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Spectrophotometric determination of tranexamic acid using vanillin
A new spectrophotometric method has been examined for the determination of the tranexamic acid (TA)by derivatization with vanillin(VAN).The molar absorptivity of TA was calculated 25 160 L·mol-1·cm-1at λ max 354 nm and obeyed the Beer's law within 0.5-2.5 μg·mL-1.The color reaction was highly stable and didnot show any change in absorbance up to 24 h.The method was applied for the analysis of TA from capsules,injections and tooth pastes.The amounts of TA found in capsules,injections and tooth pastes of various pharmaceutical companies were observed with 249.0-250.9 mg/capsule,249.3-250.7 mg/injection and 0.048%-0.049%in tooth pastes with relative standard deviation(RSD)0.2%-5.0%(n=3).
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Spectrophotometric and spectrofluorimetric methods for the determination of ropinirole content in pharmaceutical dosage forms
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Simple Spectrophotometric Methods for the Determination of Meloxicam in Presence of Its Degradation Products
Objective:To develope two simple and accurate spectrophotometric methods for the determination of meloxicam ( Ⅰ ) in presence of its degradation products, 5 - methyl - 2 - aminothiazole ( Ⅱ ) and benzothiazine carboxylic acid ( Ⅲ ). Method:Both methods are based on the formation of chelate complexes of the studied drug with uranyl acetate and ferric chloride at room temperature in a methanolic medium. Results:The resulting complexes are stable for 24 hrs and show absorption maxima at 406 nm and 580 nm for uranyl and ferric complexes respectiverecoveries of (99.44 ± 0. 48 ) % and (99. 42 ± 0. 45 ) %, and molar absorptivity of 4. 67 × 103 and 1. 029 × 103 respectively. Conclusion:Both methods are proved to be stability indicating as no interference was observed with the degradation products. The proposed methods were successfully applied to the determination of the drug in bulk powder, laboratory prepared mixtures containing different percentages of degradation products and pharmaceutical dosage forms.