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首页> 外文期刊>Журнал аналитической химии >SPECTROPHOTOMETRIC MULTICOMPONENT ANALYSIS OF A MIXTURE OF CHLORHEXIDINE HYDROCHLORIDE AND LIDOCAINE HYDROCHLORIDE IN PHARMACEUTICAL FORMULATION USING DERIVATIVE SPECTROPHOTOMETRY AND PARTIAL LEAST-SQUARES MULTWARIATE CALIBRATION
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SPECTROPHOTOMETRIC MULTICOMPONENT ANALYSIS OF A MIXTURE OF CHLORHEXIDINE HYDROCHLORIDE AND LIDOCAINE HYDROCHLORIDE IN PHARMACEUTICAL FORMULATION USING DERIVATIVE SPECTROPHOTOMETRY AND PARTIAL LEAST-SQUARES MULTWARIATE CALIBRATION

机译:偏光光度法和偏最小二乘偏光分光光度法分光光度法测定盐酸氯己定和盐酸利多卡因混合液中的分光光度

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摘要

Two spectrophotometric methods were applied to the simultaneous assay of chlorhexidine hydrochloride (CHL) and lidocaine hydrochloride (LIH) in pharmaceutical formulations. Using derivative spectropho-tometry, CHL was determined by measurement of itsfirst derivative signal at 290 nm (peak to zero amplitude) in the concentration range 5-9 mu g/mL, and LIH was analysed by measurement of its second derivative signals at 272 and 276 nm (peak to peak amplitude) in the concentration range 160-480 mu g/mL.With the partial least-squares (PLS-2), the experimental calibration matrix was constructed using 9 samples. The concentration ranges considered were 5, 6, 7 mu g/mL for CHL and 220, 240, 260 mu g/mL for LIH. The absorbances were recorded between 240 and 310 nm at every 5 nm.
机译:两种分光光度法被用于同时测定药物制剂中的盐酸洗必太(CHL)和盐酸利多卡因(LIH)。使用导数分光光度法,通过在5-9μg / mL的浓度范围内在290 nm(峰至零振幅)处测量其一阶导数信号来确定CHL,并通过在272和420 nm下测量其二阶导数信号来分析LIH。浓度范围为160-480μg / mL时为276 nm(峰峰值)。使用偏最小二乘(PLS-2),使用9个样品构建实验校准矩阵。 CHL的浓度范围为5、6、7μg / mL,LIH的浓度范围为220、240、260μg/ mL。每5 nm记录240至310 nm之间的吸光度。

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