Label-free masterful spectrofluorimetric systems for minuscule tracking of natural antioxidant vincamine in the pharmaceutical, environmental, and biological samples: Comparative greenness, whiteness, and blueness appraisal

IF 3.7 Q1 CHEMISTRY, ANALYTICAL
Eman Yosrey , Heba Elmansi , Shereen Shalan , Jenny Jeehan Nasr
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Abstract

In this work, we present two label-free spectrofluorimetric systems for the swift quantification of vincamine (VN) in various matrices without the need for knotty fluorescent dyes, drastic conditions, or expensive instrumentation, which are key merits of the quantifying procedures. The first method (Method I) relied on the direct mix-and-read assay for exploiting the intrinsic fluorescence of VN, adopting λex/em of 272/334 nm using water as a diluting solvent. The method fitted linearity across the concentrations of 1.00 – 10.00 µg mL¹. In the second method (Method II), upon turning off the photoinduced electron transfer (PET) of tertiary amine in the piperidine moiety to the indole scaffold using 0.1 M hydrochloric acid, the fluorescent signal was augmented up to 158 %. This commendable boost in the fluorescent sensitivity allowed the minute detection of VN in spiked human plasma with a standard deviation not exceeding 1.30. Using the acid-blocked PET-based probe, the fluorescent signal was linearly correlated with VN concentration across 0.25 – 6.00 µg mL¹ using λex/em of 277/323 nm. These streamlined procedures proficiently evaluated VN in both the sole and co-formulated capsules without any significant interference from capsule filler material or the co-formulated medication “piracetam”. In addition, the two submitted procedures were successfully executed to check VN through weight variation testing in the Brain-ox® capsules with good acceptance values. The constructed platforms ensemble estimated VN in the environmental samples (tap and river water) with acceptable percentage recoveries and standard deviations (0.95 – 1.65). The procedures' green, white, and blue fitness were appraised through a plethora of computational tools, including GAPI, AGREE, AGREEprep, the RGB 12 algorithm, and BAGI. The evaluation showed that the proposed works effectively strike a compromise between sustainability and functionality postulates. This highlighted that designed approaches are perfectly suited as ecological frameworks for minuscule assaying of VN in crucial pharmaceutical, biological, and environmental samples.

Abstract Image

无标签熟练的荧光光谱系统,用于制药,环境和生物样品中天然抗氧化剂长春胺的微小跟踪:比较绿色,白色和蓝色评估
在这项工作中,我们提出了两种无标记荧光光谱法系统,用于快速定量各种基质中的长春胺(VN),而不需要复杂的荧光染料,苛刻的条件或昂贵的仪器,这是定量程序的关键优点。第一种方法(方法一)采用直接混合-读取法,以水为稀释溶剂,λex/em为272/334 nm,利用VN的本征荧光。该方法在1.00 - 10.00µg mL−¹浓度范围内线性拟合。在第二种方法(方法二)中,使用0.1 M盐酸关闭哌啶部分叔胺到吲哚支架的光致电子转移(PET)后,荧光信号增强到158%。这种值得称赞的荧光灵敏度的提高使得在加药的人血浆中微小地检测到VN,标准偏差不超过1.30。使用酸阻断pet探针,在λex/em为277/323 nm的范围内,荧光信号与VN浓度在0.25 ~ 6.00µg mL−¹范围内呈线性相关。这些简化的程序熟练地评估了单独和共配制胶囊中的VN,而不受胶囊填充材料或共配制药物“吡拉西坦”的任何显著干扰。此外,提交的两个程序成功执行,通过在Brain-ox®胶囊中进行重量变化测试来检查VN,具有良好的接受值。构建的平台集合估算了环境样品(自来水和河水)中的VN,回收率和标准偏差(0.95 - 1.65)可接受。程序的绿色、白色和蓝色适应度通过大量的计算工具进行评估,包括GAPI、AGREE、AGREEprep、RGB 12算法和BAGI。评估表明,提议的作品有效地在可持续性和功能性假设之间达成妥协。这突出表明,设计的方法非常适合作为在关键的制药、生物和环境样品中微量测定VN的生态框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Talanta Open
Talanta Open Chemistry-Analytical Chemistry
CiteScore
5.20
自引率
0.00%
发文量
86
审稿时长
49 days
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