McKenna M McKay, Kensington H Fansler, Ke Liu, Dimitri Pappas
{"title":"Isolation and detection of target cells in blood <i>via</i> immunomagnetic separation and atomic emission spectroscopy.","authors":"McKenna M McKay, Kensington H Fansler, Ke Liu, Dimitri Pappas","doi":"10.1039/d5ay00937e","DOIUrl":null,"url":null,"abstract":"<p><p>The identification and quantification of cells in blood can serve to inform disease diagnosis and prognosis for patients. However, sample complexity presents a challenge for achieving sensitive and specific detection methods. Furthermore, there is a need to alleviate current standard clinical protocols from operator burden, limit the required sample volumes, and to reduce analysis timescales, all while maintaining sensitivity. This study presents a novel atomic emission cytometry assay for the detection of cells in blood with high specificity and sensitivity (LOD = 84 cells per μL), requiring only 500 μL sample volume and 1 hour of combined processing and analysis time, exhibiting the potential for broad applications in disease diagnosis. Metal nanoparticles equipped with antibodies serve as a targeted cell labeling platform, as well as an integrated method for immunomagnetic separation and subsequent quantification <i>via</i> microwave plasma-atomic emission spectroscopy (MP-AES) analysis. This assay can also be modified to include multiple types of metal-based nanoparticles and/or target multiple cell surface markers for simultaneous detection of different cell populations within the same sample. The simplicity, specificity, and efficiency of this assay mark it as a viable integrated diagnostic platform for cellular-based disease diagnosis.</p>","PeriodicalId":64,"journal":{"name":"Analytical Methods","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Methods","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5ay00937e","RegionNum":3,"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
The identification and quantification of cells in blood can serve to inform disease diagnosis and prognosis for patients. However, sample complexity presents a challenge for achieving sensitive and specific detection methods. Furthermore, there is a need to alleviate current standard clinical protocols from operator burden, limit the required sample volumes, and to reduce analysis timescales, all while maintaining sensitivity. This study presents a novel atomic emission cytometry assay for the detection of cells in blood with high specificity and sensitivity (LOD = 84 cells per μL), requiring only 500 μL sample volume and 1 hour of combined processing and analysis time, exhibiting the potential for broad applications in disease diagnosis. Metal nanoparticles equipped with antibodies serve as a targeted cell labeling platform, as well as an integrated method for immunomagnetic separation and subsequent quantification via microwave plasma-atomic emission spectroscopy (MP-AES) analysis. This assay can also be modified to include multiple types of metal-based nanoparticles and/or target multiple cell surface markers for simultaneous detection of different cell populations within the same sample. The simplicity, specificity, and efficiency of this assay mark it as a viable integrated diagnostic platform for cellular-based disease diagnosis.