086. doi: 10.3724/SP.J.1123.2024.02018.
Antimicrobials inhibit the growth and reproduction of microorganisms thereby alleviating skin and other problems caused by microorganisms. Antimicrobials are classified into different categories, including antibacterials, antifungals, and antivirals, among others, and include azoles, sulfonamides, tetracyclines, quinolones, and many other classes of synthetic and natural compound. The inappropriate or excessive use of antimicrobials can damage skin and other human organs and increase antimicrobial resistance. Relevant regulations and standards clearly state that antimicrobials are prohibited for use as ingredients in disinfection products. However, since antimicrobials enhance the disinfection or antibacterial effect of a product, with a significant short-term effect, antimicrobials are occasionally illegally added to disinfectant products, including those intended for human use. Therefore, establishing testing methods that provide technical support for enforcing regulations is an urgent objective. Herein, a method was established for the analysis of 42 antimicrobials in disinfection products, that is applicable to common types of disinfection-product matrix, including creams, gels, and aqueous solutions, using high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) combined with dispersive solid phase extraction. The 42 antimicrobials comprise antibacterials, antifungals, and antivirals, and include seven sulfonamides, ten quinolones, three lincosamides, five tetracyclines, three macrolides, eight azoles, three purine nucleoside analogs, one furan, one nonpolyene antifungal, and one steroid. Briefly, 0.2 g of a sample was first dispersed in 2 mL of water and then extracted with 10 mL of 0.5% formic acid in acetonitrile, with 3 g of anhydrous NaSO added to remove water. After centrifugation, 5 mL of the supernatant was cleaned using dispersive solid phase extraction with EMR-Lipid as the adsorbent. Lipids, waxes, surfactants, and moisturizing lubricants are commonly used as cream and gel matrices. Matrix substances containing long carbon chains dissolved in acetonitrile were removed using the EMR-Lipid adsorbent. Target analytes were separated on a Poroshell 120 EC-C18 analytical chromatography column (150 mm×3.0 mm, 2.7 μm), with 0.1% formic acid in acetonitrile and 0.1% formic acid aqueous solution used as mobile phases under gradient-elution conditions. The target analytes in the test solution were detected in positive ionization (ESI) and multi-reaction-monitoring (MRM) modes. Analytes were characterized in terms of their retention times and selected ions, and quantified using the external-standard method. The main factors affecting method response, recovery, and sensitivity, such as the extraction method and solvent, purification method and adsorbent, mobile phase, and MS conditions, were examined during sample pretreatment and instrumental analysis. The 42 antimicrobials were effectively separated under the optimized experimental conditions; the target compounds exhibited linear working curves in the 0.25-5.0 mg/kg concentration range, with correlation coefficients () greater than 0.99. Limits of detection (LODs) for the 42 antimicrobials were determined from the signal-to-noise ratios () of their chromatographic peaks. LODs of 0.03-0.10 mg/kg were determined for the three matrices using 0.2-g samples and 10-mL test solution. Recoveries of 80.3-109.8%, with relative standard deviations (RSDs) of less than 9.8%, were obtained by determining three levels of each target analyte added to the three blank matrices; this process was repeated for six parallel samples. The developed method was used to analyze antimicrobials in commercially available disinfection products, with two sample batches testing positive. The established method is simple, accurate, precise, and suitable for the rapid screening and quantification of antimicrobials in disinfection products. This study provides powerful technical support for regulating the illegal addition of related antimicrobials to disinfection products.
抗菌剂可抑制微生物的生长和繁殖,从而缓解由微生物引起的皮肤及其他问题。抗菌剂可分为不同类别,包括抗菌药、抗真菌药和抗病毒药等,涵盖唑类、磺胺类、四环素类、喹诺酮类以及许多其他类别的合成和天然化合物。抗菌剂的不当使用或过度使用会损害皮肤及人体其他器官,并增加抗菌耐药性。相关法规和标准明确规定,禁止将抗菌剂用作消毒产品的成分。然而,由于抗菌剂可增强产品的消毒或抗菌效果,且具有显著的短期效果,因此偶尔会有抗菌剂被非法添加到消毒产品中,包括用于人体的消毒产品。因此,建立能为法规执行提供技术支持的检测方法是当务之急。在此,建立了一种使用高效液相色谱 - 串联质谱法(HPLC - MS/MS)结合分散固相萃取法分析消毒产品中42种抗菌剂的方法,该方法适用于常见类型的消毒产品基质,包括乳膏、凝胶和水溶液。这42种抗菌剂包括抗菌药、抗真菌药和抗病毒药,有七种磺胺类、十种喹诺酮类、三种林可酰胺类、五种四环素类、三种大环内酯类、八种唑类、三种嘌呤核苷类似物、一种呋喃类、一种非多烯抗真菌剂和一种甾体类。简要来说,首先将0.2 g样品分散于2 mL水中,然后用10 mL 0.5%甲酸乙腈溶液萃取,并加入3 g无水硫酸钠以除去水分。离心后,取5 mL上清液,以EMR - Lipid为吸附剂通过分散固相萃取进行净化。脂质、蜡、表面活性剂和保湿润滑剂通常用作乳膏和凝胶基质。使用EMR - Lipid吸附剂可除去溶解于乙腈中的含长碳链的基质物质。目标分析物在Poroshell 120 EC - C18分析色谱柱(150 mm×3.0 mm,2.7 μm)上进行分离,以0.1%甲酸乙腈溶液和0.1%甲酸水溶液作为流动相,在梯度洗脱条件下进行。测试溶液中的目标分析物在正离子模式(ESI)和多反应监测(MRM)模式下进行检测。通过保留时间和选择离子对分析物进行表征,并采用外标法进行定量。在样品预处理和仪器分析过程中,考察了影响方法响应、回收率和灵敏度的主要因素,如萃取方法和溶剂、净化方法和吸附剂、流动相以及质谱条件等。在优化的实验条件下,42种抗菌剂得到了有效分离;目标化合物在0.25 - 5.0 mg/kg浓度范围内呈现线性工作曲线,相关系数()大于0.99。根据色谱峰的信噪比()确定了42种抗菌剂的检测限(LOD)。使用0.2 g样品和10 mL测试溶液,三种基质的检测限为0.03 - 0.10 mg/kg。通过向三种空白基质中添加三个水平的各目标分析物进行测定,回收率为80.3 - 109.8%,相对标准偏差(RSD)小于9.8%;此过程对六个平行样品重复进行。所建立的方法用于分析市售消毒产品中的抗菌剂,有两个样品批次检测呈阳性。所建立的方法简便、准确、精密,适用于消毒产品中抗菌剂的快速筛查和定量分析。本研究为规范消毒产品中相关抗菌剂的非法添加提供了有力的技术支持。