Dipartimento di Farmacia, Università degli Studi "G. d'Annunzio", Pescara, via dei Vestini 66100 Chieti, Italy.
Dipartimento di Scienze Mediche Orali e Biotecnologiche, Università degli Studi "G. d'Annunzio" Chieti, Pescara, via dei Vestini 66100 Chieti, Italy.
J Pharm Biomed Anal. 2018 Mar 20;151:266-273. doi: 10.1016/j.jpba.2017.12.039. Epub 2017 Dec 24.
An ultra high-performance liquid chromatographic (UHPLC) method with PDA detection was developed and validated for the simultaneous quantification of metronidazole, meropenem, ciprofloxacin, linezolid and piperacillin in human plasma and applied to patients suffering from hospital acquired pneumonia (HAP). The method uses an air assisted dispersive liquid-liquid microextraction for sample preparation. All parameters in the extraction step, including selection of extractant, amount of extractant, ionic strength, pH, and extraction cycles, were investigated and optimized. Chromatography was carried out using a Poroshell 120 SB C (50 × 2.1 mm I.D. 2.6 μm particle size) column and a gradient mobile phase consisting of ammonium acetate buffer (10 mM, pH 4.0) (eluent A); and a mixture of acetonitrile-methanol in a ratio (80/20)(eluent B). Ulifloxacin was used as internal standard. The method demonstrated good linearity with correlation coefficients, r > 0.9995 for the drugs, as well as high precision (RSD% ≤ 9.87%), accuracy ranged from -8.14% to +8.98. The enrichment factor (EF) obtained ranged within 87 and 121. During the validation, the concentrations of the analytes were found to be stable after 3 freeze-thaw cycles and for at least 24 h after extraction. Subsequently, this method was used to quantify the drugs in patients with HAP in order to establish if the dosage regimen given was sufficient to eradicate the infection at the target site.
建立并验证了一种超高效液相色谱(UHPLC)-光电二极管阵列(PDA)检测法,用于同时定量人血浆中的甲硝唑、美罗培南、环丙沙星、利奈唑胺和哌拉西林,并将其应用于患有医院获得性肺炎(HAP)的患者。该方法采用空气辅助分散液液微萃取进行样品前处理。对萃取步骤中的所有参数(包括萃取剂的选择、萃取剂的用量、离子强度、pH 值和萃取循环次数)进行了考察和优化。色谱分离在 Poroshell 120 SB C(50×2.1mm ID,2.6μm 粒径)柱上进行,采用由乙酸铵缓冲液(10mM,pH4.0)(洗脱剂 A)和乙腈-甲醇(80/20)混合物(洗脱剂 B)组成的梯度洗脱系统。乌洛氟沙星被用作内标。该方法对药物的线性良好,相关系数 r 均大于 0.9995,精密度高(RSD%≤9.87%),准确度在-8.14%至+8.98%之间。获得的富集因子(EF)在 87 至 121 之间。在验证过程中,发现经过 3 次冻融循环和萃取后至少 24 小时,分析物的浓度均稳定。随后,该方法用于定量 HAP 患者中的药物,以确定所给剂量方案是否足以在靶部位消除感染。