e Souza Marinês J, Bittencourt Celso F, Morsch Lisoni M
Departamento de Farmácia Industrial, Universidade Federal de Santa Maria, CEP 97, RS, Santa Maria, Brazil.
J Pharm Biomed Anal. 2002 Jun 15;28(6):1195-9. doi: 10.1016/s0731-7085(01)00673-2.
A simple, rapid and sensitive high-performance liquid chromatographic (HPLC) method was developed for the assay of enrofloxacin in raw material and injection. The validation method yielded good results and included the range, linearity, precision, accuracy, specificity, recovery, limit of detection (LOD) and limit quantification (LOQ) values. The HPLC separation was carried out by reversed phase chromatography on a C-18 absorbosphere column (150 x 4.6 mm i.d. 5 microm particle size) with a phase composed of sodium acetate (pH 4.7; 0.1 M): acetonitrile (60:40, v/v; pH 5.0), pumped isocratically at a flow rate of 1.5 ml min(-1). The effluent was monitored at 278 nm with the eluting solvent. The calibration graph for enrofloxacin was linear from 10.0 to 80.0 microg ml(-1).
建立了一种用于测定恩诺沙星原料药和注射液的简单、快速且灵敏的高效液相色谱(HPLC)方法。该验证方法取得了良好的结果,包括范围、线性、精密度、准确度、特异性、回收率、检测限(LOD)和定量限(LOQ)值。HPLC分离在C-18吸附柱(内径150×4.6mm,粒径5μm)上通过反相色谱进行,流动相由醋酸钠(pH 4.7;0.1M):乙腈(60:40,v/v;pH 5.0)组成,等度洗脱,流速为1.5ml min⁻¹。用洗脱溶剂在278nm处监测流出物。恩诺沙星的校准曲线在10.0至80.0μg ml⁻¹范围内呈线性。