Simultaneous UV-Spectrophotometric Estimation of Paracetamol and Guaiphenesin by First Order derivative Method in Combined Dosage Form
Rajan V. Rele
Abstract
Rajan V. Rele
Abstract
The objective of the study was to develop a simple, accurate, precise and rapid a UV spectrophotometric i.e. first order derivative method for the determination of paracetamol and guaiphenesin in combined dosage form i.e. tablets by using methanol as a solvent. The method was further validated by ICH guidelines. The proposed first order derivative method involves the measurement of absorbance of one drug at zero crossing point of other; hence wavelengths 230 nm and 263 nm were selected for the estimation of paracetamol and guaiphenesin respectively. The linearity of the proposed method was found in the concentration range of 1 to 10 μg/ml (r2= 0.9998) for paracetamol and 10 to 100 μg/ml (r2= 0.9993) for guaiphenesin respectively. The percentage mean recovery was found to be 99.955% for paracetamol and 99.88% for guaiphenesin respectively. The method was also statistically validated for its linearity, accuracy and precision. Both intra and inter day variations showed less percentage (%) RSD values indicating high grade of precision of this method.
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The objective of the study was to develop a simple, accurate, precise and rapid a UV spectrophotometric i.e. first order derivative method for the determination of paracetamol and guaiphenesin in combined dosage form i.e. tablets by using methanol as a solvent. The method was further validated by ICH guidelines. The proposed first order derivative method involves the measurement of absorbance of one drug at zero crossing point of other; hence wavelengths 230 nm and 263 nm were selected for the estimation of paracetamol and guaiphenesin respectively. The linearity of the proposed method was found in the concentration range of 1 to 10 μg/ml (r2= 0.9998) for paracetamol and 10 to 100 μg/ml (r2= 0.9993) for guaiphenesin respectively. The percentage mean recovery was found to be 99.955% for paracetamol and 99.88% for guaiphenesin respectively. The method was also statistically validated for its linearity, accuracy and precision. Both intra and inter day variations showed less percentage (%) RSD values indicating high grade of precision of this method.
Key concepts: Absorbance, Dosage form, Derivative (finance), Chromatography, Mathematics, Linearity, Second derivative, Accuracy and precision