Utilisation of Carbon Quantum Dots from Hazelnut Husk for Folic Acid (FA) Detection: An Innovative Approach

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ali Arda Ciritcioğlu, Erdem Elibol, Zehra Günaydın, Tuna Demirci
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Abstract

This study presents the development of a carbon quantum dot (CQD)-based fluorescence sensor for the accurate quantification of Folic Acid (FA). CQDs were synthesized from hazelnut husk using a solvothermal method and functionalized with silver ions to create an “off-state” fluorescence system. Upon mixing FA solutions, prepared from pure water and pharmaceutical tablets, with phosphate-buffered saline (PBS) and “off-state” CQDs, fluorescence emission was restored (“on-state”) in a concentration-dependent manner when excited at 360 nm. A strong linear relationship was observed between FA concentration and fluorescence intensity, with an R² value of ≈ 0.994. The samples were categorized into low (0.0376–0.7533 µM) and high (0.7533–7.533 µM) concentration groups for improved accuracy, achieving mean percentage errors of 0.70% and 1.85%, respectively, at concentrations as low as 0.565 µM. This CQD-based sensor demonstrated rapid, cost-effective, and highly sensitive detection capabilities, making it a promising alternative for FA quantification in biomedical and nutritional applications. Furthermore, the use of sustainable raw materials, such as hazelnut husk, highlights the eco-friendly and practical advantages of this method over conventional techniques.

Abstract Image

利用榛子壳碳量子点检测叶酸:一种创新方法。
本研究提出了一种基于碳量子点(CQD)的荧光传感器,用于叶酸(FA)的精确定量。以榛子壳为原料,采用溶剂热法合成了CQDs,并用银离子进行功能化,形成了一个“非稳态”荧光体系。将纯水和药片制备的FA溶液与磷酸盐缓冲盐水(PBS)和“关闭状态”的CQDs混合后,在360 nm处激发时,荧光发射以浓度依赖的方式恢复(“打开状态”)。FA浓度与荧光强度呈较强的线性关系,R²值≈0.994。为了提高准确性,将样品分为低浓度组(0.0376-0.7533µM)和高浓度组(0.7533-7.533µM),在低浓度为0.565µM时,平均百分比误差分别为0.70%和1.85%。这种基于cqd的传感器具有快速,经济,高灵敏度的检测能力,使其成为生物医学和营养应用中FA定量的有希望的替代方案。此外,使用可持续的原材料,如榛子壳,突出了这种方法比传统技术更环保和实用的优势。
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来源期刊
The Protein Journal
The Protein Journal 生物-生化与分子生物学
CiteScore
5.20
自引率
0.00%
发文量
57
审稿时长
12 months
期刊介绍: The Protein Journal (formerly the Journal of Protein Chemistry) publishes original research work on all aspects of proteins and peptides. These include studies concerned with covalent or three-dimensional structure determination (X-ray, NMR, cryoEM, EPR/ESR, optical methods, etc.), computational aspects of protein structure and function, protein folding and misfolding, assembly, genetics, evolution, proteomics, molecular biology, protein engineering, protein nanotechnology, protein purification and analysis and peptide synthesis, as well as the elucidation and interpretation of the molecular bases of biological activities of proteins and peptides. We accept original research papers, reviews, mini-reviews, hypotheses, opinion papers, and letters to the editor.
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