Development of a Simultaneous Sulfadiazine, Sulfamethoxazole, and Tetracycline Antibiotic Level Determination Method with High-Performance Liquid Chromatography

Yanulia Handayani, Iswandi, Supriyadi
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引用次数: 1

Abstract

Sulfonamides and tetracyclines are a group of synthetic antibacterials that are widely used in veterinary practice for the treatment and prevention of infections in animals that can be consumed by humans. The purpose of this study was to determine the optimum conditions for High-Performance Liquid Chromatography for simultaneous analysis of sulfadiazine, sulfamethoxazole, and tetracycline and meet the validation requirements. The research method used is the HPLC method. The instruments used are Agilent 1220 Infinity II low-pressure dual-channel gradient valve, variable wavelength detector (VWD) BI detector, the column used is Agilent 5 TC-C18 (250 x 4.6 mm), motion phase A = acetic acid 0.08%: acetonitrile (9:1) and motion phase B = methanol with a flow rate gradient of 0.5 mL/minute and UV-VIS detector at wavelength 295 hm. The results showed that the method of determining the levels of sulfadiazine, sulfamethoxazole, and tetracycline met the requirements of selectivity, accuracy, precision, linearity, LOD, and LOQ and could be applied to fish samples. The accuracy parameter test obtained recovery results between 96.99%-103.16% at all sample concentration levels of 80%, 100%, and 120%. Testing the precision parameters showed that all sample concentrations were 100% repeated for 6 times replications, fulfilling the precision requirements, namely, the concentration of ≥10 ppm was < 7.3%. The linearity test showed that the correlation coefficient of sulfadiazine was 0.999, sulfamethoxazole was 0.999, and tetracycline was 0.998. LOD and LOQ values of sulfadiazine 1.15 ppm and 3.84 ppm, sulfamethoxazole LOD 2.51 ppm and LOQ 8.37 ppm, and tetracycline LOD 3.37 ppm and LOQ 11.22 ppm. Applications to fish samples were carried out by addition and obtained levels of 14.79 ppm sulfadiazine, 14.01 ppm sulfamethoxazole, and 45.05 ppm tetracycline.   
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高效液相色谱法同时测定磺胺嘧啶、磺胺甲恶唑和四环素抗生素水平的建立
磺胺类药物和四环素类药物是一组合成抗菌素,在兽医实践中广泛用于治疗和预防可被人类食用的动物感染。本研究的目的是确定高效液相色谱法同时分析磺胺嘧啶、磺胺甲恶唑和四环素的最佳条件,并满足验证要求。研究方法采用HPLC法。所用仪器为Agilent 1220 Infinity II低压双通道梯度阀,可变波长检测器(VWD) BI检测器,色谱柱为Agilent 5 TC-C18 (250 × 4.6 mm),运动相A =乙酸0.08%:乙腈(9:1),运动相B =甲醇,流速梯度0.5 mL/min,波长295 hm UV-VIS检测器。结果表明,磺胺嘧啶、磺胺甲恶唑和四环素的含量测定方法符合选择性、准确度、精密度、线性、定量限和定量限要求,可应用于鱼类样品。在样品浓度为80%、100%和120%时,准确度参数测试的回收率在96.99% ~ 103.16%之间。精密度参数测试表明,所有样品浓度重复6次均为100%,满足精密度要求,即≥10 ppm的浓度< 7.3%。线性检验结果表明,磺胺嘧啶、磺胺甲恶唑、四环素的相关系数分别为0.999、0.999和0.998。磺胺嘧啶的LOD和LOQ分别为1.15 ppm和3.84 ppm,磺胺甲恶唑的LOD为2.51 ppm, LOQ为8.37 ppm,四环素的LOD为3.37 ppm, LOQ为11.22 ppm。通过添加对鱼样品进行应用,获得了14.79 ppm磺胺嘧啶、14.01 ppm磺胺甲恶唑和45.05 ppm四环素的水平。
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