Simultaneous Derivative Spectrophotometric Determination of Lornoxicam and Paracetamol in Tablet Dosage Forms

Bharampuram Akhil, R. K. Chaitanya, B. Venkatesh, M. M. Annapurna
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引用次数: 3

Abstract

Lornoxicam and Paracetamol in combined dosage forms (Tablets). The zero crossing point of Paracetamol (247.42 nm) has been selected for the quantification of Lornoxicam whereas the zero crossing point of Lornoxicam (233.28 nm) has been selected for the quantification of Paracetamol from the first order derivative spectrum observed in borate buffer. The method obeys Beer-Lambert’s law over the concentration range 5-50 µg/ml for Lornoxicam and 5-60 µg/ml for Paracetamol. The proposed method was validated and can be used for the analysis of tablet dosage forms containing Lornoxicam and Paracetamol. K ey words: Lornoxicam, Paracetamol, Spectrophotometry, Derivative spectroscopy, Validation.
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同时导数分光光度法测定片剂中氯诺昔康和扑热息痛的含量
氯诺昔康和扑热息痛联合剂型(片剂)。在硼酸盐缓冲液中观察到的一阶导数光谱中,对乙酰氨基酚的零点交叉点(247.42 nm)被选择用于定量氯诺昔康,而氯诺昔康的零点交叉点(233.28 nm)被选择用于定量对乙酰氨基酚。在氯诺西康5 ~ 50µg/ml和扑热息痛5 ~ 60µg/ml的浓度范围内,本方法符合Beer-Lambert定律。该方法可用于氯诺昔康和扑热息痛片剂剂型的分析。关键词:氯诺昔康,对乙酰氨基酚,分光光度法,导数光谱,验证
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