Chemosensors最新文献

{"title":"Coptisine Chloride: A Natural Isoquinoline Alkaloid as a Dual-Responsive Aggregation-Induced Emission Sensor for Heparin and Protamine","authors":"Nana Ma, Xueling Dong, Ruinan Li, Chuang Du, Yuxuan Wang, Jiaxin Bai, Run Ran, X Liu, Dianshuo Zhang, Haikui Zou","doi":"10.3390/chemosensors14020051","DOIUrl":"https://doi.org/10.3390/chemosensors14020051","url":null,"abstract":"Heparin (Hep) and its clinical antidote protamine (PRO) play essential yet antagonistic roles in anticoagulant therapy, necessitating reliable analytical tools to monitor their levels and interactions. Herein, we report that coptisine chloride (COP), a natural isoquinoline alkaloid, acts as an aggregation-induced emission (AIE) sensor enabling dual-responsive fluorescence modulation toward Hep and PRO. Owing to its rigid polycyclic and intrinsically twisted molecular framework, COP displays typical AIE behavior. In a DMSO/PBS mixture (PBS fraction = 99%, v/v), COP forms strongly emissive aggregates with Hep through electrostatically driven complexation, allowing sensitive Hep detection with a limit of detection (LOD) of 0.70 μg/mL. Subsequent competitive binding of PRO to Hep disrupts the COP–Hep aggregates, giving rise to fluorescence quenching and reversible PRO sensing (LOD: 0.49 μg/mL). Theoretical calculations together with multiple characterization techniques reveal an aggregation–disaggregation mechanism governing the dual fluorescence modulation. Moreover, COP achieves accurate Hep quantification in spiked diluted human serum, affording satisfactory linearity and recoveries (LOD = 0.71 μg/mL; recoveries 98.3–101.6%). These results demonstrate that COP, a structurally simple natural AIE luminogen, serves as a sustainable, biocompatible, and accessible tool for reversible Hep and PRO analysis in complex media.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"14 2","pages":"51-51"},"PeriodicalIF":0.0,"publicationDate":"2026-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/14/2/51/pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147382022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Rapid Smartphone Colorimetric Determination of Starch and Ultraviolet Spectrophotometry Quantification of Lignin in Chinese Chrysanthemum Teas","authors":"Wenchen Li, Weiying Lu","doi":"10.3390/chemosensors13120434","DOIUrl":"https://doi.org/10.3390/chemosensors13120434","url":null,"abstract":"Chrysanthemum, a traditional medicinal and edible plant, possesses diverse health-promoting properties attributed to its rich profile of bioactive compounds. However, the intrinsic quality, influenced by the composition of fundamental components like starch and lignin, varies significantly across different cultivars and origins. This study establishes a comprehensive phytochemical profile of 12 representative Chinese chrysanthemum cultivars by systematically quantifying their starch and lignin contents. Furthermore, it develops and validates a novel, low-cost rapid detection method for starch utilizing smartphone-based colorimetry. The starch content, determined by a colorimetric anthrone-sulfuric acid assay, ranged from 2.68 to 18.69 g/100 g, while the lignin content, measured via the acetyl bromide digestion followed by UV spectrophotometry at 280 nm, varied from 4.21 to 13.63 g/100 g, revealing substantial inter-cultivar differences. For starch analysis, a low-cost, immediate, general-purpose, and high-throughput (LIGHt) smartphone-based colorimetry was implemented. Standard curves constructed from both absorbance and the LIGHt assay demonstrated excellent linearity (R2 > 0.99). The method’s performance was evaluated under different lighting conditions and across various smartphone models. The UV spectrophotometry condenses lignin quantification to a single 30-min digestion–reading cycle, bypassing the two-day Klason protocol and increases efficiency greatly. The work successfully provides a foundational component analysis and validates a portable, high-throughput framework for on-site quality control of plant-based products, demonstrating the strong potential of smartphone-based colorimetry for rapid starch detection and a complementary laboratory-scale lignin assay.