The addition of luminescent markers into ammunition cartridges is an appealing proposal to achieve a greater individual identification of the ammunition. The lanthanide elements present in these luminescent materials act as characteristic chemical markers that, also, offer the great benefit of making gunshot residues (GSR) collection easier. Although the use of luminescent markers offers numerous advantages, and can be a reliable future option in the cartridge ammunition market, little or nothing is known about the interaction of the marker with the ammunition compounds after the shot. For the forensic laboratories, it is of utmost importance to anticipate the commercialization of tagged luminescent ammunition by knowing the type of particles produced after the discharge. That is, to investigate if markers merge with GSR to form single particles or, on the contrary, they form individual particles that travel separately from the GSR particles. In this work, conventional ammunition cartridges tagged with two types of luminescent markers were shot. Then, the particles produced were visualized under UV light on the floor, clothing targets and the shooter. The luminescent particles spread over the floor determined the shooter position and the bullet trajectory. The illumination of the shot targets allows the visualization of the GSR patterns only using a portable UV lamp, avoiding the use of colorimetric test. The GSR particles were collected and subjected to SEM-EDX and Raman spectroscopy analysis to get information about their inorganic and organic composition. The results indicated that part of the marker and the GSR merge and travel together. With this, particles composed by the marker and propellant organic compounds can be identified by Raman spectroscopy, and the unequivocal identification of the GSR and the marker can be achieved by SEM-EDX. Consequently, the luminescent particles detected under UV light improve the evidence collection and offer information about the GSR and the marker. Additionally, this study support the use of luminescent ammunition to study, for example, the transfer or persistence of GSR.
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http://dx.doi.org/10.1016/j.forsciint.2017.09.013 | DOI Listing |
Biosens Bioelectron
December 2024
Department of Academic Research, Beijing Ditan Hospital, Capital Medical University, National Center for Infectious Diseases, 8th Jingshun East Road, Beijing, 100015, China. Electronic address:
Luminescence technology is a powerful analytical tool for biomedical research as well as for marker detection. Luminescent materials with aggregation-induced emission (AIE) properties have attracted extensive research interest, and their unique luminescence characteristics, biocompatibility, and sensitivity make them useful for the development of fluorescence-turn-on biosensors with superior sensitivity. While numerous reviews have focused on the design of AIEgens, comprehensive summaries on the strategies for biosensor preparation and application fields remain limited.
View Article and Find Full Text PDFAnal Chem
December 2024
Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education Chongqing, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, People's Republic of China.
Herein, a novel zinc-organic gel with self-catalysis-enhanced electrochemiluminescence (ECL) performance was prepared as an emitter for the first time to assemble a biosensor for ultrasensitive detection of microRNA-221 (miR-221) related to liver cancer. Interestingly, Zn served as a central ion to coordinate with multidentate ligands 2,4,6-tris(4-carboxyphenyl)-1,3,5-triazine (TATB) at room temperature to form Zn-TATB-MOGs with excellent ECL intensity. More importantly, compared to metal ions (e.
View Article and Find Full Text PDFMicrolife
November 2024
Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), 07745 Jena, Germany.
Extracellular vesicles (EVs) have gained attention as facilitators of intercellular as well as interkingdom communication during host-microbe interactions. Recently we showed that upon infection, host polymorphonuclear leukocytes produce antifungal EVs targeting the clinically important fungal pathogen ; however, the small size of EVs (<1 µm) complicates their functional analysis. Here, we employed a more tractable, reporter-based system to label host alveolar epithelial cell-derived EVs and enable their visualization during interaction.
View Article and Find Full Text PDFFASEB J
December 2024
Department of Biochemistry and Molecular Cell Biology, Shanghai Key Laboratory for Tumor Microenvironment and Inflammation, Shanghai Jiao Tong University School of Medicine, Shanghai, P.R. China.
Live cell labeling of various organelles is of great demand in the research field of cell biology. However, current approaches often lack an optimal balance between efficiency and versatility. We took advantage of chemical modified mRNA to express various organelle located fluorescent proteins.
View Article and Find Full Text PDFMethods Mol Biol
December 2024
Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, China.
Genetic modification of vaccinia virus (VACV) is a fundamental and valuable research technique in elucidating the function of VACV genes, as well as the development as vaccine vectors for other infectious diseases, oncolytic therapeutics for cancers, and protein expression systems in mammalian cells. Because of the large size of poxvirus genome and noninfectious feature of the naked viral DNA, construction of recombinant VACV relies on intracellular homologous recombination between transfected DNA and replicating viral DNA in infected cells occurred in VACV infected cells. The efficiency of homologous recombination event for vaccinia virus is relatively low, and recombinant viruses only account for 0.
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