Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/165232
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dc.creatorPinho, AS-
dc.creatorPereira, R-
dc.creatorPereira, M-
dc.creatorRai, A-
dc.creatorFerreira, L-
dc.creatorMartins, MCL-
dc.creatorParreira, P-
dc.date.accessioned2025-02-10T16:31:09Z-
dc.date.available2025-02-10T16:31:09Z-
dc.date.issued2025-
dc.identifier.issn2192-2640-
dc.identifier.urihttps://hdl.handle.net/10216/165232-
dc.descriptionA.S.P., R.P., and M.P. contributed equally to this work. A.S.P. thanks FCT for the PhD Studentship 2022.12580.BD and the ICBAS Doctoral Program in Biomedical Sciences. P.P. thanks FCT for CEECIND/01210/2018 and 2023.07672.CEECIND and M.C.L.M. for LA/P/0070/2020. M.C.L.M. also acknowledges MOBILIsE Project, which has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement no. 951723. L.F. to thank the financial support of PRR project HfPT – Health from Portugal (Ref: 02/C05- i01.01/2022.PC644937233-00000047).The following i3S Scientific Platforms, all members of the national infrastructure PPBI-Portuguese Platform of Bioimaging (PPBI-POCI-01-0145-FEDER-022122) were used: Inverted Fluorescence Microscope was conducted at Bioimaging i3S Scientific Platform, Zetasizer analysis was conducted at Biointerfaces and Nanotechnology (BN) i3S Scientific Platform, Transmission electron microscopy was performed at the Histology and Electron Microscopy (HEMS) i3S Scientific Platform, with assistance from Rui Fernandes, Cláudia Machado and Sofia Pacheco.pt_PT
dc.description.abstractHelicobacter pylori chronic infection is the highest risk factor for the development of gastric cancer, being this Gram-negative bacterium classified as carcinogenic. The mounting resistance of H. pylori to antibiotics calls for innovative therapeutic strategies. Here, the proof-of-concept studies that support the development of a "trojan horse" therapeutic strategy based on cholesterol-grafted nanoparticles (Chol-NP) to counteract H. pylori infection are depicted. The bacterium ability to specifically recognize and bind to surface grafted cholesterol is demonstrated by its adhesion to cholesterol(Chol)-functionalized self-assembled monolayers (SAMs) on gold substrates (2D Chol-SAMs) in a concentration dependent manner, with optimal Chol-SAMs prepared with 25% Chol-polyethylene glycol (PEG)-thiol in solution (75% tetra(ethylene glycol)-thiol). These results further show that cholesterol functionalized gold nanoparticles (3D Chol-SAMs, Chol-NP) eradicate H. pylori at a minimum bactericidal concentration of 125 µg mL-1. Chol-NP kill H. pylori through internalization and membrane rupture, as observed by transmission electron microscopy (TEM). Chol-NP are cytocompatible (human gastric adenocarcinoma (AGS) cell line), non-hemolytic and innocuous to bacteria representative of the gut microbiota (Escherichia coli and Lactobacillus acidophilus). This study supports the further development of cholesterol functionalized biomaterials as an advanced and targeted treatment for H. pylori infection.pt_PT
dc.language.isoengpt_PT
dc.publisherWileypt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_NORTE/2022.12580.BD/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/LA%2FP%2F0070%2F2020/PT-
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/951723/EU-
dc.relation.ispartofseriesAdvanced healthcare materialspt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectHelicobacter pyloript_PT
dc.subjectAntibiotic‐free strategiespt_PT
dc.subjectBioengineeringpt_PT
dc.subjectGold nanoparticlespt_PT
dc.subjectLipidspt_PT
dc.subjectSelf‐assembled monolayerspt_PT
dc.titleCholesterol Functionalized Nanoparticles Are Effective against Helicobacter pylori, the Gastric Bug: A Proof-of-Concept Studypt_PT
dc.typeArtigo em Revista Científica Internacionalpt_PT
dc.contributor.uportoInstituto de Investigação e Inovação em Saúdept_PT
dc.identifier.doi10.1002/adhm.202404065-
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/10.1002/adhm.202404065-
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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