The potential of metal-organic framework MIL-101(Al)-NH2 in the forefront of antiviral protection of cells via interaction with SARS-CoV-2 spike RBD protein and their antibacterial action mediated with hypericin and photodynamic treatment

. 2025 Aug ; 691 () : 137454. [epub] 20250326

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid40168900
Odkazy

PubMed 40168900
DOI 10.1016/j.jcis.2025.137454
PII: S0021-9797(25)00845-8
Knihovny.cz E-zdroje

The global pandemic of SARS-CoV-2 has highlighted the necessity for innovative therapeutic solutions. This research presents a new formulation utilising the metal-organic framework MIL-101(Al)-NH2, which is loaded with hypericin, aimed at addressing viral and bacterial challenges. Hypericin, recognised for its antiviral and antibacterial efficacy, was encapsulated to mitigate its hydrophobicity, improve bioavailability, and utilise its photodynamic characteristics. The MIL-101(Al)-NH2 Hyp complex was synthesised, characterised, and evaluated for its biological applications for the first time. The main objective of this study was to demonstrate the multimodal potential of such a construct, in particular the effect on SARS-CoV-2 protein levels and its interaction with cells. Both in vitro and in vivo experiments demonstrated the effective transport of hypericin to cells that express ACE2 receptors, thereby mimicking mechanisms of viral entry. In addition, hypericin found in the mitochondria showed selective phototoxicity when activated by light, leading to a decrease in the metabolic activity of glioblastoma cells. Importantly, the complex also showed antibacterial efficacy by selectively targeting Gram-positive Staphylococcus epidermidis compared to Gram-negative Escherichia coli under photodynamic therapy (PDT) conditions. To our knowledge, this study was the first to demonstrate the interaction between hypericin, MIL-101(Al)-NH2 and the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein, which inhibits cellular uptake and colocalises with ACE2-expressing cells. Therefore, the dual functionality of the complex - targeting the viral RBD and the antibacterial effect via PDT - emphasises its potential to mitigate complications of viral infections, such as secondary bacterial infections. In summary, these results suggest that MIL-101(Al)-NH2 Hyp is a promising multifunctional therapeutic agent for antiviral and antibacterial applications, potentially contributing to the improvement of COVID-19 treatment protocols and the treatment of co-infections.

Center for Interdisciplinary Biosciences Technology and Innovation Park P J Šafárik University in Košice Jesenná 5 SK 041 54 Košice Slovak Republic

Center for Interdisciplinary Biosciences Technology and Innovation Park P J Šafárik University in Košice Jesenná 5 SK 041 54 Košice Slovak Republic; Department of Biochemistry Faculty of Science P J Šafárik University in Košice Moyzesova 11 SK 041 54 Košice Slovak Republic

Center for Interdisciplinary Biosciences Technology and Innovation Park P J Šafárik University in Košice Jesenná 5 SK 041 54 Košice Slovak Republic; Department of Biophysics Faculty of Science P J Šafárik University in Košice Jesenná 5 SK 041 54 Košice Slovak Republic

Center for Interdisciplinary Biosciences Technology and Innovation Park P J Šafárik University in Košice Jesenná 5 SK 041 54 Košice Slovak Republic; Institute of Animal Biochemistry and Genetics Centre of Biosciences Slovak Academy of Sciences Dúbravská cesta 9 SK 840 05 Bratislava Slovak Republic

Depart of Condensed Matter Physics Faculty of Science P J Šafárik University in Košice Jesenná 5 SK 041 54 Košice Slovak Republic

Department of Biophysics and Cell Biology Faculty of Medicine University of Debrecen Doctoral School of Molecular Medicine Egyetem tér 1 H 4032 Debrecen Hungary

Department of Chemistry Faculty of Science University of Ostrava 30 Dubna 22 CZ 702 00 Ostrava Czech Republic

Department of Inorganic Chemistry Faculty of Science P J Šafárik University in Košice Moyzesova 11 SK 041 54 Košice Slovak Republic

Department of Inorganic Chemistry Faculty of Science P J Šafárik University in Košice Moyzesova 11 SK 041 54 Košice Slovak Republic; BovaChem s r o Laboratory 1 Kirejevská 22 SK 979 01 Rimavská Sobota Slovak Republic

Institute of Experimental Physics Slovak Academy of Sciences Watsonova 47 SK 040 01 Košice Slovak Republic

Laboratory for Functional and Metabolic Imaging Institute of Physics Swiss Federal Institute of Technology in Lausanne Station 3 Building PH CH 1015 Lausanne Switzerland

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