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 12","pages":"434-434"},"PeriodicalIF":0.0,"publicationDate":"2025-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/13/12/434/pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147333879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Plasmonic Nanopore Sensing to Probe the DNA Loading Status of Adeno-Associated Viruses.","authors":"Scott Renkes, Steven J Gray, Minjun Kim, George Alexandrakis","doi":"10.3390/chemosensors13120418","DOIUrl":"10.3390/chemosensors13120418","url":null,"abstract":"<p><p>Adeno-associated viruses (AAVs) are a leading vector for gene therapy, yet their clinical utility is limited by the lack of robust quality control methods to distinguish between empty (AAV_empty), partially loaded (AAV_partial), and fully DNA loaded (AAV_full) capsids. Current analytical techniques provide partial insights but remain limited in sensitivity, throughput, or resolution. Here we present a multimodal plasmonic nanopore sensor that integrates optical trapping with electrical resistive-pulse sensing to characterize AAV9 capsids at the single-particle level in tens of μL sample volumes and fM range concentrations. As a model system, we employed AAV9 capsids not loaded with DNA, capsids loaded with a self-complementary 4.7 kbp DNA (AAV_scDNA), and ones loaded with single-stranded 4.7 kbp DNA (AAV_ssDNA). Ground-truth validation was performed with analytical ultracentrifugation (AUC). Nanosensor data were acquired concurrently for optical step changes (occurring at AAV trapping and un-trapping) both in transmittance and reflectance geometries, and electrical nanopore resistive pulse signatures, making for a total of five data dimensions. The acquired data was then filtered and clustered by Gaussian mixture models (GMMs), accompanied by spectral clustering stability analysis, to successfully separate between AAV species based on their DNA load status (AAV_empty, AAV_partial, AAV_full) and DNA load type (AAV_scDNA versus AAV_ssDNA). The motivation for quantifying the AAV_empty and AAV_partial population fractions is that they reduce treatment efficacy and increase immunogenicity. Likewise, the motivation to identify AAV_scDNA population fractions is that these have much higher transfection rates. Importantly, the results showed that the nanosensor could differentiate between AAV_scDNA and AAV_ssDNA despite their identical masses. In contrast, AUC could not differentiate between AAV_scDNA and AAV_ssDNA. An equimolar mixture of AAV_scDNA, AAV_ssDNA and AAV_empty was also measured with the sensor, and the results showed the expected population fractions, supporting the capacity of the method to differentiate AAV load status in heterogeneous solutions. In addition, less common optical and electrical signal signatures were identified in the acquired data, which were attributed to debris, rapid entry re-entry to the optical trap, or weak optical trap exits, representing critical artifacts to recognize for correct interpretation of the data. Together, these findings establish plasmonic nanopore sensing as a promising platform for quantifying AAV DNA loading status and genome type with the potential to extend ultra-sensitive single-particle characterization beyond the capabilities of existing methods.</p>","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 12","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13132496/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147811317","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A Label-Free Fluorescence Polarization for Protein Detection Based on Albumin Nanoparticles","authors":"Yunshu Wang, Ruixin An, Fengwei Liu, Zhongyun Dong, Yang Sheng, Siyu Liu","doi":"10.3390/chemosensors13110396","DOIUrl":"https://doi.org/10.3390/chemosensors13110396","url":null,"abstract":"Human serum albumin (HSA), an endogenous protein, was employed in the synthesis of nanoparticles. The treatment of an HSA solution with ethanol and glutaraldehyde resulted in the formation of human serum albumin nanoparticles (HSA NPs), which exhibited a weak fluorescence emission peak at 515 nm upon excitation at 360 nm. Importantly, these synthesized HSA NPs displayed a pronounced fluorescence polarization (FP) signal under identical excitation and emission conditions. Furthermore, incubation of the HSA NPs with specific DNA aptamers targeting lysozyme and thrombin led to a significant decrease in the FP values. This reduction in FP was effectively reversed upon the addition of lysozyme and thrombin. Based on these observations, a label-free fluorescence polarization-based detection platform for lysozyme and thrombin was developed utilizing HSA NPs and a DNA aptamer system.