Pub Date : 2025-10-15DOI: 10.1016/j.trac.2025.118498
Lu Shen , Fei Gao , Jing Wei , Die Gao , Dalian Qin , Xiao Wang , Yujiao Ji , Xiaobing An , Xiaogang Zhou , Jianming Wu , Jianing Mi , Lixian Li , Bin Huang , Anguo Wu
The growing interest in natural medicines highlights the need for rapid and accurate analytical methods to identify bioactive compounds. Conventional techniques such as high-performance liquid chromatography, mass spectrometry, and nuclear magnetic resonance are precise but limited by time, cost, and complexity, restricting their use in high-throughput screening. Biosensor technologies offer real-time, label-free, and highly sensitive detection, emerging as powerful alternatives. This review summarizes recent advances in optical, electrochemical, and microfluidic-integrated biosensors, along with their applications in screening antiviral, anti-inflammatory, anticancer, neuroprotective, and nucleic acid-targeting compounds. Key challenges, including matrix interference, specificity, sensitivity, throughput, and standardization, are discussed. Future directions focus on enhancing sensor performance through surface modifications, improved sample processing, multiplexing, and artificial intelligence-assisted data integration. These strategies aim to fully realize the potential of biosensors in accelerating the discovery of novel and effective therapeutic agents from natural sources.
{"title":"Biosensor technologies for natural medicine discovery: current advances, challenges, and future directions","authors":"Lu Shen , Fei Gao , Jing Wei , Die Gao , Dalian Qin , Xiao Wang , Yujiao Ji , Xiaobing An , Xiaogang Zhou , Jianming Wu , Jianing Mi , Lixian Li , Bin Huang , Anguo Wu","doi":"10.1016/j.trac.2025.118498","DOIUrl":"10.1016/j.trac.2025.118498","url":null,"abstract":"<div><div>The growing interest in natural medicines highlights the need for rapid and accurate analytical methods to identify bioactive compounds. Conventional techniques such as high-performance liquid chromatography, mass spectrometry, and nuclear magnetic resonance are precise but limited by time, cost, and complexity, restricting their use in high-throughput screening. Biosensor technologies offer real-time, label-free, and highly sensitive detection, emerging as powerful alternatives. This review summarizes recent advances in optical, electrochemical, and microfluidic-integrated biosensors, along with their applications in screening antiviral, anti-inflammatory, anticancer, neuroprotective, and nucleic acid-targeting compounds. Key challenges, including matrix interference, specificity, sensitivity, throughput, and standardization, are discussed. Future directions focus on enhancing sensor performance through surface modifications, improved sample processing, multiplexing, and artificial intelligence-assisted data integration. These strategies aim to fully realize the potential of biosensors in accelerating the discovery of novel and effective therapeutic agents from natural sources.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118498"},"PeriodicalIF":12.0,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145360141","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-15DOI: 10.1016/j.trac.2025.118501
Enrico Taglioni, Chiara Cavaliere, Andrea Cerrato, Aldo Laganà, Carmela Maria Montone, Anna Laura Capriotti
Microextraction techniques are increasingly valued for their low sample requirements and consistency with green chemistry principles. Over time, several formats have been developed, enabling faster and automated analytical workflows. Among them, in tube-solid phase microextraction (IT-SPME) stands out as a powerful sample preparation technique, offering direct online coupling with chromatographic systems, automation, and reduced solvent use. This review critically examines the main strategies for IT-SPME sorbent fabrication, including fiber-filled, monolithic, coated, and particle-packed capillaries. Emphasis is set on the underlying chemistry of sorbent synthesis, radical polymerization, sol-gel processes, hydrothermal reactions, and click chemistry, while assessing efficiency, scalability, and environmental impact. Challenges such as complex syntheses, hazardous reagents, and artisanal protocols are discussed. The review offers the analytical community a practical guide to reproducible and sustainable strategies for developing IT-SPME devices that are well-suited to automated workflows.
