Abdel-Hakim Ali, Belal Fathalla, Hammad Mohamed A, Elgaml Abdelaziz, El-Maghrabey Mahmoud
Department of Analytical Chemistry, Faculty of Pharmacy, University of Sadat City, Sadat City, 32897, Monufia, Egypt; Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.
Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.
Anal Chim Acta. 2025 Feb 1;1337:343539. doi: 10.1016/j.aca.2024.343539. Epub 2024 Dec 10.
The current synthetic strategies for carbon dots (CDs) are usually time-consuming, rely on complicated processes, and need high temperatures and energy. Recent studies have successfully synthesized CDs at room temperature. Unfortunately, most CDs synthesized at room temperature are obtained under harsh reaction conditions, prepared using aromatic precursors, or need a long time to generate. Therefore, an energy-free room-temperature rapid synthesis of CDs under mild conditions using aliphatic substrates is important. We aim to provide an innovative approach to synthesizing CDs to be used to develop the first fluorescence-based assay of the non-fluorescent anti-hyperlipidemic drug, fenofibrate.
We report an innovative, energy-free, and room-temperature preparation of fluorescent N-doped CDs utilizing aliphatic substrates in only 20 min. The synthesis was based on a self-exothermic Schiff base condensation reaction between methylglyoxal and ethylenediamine. The prepared CDs' antibacterial properties, biocompatibility, and cell-imaging ability were investigated. The fluorescence signal of the CDs was quantitively quenched upon adding increasing concentrations of fenofibrate in the range of 0.50-15.0 μg/mL. Therefore, the prepared CDs were applied as a nanosensor to develop the first fluorescence-based assay of fenofibrate. The reliability of the synthesized nanosensor was confirmed by the successful quantification of fenofibrate in pharmaceutical dosage forms, environmental water, weight loss herbal products, and dietary supplements. The obtained recovery ranged from 95.33 to 104.58 %. In addition, the minimal environmental impact of the developed fenofibrate sensing strategy was confirmed using the recently reported metrics.
The key advantage of this work is the use of an energy-free approach to synthesize CDs rapidly under mild conditions without aromatic substrates. This opens a new window for the eco-friendly synthesis of CDs that avoids the drawbacks of the traditional methods. Additionally, it is the first fluorescence nanosensor for sensing fenofibrate in various matrices, avoiding the limitations of the previous methods, such as high cost, poor selectivity, and low sensitivity.
目前碳点(CDs)的合成策略通常耗时,依赖复杂的过程,且需要高温和能源。最近的研究已成功在室温下合成碳点。不幸的是,大多数在室温下合成的碳点是在苛刻的反应条件下获得的,使用芳香族前体制备,或者需要很长时间才能生成。因此,利用脂肪族底物在温和条件下无能量室温快速合成碳点很重要。我们旨在提供一种创新方法来合成碳点,用于开发首个基于荧光的非荧光抗高血脂药物非诺贝特的检测方法。
我们报道了一种创新的、无能量的室温制备方法,利用脂肪族底物仅在20分钟内即可制备出荧光N掺杂碳点。该合成基于甲基乙二醛和乙二胺之间的自热席夫碱缩合反应。研究了制备的碳点的抗菌性能、生物相容性和细胞成像能力。在0.50 - 15.0μg/mL范围内加入浓度不断增加的非诺贝特时,碳点的荧光信号被定量猝灭。因此,制备的碳点被用作纳米传感器来开发首个基于荧光的非诺贝特检测方法。通过成功定量药物剂型、环境水、减肥草药产品和膳食补充剂中的非诺贝特,证实了合成纳米传感器的可靠性。获得的回收率在95.33%至104.58%之间。此外,使用最近报道的指标证实了所开发的非诺贝特传感策略对环境的影响最小。
这项工作的关键优势在于使用无能量方法在温和条件下快速合成碳点,且无需芳香族底物。这为碳点的环保合成打开了一扇新窗口,避免了传统方法的缺点。此外,它是首个用于检测各种基质中非诺贝特的荧光纳米传感器,避免了先前方法的局限性,如成本高、选择性差和灵敏度低。