TRAC-TRENDS IN ANALYTICAL CHEMISTRY分析化学趋势

TRAC-TRENDS IN ANALYTICAL CHEMISTRY(英文缩写 TRAC-TREND ANAL CHEM),ISSN 0165-9936,eISSN 1879-3142,中文译名:分析化学趋势 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
13.500
JCR 分区
Q1
CAS 分区
B1
近一年发文量
2
本站 PubMed 收录统计

发文量统计区间:2025-11-01 至 2026-10-31,按本站收录文献的发表日期统计。

ISSN: 0165-9936 · eISSN: 1879-3142 · 缩写: TRAC-TREND ANAL CHEM ·中文: 分析化学趋势

期刊介绍

选择期刊介绍栏目

期刊简介

《TrAC-Trends in Analytical Chemistry》是分析化学领域具有国际影响力的综述期刊,聚焦分析科学与技术的前沿进展。内容涵盖仪器方法、传感与检测、分离科学、组学分析、环境与生物分析等方向,读者群包括分析化学研究者、方法开发人员及跨学科应用科学家。

研究方向

主要发表分析化学各分支的综述、评论与前瞻性文章,主题涉及新型分析技术、样品前处理、化学计量学、生物传感、质谱与光谱方法、微纳尺度分析及环境、临床、食品等应用领域,也关注方法学趋势与跨学科融合。

期刊特色

以约稿和主动投稿的综述为主,强调对领域发展脉络的梳理与批判性评价,而非单篇原创研究。文章信息密度高、引用广泛,适合希望快速把握方向动态的研究生、课题负责人及工业研发人员阅读参考。

投稿难度

投稿难度较高,通常需要作者在对应方向有系统积累,并对文献进行深入整合与观点提炼。建议先与编辑沟通选题,突出综述的新颖视角与时效性,避免简单罗列文献;录用与否更取决于选题价值和写作质量,而非单一指标。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
202114.908Q1
202213.100Q1
202311.800Q1
202412.000Q1
202513.500Q1

TRAC-TRENDS IN ANALYTICAL CHEMISTRY 最新收录文献

  1. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    1. Ambient high-spatial-resolution mass spectrometry imaging: recent advances in technologies and metabolomics studies.

    1. 常压高空间分辨率质谱成像:技术与代谢组学研究的最新进展
    作者:
    Dan Chen, Nathan Colwell, Zhibo Yang
    日期:
    2026-02-27

    Achieving high-spatial-resolution in ambient mass spectrometry imaging (MSI) is critical in accurately characterizing the spatial distribution of biomolecules. Ambient MSI enables in situ mapping spatial heterogeneity of metabolites under ambient conditions, facilitating molecular imaging from multicellular structure down to subcellular level. In this review, we first summarized the strategies developed to enhance spatial resolution in ambient MSI, including technological innovations, advances in sample preparation, and data-driven approaches. We then discussed the applications of these techniques in metabolomics studies and addressed current challenges and limitations. Finally, we highlighted emerging opportunities and future directions for achieving ambient high-spatial-resolution MSI.

  2. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    2. Multifunctional Nanobody Fusion Proteins in Immunoassays: Diverse Strategies for Enhanced Analytical Performance.

    作者:
    Qiyi He, Junkang Pan, Yijia Zhang, Zhihao Xu, Christophe Morisseau, Bruce D Hammock, Dongyang Li
    日期:
    2025-08-02

    Nanobodies, derived from camelid heavy-chain antibodies, offer exceptional specificity, stability, and solubility, enabling rapid and sensitive immunoassays. Their small size makes them ideal scaffolds for genetic fusion with reporter proteins, functional peptides, and signal amplification modules. In contrast to conventional antibodies, nanobodies can be precisely engineered at the gene level, allowing directional conjugation and efficient incorporation of signal-enhancing elements. This tunability simplifies assay design and reduces processing steps. Additionally, recombinant expression systems enable stable, scalable, and standardized production of nanobody-based immunoreagents, ensuring reproducibility in diagnostics. In this review, we summarize recent advances in the engineering and application of nanobody fusion proteins in immunoassays, with a particular focus on three main strategies: signal reporting, site-oriented strategies, and multivalency. We highlight how these approaches enhance sensitivity, shorten assay time, and enable multiplex detection. Finally, we discuss future perspectives and remaining challenges in the design and application of nanobody-based platforms for diagnostics.

  3. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    3. Nanoplasmonics biosensors: At the frontiers of biomedical diagnostics.