{"title":"Towards an efficient and sustainable technique: A review on the preparation and synthesis of sorbents for in-tube solid-phase microextraction","authors":"Enrico Taglioni, Chiara Cavaliere, Andrea Cerrato, Aldo Laganà, Carmela Maria Montone, Anna Laura Capriotti","doi":"10.1016/j.trac.2025.118501","DOIUrl":"10.1016/j.trac.2025.118501","url":null,"abstract":"<div><div>Microextraction techniques are increasingly valued for their low sample requirements and consistency with green chemistry principles. Over time, several formats have been developed, enabling faster and automated analytical workflows. Among them, in tube-solid phase microextraction (IT-SPME) stands out as a powerful sample preparation technique, offering direct online coupling with chromatographic systems, automation, and reduced solvent use. This review critically examines the main strategies for IT-SPME sorbent fabrication, including fiber-filled, monolithic, coated, and particle-packed capillaries. Emphasis is set on the underlying chemistry of sorbent synthesis, radical polymerization, sol-gel processes, hydrothermal reactions, and click chemistry, while assessing efficiency, scalability, and environmental impact. Challenges such as complex syntheses, hazardous reagents, and artisanal protocols are discussed. The review offers the analytical community a practical guide to reproducible and sustainable strategies for developing IT-SPME devices that are well-suited to automated workflows.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118501"},"PeriodicalIF":12.0,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334165","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
As the body's largest organ, skin plays essential roles in maintaining physiological homeostasis. While indispensable for research and product development, conventional in vitro skin models cannot fully recapitulate recapitulate three-dimensional microenvironments, dynamic perfusion, and multicellular interactions, impeding accurate modeling of barrier functions, immune regulation, and drug permeation. Emerging skin-on-a-chip (SoC) technologies overcome these constraints through innovative microfluidic architectures, controlled fluidics, and multicellular integration, enabling the reconstruction of hierarchical skin structures. However, challenges remain, including material adsorption, absence of appendages, incomplete functional characterization, and a lack of standardized protocols. This review systematically evaluates technological advancements and translational barriers in SoC development. We first outline the native skin's layered architecture and cellular heterogeneity to reveal current modeling limitations. Subsequent analysis focuses on key innovations: biomimetic structural design, advanced biomaterials, biomechanical simulation, and microfluidic regulation. We further examine characterization methodologies and application scenarios. By integrating current findings, we demonstrate the potential of SoC platforms to revolutionize skin pathology research via omics-enabled spatiotemporal profiling and to serve as standardized platforms for product testing and health monitoring. Realizing this potential will require interdisciplinary collaboration to overcome critical bottlenecks in appendage integration, high-throughput detection, and manufacturing standardization—advances poised to transform conventional evaluation paradigms.
{"title":"Advances in skin-on-a-chip technology: Functional innovations and translational challenges","authors":"Jingfan Zhang , Qingwen Zhang , Xiang Fang , Guangsheng Guo , Xiayan Wang","doi":"10.1016/j.trac.2025.118500","DOIUrl":"10.1016/j.trac.2025.118500","url":null,"abstract":"<div><div>As the body's largest organ, skin plays essential roles in maintaining physiological homeostasis. While indispensable for research and product development, conventional in vitro skin models cannot fully recapitulate recapitulate three-dimensional microenvironments, dynamic perfusion, and multicellular interactions, impeding accurate modeling of barrier functions, immune regulation, and drug permeation. Emerging skin-on-a-chip (SoC) technologies overcome these constraints through innovative microfluidic architectures, controlled fluidics, and multicellular integration, enabling the reconstruction of hierarchical skin structures. However, challenges remain, including material adsorption, absence of appendages, incomplete functional characterization, and a lack of standardized protocols. This review systematically evaluates technological advancements and translational barriers in SoC development. We first outline the native skin's layered architecture and cellular heterogeneity to reveal current modeling limitations. Subsequent analysis focuses on key innovations: biomimetic structural design, advanced biomaterials, biomechanical simulation, and microfluidic regulation. We further examine characterization methodologies and application scenarios. By integrating current findings, we demonstrate the potential of SoC platforms to revolutionize skin pathology research via omics-enabled spatiotemporal profiling and to serve as standardized platforms for product testing and health monitoring. Realizing this potential will require interdisciplinary collaboration to overcome critical bottlenecks in appendage integration, high-throughput detection, and manufacturing standardization—advances poised to transform conventional evaluation paradigms.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118500"},"PeriodicalIF":12.0,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334161","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-14DOI: 10.1016/j.trac.2025.118493
Liyuan Wang , Xiaofeng Hu , Shenling Wang , Wenqin Wu , Kaiming Wu , Li Yu , Peiwu Li , Zhaowei Zhang
As urgent public health challenges, food safety and environmental monitoring have drawn growing attention. Point-of-care testing (POCT) represents a cost-effective, rapid, accurate, and convenient means of quantitative detection. The unique fluorescent phenomenon induced by aggregation-induced emission (AIE) holds substantial promise for enhancing POCT capabilities in detecting food and environmental contaminants. This work reviewed recent advancements and challenges in developing the AIE-enhanced POCT method. Firstly, the principles and advantages of the AIE-powered POCT method were discussed. Subsequently, the applications of the AIE-enhanced POCT method in detecting environmental and food contamination were summarized. Finally, the potential commercialization and challenges associated with AIE-powered POCT methods are discussed. This review refreshes the perspective to develop portable, cost-effective sensing solutions and encourages collaborative efforts to advance sensing technology.
