Simultaneous Chromatographic Estimation of Vildagliptin and Dapagliflozin Using Hybrid Principles of White Analytical Chemistry and Analytical Quality by Design.

IF 1.7 4区 农林科学 Q3 CHEMISTRY, ANALYTICAL
Pintu Prajapati, Bageshree Rana, Veera Shakar Pulusu, Shailesh Shah
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引用次数: 0

Abstract

Background: The fixed-dose combination of vildagliptin (VDG) and dapagliflozin (DGZ) is used in the treatment of type 2 diabetes mellitus. According to the literature survey, RP-HPLC and HPTLC methods have been reported for routine analysis of VDG and DGZ. These chromatographic methods have been developed using potentially neurotoxic and teratogenic solvents, which are unsafe for human and aquatic animal life and hazardous to the environment. These types of organic solvents shall be replaced or reduced during chromatographic analysis of drugs for the safety of human and aquatic animal life and the protection of the environment. The novel white analytical chemistry (WAC) approach has been introduced, which emphasizes robust, green, user-friendly, economical, and rapid analysis of drug samples.

Objective: Hence, the WAC-based RP-HPLC method has been developed for the estimation of VDG and DGZ using lower toxic and economical solvents.

Method: The development of the RP-HPLC method includes the implementation of the analytical quality by design approach using principles of design of experiments to reduce organic waste generation and regulatory compliance of analytical method. The central composite design was applied for response surface modeling (RSM) and optimization of the RP-HPLC method. The method validation was carried out according to ICH Q2 (R1) guidelines.

Results: The fixed-dose combinations of VDG and DGZ were assayed, and results were found in compliance with their labeled claim. The published and proposed RP-HPLC methods were assessed for chromatographic analysis of VDG and DGZ using the Red-Green-Blue (RGB) model, AGREE calculator, Eco-Scale Assessment tool, GAPI software, and NEMI standards.

Conclusions: The proposed method was found to be robust, green, economical, and user-friendly for chromatographic analysis of VDG and DGZ. The proposed method can be an economical and eco-friendly analytical tool in the pharmaceutical industry for quality control and routine analysis of fixed-dose combinations of VDG and DGZ.

Highlights: Hybrid principles of WAC and analytical quality by design to RP-HPLC method for simultaneous estimation of VDG and DGZ in their fixed-dose combinations.

利用白分析化学和设计分析质量的混合原理同时色谱法估算维达列汀和达帕格列汀
背景:维达列汀(VDG)和达帕格列净(DGZ)的固定剂量复方制剂用于治疗2型糖尿病。根据文献调查,目前已有用于常规分析 VDG 和 DGZ 的 RP-HPLC 和 HPTLC 方法的报道。这些色谱法使用的溶剂可能具有神经毒性和致畸性,对人类和水生动物的生命不安全,而且对环境有害。为了人类和水生动物的生命安全和保护环境,在对药物进行色谱分析时,应替换或减少这些类型的有机溶剂。因此,我们开发了基于白分析化学(WAC)的 RP-HPLC 方法,使用毒性较低且经济的溶剂来估算 VDG 和 DGZ:方法:RP-HPLC 方法的开发包括利用实验设计原则实施分析质量设计方法,以减少有机废物的产生并使分析方法符合法规要求。中心复合设计用于响应面建模(RSM)和 RP-HPLC 方法的优化。根据 ICH Q2 (R1) 指南进行了方法验证:结果:对VDG和DGZ的固定剂量复方制剂进行了检测,结果符合其标签要求。采用红-绿-蓝(RGB)模型、AGREE 计算器、生态尺度评估工具、GAPI 软件和 NEMI 标准,对已公布和拟议的 RP-HPLC 方法进行了评估,以对 VDG 和 DGZ 进行色谱分析:结论:所提出的方法在色谱分析 VDG 和 DGZ 方面具有稳健、绿色、经济和用户友好的特点。结论:所提出的方法在 VDG 和 DGZ 固定剂量复方制剂的色谱分析中具有稳健性、绿色性、经济性和用户友好性,可作为制药行业中一种经济、环保的分析工具,用于质量控制和常规分析:将WAC和分析质量的混合原理应用于RP-HPLC方法,用于同时估算VDG和DGZ的固定剂量复方制剂。
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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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