首页> 外文期刊>Acta Poloniae Pharmaceutica: Durg Research >UV/VIS spectrophotometric methods for determination of caffeine and phenylephrine hydrochloride in complex pharmaceutical preparations. Validation of the methods.
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UV/VIS spectrophotometric methods for determination of caffeine and phenylephrine hydrochloride in complex pharmaceutical preparations. Validation of the methods.

机译:紫外/可见分光光度法测定复杂药物制剂中的咖啡因和盐酸去氧肾上腺素。方法的验证。

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摘要

The contents of active substances were determined in a preparation TP-4 (tablets) containing paracetamol, ascorbic acid, caffeine and phenylephrine hydrochloride. For determination of caffeine and phenylephrine hydrochloride, UV/VIS spectrophotometric method was used. The VIS spectrophotometric method based on the reaction of phenylephrine with ninhydrine in sulphuric acid (1.127 kg/l). Validation of methods performed for model mixtures proved those methods were accurate, precise, repeatable and linear in the range from 50% to 150% of the amount declared in the preparation. The content of caffeine and phenylephrine hydrochloride in TP-4, Thompyrin, Panadol Extra, Ring N satisfies the FP V demands.
机译:在含有对乙酰氨基酚,抗坏血酸,咖啡因和盐酸去氧肾上腺素的制剂TP-4(片剂)中测定活性物质的含量。为了测定咖啡因和盐酸去氧肾上腺素,使用了UV / VIS分光光度法。 VIS分光光度法,基于去氧肾上腺素与茚三酮在硫酸(1.127 kg / l)中的反应。对模型混合物进行的方法的验证证明,这些方法准确,准确,可重复且线性,范围为制剂中声明量的50%至150%。 TP-4,Thompyrin,Panadol Extra,N环N中的咖啡因和盐酸去氧肾上腺素的含量满足FP V的要求。

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