    3. 纳米等离子体生物传感器:生物医学诊断的前沿
    作者:
    Aidan J Canning, Joy Q Li, Supriya Atta, Hsin-Neng Wang, Tuan Vo-Dinh
    日期:
    2024-09-18

    This article presents an overview of various nanoplasmonics biosensors and their diverse applications, focusing on recent developments in our laboratory. We describe the versatility and effectiveness of different plasmonics-active platforms, ranging from solid substrates to adaptable nanoparticles like gold nanostars and nanorattles. The "Inverse Molecular Sentinel" (iMS) biosensing technology uses surface-enhanced Raman scattering (SERS) to detect nucleotide biomarkers associated with diseases ranging from acute infections to several types of cancer. We have also developed SERS-based nanochip systems capable of detecting DNA targets related to infectious disease biomarkers such as HIV, malaria, and dengue, promising advancements in global health diagnostics. Further, nanorattle-based biosensors are designed as "lab-in-a-stick" devices for rapid head and neck cancer diagnosis. Other technologies include plasmonics-enhanced lateral flow immunoassay systems, smartphone-based biosensing, and implantable biosensors or "smart tattoo" systems. These nanoplasmonics biosensors open new frontiers to rapid, simple, and effective detection systems for biomedical diagnostics.

  4. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    4. A Reproducibility Crisis for Clinical Metabolomics Studies.

    作者:
    Darcy Cochran, Mai NourEldein, Dominika Bezdekova, Aaron Schram, Réka Howard, Robert Powers
    日期:
    2024-08-19

    Cancer is a leading cause of world-wide death and a major subject of clinical studies focused on the identification of new diagnostic tools. An in-depth meta-analysis of 244 clinical metabolomics studies of human serum samples highlights a reproducibility crisis. A total of 2,206 unique metabolites were reported as statistically significant across the 244 studies, but 72% (1,582) of these metabolites were identified by only one study. Further analysis shows a random disparate disagreement in reported directions of metabolite concentration changes when detected by multiple studies. Statistical models revealed that 1,867 of the 2,206 metabolites (85%) are simply statistical noise. Only 3 to 12% of these metabolites reach the threshold of statistical significance for a specific cancer type. Our findings demonstrate the absence of a detectable metabolic response to cancer and provide evidence of a serious need by the metabolomics community to establish widely accepted best practices to improve future outcomes.

  5. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    5. Multi-adductomics: Advancing mass spectrometry techniques for comprehensive exposome characterization.

    5. 多加合物组学:推进质谱技术以全面表征暴露组
    作者:
    Mu-Rong Chao, Yuan-Jhe Chang, Marcus S Cooke, Chiung-Wen Hu
    日期:
    2024-08-05

    Adductomics, an emerging field within the 'omics sciences, focuses on the formation and prevalence of DNA, RNA, and protein adducts induced by endogenous and exogenous agents in biological systems. These modifications often result from exposure to environmental pollutants, dietary components, and xenobiotics, impacting cellular functions and potentially leading to diseases such as cancer. This review highlights advances in mass spectrometry (MS) that enhance the detection of these critical modifications and discusses current and emerging trends in adductomics, including developments in MS instrument use, screening techniques, and the study of various biomolecular modifications from mono-adducts to complex hybrid crosslinks between different types of biomolecules. The review also considers challenges, including the need for specialized MS spectra databases and multi-omics integration, while emphasizing techniques to distinguish between exogenous and endogenous modifications. The future of adductomics possesses significant potential for enhancing our understanding of health in relation to environmental exposures and precision medicine.

  6. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    6. Artificial Intelligence in Metabolomics: A Current Review.

    作者:
    Jinhua Chi, Jingmin Shu, Ming Li, Rekha Mudappathi, Yan Jin, Freeman Lewis, Alexandria Boon, Xiaoyan Qin, Li Liu, Haiwei Gu
    日期:
    2024-07-03

    Metabolomics and artificial intelligence (AI) form a synergistic partnership. Metabolomics generates large datasets comprising hundreds to thousands of metabolites with complex relationships. AI, aiming to mimic human intelligence through computational modeling, possesses extraordinary capabilities for big data analysis. In this review, we provide a recent overview of the methodologies and applications of AI in metabolomics studies in the context of systems biology and human health. We first introduce the AI concept, history, and key algorithms for machine learning and deep learning, summarizing their strengths and weaknesses. We then discuss studies that have successfully used AI across different aspects of metabolomic analysis, including analytical detection, data preprocessing, biomarker discovery, predictive modeling, and multi-omics data integration. Lastly, we discuss the existing challenges and future perspectives in this rapidly evolving field. Despite limitations and challenges, the combination of metabolomics and AI holds great promises for revolutionary advancements in enhancing human health.

  7. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    7. Frontiers in Mass Spectrometry-Based Spatial Metabolomics: Current Applications and Challenges in the Context of Biomedical Research.