{"title":"Aggregation-induced emission-enhanced point-of-care testing method for food safety and environmental monitoring","authors":"Liyuan Wang , Xiaofeng Hu , Shenling Wang , Wenqin Wu , Kaiming Wu , Li Yu , Peiwu Li , Zhaowei Zhang","doi":"10.1016/j.trac.2025.118493","DOIUrl":"10.1016/j.trac.2025.118493","url":null,"abstract":"<div><div>As urgent public health challenges, food safety and environmental monitoring have drawn growing attention. Point-of-care testing (POCT) represents a cost-effective, rapid, accurate, and convenient means of quantitative detection. The unique fluorescent phenomenon induced by aggregation-induced emission (AIE) holds substantial promise for enhancing POCT capabilities in detecting food and environmental contaminants. This work reviewed recent advancements and challenges in developing the AIE-enhanced POCT method. Firstly, the principles and advantages of the AIE-powered POCT method were discussed. Subsequently, the applications of the AIE-enhanced POCT method in detecting environmental and food contamination were summarized. Finally, the potential commercialization and challenges associated with AIE-powered POCT methods are discussed. This review refreshes the perspective to develop portable, cost-effective sensing solutions and encourages collaborative efforts to advance sensing technology.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118493"},"PeriodicalIF":12.0,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145359987","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-14DOI: 10.1016/j.trac.2025.118499
Ganping Cai , Huifeng Zhang , Ran Zhu , Yongcun Zou , Qiong Jia
The deep integration of molecularly imprinted polymers (MIPs) with optical sensing technologies demonstrates promising potential in the analysis of disease biomarkers. By incorporating multimodal optical sensing approaches including fluorescence (FL), surface-enhanced Raman scattering (SERS), surface plasmon resonance (SPR), colorimetry (CM), optics fiber (OF), photonic crystals (PC), and electrochemiluminescence (ECL), MIP-based optical sensors have enabled precise identification of disease biomarkers (e.g., proteins, extracellular vesicles, small molecules, and microorganisms). This review systematically summarizes recent advances in MIPs-based optical sensors, focusing on their design principles, construction strategies, and applications in diagnosing cancers, cardiovascular diseases, neurodegenerative diseases, and bacterial infectious diseases, while also discussing future development trends.
