开发两种绿色高通量微孔光谱平台,用于测定 Reboxetine(美国 FDA 批准的第一种选择性去甲肾上腺素再摄取抑制剂抗抑郁药物)。

Ibrahim A Darwish, Mohammed S Alsalhi
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引用次数: 0

摘要

背景介绍瑞波西汀(RBX)是美国食品和药物管理局批准的第一种选择性去甲肾上腺素再摄取抑制剂类抗抑郁药物。目前亟需一种方便的分析工具来定量检测其剂型中的瑞波西汀:本研究旨在开发和验证两种用于 RBX 药物分析的绿色高通量微孔光谱平台:这两个平台分别简称为 MW-AB 和 MW-FL,采用微孔分析技术,并配有多功能微孔板读数器,分别测量吸光度和荧光信号。MW-AB 和 MW-FL 平台涉及 RBX 分别与氧化焦儿茶酚试剂(OPC)和四氰基二甲氧基醌(TCNQ)反应生成有色和荧光衍生物。有色 RBX-OPC 衍生物的吸光度为 520 纳米,RBX-TCNQ 电荷转移复合物的荧光激发和发射波长分别为 283 纳米和 484 纳米。建立了两种反应的最佳条件,确定了它们的摩尔比,并推测了反应机理:结果:根据国际协调理事会的指导方针,对两个平台进行了优化和验证。MW-AB 和 MW-FL 的定量限分别为 19.6 µg/mL 和 27 ng/mL。这两种平台均可用于定量检测 Edranox® 片剂中的 RBX 含量及其药物均匀性,可靠性极佳。两个平台的绿色程度均通过两种综合工具进行了评估,结果证实两个平台的绿色程度都很高:结论:两种平台都涉及一步反应、微孔分析和同时处理大量样品。结论:这两个平台都是一步反应,适合微孔分析,可同时处理大量样品,因此具有绿色环保和高通量分析的优点:亮点:所提出的两种平台是快速定量 RBX 的重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Two Green and High-Throughput Microwell Spectrometric Platforms for Determination of Reboxetine, the First FDA-Approved Selective Noradrenaline Reuptake Inhibitor Antidepressant Drug.

Background: Reboxetine (RBX) is the first FDA-approved antidepressant drug of the selective noradrenaline reuptake inhibitors class. There is a serious need for a convenient analytical tool for the quantitation of RBX in its dosage form.

Objective: This study aims toward the development and validation of two green and high-throughput microwell spectrometric platforms for the pharmaceutical analysis of RBX.

Methods: The two platforms, abbreviated as MW-AB and MW-FL, involved microwell-based analysis assisted with a multifunction microplate plate reader for measuring absorbance and fluorescence signals, respectively. The MW-AB and MW-FL platforms involved the formation of colored and fluorescent derivatives upon the reaction of RBX with oxidized pyrocatechol reagent (OPC) and tetracyanoquinodimethane (TCNQ), respectively. The absorbance of colored RBX-OPC derivative at 520 nm, and the fluorescence of RBX-TCNQ charge transfer complex at 283 and 484 nm for excitation and emission, respectively. The optimum conditions of both reactions were established, their molar ratios were determined, and reaction mechanisms were postulated.

Results: Both platforms were optimized and validated according to the guidelines of the International Council on Harmonization. The limits of quantitation were 19.6 µg/mL and 27 ng/mL for MW-AB and MW-FL, respectively. Both platforms were applied with excellent reliability to the quantitation of RBX content in Edranox® tablets and their drug uniformity. The greenness levels of both platforms were assessed by two comprehensive tools, and the results confirmed the high level of greenness for both platforms.

Conclusions: Both platforms involved one-step reactions, adapted microwell analysis, and simultaneous handling of large number of samples. Therefore, they have the advantages of greenness and high-throughput analysis.

Highlights: The proposed two platforms are valuable tools for the rapid quantitation of RBX.

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