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This study aimed to evaluate the use of electrochemistry to generate the oxidation and reduction products of active pharmaceutical ingredients (APIs) with a hydrazone group, including dantrolene, nitrofurantoin, furazidine, and nitrofural. In the first step, cyclic voltammetry was employed to assess the electroactivity of these compounds. In the second step, the transformation products of selected APIs following electrochemical oxidation and reduction were analyzed using the ROXY EC System equipped with a µ-PrepCell™ 2.0, coupled with a high-resolution Q-TOF mass spectrometer. The identification of transformation products was based on accurate mass, isotopic distribution, and fragmentation pattern. Seventeen API impurities were identified in this study, contributing to insights into drug stability and potential risks associated with their manufacture. Experimental findings were supported by the quantum mechanical DFT calculations of the molecular energies. In addition, using commercially available in silico software, the predicted metabolic products were compared with those obtained by experimental methods. The electrochemical approach proved useful as a test for determining the stability of compounds, the detection of new impurities and structure determination using high-resolution mass spectrometry.
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http://dx.doi.org/10.3390/ijms26094295 | DOI Listing |
Bioimpacts
August 2025
Department of Biochemistry, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand.
Introduction: Hepatocellular carcinoma (HCC) remains a major cause of cancer mortality, and effective therapeutic options are limited. MicroRNA‑372‑3p (miR‑372‑3p) has been implicated in HCC, yet its exact role is unclear.
Methods: We established miR‑372‑3p‑overexpressing HCC cell lines (HepG2, SNU‑449, JHH‑4) via lentiviral transduction.
Scand J Med Sci Sports
September 2025
Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Dietary intake has an important influence on rates of fuel use during exercise, but the extent to which short-term diet changes affect peak fat oxidation (PFO) and the intensity at which this occurs (Fat) is unknown. This study examined the impact of diet-induced changes in substrate availability on PFO and Fat and the expression of key lipid-regulatory genes and proteins in skeletal muscle. Forty moderately to well-trained males (27 ± 5 years, V̇O 56.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
Earth and Environmental Sciences, University of Minnesota-Twin Cities, Minneapolis, Minnesota 55455, United States.
Mining metals for the advancement of society requires innovative and cost-effective remediation strategies that protect the environment and, ideally, allow for concentration and recovery of metals from waste streams. Microbially mediated strategies that remove metals from aqueous waste streams via sorption and/or oxidation-reduction reactions show promise as eco-friendly, cost-effective solutions. Our objective was to use Mn-oxidizing fungi, isolated from the Soudan Underground Mine State Park, MN, a high-salinity, mine-impacted environment, to sequester transition metals Mn, Co, Cu, and Ni.
View Article and Find Full Text PDFAnim Sci J
September 2025
Department of Animal Science and Technology, National Taiwan University, Taipei, Taiwan.
Dietary n-6 and n-3 polyunsaturated fatty acid (PUFA) balance critically modulates various physiological processes, including inflammation and cell death. This study investigated the effects of different n-6 PUFA ratios (1:1, 5:1, 10:1, 20:1) on ferroptosis in porcine IPEC-J2 intestinal epithelial cells. Cells treated with varying PUFA ratios showed a significant reduction in cell viability, which was alleviated by the ferroptosis inhibitor ferrostatin-1 (fer-1).
View Article and Find Full Text PDFJ Biochem Mol Toxicol
September 2025
Biochemistry Division, Chemistry Department, Faculty of Science, Tanta University, Tanta, Egypt.
Breast cancer is one of the most lethal cancers in women worldwide. Tamoxifen (TAM), a nonsteroidal antiestrogen, is a highly successful treatment for breast cancer. However, developed resistance to TAM can substantially impair chemotherapy efficacy, resulting in poor prognosis and cancer recurrence.
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