{"title":"Molecularly imprinted optical sensors for disease biomarker analysis: current progress and future trends","authors":"Ganping Cai , Huifeng Zhang , Ran Zhu , Yongcun Zou , Qiong Jia","doi":"10.1016/j.trac.2025.118499","DOIUrl":"10.1016/j.trac.2025.118499","url":null,"abstract":"<div><div>The deep integration of molecularly imprinted polymers (MIPs) with optical sensing technologies demonstrates promising potential in the analysis of disease biomarkers. By incorporating multimodal optical sensing approaches including fluorescence (FL), surface-enhanced Raman scattering (SERS), surface plasmon resonance (SPR), colorimetry (CM), optics fiber (OF), photonic crystals (PC), and electrochemiluminescence (ECL), MIP-based optical sensors have enabled precise identification of disease biomarkers (e.g., proteins, extracellular vesicles, small molecules, and microorganisms). This review systematically summarizes recent advances in MIPs-based optical sensors, focusing on their design principles, construction strategies, and applications in diagnosing cancers, cardiovascular diseases, neurodegenerative diseases, and bacterial infectious diseases, while also discussing future development trends.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118499"},"PeriodicalIF":12.0,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-13DOI: 10.1016/j.trac.2025.118497
Yijia Zheng, Xinyi Sun, Xijiao Li, Jing Lei, Erqun Song
The effective detection of pathogenic bacteria is crucial for safeguarding human health, as these pathogenic bacteria cause a wide range of diseases. Conventional detection methods are often limited by their specificity, sensitivity, and speed, hindering timely detection of pathogenic bacteria. In recent years, the CRISPR/Cas system-comprising clustered regularly interspaced short palindromic repeats (CRISPR) and its associated protein (Cas) - has emerged as a powerful platform for developing such detection methods for pathogenic bacteria, owing to its high specificity in recognizing and cleaving nucleic acid sequences. This manuscript begins with a brief introduction to the origin, classification, working principle, and characteristics of the CRISPR/Cas system. It then comprehensively reviews the recent advances of CRISPR/Cas-based methods integrated with various signal output modalities for the detection of pathogenic bacteria. Finally, the advantages, current limitations, and future prospects of CRISPR/Cas system-based methods for pathogenic bacteria assay are discussed.
{"title":"CRISPR/Cas system-based strategies for pathogenic bacteria detection","authors":"Yijia Zheng, Xinyi Sun, Xijiao Li, Jing Lei, Erqun Song","doi":"10.1016/j.trac.2025.118497","DOIUrl":"10.1016/j.trac.2025.118497","url":null,"abstract":"<div><div>The effective detection of pathogenic bacteria is crucial for safeguarding human health, as these pathogenic bacteria cause a wide range of diseases. Conventional detection methods are often limited by their specificity, sensitivity, and speed, hindering timely detection of pathogenic bacteria. In recent years, the CRISPR/Cas system-comprising clustered regularly interspaced short palindromic repeats (CRISPR) and its associated protein (Cas) - has emerged as a powerful platform for developing such detection methods for pathogenic bacteria, owing to its high specificity in recognizing and cleaving nucleic acid sequences. This manuscript begins with a brief introduction to the origin, classification, working principle, and characteristics of the CRISPR/Cas system. It then comprehensively reviews the recent advances of CRISPR/Cas-based methods integrated with various signal output modalities for the detection of pathogenic bacteria. Finally, the advantages, current limitations, and future prospects of CRISPR/Cas system-based methods for pathogenic bacteria assay are discussed.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118497"},"PeriodicalIF":12.0,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334163","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-13DOI: 10.1016/j.trac.2025.118496
Muyang Liu , Bingxin Zheng , Mengqiu Xiong , Bangshun He , Chunlan Qiu , Tao Li , Ying Li
With the continuous advancement of molecular diagnostic technologies, CRISPR-based nucleic acid detection platforms have emerged as powerful tools due to their programmability, sensitivity, and operational simplicity. While conventional ssDNA and ssRNA probes are widely used, recent studies have demonstrated that advanced nucleic acid probes, such as hairpins, G-triplexes, and G-quadruplexes, can further enhance CRISPR detection by improving signal stability, mismatch discrimination, and amplification-free sensitivity. However, their role has not been comprehensively reviewed. This article provides a systematic summary of these high-order probes, classifying them by structure and signal mechanism, and analyzing their contributions to Cas12/Cas13-based systems. We also highlight how these innovations address key challenges such as low trans-cleavage turnover and background noise, enabling CRISPR diagnostics to achieve greater robustness, specificity, and real-world clinical potential. By integrating molecular design with diagnostic function, these probes represent a promising direction for advancing CRISPR-based detection toward next-generation applications in point-of-care testing.
