Mahaparale Sonali, Telekone R S, Raut R P, Damle S S, Kasture P V
Dr. D. Y. Patil College of Pharmacy, Akurdi, Pune-411 044, India.
Indian J Pharm Sci. 2010 Jan;72(1):133-6. doi: 10.4103/0250-474X.62241.
Two simple, accurate and reproducible spectrophotometric methods; Q analysis and first order derivative method have been described for the simultaneous estimation of drotaverine hydrochloride and paracetamol in combined tablet dosage form. Absorption maxima of drotaverine hydrochloride and paracetamol in distilled water were found to be 303.5 nm and 243.5 nm respectively. Beer's law was obeyed in the concentration range 5-50 mug/ml for drotaverine and 5-60 mug/ml for paracetamol. In Q analysis method, two wavelengths were selected at isobestic point (277 nm) and lambda(max) of paracetamol (243.5 nm). In first order derivative method, zero crossing point for drotaverine hydrochloride and paracetamol were selected at 303.5 nm and 243.5 nm, respectively. The results of two methods were validated statistically and recovery studies were found to be satisfactory.
已经描述了两种简单、准确且可重复的分光光度法;Q 分析法和一阶导数法,用于同时测定复方片剂剂型中盐酸屈他维林和对乙酰氨基酚的含量。发现盐酸屈他维林和对乙酰氨基酚在蒸馏水中的最大吸收波长分别为 303.5 nm 和 243.5 nm。盐酸屈他维林在 5 - 50 μg/ml 浓度范围内、对乙酰氨基酚在 5 - 60 μg/ml 浓度范围内遵守比尔定律。在 Q 分析法中,在等吸收点(277 nm)和对乙酰氨基酚的 λ(max)(243.5 nm)处选择了两个波长。在一阶导数法中,盐酸屈他维林和对乙酰氨基酚的零交叉点分别选择在 303.5 nm 和 243.5 nm 处。两种方法的结果经统计学验证,回收率研究结果令人满意。