Chandra Preeti, Rathore Atul Singh, Lohidasan Sathiyanarayanan, Mahadik Kakasaheb Ramoo
Department of Pharmaceutical Chemistry, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Erandwane, Pune-411038, Maharashtra, India.
Sci Pharm. 2012 Apr-Jun;80(2):337-51. doi: 10.3797/scipharm.1108-04. Epub 2012 Jan 31.
A simple, precise and accurate reversed-phase liquid chromatographic method has been developed for the simultaneous estimation of aceclofenac (ACF), paracetamol (PCM) and tramadol hydrochloride (TRM) in pharmaceutical dosage form. The chromatographic separation was achieved on a HiQ-Sil™ HS C18 column (250×4.6 mm i.d., 5 μm particle size), kromatek analytical column at ambient temperature. The mobile phase consisted of 40: 60 (v/v); phosphate buffer (pH 6.0): methanol. The flow rate was set to 1.0 mL min(-1) and UV detection was carried out at 270 nm. The retention time (t(R)) for ACF, PCM and TRM were found to be 14.567 ± 0.02, 3.133 ± 0.01 and 7.858 ± 0.02 min, respectively. The validation of the proposed method was carried out for linearity, precision, robustness, limit of detection, limit of quantitation, speci city, accuracy and system suitability. The linear dynamic ranges were from 40-160 μg mL(-1) for ACF, 130-520 μg mL(-1) for PCM and 15-60 μg mL(-1) for TRM. The developed method can be used for routine quality control analysis of titled drugs in pharmaceutical dosage form.
已开发出一种简单、精确且准确的反相液相色谱法,用于同时测定药物剂型中醋氯芬酸(ACF)、对乙酰氨基酚(PCM)和盐酸曲马多(TRM)的含量。色谱分离在HiQ-Sil™ HS C18柱(内径250×4.6 mm,粒径5μm)、kromatek分析柱上于室温下进行。流动相由40:60(v/v)的磷酸盐缓冲液(pH 6.0):甲醇组成。流速设定为1.0 mL min(-1),紫外检测在270 nm波长下进行。ACF、PCM和TRM的保留时间(t(R))分别为14.567±0.02、3.133±0.01和7.858±0.02分钟。对所提出方法的线性、精密度、稳健性、检测限、定量限、特异性、准确度和系统适用性进行了验证。ACF的线性动态范围为40 - 160μg mL(-1),PCM为130 - 520μg mL(-1),TRM为15 - 60μg mL(-1)。所开发的方法可用于药物剂型中上述药物的常规质量控制分析。