    作者:
    Kate Wheeler, Camil Gosmanov, Michael Jimenez Sandoval, Zhibo Yang, Laura-Isobel McCall
    日期:
    2024-04-18

    Metabolites are critical products and mediators of cellular and tissue function, and key signals in cell-to-cell, organ-to-organ and cross-organism communication. Many of these interactions are spatially segregated. Thus, spatial metabolomics can provide valuable insight into healthy tissue function and disease pathogenesis. Here, we review major mass spectrometry-based spatial metabolomics techniques and the biological insights they have enabled, with a focus on brain and microbiota function and on cancer, neurological diseases and infectious diseases. These techniques also present significant translational utility, for example in cancer diagnosis, and for drug development. However, spatial mass spectrometry techniques still encounter significant challenges, including artifactual features, metabolite annotation, open data, and ethical considerations. Addressing these issues represent the future challenges in this field.

  8. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    8. Current smartphone-assisted point-of-care cancer detection: Towards supporting personalized cancer monitoring.

    8. 当前智能手机辅助的即时癌症检测:迈向支持个性化癌症监测
    作者:
    Linh Thi Phuong Le, Anh Hoang Quan Nguyen, Le Minh Tu Phan, Hien Thi Thanh Ngo, Xing Wang, Brian Cunningham, Enrique Valera, Rashid Bashir, Andrew W Taylor-Robinson, Cuong Danh Do
    日期:
    2024-04-09

    With the rising incidence of cancer-related mortality, new enabling technologies are necessary to offer comprehensive molecular profiles of patients in order to assist clinicians to establish an early presumptive diagnosis. Biosensors that are technically comparable to conventional laboratory diagnostics have been developed. However, because the manufacture and operation processes of these biosensors were not well adjusted for end-users as patients, the approach is not optimized in these newly built platforms. Hence, smartphone-assisted biosensors have been developed for point-of-care utilization. They are faster, simpler, and more affordable than standard examinations and first-generation biosensors, however, they raise numerous concerns regarding their applicability for early cancer detection. Therefore, this review focuses primarily on cutting edge developments in smartphone-assisted biosensing platforms that are most relevant to early cancer diagnosis, including optical and electrochemical biosensors, and cancer imaging. What is needed to bring this important technology to realization as early cancer diagnosis tool is discussed.

  9. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    9. Single Cell mass spectrometry: Towards quantification of small molecules in individual cells.

    作者:
    Yunpeng Lan, Zhu Zou, Zhibo Yang
    日期:
    2024-03-19

    Studying cell heterogeneity can provide a deeper understanding of biological activities, but appropriate studies cannot be performed using traditional bulk analysis methods. The development of diverse single cell bioanalysis methods is in urgent need and of great significance. Mass spectrometry (MS) has been recognized as a powerful technique for bioanalysis for its high sensitivity, wide applicability, label-free detection, and capability for quantitative analysis. In this review, the general development of single cell mass spectrometry (SCMS) field is covered. First, multiple existing SCMS techniques are described and compared. Next, the development of SCMS field is discussed in a chronological order. Last, the latest quantification studies on small molecules using SCMS have been described in detail.

  10. JCR分区: Q1 CAS分区: B1 影响因子: 13.5

    10. Best Practices in NMR Metabolomics: Current State.

    10. 核磁共振代谢组学的最佳实践:现状
    作者:
    Robert Powers, Erik R Andersson, Amanda L Bayless, Robert B Brua, Mario C Chang, Leo L Cheng, Chaevien S Clendinen, Darcy Cochran, Valérie Copié, John R Cort, Alexandra A Crook, Hamid R Eghbalnia, Anthony Giacalone, Goncalo J Gouveia, Jeffrey C Hoch, Micah J Jeppesen, Amith S Maroli, Matthew E Merritt, Wimal Pathmasiri, Heidi E Roth, Anna Rushin, Isin T Sakallioglu, Saurav Sarma, Tracey B Schock, Lloyd W Sumner, Panteleimon Takis, Mario Uchimiya, David S Wishart
    日期:
    2023-12-12

    A literature survey was conducted to identify current practices used by NMR metabolomics investigators when conducting and reporting their metabolomics studies. A total of 463 papers from 2020 and 80 papers from 2010 were selected from PubMed and were manually analyzed by a team of investigators to assess the extent and completeness of the experimental procedures and protocols reported. A significant number of the papers did not report on essential experimental details, incompletely stated which statistical methods were used, improperly applied supervised multivariate statistical analyses, or lacked validation of statistical models. A large diversity of protocols and software were identified, which suggests a lack of consensus and a relatively limited use of commonly agreed upon standards for conducting and reporting NMR metabolomics studies. The overall intent of the survey is to inform and encourage the NMR metabolomics community to develop and adopt best-practices for the field.

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