一种新的、可持续的、生态友好的分光光度和化学计量学方法,通过统一的回归方程来确定严重重叠的光谱:绿度和白度评估。

IF 1.7 4区 农林科学 Q3 CHEMISTRY, ANALYTICAL Journal of AOAC International Pub Date : 2023-09-01 DOI:10.1093/jaoacint/qsad037
Ragaa Magdy, Nermine V Fares, Maha Farouk, Ahmed Hemdan
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引用次数: 1

摘要

背景:奈比洛尔和缬沙坦(VAL)联合用药可成功控制血压,改善高血压患者预后。目的:建立创新、简便、可持续的纳比洛尔和缬沙坦的分光光度同时分析方法。方法:改进的差分调幅(MD-AM)方法只使用统一的回归方程,不需要任何分辨率技术。其他不同的方法也适用于同一混合物的测定,包括单变量和多变量分光光度法。多变量方法为PLS和PCR,单变量方法为导数比(DD1)、比差(RD)、恒中心(CC)、恒中心谱减(CC- ss)、恒值与幅差耦合(CV-AD)、超前浓度值(ACV)和幅差(AD)。所提出的方法使用绿色溶剂;因此,使用六种知名的评估工具对所提出的程序的环境影响进行了定性和定量评估。结果:所有方法均成功地用于分析所研究药物的散装粉剂、Byvalson®制剂剂型以及在USP溶出度仪下肠道pH(7.4)的体外释放度。所得结果与文献报道的方法进行统计比较,并采用单因素方差分析(one-way ANOVA)进行统计检验,均无显著差异。结论:所有的绿色和白色分析化学评价工具结果都证实了该方法的安全性、可持续性和成本效益,表明该方法是绿色和可持续的。结果令人满意,鼓励其在剂型质量控制实验室的适用性,并使这些方法成为该联合剂型分析和溶出谱评估的环保替代品。重点:首次使用统一的回归方程确定了严重重叠的光谱,而不需要扩展部分或零贡献区域。该方法是第一个研究盐酸奈比洛尔(nebivolol hydrochloride, NEB)和VAL的体外溶出度的方法,也是第一个在不影响分析标准的情况下应用的可持续的绿色方法。
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A Novel, Sustainable, and Eco-Friendly Spectrophotometric and Chemometric Approach for Determination of Severely Overlapped Spectrum via Unified Regression Equation: Greenness and Whiteness Assessment.

Background: Nebivolol and valsartan (VAL) in combination with each other successfully control blood pressure and improve hypertension patient outcomes.

Objective: To develop and validate innovative, simple, and sustainable spectrophotometric methods for the simultaneous analysis of nebivolol and valsartan.

Method: The new modified difference amplitude modulation (MD-AM) method uses only unified regression equation and does not require any resolution techniques. Other different approaches were also applied for the determination of the same mixture including univariate and multivariate spectrophotometric methods. The multivariate methods were PLS and PCR, whereas the univariate methods were derivative ratio (DD1), ratio difference (RD), constant center (CC), constant center spectrum subtraction (CC-SS), constant value coupled with amplitude difference (CV-AD), advanced concentration value (ACV), and amplitude difference (AD). The proposed methods use a green solvent; thus, the environmental impact of the presented procedures was evaluated qualitatively and quantitatively using six well-known evaluation tools.

Results: All methods were applied successfully for the analysis of the studied drugs in their bulk powder, pharmaceutical dosage form Byvalson®, and in vitro release at intestinal pH (7.4) using a USP dissolution tester. Results obtained were compared statistically with the reported method and with each other using a one-way ANOVA statistical test, and no significant differences were found.

Conclusions: All green and white analytical chemistry evaluation tools results confirm the safety, sustainability, and cost-effectiveness of the approaches, indicating that the methods are regarded green and sustainable. Results were agreeable, encouraging their applicability in quality control laboratories for dosage form and making these methods an eco-friendly substitute for the analysis of this combined dosage form and for evaluating the dissolution profile.

Highlights: For the first time, a severely overlapped spectrum was determined using a unified regression equation without the need of extended part or zero contribution regions by the novel method MD-AM. The proposed methods are the first study of in vitro dissolution profiling of nebivolol hydrochloride (NEB) and VAL and the first sustainable and green methods applied without compromising the analytical criteria.

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来源期刊
Journal of AOAC International
Journal of AOAC International 医学-分析化学
CiteScore
3.10
自引率
12.50%
发文量
144
审稿时长
2.7 months
期刊介绍: The Journal of AOAC INTERNATIONAL publishes the latest in basic and applied research in analytical sciences related to foods, drugs, agriculture, the environment, and more. The Journal is the method researchers'' forum for exchanging information and keeping informed of new technology and techniques pertinent to regulatory agencies and regulated industries.
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