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DOI 10.1016/j.saa.2024.124470

Медицинская библиотека · Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy · 2024

Design of new boron-doped carbon dots for nano-level assay of nebivolol in human plasma and commercial products; Application to greenness assessments.

AlSalem Huda Salem, Alharbi Sara Naif, Al-Goul Soha Talal, Salman Baher I, Hassan Yasser F, Abdel-Lateef Mohamed A

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Recently, nanomaterials have attracted a lot of attention due to their potential as effective fluorescent nano-sensor probes. They were distinguishing substitutes for other luminescent techniques, such as fluorescent dyes and luminous derivatization, because of their affordability, environmental friendliness, and special photocatalytic properties. In the suggested work, a straightforward method was used to create boron and nitrogen carbon dots (B@CDs) with a good quantum yield value of 31.15 % utilizing boric acid and di-sodium EDTA. For the purpose of characterizing QDs, a variety of instruments were employed, such as transmission electron microscopy, fluorescence spectroscopy, X-ray FTIR, and UV-VIS spectroscopy. Nebivolol (NEB) is a cardiovascular medication used globally to treat congestive heart failure and hypertension, is in the meantime. For this reason, a brand-new, environmentally friendly analytical technique was created to determine the amount of human plasma, uniformity test, and commercial nebivolol (NEB) tablets. After gradually adding NEB, the response of B@CQDs was enhanced at 438 nm (excitation at 371 nm). The calibration graph ranged between 20 and 500 ng mL-1 with a quantification limit (LOQ) of 2.50 ng mL-1 and a detection limit (LOD) of 0.82 ng mL-1.

Для цитирования: AlSalem Huda Salem, Alharbi Sara Naif, Al-Goul Soha Talal, Salman Baher I, Hassan Yasser F, Abdel-Lateef Mohamed A. Design of new boron-doped carbon dots for nano-level assay of nebivolol in human plasma and commercial products; Application to greenness assessments.. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2024. DOI: 10.1016/j.saa.2024.124470.

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