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 11","pages":"396-396"},"PeriodicalIF":0.0,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/13/11/396/pdf?version=1762942371","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147332508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"High-Intensity In Situ Fluorescence Imaging of MicroRNA in Cells Based on Y-Shaped Cascade Assembly","authors":"Yan Liu, Xu Fan, Xinying Zhou, Zhiqi Zhang, Qi Yang, Rongjie Yang, Yingxue Li, Anran Zheng, Lianqun Zhou, Wei Zhang, Jinze Li","doi":"10.3390/chemosensors13090343","DOIUrl":"https://doi.org/10.3390/chemosensors13090343","url":null,"abstract":"MicroRNAs are closely associated with various physiological and pathological processes, making their in situ fluorescence imaging crucial for functional studies and disease diagnosis. Current methods for the in situ fluorescence imaging of microRNA predominantly rely on linear signal amplification, resulting in relatively weak imaging signals. This study introduces a Y-shaped cascade assembly (YCA) method for high-brightness microRNA imaging in cells. Triggered by target microRNA, catalytic hairpin assembly forms double-stranded DNA (H). Through annealing and hybridization, a Y-shaped structure (P) is created. These components assemble into DNA nanofluorescent particles with multiple FAM fluorophores, significantly amplifying fluorescence signals. Optimization experiments revealed that a 1:1 ratio of P to H and an assembly time of 60 min yielded the best results. Under these optimal conditions, the resulting fluorescent nanoparticles exhibited diameters of 664.133 nm, as observed by DLS. In Huh7 liver cancer cells, YCA generated DNA nanoparticles with a fluorescence intensity increase of 117.77%, triggered by target microRNA-21, producing high-intensity fluorescence images and enabling qualitative detection of microRNA-21. The YCA in situ imaging method offers excellent imaging quality and high efficiency, providing a robust and reliable analytical tool for the diagnosis and monitoring of microRNA-related diseases.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 9","pages":"343-343"},"PeriodicalIF":0.0,"publicationDate":"2025-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/13/9/343/pdf?version=1757313664","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147331941","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Development of Polydopamine–Chitosan-Modified Electrochemical Immunosensor for Sensitive Detection of 7,12-Dimethylbenzo[a]anthracene in Seawater","authors":"Huili Hao, Chengjun Qiu, Wei Qu, Yuan Zhuang, Zizi Zhao, Haozheng Liu, Wenhao Wang, Jiarui Su, Wei Tao","doi":"10.3390/chemosensors13070263","DOIUrl":"https://doi.org/10.3390/chemosensors13070263","url":null,"abstract":"7,12-Dimethylbenzo[a]anthracene (DMBA-7,12), a highly toxic and environmentally persistent polycyclic aromatic hydrocarbon (PAH), poses significant threats to marine biodiversity and human health due to its bioaccumulation through the food chain. Conventional chromatographic methods, while achieving comparable detection limits, are hindered by the need for expensive instrumentation and prolonged analysis times, rendering them unsuitable for rapid on-site monitoring of DMBA-7,12 in marine environments. Therefore, the development of novel, efficient detection techniques is imperative. In this study, we have successfully developed an electrochemical immunosensor based on a polydopamine (PDA)–chitosan (CTs) composite interface to overcome existing technical limitations. PDA provides a robust scaffold for antibody immobilization due to its strong adhesive properties, while CTs enhances signal amplification and biocompatibility. The synergistic integration of these materials combines the high efficiency of electrochemical detection with the specificity of antigen–antibody recognition, enabling precise qualitative and quantitative analysis of the target analyte through monitoring changes in the electrochemical properties at the electrode surface. By systematically optimizing key experimental parameters, including buffer pH, probe concentration, and antibody loading, we have constructed the first electrochemical immunosensor for detecting DMBA-7,12 in seawater. The sensor achieved a detection limit as low as 0.42 ng/mL. In spiked seawater samples, the recovery rates ranged from 95.53% to 99.44%, with relative standard deviations (RSDs) ≤ 4.6%, demonstrating excellent accuracy and reliability. This innovative approach offers a cost-effective and efficient solution for the in situ rapid monitoring of trace carcinogens in marine environments, potentially advancing the field of marine pollutant detection technologies.