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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Determination of chlorprothixene and amitryptyline hydrochlorides by UV-derivative spectrophotometry and UV-solid-phase spectrophotometry
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Determination of chlorprothixene and amitryptyline hydrochlorides by UV-derivative spectrophotometry and UV-solid-phase spectrophotometry

机译:紫外导数分光光度法和紫外固相分光光度法测定氯噻吨烯和盐酸氨苄替林

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摘要

Two methods for spectrophotometric determination of chlorprothixene and amitryptyline hydrochlorides were proposed. One of them is based on spectral analysis of their derivative spectra. The measurement of the value at 316.0 nm of first derivative was used for construction of calibration graph for chlorprothixene. The Beer law was obeyed in the concentration range 0.5-50.0 mug ml(-1). The amplitude of the second derivative at 261.4 nm was used for determination of amitryptyline in the range 0.5-75.0 mug ml(-1). The second proposed method is utilized the use of solid sorbent for simultaneous preconcentration and assay of studied compounds. For this purpose the filtration gel Sephadex G100 was applied. The elaborated solid-phase spectrophotometric method was used for determination of chlorprothixene at 268.0 nm in the range 2.5-75.0 mug ml(-1) and amitryptyline at 238.0 nm in the concentration range 10.0-75.0 mug ml(-1). (C) 2004 Elsevier B.V. All rights reserved.
机译:提出了两种分光光度法测定氯丙噻吨和盐酸阿米替林的方法。其中之一是基于其派生光谱的光谱分析。一阶导数在316.0 nm处的测量值用于构建氯噻吨的校正图。在0.5-50.0马克杯ml(-1)的浓度范围内遵守啤酒法。二阶导数在261.4 nm处的振幅用于确定阿米替林在0.5-75.0马克杯ml(-1)范围内。拟议的第二种方法是利用固体吸附剂同时预浓缩和分析所研究的化合物。为此目的,使用了Sephadex G100过滤胶。精细的固相分光光度法用于测定268.0 nm处的氯丙噻烯在2.5-75.0毫升/毫升(-1)的范围内和阿米替林在238.0 nm处的浓度在10.0-75.0毫升/毫升(-1)的范围内。 (C)2004 Elsevier B.V.保留所有权利。

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