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在二甲基苯胺存在下测定盐酸利多卡因和十六烷基氯化吡啶二元混合物的绿色分光光度法。

Green spectrophotometric methods for the determination of a binary mixture of lidocaine hydrochloride and cetylpyridinium chloride in the presence of dimethylaniline.

作者信息

Merey Hanan A, Ramadan Nesrin K, Diab Sherine S, Moustafa Azza A

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El Aini Post, 11562 Cairo, Egypt.

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El Aini Post, 11562 Cairo, Egypt.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2020 Dec 5;242:118743. doi: 10.1016/j.saa.2020.118743. Epub 2020 Jul 20.

Abstract

Three green, simple, precise, accurate and sensitive spectrophotometric methods were developed for the determination of a binary mixture of lidocaine hydrochloride (LDC) and cetylpyridinium chloride (CPC) in the presence of dimethylaniline (DMA). In the three methods, the interference of DMA spectrum is eliminated using the ratio subtraction method. Method (A) depended on determining LDC and CPC by measuring the first derivative of the ratio spectra (DD) at 271.0 and 268.4 nm, respectively. Method (B) was the ratio difference (RD), based on dividing the absorption spectrum of the binary mixture by a standard spectrum of CPC or LDC, then measuring the amplitude difference of the ratio spectra (∆P) between 231.2 and 240.0 nm for LDC and between 242.8 and 258.0 nm for CPC. Method (C) based on the application of dual wavelength coupled with the isoabsorptive point method. This was achieved by measuring the absorbance difference (∆A) between 243.0 and 268.6 nm for the determination of LDC, followed by application of isoabsorptive point method comprised of measurement the total content of the mixture of LDC and CPC at their isoabsorptive point at 240.0 nm. The content of CPC was obtained by subtraction. The specificity of the developed methods was investigated by analyzing laboratory prepared mixtures containing different ratios of LDC and CPC in presence of DMA. The proposed methods displayed useful analytical characteristics for the determination of LDC and CPC in bulk powder and their combined dosage form. The obtained results were statistically compared with those obtained by the official methods, showing no significant difference with respect to accuracy and precision.

摘要

开发了三种绿色、简单、精确、准确且灵敏的分光光度法,用于在存在二甲基苯胺(DMA)的情况下测定盐酸利多卡因(LDC)和十六烷基吡啶氯化物(CPC)的二元混合物。在这三种方法中,使用比率减法消除了DMA光谱的干扰。方法(A)通过分别在271.0和268.4 nm处测量比率光谱的一阶导数(DD)来测定LDC和CPC。方法(B)是比率差(RD)法,基于将二元混合物的吸收光谱除以CPC或LDC的标准光谱,然后测量LDC在231.2和240.0 nm之间以及CPC在242.8和258.0 nm之间的比率光谱的幅度差(∆P)。方法(C)基于双波长结合等吸收点法的应用。这是通过测量243.0和268.6 nm之间的吸光度差(∆A)来测定LDC,然后应用等吸收点法,该方法包括在240.0 nm的等吸收点测量LDC和CPC混合物的总含量。通过减法获得CPC的含量。通过分析在DMA存在下含有不同比例LDC和CPC的实验室制备混合物,研究了所开发方法的特异性。所提出的方法对散装粉末及其复方剂型中的LDC和CPC测定显示出有用的分析特性。将获得的结果与官方方法获得的结果进行统计学比较,在准确度和精密度方面没有显著差异。

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