Pawar Rajendra-Prasad, Sharma Girraj, Durgbanshi Abhilasha, Bose Devasish, Peris-Vicente Juan, Roca-Genovés Pasqual, Carda-Broch Samuel
Department of Criminology and Forensic Science, Doctor Harisingh Gour Vishwavidyalaya (A Central University), Sagar, Madhya Pradesh, India.
Department of Chemistry, Doctor Harisingh Gour Vishwavidyalaya (A Central University), Sagar, Madhya Pradesh, India.
Electrophoresis. 2024 Feb;45(3-4):212-217. doi: 10.1002/elps.202200273. Epub 2023 Feb 9.
A procedure to determine albendazole and ivermectin in veterinary formulations, like tablet, bolus, oral suspensions, and injections by micellar liquid chromatography, has been developed. Sample preparation was a batch solid-to-liquid extraction in mobile phase, consisting of a stirring step (15 min), followed by ultrasonication (15 min) and filtration of the obtained supernatant, to reach a target concentration of 2 mg/L for both analytes. Using a mobile phase of 0.15 M sodium dodecyl sulfate-6% 1-pentanol buffered at pH 3 with a 0.01 M phosphate salt, running at 1 mL/min through a C18 column, both drugs were resolved in less than 10 min. Absorbance detection wavelength was 292 nm. Procedure was validated by the guidelines of the International Council on Harmonization in terms of specificity, calibration range (0.025-5 mg/L), trueness (97.8%-102.6%), precision (<2.2%), and system suitability. The method was found easy-to-handle, low cost, safe, green, and with high sample-throughput, thus useful for routine analysis. Therefore, it represents a valuable alternative for quality control of veterinary formulations. It was applied to samples of veterinary formulations purchased from local chemists and veterinarians, and label claims were inside the acceptance criteria (95%-105%).
已开发出一种通过胶束液相色谱法测定兽用制剂(如片剂、大丸剂、口服混悬液和注射液)中阿苯达唑和伊维菌素的方法。样品制备是在流动相中进行批量固液萃取,包括搅拌步骤(15分钟),随后超声处理(15分钟)并过滤所得上清液,以使两种分析物的目标浓度达到2mg/L。使用0.15M十二烷基硫酸钠 - 6% 1 - 戊醇的流动相,用0.01M磷酸盐缓冲至pH 3,以1mL/min的流速通过C18柱,两种药物在不到10分钟内分离。吸光度检测波长为292nm。该方法按照国际协调理事会的指导原则在特异性、校准范围(0.025 - 5mg/L)、准确性(97.8% - 102.6%)、精密度(<2.2%)和系统适用性方面进行了验证。该方法易于操作、成本低、安全、绿色且样品通量高,因此可用于常规分析。所以,它是兽用制剂质量控制的一种有价值的替代方法。它被应用于从当地药剂师和兽医处购买的兽用制剂样品,标签声明在验收标准(95% - 105%)范围内。