基于量子点的新型测定法,用于测定不同基质中的抗高血压药物米诺地尔和噻吗洛尔。

Esraa S Ahmed, Eman A Bahgat, Hanaa Saleh, Mona E El Sharkasy, Fathalla Belal
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引用次数: 0

摘要

本研究报告了一种灵敏、经济、生态友好的光谱荧光法,用于评估两种抗高血压药物,即米诺地尔和噻吗洛尔。通过对可溶性淀粉和硫脲进行 15 分钟的微波处理,生成了蓝色发光的硫氮共掺杂碳量子点(S,N-CQDs)。制备的纳米点在 276/430 纳米波长处显示荧光,量子产率为 22%。对制备的纳米传感器的检测证实,它们掺杂了氮和硫,尺寸在 4.5-9.03 纳米之间。所提议的方法在 0.20 至 5.0 和 2.0 至 30.0 µg/mL 范围内具有直线性,米诺地尔和噻吗洛尔的 LOQ 分别为 0.16 和 0.82 µg/mL。所开发的方法可用于评估药物制剂中米诺地尔和噻吗洛尔的浓度,回收率在99.00%和101.94%之间,RSD值较低(小于2%)。所开发的方法灵敏度高,可用于人工水溶液中噻吗洛尔的测定,回收率在 97.60 % 至 101.57 % 之间。研究进一步考察了每种分析物如何与制备的点相互作用,从而导致其荧光淬灭。此外,还进行了干扰研究,通过确定常见添加剂、共同配制药物和共同给药药物中的分析物水平,评估所提出方法的特异性。分析生态尺度、GAPI 和 AGREE 评估技术被用来确认所建议方法的绿色性。
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Novel quantum dots-based assay for the determination of anti-hypertensive drugs minoxidil and timolol in different matrices.

The present work reports a sensitive, affordable, and ecologically friendly spectrofluorimetric method for the assessment of two antihypertensive medications, namely minoxidil and timolol. Blue-emitting sulfur and nitrogen co-doped carbon quantum dots (S,N-CQDs) were generated by exposing soluble starch and thiourea to a 15-minute microwave treatment. The so- prepared nanodots displayed fluorescence at 276/430 nm with a quantum yield of 22 %. Inspection of the so-prepared nano-sensor verified their doping with nitrogen and sulfur, and their size was in the range of 4.5-9.03 nm. The proposed method was found to be rectilinear in the range of 0.20-5.0 and 2.0-30.0 µg/mL, with LOQs of 0.16 and 0.82 µg/mL for minoxidil and timolol, respectively. The developed method was employed to assess the concentrations of minoxidil and timolol in their pharmaceutical formulations, with %recoveries varying between 99.00 % and 101.94 %, and low RSD values (less than 2 %). The high sensitivity of the developed method allowed its use for timolol measurement in artificial aqueous humor, with % recoveries between 97.60 %.and 101.57 %. The study further examined how each analyte interacted with the prepared dots, leading to a quenching of their fluorescence. Additionally, an interference study was utilized to evaluate the specificity of the proposed approach through determining analyte levels in the existence of common additives, co-formulated drugs, and co-administered drugs. The analytical eco-scale, GAPI and AGREE assessment techniques were utilized to confirm the suggested method greenness.

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