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 7","pages":"263-263"},"PeriodicalIF":0.0,"publicationDate":"2025-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/13/7/263/pdf?version=1752998238","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147332413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Electrostatic Self-Assembly of Heterostructured In2O3/Ti3C2Tx Nanocomposite for High-Selectivity NO2 Gas Sensing at Room Temperature","authors":"Yongjing Guo, Zhengxin Zhang, Hangshuo Feng, Qiuyan Dai, Qiuni Zhao, Zaihua Duan, Shenghui Guo, Yang Li, Ming Hou, Yi Xia","doi":"10.3390/chemosensors13070249","DOIUrl":"https://doi.org/10.3390/chemosensors13070249","url":null,"abstract":"Owing to high electrical conductivity, layered structure, and abundant surface functional groups, transition metal carbides/nitrides (MXenes) have received enormous interest in the field of gas sensors at room temperature. In this work, we synthesize a heterostructured nanocomposite with indium oxide (In2O3) decorated on titanium carbide (Ti3C2Tx) nanosheets by electrostatic self-assembly and develop it for high-selectivity NO2 gas sensing at room temperature. Self-assembly formation of multiple heterojunctions in the In2O3/Ti3C2Tx composite provide abundant NO2 gas adsorption sites and high electron transfer activity, which is conducive to improving the gas-sensing response of the In2O3/Ti3C2Tx gas sensor. Assisted by rich adsorption sites and hetero interface, the as-fabricated In2O3/Ti3C2Tx gas sensor exhibits the highest response to NO2 among various interference gases. Meanwhile, a detection limit of 0.3 ppm, and response/recovery time (197.62/93.84 s) is displayed at room temperature. Finally, a NO2 sensing mechanism of In2O3/Ti3C2Tx gas sensor is constructed based on PN heterojunction enhancement and molecular adsorption. This work not only expands the gas-sensing application of MXenes, but also demonstrates an avenue for the rational design and construction of NO2-sensing materials.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 7","pages":"249-249"},"PeriodicalIF":0.0,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/13/7/249/pdf?version=1752145297","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147333930","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Electrochemical Detection of Bisphenol S Based on Molecularly Imprinted Polymers Grafted on Functionalized Multiwalled Carbon Nanotubes: A Facile Sensor Fabrication Approach","authors":"Christopher Mwanza, Lin Zhao, Qing Zhang, Shou‐Nian Ding","doi":"10.3390/chemosensors13070236","DOIUrl":"https://doi.org/10.3390/chemosensors13070236","url":null,"abstract":"Bisphenol S (BPS), a key ingredient in polycarbonate plastics and epoxy resins, is a known endocrine-disrupting compound that poses significant risks to human health and the environment. As such, the development of rapid and reliable analytical techniques for its detection is essential. In this work, we present a newly engineered electrochemical sensor designed for the sensitive and selective detection of BPS using a straightforward and effective fabrication approach. The sensor was constructed by grafting molecularly imprinted polymers (MIPs) onto vinyl-functionalized multiwalled carbon nanotubes (f-MWCNTs). Ethylene glycol dimethacrylate and acrylamide were used as the cross-linker and functional monomer, respectively, in the synthesis of the MIP layer. The resulting MIP@f-MWCNT nanocomposite was characterized using Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). The MIP@f-MWCNT material was then combined with chitosan, a biocompatible binder, to fabricate the final MIP@f-MWCNT/chitosan-modified glassy carbon electrode (GCE). Electrochemical evaluation showed a broad linear detection range from 1 to 60 µM (R2 = 0.992), with a sensitivity of 0.108 µA/µM and a detection limit of 2.00 µM. The sensor retained 96.0% of its response after four weeks and exhibited high selectivity against structural analogues. In spiked plastic extract samples, recoveries ranged from 95.6% to 105.0%. This robust, cost-effective, and scalable sensing platform holds strong potential for environmental monitoring, food safety applications, and real-time electrochemical detection of endocrine-disrupting compounds like BPS.