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基于曙红 Y 离子缔合作用分光光度法和荧光光度法分析两种肿瘤药物福替替尼和卡培他滨。

Analysis of Two Oncological Drugs Futibatinib and Capivasertib via Ion-Pairing With Eosin Y as a Spectrofluorimetric and Spectrophotometric Probe.

机构信息

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

出版信息

Luminescence. 2024 Oct;39(10):e4919. doi: 10.1002/bio.4919.

Abstract

Using spectroscopy, two quick and sensitive analytical methods based on eosin Y ion pairing were developed and assessed in order to determine capivasertib and futibatinib with high selectivity and sensitivity. The quenching impact of futibatinib or capivasertib on the eosin Y's fluorescence at a pH 3.8 and 3.3 for futibatinib and capivasertib, respectively, in 0.1-M acetate buffer solution was observed using two spectrofluorometric techniques. These techniques are regarded as the original spectrofluorometric techniques for the assay of futibatinib and capivasertib. For futibatinib and capivasertib, the quenching effect on fluorescence was ranged from 100 to 1000 and 150 to 1500 ng mL, respectively. The absorbance of the generated ion-pair was measured using two different spectrophotometric methods at 550 nm in aqueous buffered solutions with pH values of 3.8 and 3.3 for futibatinib and capivasertib, respectively. In the concentration range of 1.0-10.0 and 2.0-10.0 μg mL, Beer's law was followed. The four approaches were applied to the analysis of dosage forms with a high percent recovery successfully, and they were assessed in compliance with ICH guidelines.

摘要

利用光谱学,开发并评估了两种基于曙红 Y 离子缔合的快速灵敏分析方法,以高选择性和灵敏度来测定卡比沙替尼和呋替尼。在 pH 3.8 和 3.3(分别对应呋替尼和卡比沙替尼)下,在 0.1-M 乙酸盐缓冲溶液中,观察到呋替尼或卡比沙替尼对曙红 Y 荧光的猝灭作用,分别采用两种荧光分光光度技术。这两种技术被认为是检测呋替尼和卡比沙替尼的原始荧光分光光度技术。对于呋替尼和卡比沙替尼,荧光猝灭效应的范围分别为 100 至 1000 和 150 至 1500ng/mL。在 pH 值分别为 3.8 和 3.3 的水缓冲溶液中,使用两种不同的分光光度法在 550nm 处测量生成的离子对的吸光度。在 1.0-10.0 和 2.0-10.0μg/mL 的浓度范围内,遵循比尔定律。四种方法均成功应用于制剂的分析,且回收率高,均符合 ICH 指南的要求。

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