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Carbamazepine (CBZ) is a widely used pharmaceutical for various purposes, including as an anticonvulsant, antibiotic, and antiepileptic agent, and it undergoes diverse metabolic pathways in both the environment and the human body. Therefore, this study aimed to explore the distribution of CBZ, the presence of its transformation products (TPs), and the transformation pathways in the Mangyeong and Dongjin Rivers in the Saemangeum watershed of Korea using non-targeted screening. The concentration distribution results for CBZ and its TPs showed that the average concentrations in the Mangyeong and Dongjin Rivers were 128.8 ng/L and 89.0 ng/L, respectively. The Mangyeong River exhibited a higher CBZ concentration than the Dongjin River, which was similar to those of the reported CBZ concentrations in other major domestic and international rivers. The types and detection frequencies of the identified TPs exhibited similar trends. The detection frequencies of the TPs decreased in the following order: CBZ-EP > DiOH-CBZ > 10OH-CBZ > 2OH-CBZ > 9-carboxyacridine > 9-acridinecarboxaldehyde. The detection frequency of the main TPs was high, and some were believed to be generated during the water treatment process. The presence of additional TPs (CBZ-O-quinone, acridine, and iminostilbene) was confirmed by the generated molecular networks. This study presents the transformation pathway of the CBZ and provides foundational data for understanding the environmental behavior of TPs, improving wastewater treatment plants, managing water quality, and establishing water environmental policies. [ABSTRACT FROM AUTHOR]

To avoid fraudulent practices, LC-Orbitrap and FT-NIRS combined with multivariate analysis was used to distinguish between 53 Korean and foreign Boston butt samples; forty were used to establish the calibration model and 13 were used as an external validation set. Twenty metabolites were determined to be good indicators of geographic origin. Both LC-Orbitrap with CDA model based on 20 metabolites and FT-NIRS with PLS achieved 100% efficiency in identifying Korean and foreign samples; overall predictive rates for LC-Orbitrap (94.9%) and FT-NIRS (100%). Thus, combined use of LC-Orbitrap and FT-NIRS could be proposed to determine reliably discriminate geographic origins of pork samples.

Triptorelin, a synthetic gonadotrophin-releasing hormone (GnRH), is mainly used in the clinical treatment of prostate cancer. The mechanism initially stimulates luteinizing hormone (LH) and testosterone secretion followed by suppression, resulting in a reduction in cancer progression. However, GnRHs are prohibited in doping control because of the indirect surge of LH and testosterone. Therefore, GnRH analog detection and confirmation are enforced by World Anti-Doping Agency (WADA) requirements. The effects of triptorelin on LH and endogenous steroid levels in urine and serum of five prostate cancer patients taking triptorelin for the first time were investigated and compared with leuprorelin. The samples were collected at 0.0 h, 3.0 h, 6.0 h, 1 month, and 3 months later after drug administration. The effect of triptorelin on LH levels was measured using a sandwich enzyme-linked immunoassay (ELISA). Testosterone and endogenous steroid levels were monitored using gas chromatography coupled with mass spectrometry (GC/MS). Triptorelin showed an advantage over leuprorelin on LH and testosterone suppression, which is preferable to use for prostate cancer treatment. In this study, triptorelin (5-10), a unique in vivo metabolite, was found in urine and serum and verified with synthetic triptorelin (5-10). The metabolite was analyzed using liquid chromatography combined with Orbitrap (LC-Orbitrap) and liquid chromatography coupled with ion trap/time-of-flight mass spectrometry (LC/MS-IT-TOF). When triptorelin levels are undetectable, the presence of triptorelin (5-10) in human urine can be used as evidence that triptorelin is being misused in doping control., (© 2025 The Author(s). Drug Testing and Analysis published by John Wiley & Sons Ltd.)

Dissolved organic matter (DOM) in aquatic systems is a highly heterogeneous mixture of water-soluble organic compounds, acting as a major carbon reservoir driving biogeochemical cycles. Understanding DOM molecular composition is thus of vital interest for the health assessment of aquatic ecosystems, yet its characterization poses challenges due to its complex and dynamic chemical profile. Here, we performed a comprehensive chemical analysis of DOM from highly urbanized river and seawater sources and compared it to drinking water. Extensive analyses by nontargeted direct infusion (DI) and liquid chromatography (LC) high-resolution mass spectrometry (HRMS) through Orbitrap were integrated with novel computational workflows to allow molecular- and structural-level characterization of DOM. Across all water samples, over 7000 molecular formulas were calculated using both methods (∼4200 in DI and ∼3600 in LC). While the DI approach was limited to molecular formula calculation, the downstream data processing of MS2 spectral information combining library matching and in silico predictions enabled a comprehensive structural-level characterization of 16% of the molecular space detected by LC-HRMS across all water samples. Both analytical methods proved complementary, covering a broad chemical space that includes more highly polar compounds with DI and more less polar ones with LC. The innovative integration of diverse analytical techniques and computational workflow introduces a robust and largely available framework in the field, providing a widely applicable approach that significantly contributes to understanding the complex molecular composition of DOM.