Sodium ibuprofenate: antibacterial activities and potential β-lactamase inhibition in critical Gram-negative bacteria

To evaluate the antibacterial and antibiofilm activities of sodium ibuprofenate (NaI) and its hypertonic variant (NaIHS) against multidrug-resistant Gram-negative bacteria (MDR-GNB) and explore their potential to inhibit β-lactamase enzymes. Antibacterial activity was assessed using minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and time-kill assays. Antibiofilm activity was evaluated by measuring bacterial viability and biomass reduction in preformed biofilms. Scanning electron microscopy (SEM) was used to observe membrane effects. Molecular docking and molecular dynamics simulations were conducted to analyze the binding affinity of ibuprofen to the active sites of β-lactamases (CTX-M-15, KPC-2, OXA-23). NaI exhibited bactericidal activity at concentrations of 25–75 mm, with <i>Acinetobacter baumannii</i> being the most susceptible. NaCl (≥0.5 M) enhanced bactericidal efficacy and lowered MBCs. Time-kill assays indicated rapid bacterial eradication within 2 hours, with NaIHS achieving similar results at lower concentrations. SEM confirmed membrane disruption. Both formulations reduced bacterial viability in biofilms, with NaIHS showing greater efficiency. <i>In silico</i> studies suggest ibuprofen may inhibit β-lactamases, with enhanced interactions in saline environments. Sodium ibuprofenate, particularly in its hypertonic form, demonstrates strong antibacterial, antibiofilm, and potential β-lactamase inhibitory activity, making it a promising candidate for treating MDR-GNB infections. Some bacteria, called “superbugs,” are very hard to treat because they resist most antibiotics. These superbugs can cause serious infections, so it’s important to find new ways to fight them. In this study, we tested a special type of ibuprofen, called sodium ibuprofenate, to see if it could help fight superbugs. We also looked at whether it could affect two ways these bacteria protect themselves: biofilms, where they form a protective layer, and enzymes that make them resistant to antibiotics. We found that sodium ibuprofenate, especially when mixed with salt, can kill bacteria both in biofilms and on their own. It also weakens the biofilms and may help antibiotics work better. These results are important because this combination could be a new way to treat infections caused by resistant bacteria, but more research is needed.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28561846
Primary Topic
Scientific Computing and Data Management
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article
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article

Sodium ibuprofenate: antibacterial activities and potential β-lactamase inhibition in critical Gram-negative bacteria

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Scientific Computing and Data Management
article

Sodium ibuprofenate: antibacterial activities and potential β-lactamase inhibition in critical Gram-negative bacteria

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Abstract

To evaluate the antibacterial and antibiofilm activities of sodium ibuprofenate (NaI) and its hypertonic variant (NaIHS) against multidrug-resistant Gram-negative bacteria (MDR-GNB) and explore their potential to inhibit β-lactamase enzymes. Antibacterial activity was assessed using minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and time-kill assays. Antibiofilm activity was evaluated by measuring bacterial viability and biomass reduction in preformed biofilms. Scanning electron microscopy (SEM) was used to observe membrane effects. Molecular docking and molecular dynamics simulations were conducted to analyze the binding affinity of ibuprofen to the active sites of β-lactamases (CTX-M-15, KPC-2, OXA-23). NaI exhibited bactericidal activity at concentrations of 25–75 mm, with <i>Acinetobacter baumannii</i> being the most susceptible. NaCl (≥0.5 M) enhanced bactericidal efficacy and lowered MBCs. Time-kill assays indicated rapid bacterial eradication within 2 hours, with NaIHS achieving similar results at lower concentrations. SEM confirmed membrane disruption. Both formulations reduced bacterial viability in biofilms, with NaIHS showing greater efficiency. <i>In silico</i> studies suggest ibuprofen may inhibit β-lactamases, with enhanced interactions in saline environments. Sodium ibuprofenate, particularly in its hypertonic form, demonstrates strong antibacterial, antibiofilm, and potential β-lactamase inhibitory activity, making it a promising candidate for treating MDR-GNB infections. Some bacteria, called “superbugs,” are very hard to treat because they resist most antibiotics. These superbugs can cause serious infections, so it’s important to find new ways to fight them. In this study, we tested a special type of ibuprofen, called sodium ibuprofenate, to see if it could help fight superbugs. We also looked at whether it could affect two ways these bacteria protect themselves: biofilms, where they form a protective layer, and enzymes that make them resistant to antibiotics. We found that sodium ibuprofenate, especially when mixed with salt, can kill bacteria both in biofilms and on their own. It also weakens the biofilms and may help antibiotics work better. These results are important because this combination could be a new way to treat infections caused by resistant bacteria, but more research is needed.

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Scientific Computing and Data Management
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