{"title":"Advanced nucleic acid probes for enhanced CRISPR diagnostics","authors":"Muyang Liu , Bingxin Zheng , Mengqiu Xiong , Bangshun He , Chunlan Qiu , Tao Li , Ying Li","doi":"10.1016/j.trac.2025.118496","DOIUrl":"10.1016/j.trac.2025.118496","url":null,"abstract":"<div><div>With the continuous advancement of molecular diagnostic technologies, CRISPR-based nucleic acid detection platforms have emerged as powerful tools due to their programmability, sensitivity, and operational simplicity. While conventional ssDNA and ssRNA probes are widely used, recent studies have demonstrated that advanced nucleic acid probes, such as hairpins, G-triplexes, and G-quadruplexes, can further enhance CRISPR detection by improving signal stability, mismatch discrimination, and amplification-free sensitivity. However, their role has not been comprehensively reviewed. This article provides a systematic summary of these high-order probes, classifying them by structure and signal mechanism, and analyzing their contributions to Cas12/Cas13-based systems. We also highlight how these innovations address key challenges such as low <em>trans</em>-cleavage turnover and background noise, enabling CRISPR diagnostics to achieve greater robustness, specificity, and real-world clinical potential. By integrating molecular design with diagnostic function, these probes represent a promising direction for advancing CRISPR-based detection toward next-generation applications in point-of-care testing.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118496"},"PeriodicalIF":12.0,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-12DOI: 10.1016/j.trac.2025.118494
Jingrui Yuan , Liang Huang , Jing Wang
Enhancing the sensitivity of lateral flow immunoassays (LFIA) is pivotal for advancing point-of-care diagnosis, primarily by improving the signal to noise (S/N) ratio. This review comprehensively summarizes recent strategies aimed at both amplifying signals and suppressing background noise. Signal enhancement approaches encompass sample amplification (target pre-amplification and enrichment), optimization of immune recognition efficiency (through kinetic regulation and increased reaction probability), and diverse signal amplification techniques (e.g., assembly-based amplification, metal-enhanced fluorescence, advanced detection modalities). Methods to reduce background interference involve low-excitation background strategies (chemiluminescence, magnetically modulated luminescence), low-optical detection background techniques (e.g., time-gated noise suppression, wavelength-selective noise reduction, and scattered light detection). The review also traces the evolution of these methodologies, offering context for their development and guiding researchers in navigating the LFIA platform. Overall, this work serves as an essential resource for enhancing the S/N ratio in LFIA and provides valuable perspectives for the design of next-generation LFIA systems.
{"title":"Strategies for enhancing the signal-to-noise ratio in optical lateral flow immunoassay: A review","authors":"Jingrui Yuan , Liang Huang , Jing Wang","doi":"10.1016/j.trac.2025.118494","DOIUrl":"10.1016/j.trac.2025.118494","url":null,"abstract":"<div><div>Enhancing the sensitivity of lateral flow immunoassays (LFIA) is pivotal for advancing point-of-care diagnosis, primarily by improving the signal to noise (S/N) ratio. This review comprehensively summarizes recent strategies aimed at both amplifying signals and suppressing background noise. Signal enhancement approaches encompass sample amplification (target pre-amplification and enrichment), optimization of immune recognition efficiency (through kinetic regulation and increased reaction probability), and diverse signal amplification techniques (e.g., assembly-based amplification, metal-enhanced fluorescence, advanced detection modalities). Methods to reduce background interference involve low-excitation background strategies (chemiluminescence, magnetically modulated luminescence), low-optical detection background techniques (e.g., time-gated noise suppression, wavelength-selective noise reduction, and scattered light detection). The review also traces the evolution of these methodologies, offering context for their development and guiding researchers in navigating the LFIA platform. Overall, this work serves as an essential resource for enhancing the S/N ratio in LFIA and provides valuable perspectives for the design of next-generation LFIA systems.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118494"},"PeriodicalIF":12.0,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334100","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-12DOI: 10.1016/j.trac.2025.118495
Ximei Zhang, Guangmin Zhang, Lanzhen He, Lanlan Chen, Huanghao Yang
Recent advancements in nucleic acid-based nanoprobes have revolutionized targeted subcellular imaging, offering unprecedented precision and versatility in visualizing cellular components. This review highlights the design and application of these probes, which leverage their high specificity to bind target molecules, enabling accurate imaging and dynamic tracking of organelles such as mitochondria, lysosomes, and the endoplasmic reticulum. By integrating signal amplification and fluorescence modules, these probes significantly enhance imaging sensitivity, making them invaluable tools in disease diagnosis, drug development, and biomedical research. Furthermore, their cross-disciplinary potential extends to gene expression regulation, disease mechanism elucidation, and personalized therapy. This comprehensive overview underscores the transformative impact of nucleic acid-based probes in advancing analytical chemistry and life sciences, paving the way for future innovations in subcellular imaging and therapeutic applications.
