{"title":"The FRET-Based APTA Sensor/Cy3 Complex for Glucose Determination","authors":"Ghasem Rezanejade Bardajee, Afsaneh Rahimi Chahrogh, Mojdeh Atashkadi","doi":"10.1002/bio.70097","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>This study developed a sensitive and cost-effective fluorescent probe based on the Förster Resonance Energy Transfer (FRET) method to monitor blood glucose levels. The APTA sensor/Cy3 probe consisted of cadmium telluride quantum dots modified with thioglycolic acid (CdTe-TGA QDs), a thiol-glucose-aptamer, and a Cy3-labeled aptamer. Due to the well-matched emission spectrum of the CdTe QDs and the absorption spectrum of Cy3, the FRET system decreased fluorescence intensity. However, glucose molecules quenched it when introduced to the system. The linear relationship between fluorescence intensity and glucose concentration was established with a detection limit of 7.72 × 10<sup>−9</sup> M. The APTA sensor/Cy3 complex demonstrated excellent selectivity and specificity toward glucose and a high recovery rate of 96.00–101.11% in human serum and urine using the spiking method. The structural and morphological characteristics of the APTA sensor/Cy3 complex were confirmed by UV–visible spectroscopy, Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), atomic force microscopy (AFM), and dynamic light scattering (DLS) analyses. The results suggest that the FRET-based APTA sensor/Cy3 complex would lead to the development of fluorescent probes for screening biological metabolites in clinical diagnostics and research.</p>\n </div>","PeriodicalId":49902,"journal":{"name":"Luminescence","volume":"40 2","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Luminescence","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bio.70097","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
This study developed a sensitive and cost-effective fluorescent probe based on the Förster Resonance Energy Transfer (FRET) method to monitor blood glucose levels. The APTA sensor/Cy3 probe consisted of cadmium telluride quantum dots modified with thioglycolic acid (CdTe-TGA QDs), a thiol-glucose-aptamer, and a Cy3-labeled aptamer. Due to the well-matched emission spectrum of the CdTe QDs and the absorption spectrum of Cy3, the FRET system decreased fluorescence intensity. However, glucose molecules quenched it when introduced to the system. The linear relationship between fluorescence intensity and glucose concentration was established with a detection limit of 7.72 × 10−9 M. The APTA sensor/Cy3 complex demonstrated excellent selectivity and specificity toward glucose and a high recovery rate of 96.00–101.11% in human serum and urine using the spiking method. The structural and morphological characteristics of the APTA sensor/Cy3 complex were confirmed by UV–visible spectroscopy, Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), atomic force microscopy (AFM), and dynamic light scattering (DLS) analyses. The results suggest that the FRET-based APTA sensor/Cy3 complex would lead to the development of fluorescent probes for screening biological metabolites in clinical diagnostics and research.
期刊介绍:
Luminescence provides a forum for the publication of original scientific papers, short communications, technical notes and reviews on fundamental and applied aspects of all forms of luminescence, including bioluminescence, chemiluminescence, electrochemiluminescence, sonoluminescence, triboluminescence, fluorescence, time-resolved fluorescence and phosphorescence. Luminescence publishes papers on assays and analytical methods, instrumentation, mechanistic and synthetic studies, basic biology and chemistry.
Luminescence also publishes details of forthcoming meetings, information on new products, and book reviews. A special feature of the Journal is surveys of the recent literature on selected topics in luminescence.