Mass Spectroscopy in Analytical and Bioanalytical Chemistry

A special issue of Chemosensors (ISSN 2227-9040). This special issue belongs to the section "Analytical Methods, Instrumentation and Miniaturization".

Deadline for manuscript submissions: 15 June 2025 | Viewed by 933

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Guest Editor
Major in Materials Science and Engineering, Hallym University, Chuncheon-si, Gangwon-do 24252, Republic of Korea
Interests: MALDI-TOF MS; nanomaterials; biosensors; antibiotic susceptibility tests; small biomarker detection; bacteriophages
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Special Issue Information

Dear Colleagues,

Mass spectroscopy is an analysis technology that enables the detection of high sensitivity to mass via the ionization, acceleration, separation, and detection of samples. Mass spectroscopy technologies such as LC-MS, GC-MS, MALDI-TOF MS, and tandem mass spectroscopy have been developed for various fields, including molecular structural analysis, quality control for industrial products, environmental monitoring, drug analysis, and biological analysis. Mass spectroscopy, which can provide rapid analysis, small-volume analysis, and sensitive analysis, has already been accepted as an advanced tool in analytical chemistry and exhibits the potential to grow as a novel diagnostic paradigm in the biomedical field.

This Special Issue aims to provide an overview of recent advances in mass spectroscopy in analytical and bioanalytical chemistry. We therefore welcome the submission of articles whose scope includes, but is not limited to, sample pretreatment methods, novel chromatography approaches, and novel mass spectrometric techniques. In addition to the subject areas outlined in the keywords below, we welcome all studies that perform analytical and bioanalytical analysis using mass spectroscopy. Both review articles and original research papers will be considered for publication.

Dr. Jong-Min Park
Guest Editor

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Keywords

  • sample preparation
  • elemental analysis
  • small-molecule detection
  • environmental monitoring
  • therapeutic drug monitoring
  • novel matrices for molecular ionization
  • mass spectrometry imaging for battery, display, and biological tissue analysis
  • AI approaches for analytical mass spectroscopy

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Published Papers (1 paper)

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Research

13 pages, 2639 KiB  
Article
Development and Validation of a High-Performance Liquid Chromatography-Inductively Coupled Plasma Mass Spectrometry Method for the Simultaneous Determination of Arsenic and Mercury Species in Human Urine
by Chenyang Zheng, Jun Tang, Xiaodong Pan, Haitao Shen, Zhengyan Hu, Jingshun Zhang, Luxuan Wang, Pinggu Wu and Ying Tan
Chemosensors 2025, 13(3), 78; https://doi.org/10.3390/chemosensors13030078 - 1 Mar 2025
Cited by 1 | Viewed by 730
Abstract
The simultaneous determination of arsenic and mercury species in human urine is critical for clinical diagnostics and therapeutic monitoring because it reduces the costs, time, and consumption of samples. This study proposes a method of utilizing high-performance liquid chromatography-inductively coupled plasma mass spectrometry [...] Read more.
The simultaneous determination of arsenic and mercury species in human urine is critical for clinical diagnostics and therapeutic monitoring because it reduces the costs, time, and consumption of samples. This study proposes a method of utilizing high-performance liquid chromatography-inductively coupled plasma mass spectrometry (HPLC-ICP-MS) for the concurrent analysis of arsenic and mercury species in urine samples. The separation was performed using a Hepu AR 5 μm C18 (250 × 4.6 mm) column, employing a mobile phase composed of 0.1% L-cysteine, 5 mM NH4H2PO4, and 4 mM tetrabutylammonium hydroxide (TBAH). The samples were diluted with water, and matrix interference was reduced through the application of a kinetic energy discrimination (KED) mode. Calibration curves for four arsenic species and three mercury species exhibited strong linearity within the range of 1–20 μg L−1, with correlation coefficients (r) above 0.999. The limits of detection (LOD) ranged from 0.030 to 0.086 μg L−1, while the limits of quantitation (LOQ) were observed to range from 0.10 to 0.29 μg L−1. The spiking recoveries for all species varied from 87.0% to 110.3%, and the intra-day and inter-day relative standard deviations (RSD) were determined to be 1.1–6.0%, and 0.8–9.2%, respectively. These results indicate that the developed method achieves high precision, accuracy, and suitability for clinical applications, offering valuable insights for the diagnosis and treatment of heavy metal exposure. Full article
(This article belongs to the Special Issue Mass Spectroscopy in Analytical and Bioanalytical Chemistry)
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