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Ethanol abuse is increasingly becoming a global issue, adversely affecting both society and families. In blood alcohol concentration (BAC) detection, traditional techniques have long experimental cycles and harsh experimental conditions and often fail to produce timely results. Consequently, achieving swift and precise on-site detection of ethanol poisoning in humans poses a formidable challenge in analytical science. We designed a novel assay for swift on-site analysis of ethanol and BTEX (benzene, toluene, ethylbenzene, and xylene) poisoning in humans using a custom portable headspace injector (portable HS) and portable gas chromatography-mass spectrometry (portable GC-MS). This setup, known for its lightweight design and speed, allows on-site sampling and delivers rapid results. We established a calibration curve (R2 > 0.99) for ethanol in blood using portable gas chromatography-mass spectrometry (portable GC-MS). This on-site blood alcohol concentration (BAC) assay proves simpler than traditional methods, enabling rapid analysis of each sample within a short timeframe and requiring only a small blood volume (0.1 ml). In addition to our investigation on ethanol, we developed a portable method for detecting BTEX in blood. This method provides a favorable coefficient of determination (R2 > 0.99) for various substances, thereby broadening the utility of portable mass spectrometry in areas such as traffic inspection and forensic identification. [ABSTRACT FROM AUTHOR]

A compact in-trap single photon ionization (SPI) system, termed discontinuous atmospheric pressure interface (DAPI) ion trap mass spectrometry (ITMS), for the rapid determination of trace volatile organic compounds (VOCs). DAPI enables the maintenance of high analyte pressure in the SPI source while preserving the vacuum. Utilizing vacuum ultraviolet (VUV) lamp as the ion source, we ionize the analyte within an enclosed miniature 3D ion trap for efficient analysis. Experimental findings demonstrate that the system achieves a mass resolution of less than 0.5 atomic mass units for full width at half maxima (FWHM), providing unit resolution. For the response for benzene, the system achieves almost instantaneous response, with rise and fall times of only 2 s, which is a significant advantage compared to the membrane inlet (MI) approach necessary for on-site detection. Additionally, tandem mass spectrometry (MS/MS) with unit m/z isolation window was achieved and resolved dimethyl disulfide and phenol with similar molecular weights. Our results demonstrate that the system provides excellent performance and we anticipate its application in rapidly determining VOCs. [ABSTRACT FROM AUTHOR]

Peak detection is an important step in mass spectrometry as accurately identifying characteristic peaks is key to data analysis. In order to address the issue of false peak detection, while simultaneously ensuring accurate detection of weak and overlapped peaks, this paper introduces an improved algorithm for mass spectrometry integrating weighted continuous wavelet transform with particle swarm optimization-based Otsu (WWTPO). The algorithm applies the weighted continuous wavelet transform (WCWT) to compress the frequency spectrum signal into a smaller scale range, which allows for the acquisition of more distinct and informative peak information. Moreover, the algorithm employs the particle swarm optimization (PSO) algorithm to iteratively evaluate the optimal image segmentation threshold, which addresses the challenge of inaccurate Otsu image segmentation. The method was applied to detect simulated peaks as well as matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) datasets. The performance evaluation was conducted using receiver operating characteristic (ROC) curves, F1 measure and F-scores. Through comparison with continuous wavelet transform (CWT) and genetic algorithm-based threshold segmentation (WSTGA), multi-scale peak detection (MSPD) and CWT and image segmentation (CWT-IS), the results demonstrate that WWTPO exhibits excellent performance in peak detection. The determination of 4-isopropyltoluene also demonstrates that WWTPO has excellent practical application. This method not only maintains a low false peak identification rate but also detects more weak peaks and overlapping peaks, further improving the accuracy and efficiency of peak detection in mass spectrometry. [ABSTRACT FROM AUTHOR]

Mass spectrometry data may be affected by random noise and baseline drift due to experimental instruments and conditions, posing significant challenges for detecting spectral peaks, particularly when identifying weak and separating overlapping peaks. To increase the sensitivity and enhance the resolution, we propose a mass spectral peak detection algorithm that integrates resolution enhancement and image segmentation. Initially, the extended Mexican hat wavelet is proposed by integrating the peak sharpening method with its wavelet. This approach accurately transforms mass spectra into wavelet space using the continuous wavelet transform. Subsequently, the triangular single-peak thresholding method, a more suitable threshold segmentation approach for spectral analysis, is introduced to identify ridges in the two-dimensional wavelet space. Compared to traditional Otsu and its improved variants, long-tailed single-peaked histograms are more effectively processed by this method with lower computational complexity, enabling faster identification of segmentation thresholds and image segmentation. Ultimately, peak positions are determined by utilizing ridge and valley lines in wavelet space along with the original spectrum. To evaluate the performance of the peak recognition algorithm, two metrics are introduced: the receiver operating characteristic (ROC) curve and the balanced F score (F1 score). When compared to multi-scale peak detection (MSPD), continuous wavelet transform and image segmentation (CWT-IS), the developed approach is more suitable for weak and highly overlapping peaks. The robustness and practicality of the method are verified through peak detection using matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectra. [ABSTRACT FROM AUTHOR]

A novel nano-floral inter-polymeric material (λ-Carr-Ag-SA) was developed to effectively capture N-linked glycopeptides from biological samples. A simple one-step reduction of silver ions was involved in the synthesis of the material in which λ-carrageenan and sodium alginate, with abundant hydrophilic groups, were used as the reducing agent and stabilizer. The performance of λ-Carr-Ag-SA was evaluated experimentally by enriching glycopeptides from horse radish peroxidase (HRP) and human serum. All the results demonstrated that λ-Carr-Ag-SA had a great selectivity, low detection limit and a large binding capacity toward glycopeptides. The successful application exhibits great potential of λ-Carr-Ag-SA for further glycoproteome analysis. [ABSTRACT FROM AUTHOR]