Garcia Cássia V, Costa Gislaine R, Mendez Andreas S L
Departamento de Produção e Controle de Medicamentos, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul (UFRGS). Av. Ipiranga, 2752. Sala 406. CEP 90610-000, Porto Alegre/RS, Brazil.
Sci Pharm. 2012 Apr-Jun;80(2):317-27. doi: 10.3797/scipharm.1111-11. Epub 2012 Mar 12.
A stability-indicating liquid chromatographic (LC) method was developed for the determination of posaconazole in bulk. Chromatographic separation was achieved using an isocratic elution in a reversed-phase system, with a mobile phase composed of methanol-water (75:25, v/v), at 1.0 mL min(-1) flow. Samples were exposed to degradation under thermal, oxidative and acid/basic conditions, and no interference in the analysis was observed. System suitability was evaluated and results were satisfactory (N = 4,900.00 tailing factor 1.04; RSD between injections = 0.65). The retention time of posaconazole was about 8.5 min and the method was validated within the concentration range 5-60 μg mL(-1) (r = 0.9996). Adequate results were obtained for repeatability (RSD % = 0.86-1.22), inter-day precision (RSD % = 1.21) and accuracy (98.13% mean recovery). Robustness was also determined to be satisfactory after evaluation. The proposed method was successfully applied to posaconazole bulk quantification, showing the method is useful for determination of the drug in routine analysis.
建立了一种用于测定泊沙康唑原料药的稳定性指示液相色谱(LC)方法。采用反相系统等度洗脱实现色谱分离,流动相由甲醇 - 水(75:25,v/v)组成,流速为1.0 mL min⁻¹。样品在热、氧化及酸/碱条件下进行降解,分析过程中未观察到干扰。对系统适用性进行了评估,结果令人满意(N = 4,900.00,拖尾因子1.04;进样间相对标准偏差 = 0.65)。泊沙康唑的保留时间约为8.5分钟,该方法在5 - 60 μg mL⁻¹浓度范围内进行了验证(r = 0.9996)。重复性(相对标准偏差% = 0.86 - 1.22)、日间精密度(相对标准偏差% = 1.21)和准确度(平均回收率98.13%)均获得了满意结果。评估后确定该方法的稳健性也令人满意。所提出的方法成功应用于泊沙康唑原料药的定量分析,表明该方法在常规分析中可用于该药物的测定。