{"title":"Recent advances in nucleic acid-based probes for organelle-specific imaging","authors":"Ximei Zhang, Guangmin Zhang, Lanzhen He, Lanlan Chen, Huanghao Yang","doi":"10.1016/j.trac.2025.118495","DOIUrl":"10.1016/j.trac.2025.118495","url":null,"abstract":"<div><div>Recent advancements in nucleic acid-based nanoprobes have revolutionized targeted subcellular imaging, offering unprecedented precision and versatility in visualizing cellular components. This review highlights the design and application of these probes, which leverage their high specificity to bind target molecules, enabling accurate imaging and dynamic tracking of organelles such as mitochondria, lysosomes, and the endoplasmic reticulum. By integrating signal amplification and fluorescence modules, these probes significantly enhance imaging sensitivity, making them invaluable tools in disease diagnosis, drug development, and biomedical research. Furthermore, their cross-disciplinary potential extends to gene expression regulation, disease mechanism elucidation, and personalized therapy. This comprehensive overview underscores the transformative impact of nucleic acid-based probes in advancing analytical chemistry and life sciences, paving the way for future innovations in subcellular imaging and therapeutic applications.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118495"},"PeriodicalIF":12.0,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334159","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A major concern for patients with blood-based disorders is their requirement for frequent blood transfusions, which is one of the primary causes of increased morbidity and mortality among these groups, especially in low- and middle-income countries. Various efforts have been made to extend blood grouping, genotyping, and compatibility testing to improve blood transfusion practices, especially for patients affected with β-thalassemia, sickle cell disease, aplastic anemia, and cancer. Precise blood typing will assist in optimizing donor-recipient compatibility testing, thereby reducing alloimmunization risk and post-transfusion complications. Different Point-of-Care-Testing (POCT) devices have been transformed into trailblazers, opening various avenues in transfusion medicine practices as they automate, reduce the number of steps, and have a profound ability to reproduce results rapidly with high economic benefits that contribute significantly to the healthcare sectors. The current state-of-the-art POCTs include wearables, flexible, paper-based, chip-based, printed-type, microfluidics, and lateral flow-based assays, as discussed in this review article. In addition, exciting insights into various other applications of POCTs in hemoglobin and hematocrit measurement, identifying storage lesions, and monitoring of bacterial contamination prior to platelet transfusion among others have been comprehensively discussed. This review thus intends to provide a critical perspective focusing on the future direction of POCTs for the efficient practice of transfusion medicine.
{"title":"Recent advances in point-of-care testing devices for transfusion medicine","authors":"Rijo Rajeev , Paresh Mohanty , Suvro Sankha Datta , Parikshit Moitra","doi":"10.1016/j.trac.2025.118490","DOIUrl":"10.1016/j.trac.2025.118490","url":null,"abstract":"<div><div>A major concern for patients with blood-based disorders is their requirement for frequent blood transfusions, which is one of the primary causes of increased morbidity and mortality among these groups, especially in low- and middle-income countries. Various efforts have been made to extend blood grouping, genotyping, and compatibility testing to improve blood transfusion practices, especially for patients affected with β-thalassemia, sickle cell disease, aplastic anemia, and cancer. Precise blood typing will assist in optimizing donor-recipient compatibility testing, thereby reducing alloimmunization risk and post-transfusion complications. Different Point-of-Care-Testing (POCT) devices have been transformed into trailblazers, opening various avenues in transfusion medicine practices as they automate, reduce the number of steps, and have a profound ability to reproduce results rapidly with high economic benefits that contribute significantly to the healthcare sectors. The current state-of-the-art POCTs include wearables, flexible, paper-based, chip-based, printed-type, microfluidics, and lateral flow-based assays, as discussed in this review article. In addition, exciting insights into various other applications of POCTs in hemoglobin and hematocrit measurement, identifying storage lesions, and monitoring of bacterial contamination prior to platelet transfusion among others have been comprehensively discussed. This review thus intends to provide a critical perspective focusing on the future direction of POCTs for the efficient practice of transfusion medicine.</div></div>","PeriodicalId":439,"journal":{"name":"Trends in Analytical Chemistry","volume":"194 ","pages":"Article 118490"},"PeriodicalIF":12.0,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145334098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}