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用于含硫醇药物可行且可靠检测的绿色创新荧光方法;以卡托普利为例

Green innovative fluorescence approach for the feasible and reliable assay of thiol-containing drugs; captopril as a model.

作者信息

Derayea Sayed M, Nagy Dalia M, Badr El-Din Khalid M, Attia Tamer Z, Samir Ebtihal, Mohamed Abobakr A, Hamad Ahmed A

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Minia University 61519-Minia Egypt.

Analytical Chemistry Department, Faculty of Pharmacy, Deraya University New-Minia 61519-Minia Egypt.

出版信息

RSC Adv. 2022 Jun 14;12(27):17607-17616. doi: 10.1039/d2ra02408j. eCollection 2022 Jun 7.

Abstract

In the present study, a novel spectrofluorimetric approach was designed for the analysis of captopril as a thiol-containing compound. The approach is based on the formation of a ternary fluorescent compound between the target thiol compound, -phthaldehyde, and a suitable primary amine-containing compound. The produced 1-thio-alkyl-isoindole derivative exhibited very high emission activity in a faintly alkaline aqueous solution that could be monitored at 448 nm (excitation at 334 nm). 2-Amino-6-methyl-6-hydroxy-heptane was selected as the primary amine candidate that gave the high fluorescence intensity with the stability of the formed product. At the optimal experimental condition, the intensity of fluorescence of the formed product was linearly related to the concentration of captopril in 20-450 ng mL range. Commercial pharmaceutical tablets were analyzed, and the obtained results agreed with those of the published method regarding precision and accuracy. The mechanism of the reaction was discussed. In addition, the greenness of the approach was rated following eco-scale criteria.

摘要

在本研究中,设计了一种新型荧光光谱法用于分析含硫醇的化合物卡托普利。该方法基于目标硫醇化合物、邻苯二甲醛和合适的含伯胺化合物之间形成三元荧光化合物。生成的1-硫代烷基异吲哚衍生物在弱碱性水溶液中表现出非常高的发射活性,可在448nm处监测(激发波长为334nm)。选择2-氨基-6-甲基-6-羟基庚烷作为伯胺候选物,其形成的产物具有高荧光强度和稳定性。在最佳实验条件下,生成产物的荧光强度在20-450ng/mL范围内与卡托普利浓度呈线性关系。对市售药片片剂进行了分析,所得结果在精密度和准确度方面与已发表方法的结果一致。讨论了反应机理。此外,根据生态规模标准对该方法的绿色度进行了评级。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e82/9194952/e6c5f8a1ed36/d2ra02408j-f1.jpg

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