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用于处理和放大白多分量系统中关键浓度产生的弱光谱信号的先进方法。

Advanced approaches for the treatment and amplification of weak spectral signals produced by critical concentrations in white multicomponent systems.

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr-El Aini Street, 11562 Cairo, Egypt; Pharmaceutical Chemistry Department, Faculty of Pharmaceutical Sciences & Pharmaceutical Industries, Future University in Egypt, 12311, Cairo, Egypt.

Analytical Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), 11787 6(th) October, Egypt.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2020 Jan 5;224:117339. doi: 10.1016/j.saa.2019.117339. Epub 2019 Jul 8.

Abstract

An analytical investigation was carried out to study the treatment and amplification of the spectral signals produced by critical concentrations with high accuracy and precision using two advanced approaches. The factorized-spectrum approach was applied through two novel methods which were: absorptivity centering technique via both: factorized zero order absorption spectrum (ACT-FSD) and factorized ratio spectrum (ACT-FSR). The proposed methods were found to be linear in the ranges of (15-100 μg/mL) and (3-40 μg/mL) for ASP and MTO, respectively. Those methods were compared to the methods following the geometrical standard addition approach: ratio H-point standard addition method (RHPSAM) and geometrical induced amplitude modulation (GIAM). The approaches were applied for the determination of the minor component metoclopramide in its mixture with the major component aspirin in the challengeable ratio of (1,90) respectively in a white multicomponent system. The results obtained from the proposed approaches were statistically compared with each other. The methods were validated according to ICH guidelines where the results were found to be within the acceptable limits. The methods were found to be accurate and reliable for the determination of metoclopramide critical concentration besides aspirin concentration. The results of single factor ANOVA analysis indicated that there is no significant difference among the developed methods. These methods provided simple resolution of this binary combination from synthetic mixtures and pharmaceutical preparation and can be conveniently adopted for routine quality control analysis.

摘要

采用两种先进方法对高浓度临界浓度产生的光谱信号进行了分析研究,以实现治疗和放大,具有高精度和高精准度。通过两种新颖的方法应用了分解光谱方法:通过:分解零阶吸收光谱(ACT-FSD)和分解比光谱(ACT-FSR)的吸收率中心化技术。发现该方法在 ASP 和 MTO 的(15-100μg/mL)和(3-40μg/mL)范围内呈线性。将这些方法与遵循几何标准添加方法的方法进行了比较:比率 H 点标准添加法(RHPSAM)和几何诱导幅度调制(GIAM)。这些方法用于在白色多组分系统中分别以挑战性比例(1,90)测定混合有主要成分阿司匹林的次要成分甲氧氯普胺。将所得结果进行了统计学比较。根据 ICH 指南对这些方法进行了验证,结果在可接受范围内。这些方法对于测定甲氧氯普胺的临界浓度(除了阿司匹林浓度)以及精确可靠。单因素方差分析的结果表明,所开发的方法之间没有显着差异。这些方法为从合成混合物和药物制剂中简单地解析这种二元混合物提供了便利,并可方便地用于常规质量控制分析。

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