Antipathogenic Activity of Betainized Polyethyleneimine Sprays Without Toxicity
dc.authorid | Şahiner, Nurettin / 0000-0003-0120-530X | |
dc.authorid | Sağbaş Suner, Selin / 0000-0002-3524-0675 | |
dc.contributor.author | Sağbaş Suner, Selin | |
dc.contributor.author | Ayyala, Ramesh S. | |
dc.contributor.author | Şahiner, Nurettin | |
dc.date.accessioned | 2025-01-27T20:54:07Z | |
dc.date.available | 2025-01-27T20:54:07Z | |
dc.date.issued | 2024 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | Background/Objectives: The design of alternative antipathogenic sprays has recently attracted much attention due to the limitations of existing formulations, such as toxicity and low and narrow efficacy. Polyethyleneimine (PEI) is a great antimicrobial polymer against a wide range of pathogens, but toxicity limits its use. Here, betainized PEI (B-PEI) was synthesized to decrease the toxicity of PEI and protonated with citric acid (CA), boric acid (BA), and HCl to improve antimicrobial activity. Methods: Cytotoxicity of the PEI-based solutions was determined on L929 fibroblast cells. Antibacterial/fungal activity of PEI-based antipathogenic sprays was investigated by microtiter and disc diffusion assays, in addition to bacterial viability and adhesion % of common bacteria and fungi on the PEI-treated masks. Furthermore, the antiviral effect of the PEI-based solutions was determined against SARS-CoV-2 virus. Results: The biosafe concentration of PEI was determined as 1 mu g/mL with 75 +/- 11% cell viability, but B-PEI and its protonated forms had great biocompatibility even at 1000 mu g/mL with more than 85% viability. The antibacterial/fungal effect of non-toxic B-PEI was improved by protonation with BA and HCl with 2.5-10 mg/mL minimum bactericidal/fungicidal concentrations (MBCs/MFCs). Bacterial/fungal viability and adhesion on the mask was almost eliminated by using 50 mu L with 5-10 mg/mL of B-PEI-BA. Both protonated bare and betainized PEI show potent antiviral activity against SARS-CoV-2 virus. Conclusions: The toxicity of PEI was overcome by using betainized forms of PEI (B-PEI). Furthermore, the antimicrobial and antiviral efficacy of PEI and B-PEI was improved by protonation with CA, BA, and HCl of amine groups on B-PEI. B-PEI-BA spray solution has great potential as an antipathogenic spray with broad-spectrum antimicrobial potency against harmful bacteria, fungi, and viruses without any toxicity. | |
dc.description.sponsorship | Department of Ophthalmology, Morsani College of Medicine, University of South Florida | |
dc.description.sponsorship | This research was funded by a startup fund from the Department of Ophthalmology, Morsani College of Medicine, University of South Florida. | |
dc.identifier.doi | 10.3390/biomedicines12112462 | |
dc.identifier.issn | 2227-9059 | |
dc.identifier.issue | 11 | |
dc.identifier.pmid | 39595028 | |
dc.identifier.scopus | 2-s2.0-85210432941 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.uri | https://doi.org/10.3390/biomedicines12112462 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/25980 | |
dc.identifier.volume | 12 | |
dc.identifier.wos | WOS:001366835900001 | |
dc.identifier.wosquality | N/A | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | Mdpi | |
dc.relation.ispartof | Biomedicines | |
dc.relation.publicationcategory | info:eu-repo/semantics/openAccess | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.snmz | KA_WoS_20250125 | |
dc.subject | polyethyleneimine | |
dc.subject | betainized polyethyleneimine | |
dc.subject | antipathogenic sprays | |
dc.subject | biocompatible | |
dc.subject | antimicrobial | |
dc.subject | antiviral | |
dc.title | Antipathogenic Activity of Betainized Polyethyleneimine Sprays Without Toxicity | |
dc.type | Article |
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