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 7","pages":"236-236"},"PeriodicalIF":0.0,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/13/7/236/pdf?version=1751297036","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147331594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"An Electrochemical Sensor Based on AuNPs@Cu-MOF/MWCNTs Integrated Microfluidic Device for Selective Monitoring of Hydroxychloroquine in Human Serum","authors":"X Y Feng, Jiaqi Zhao, Shiwei Wu, Ying Kan, H. Li, Weifei Zhang","doi":"10.3390/chemosensors13060200","DOIUrl":"https://doi.org/10.3390/chemosensors13060200","url":null,"abstract":"Hydroxychloroquine (HCQ), a cornerstone therapeutic agent for autoimmune diseases, requires precise serum concentration monitoring due to its narrow therapeutic window. Current HCQ monitoring methods such as HPLC and LC-MS/MS are sensitive but costly and complex. While electrochemical sensors offer rapid, cost-effective detection, their large chambers and high sample consumption hinder point-of-care use. To address these challenges, we developed a microfluidic electrochemical sensing platform based on a screen-printed carbon electrode (SPCE) modified with a hierarchical nanocomposite of gold nanoparticles (AuNPs), copper-based metal–organic frameworks (Cu-MOFs), and multi-walled carbon nanotubes (MWCNTs). The Cu-MOF provided high porosity and analyte enrichment, MWCNTs established a 3D conductive network to enhance electron transfer, and AuNPs further optimized catalytic activity through localized plasmonic effects. Structural characterization (SEM, XRD, FT-IR) confirmed the successful integration of these components via π-π stacking and metal–carboxylate coordination. Electrochemical analyses (CV, EIS, DPV) revealed exceptional performance, with a wide linear range (0.05–50 μM), a low detection limit (19 nM, S/N = 3), and a rapid response time (&lt;5 min). The sensor exhibited outstanding selectivity against common interferents, high reproducibility (RSD = 3.15%), and long-term stability (98% signal retention after 15 days). By integrating the nanocomposite-modified SPCE into a microfluidic chip, we achieved accurate HCQ detection in 50 μL of serum, with recovery rates of 95.0–103.0%, meeting FDA validation criteria. This portable platform combines the synergistic advantages of nanomaterials with microfluidic miniaturization, offering a robust and practical tool for real-time therapeutic drug monitoring in clinical settings.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 6","pages":"200-200"},"PeriodicalIF":0.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2227-9040/13/6/200/pdf?version=1748766559","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147332734","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Evaluating the Intensity of Bitter–Astringent Interactive Perception in Green Tea Based on the Weber–Fechner Law","authors":"Siying Li, Dongdong Du, Shaoming Cheng, Zhenbo Wei","doi":"10.3390/chemosensors13040137","DOIUrl":"https://doi.org/10.3390/chemosensors13040137","url":null,"abstract":"This study aimed to quantify the bitter–astringent interactive perceived intensity (BAIPI) of green tea based on the Weber–Fechner law by two-alternative forced choice test. Caffeine, (-)-epigallocatechin-3-gallate (EGCG), and Quercetin-3-o-rutinoside (Que-rut) were identified as the key bitter–astringent compounds. Then, BAIPI values were assessed based on the concentration ratios and ranges of caffeine, EGCG, and Que-rut in green tea according to the Weber–Fechner law. The BAIPI values were further fitted to a logarithmic curve: yBAIPIvalue=a×lnxconcentration of caffeine−b−⁡c+IVinitialBAIPIvalue−1. The constant terms a, b, and c were derived from the ratio of caffeine to EGCG, as the slope and X-intercept of the curves correlated exponentially with this ratio. The initial BAIPI value (IV) was calculated as: IVinitialBAIPIvalue=18.7960−0.3956q(the ratio of caffeine to Que−rut). Validation showed a standard error of 1.5865 between estimated and actual BAIPI values. This method enables the estimation of bitter–astringent intensity in green tea by analyzing the concentrations of caffeine, EGCG, and Que-rut.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"13 4","pages":"137-137"},"PeriodicalIF":0.0,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147331335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}