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Study on the supramolecular interaction of astemizole with cucurbit[7]uril and its analytical application

机译:阿司咪唑与葫芦[7] uril的超分子相互作用研究及其分析应用

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摘要

Astemizole (AST) is non-fluorescent in aqueous solution. This property makes its determination through direct fluorescence methods difficult. Reaction and supramolecular interaction mechanisms, between AST and palmatine (PAL) as they compete for occupancy of the cucurbit[7]uril (CB[7]) cavity, were studied using spectrofluorimetry, ~1H NMR, and molecular modeling calculations. The association constants of the complexes formed between the host and the guest were determined. Based on the significant quenching of the supramolecular complex fluorescence intensity, a fluorescent probe method of high sensitivity and selectivity was developed to determine AST in its pharmaceutical dosage forms and in urine samples with good precision and accuracy. The linear range of the method was from 0.02 ng mL~(-1) to 2.2 ng mL~(-1). The detection limit was 0.007 ng mL~(-1). This shows that the proposed method has promising potential for therapeutic monitoring and pharmacokinetics and for clinical application.
机译:Astemizole(AST)在水溶液中不发荧光。该性质使其难以通过直接荧光法测定。使用分光荧光法,〜1H NMR和分子模型计算研究了AST和棕榈碱(PAL)之间竞争葫芦[7] uril(CB [7])空腔的反应和超分子相互作用机理。确定了主体和客体之间形成的配合物的缔合常数。基于超分子复合荧光强度的显着猝灭,开发了一种高灵敏度和选择性的荧光探针方法,以测定其药物剂型和尿液样品中的AST,具有良好的准确性和准确性。该方法的线性范围为0.02 ng mL〜(-1)至2.2 ng mL〜(-1)。检出限为0.007 ng mL〜(-1)。这表明所提出的方法在治疗监测和药代动力学以及临床应用方面具有广阔的前景。

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