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亲核取代反应在阿立哌唑制剂和血浆基质中荧光分光光度法测定中的应用;绿色度评估。

Application of a nucleophilic substitution reaction for spectrofluorimetric determination of aripiprazole in pharmaceutical dosage form and plasma matrix; greenness assessment.

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Northern Border University, Rafha 91911, Saudi Arabia.

Pharmaceutical Chemistry Department, College of Pharmacy, Umm Al-Qura University, Makkah, Saudi Arabia.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2023 Dec 15;303:123238. doi: 10.1016/j.saa.2023.123238. Epub 2023 Aug 5.

DOI:10.1016/j.saa.2023.123238
PMID:37562210
Abstract

Aripiprazole is an antipsychotic medicine used to treat a variety of mental disorders, including irritability linked with autism disorder in children. Herein, a green and highly sensitive spectrofluorimetric method was developed for the determination of aripiprazole in pharmaceutical dosage form and plasma matrix. The method based on the formation of a fluorescent adduct from the nucleophilic substitution reaction of 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole (NBD-chloride) with aripiprazole, which can be detected at 542 nm following excitation at 481 nm. Factors that affect the development and fluorescence sensitivity of the reaction product were investigated and optimized. The reaction yielded the most optimal fluorescence responses when it was performed using 1.5 mL of 0.2 % w/v NBD-chloride, 1.5 mL of borate buffer pH 9, heating at 80 °C for 20 min, and ethanol as a diluting solvent. The method was validated as per ICH guidelines for analytical and bioanalytical procedures. Good linearity was established between the fluorescence responses of the reaction product and aripiprazole concentrations in the range of 100-1200 ng/mL with adequate accuracy and precision results. The applied method was very sensitive and selectively determined aripiprazole in pharmaceutical and plasma matrices with no interferences. Furthermore, the compliance of the proposed method with the principles of green analytical chemistry was evaluated in comparison with the reported method using analytical eco-scale and AGREE metrics. The outputs proved that the proposed method complied more with the principles of green analytical chemistry than the reported method.

摘要

阿立哌唑是一种抗精神病药物,用于治疗多种精神障碍,包括与儿童自闭症相关的易怒症。在此,开发了一种用于测定药物制剂和血浆基质中阿立哌唑的绿色、高灵敏度分光荧光法。该方法基于亲核取代反应,即 4-氯-7-硝基苯并-2-氧代-1,3-二唑(NBD-氯)与阿立哌唑的反应,生成荧光加合物,在 481nm 激发下,可在 542nm 处检测到。研究并优化了影响反应产物形成和荧光灵敏度的因素。当使用 1.5mL 0.2%w/v NBD-氯、1.5mL 硼酸缓冲液 pH 9、在 80°C 加热 20min 并使用乙醇作为稀释溶剂时,反应产生了最佳的荧光响应。该方法按照 ICH 分析和生物分析程序指南进行了验证。反应产物的荧光响应与阿立哌唑浓度在 100-1200ng/mL 范围内呈良好的线性关系,具有足够的准确性和精密度。该方法对药物和血浆基质中的阿立哌唑具有很高的灵敏度和选择性,无干扰。此外,通过分析生态标度和 AGREE 指标与已报道的方法进行比较,评估了所提出方法与绿色分析化学原则的符合程度。结果表明,与已报道的方法相比,所提出的方法更符合绿色分析化学原则。

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