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Query: "author" (Primož Šket) .

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Green synthesis of a magnetite/graphitic carbon nitride 2D nanocomposite for efficient ▫$Hg^{2+}$▫ remediation
Raghuraj S. Chouhan, Jan Gačnik, Igor Živković, Sreekanth Vijayakumaran Nair, Nigel Willy Van de Velde, Alenka Vesel, Primož Šket, Sonu Gandhi, Ivan Jerman, Milena Horvat, 2023, original scientific article

Abstract: Novel nanoadsorbents demonstrate the potential to efficiently eliminate harmful substances, such as Hg2+, from the environment while preserving ecological balance. However, the search for environmentally-friendly nanomaterials as ideal adsorbents, as well as the development of suitable synthesis protocols, remains a challenge. This study presents an effective thermal-sonication technique for producing unique de novo tris-s-triazine carbon nitride nanosheets decorated with magnetite nanoparticles (M-g-CN). The structural integrity and chemical properties of the M-g-CN nanocomposite were extensively characterized using a battery of analytical instruments, including FTIR, SEM, TEM, XRD, XPS, AFM, Raman, and NMR. The obtained data, along with the analysis results, are discussed in detail. The novel synthesis method yields a high percentage (97.7%) of stable, highly selective, and reusable M-g-CN (40 mg mL−1). The resulting M-g-CN effectively binds Hg2+, with binding efficiencies of 96.0%, 97.5%, 98.2%, and 99.4% for Hg2+ concentrations of 50 pg mL−1 in marine, stream, precipitation, and ultra-pure matrices, respectively. Also, the magnetite-decorated particles can be easily retrieved using an applied magnetic field. This greener and scalable synthesis method does not require harsh chemicals, making it cost-effective, eco-friendly, and non-toxic compared to other technologies such as carbon filters, ion exchange resins, chemical precipitation, membrane filtration, electrochemical methods, and biological remediation. Overall, the synthesized M-g-CN exhibits wide-ranging potential applications, particularly as a green adsorbent in passive samplers or materials for remediation purposes.
Keywords: mercury, elimination, nanoadsorbents, nanocomposites
Published in DiRROS: 05.01.2026; Views: 84; Downloads: 33
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2.
Glyoxal as single crosslinker for mechanically blown, condensed and hydrolyzable tannin foams
Jonas Eckardt, Michele De Nato, Elena Colusso, Lorenzo Moro, Primož Šket, Samuele Giovando, Gianluca Tondi, 2025, original scientific article

Published in DiRROS: 05.12.2025; Views: 202; Downloads: 84
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A novel glucosamine-based cannabidiol complex based on intermolecular bonding with improved water solubility
Mitja Križman, Jure Zekič, Primož Šket, Alojz Anžlovar, Barbara Zupančič, Jože Grdadolnik, 2025, original scientific article

Published in DiRROS: 26.08.2025; Views: 453; Downloads: 211
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Thiol-reactive or redox-active : revising a repurposing screen led to a new invalidation pipeline and identified a true noncovalent inhibitor against papain-like protease from SARS-CoV-2
Maria Kuzikov, Stefano Morasso, Jeanette Reinshagen, Markus Wolf, Vittoria Monaco, Flora Cozzolino, Simona Golič Grdadolnik, Primož Šket, Janez Plavec, Daniela Iaconis, 2025, original scientific article

Abstract: The SARS-CoV-2 papain-like protease PLpro has multiple roles in the viral replication cycle, related to both its polypeptide cleavage function and its ability to antagonize the host immune response. Targeting the PLpro function is recognized as a promising mechanism to modulate viral replication, while supporting host immune responses. However, the development of PLpro-specific inhibitors remains challenging. Comprehensive investigations utilizing enzymatic, binding studies, and cellular assays revealed the previously reported inhibitors to act in an unspecific manner. At present, GRL-0617 and its derivatives remain the best-validated compounds with demonstrated antiviral activity in cells and in mouse models. In this study, we refer to the pitfalls of the redox sensitivity of PLpro. Using a screening-based approach to identify inhibitors of PLpro’s proteolytic activity, we made extensive efforts to validate active compounds over a range of conditions and readouts, emphasizing the need for comprehensive orthogonal data when profiling putative PLpro inhibitors. The remaining active compound, CPI-169, was shown to be a noncovalent inhibitor capable of competing with GRL-0617 in NMR-based experiments, suggesting that it occupied a similar binding site and inhibited viral replication in Vero-E6 cells, opening new design opportunities for further development as antiviral agents.
Keywords: SARS-CoV-2, drug repurposing, papain-like protease, redox, STD-NMR, CPI-169, GRL-0617
Published in DiRROS: 20.08.2025; Views: 410; Downloads: 187
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Comparing hydrolysable and condensed tannins for tannin protein-based foams
Jonas Eckardt, Lorenzo Moro, Elena Colusso, Primož Šket, Samuele Giovando, Gianluca Tondi, 2025, original scientific article

Published in DiRROS: 30.01.2025; Views: 877; Downloads: 378
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