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绿色化学在可持续荧光衍生方法中的应用,用于定量测定药物制剂和加标人血浆中作为抗肿瘤药物的达罗他胺的荧光分光光度法。

Utility of green chemistry for sustainable fluorescence derivatization approach for spectrofluorimetric quantification of Darolutamide as antineoplastic drug in pharmaceutical formulation and spiked human plasma.

机构信息

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Deraya University, New Minia, Egypt.

Faculty of Pharmacy, Deraya University, New Minia, Egypt.

出版信息

Luminescence. 2024 Mar;39(3):e4704. doi: 10.1002/bio.4704.

DOI:10.1002/bio.4704
PMID:38433336
Abstract

Darolutamide is an oral nonsteroidal androgen receptor antagonist used to delay the process of prostate cancer to metastatic disease and to increase the quality of life for people with advanced prostate cancer. Here, a second spectrofluorimetric method was advanced for quantifying Darolutamide in pharmaceutical formulation and spiked human plasma. This method depends on the fluorescence derivatization of Darolutamide with 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole (NBD-Cl) at 75°C in a (pH 9) of borate buffer to produce a fluorescent derivative that can be detected at 520 nm after excitation at 460 nm. The method has been validated using ICH criteria, and it demonstrated linearity in the range 5-200 ng ml The limit of detection (LOD) and limit of quantitation (LOQ) were 1.15 and 3.84 nm, respectively. The proposed method was applied precisely and accurately for quantifying Darolutamide within the pharmaceutical formulation and spiking human plasma without any interferences. Moreover, the method's sustainability was evaluated and compared with the published method using two greenness assessment tools termed analytical eco-scale and Analytical GREEnness (AGREE). These findings suggest that the method is more sustainable than the published method.

摘要

达罗他胺是一种口服非甾体雄激素受体拮抗剂,用于延缓前列腺癌向转移性疾病的发展进程,并提高晚期前列腺癌患者的生活质量。在此,提出了第二种分光荧光法,用于定量测定药物制剂和加标人血浆中的达罗他胺。该方法依赖于达罗他胺在硼酸盐缓冲液(pH 9)中与 4-氯-7-硝基苯并-2-氧杂-1,3-二唑(NBD-Cl)在 75°C 下进行荧光衍生化,以产生可在 460nm 激发后在 520nm 处检测到的荧光衍生物。该方法已根据 ICH 标准进行了验证,并且在 5-200ng ml 的范围内表现出线性关系。检测限(LOD)和定量限(LOQ)分别为 1.15 和 3.84ng ml。该方法可精确且准确地用于定量测定药物制剂中的达罗他胺和加标人血浆中的达罗他胺,无任何干扰。此外,还使用两种称为分析生态标度和分析绿色度(AGREE)的绿色评估工具评估和比较了该方法的可持续性与已发表方法。这些发现表明,该方法比已发表的方法更具可持续性。

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