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. 2023 Apr 21;14:1135579. doi: 10.3389/fmicb.2023.1135579

Table 2.

Nanoparticles and their mechanism of action at the NP-bacterial membrane interface.

S. No. Nanoparticle Investigated bacteria Interaction with/membrane target Mechanism of nanoparticle action Reference
1. Ag NPs E. coli LPS and L- α -phosphatidyl-ethanolamine (PE)
  • NP interacted with O-antigen part of LPS via hydrogen bonding

  • Ag NP broke phosphodiester bond of PE into phosphate monoesters to form highly disordered alkyl chain

Ansari et al. (2014a)
2. Al2O3 NPs E. coli LPS and L- α -phosphatidyl-ethanolamine (PE)
  • LPS binding to Al2O3 NPs through hydrogen bonding and ligand exchange

  • structural changes in phospholipids led to loss of amphiphilic properties

Ansari et al. (2014b)
3. Au NPs functionalized with branched polyethylenimine B. subtilis Teichoic acid
  • Electrostatic interaction between NPs and teichoic acid

  • No interaction with mutant having teichoic acid but lacking alanine

Caudill et al. (2020)
4. Ampicillin- chitosan–polyanion nanoparticles S. aureus strains (ATCC25923, ATCC29213 and ATCC43300) Lipoteichoic acid (LTA)
  • Electrostatic interaction between chitosan and LTA leads to disturbance in membrane homeostasis

  • MIC for free and NP-encapsulated Ampicillin was 0.26 μg/ml and 0.13 μg/ml respectively

Ciro et al. (2019)
5. Curcumin-functionalized poly(lactic-co-glycolic acid)-dextran micelles P. putida (PCL 1482) and P. fuorescens (PCL 1701) biofilms Exopolysaccharide (EPS)
  • Micelle possibly altered surface hydrophobicity in bacteria

  • Disruption of established biofilms induced electrostatic interaction between micelles and EPS to weaken overall architecture

Barros et al. (2021)
6. CTAB-coated gold nanoshell S. aureus, E. coli, S. enterica and P. aeruginosa Cell wall
  • The aim was to use gold nanoshells as sensors for bacterial detection

  • Both enzyme β-galactosidase and bacteria competed to interact with gold nanoshells

  • Electrostatic interaction with LPS led to formation of gold nanoshell aggregates in cell wall causing cell death

Tanvir et al. (2017)
7. Spherical and Rod-shaped Ag NPs E. coli (ATCC25922) and S. aureus (ATCC25923). B. subtilis (AST5-2), P. aeruginosa (AL2-14B32) and K. pneumoniae (AWD5) Cell wall
  • FESEM analysis suggested rupture of cell wall

  • Rod-shaped Ag NPs showed enhanced antibacterial activity

Acharya et al. (2018)
8. Curcumin loaded Solid Lipid Nanoparticles E. coli (ATCC25922)
S. aureus (ATCC25923)
Cell permeability
  • Combination of cholesterol-curcumin exhibited stronger antibacterial activity and led to enhanced cell membrane penetration and leakage

Jourghanian et al. (2016)
9. Triclosan-loaded micellar nanocarriers S. aureus (ATCC12600GFP) and bioluminescent S. aureus Xen36 Cell permeability
  • Enhanced biofilm penetration of micelle and accumulation due to electrostatic interaction with bacterial cell surface at acidic pH

  • Triclosan release due to micelle degradation by bacterial lipase

Liu et al. (2016)
10. Graphene oxide Ag Nanocomposite Enterobacter cloacae
Staphylococcus mutans
Cell leakage
  • Protein leakage was assessed and found to be significant in Gram – than in Gram +

  • Gram + has thicker cell wall and posed barrier to nanocomposite penetration

Kulshrestha et al. (2017)
11. Au NP capped with pyrimidine (Au-DAPT) 4,6-Diamino-2-pyrimidinethiol MDR clinical isolates- E. coli and P. aeruginosa Membrane Ions: Mg2+ and Ca2+ ion of outer membrane vesicle (OMV)
  • Sequestration or chelation of Mg2+ and Ca2+caused by Au-DAPT lead to the disruption of membrane integrity which lead to leakage of cellular components

Zhao et al. (2010)
12. Poly(acrylic acid; PAA)-coated iron oxide (magnetite) nanoparticles (PAA-MNPs) and Rifampicin (TB drug) Mycobacterium smegmatis Efflux pump
  • Iron oxide NPs acted as efflux pump inhibitor which resulted in up to a 3-fold-increased accumulation of rifampicin inside Mycobacterium

Padwal et al. (2014)
13. Cu NPs Wild type- S. aureus and P. aeruginosa. MRSA and drug resistant mutant- S. aureus Efflux pump
  • Exhibited remarkable efflux inhibition activity

  • Reverse the MIC of the mutant S. aureus strain for ciprofloxacin by 4-fold

Christena et al. (2015)
14. CuI NPs B. subtilis (ATCC6633) and E. coli DHF 5α (ATCC10536), Shigella dysenteriae (ATCC12039) ROS generation
  • Bactericidal activity due to ROS formation of the surface of CuI NP due to interaction with amine functional group of various biomolecules on cell membrane

Pramanik et al. (2012)
15. TiO2 NPs MRSA, E. coli and P. aeruginosa ROS generation
  • NP interaction with membrane protein and lipid leads to generation of ROS followed by cell death

Alhadrami and Shoudri (2020)
16. ZnO NPs Vibrio cholera ROS generation and membrane disruption
  • NPs increased fluidity and depolarization of membrane, protein leakage leading to bacterial death

Sarwar et al. (2016)
17. Chlorohexidine acetate nanoemulsion (CNE) Skin burn wound MRSA infection Ion leakage and membrane disruption
  • CNE treatment led to leakage of K+, Mg2+ Ions, DNA and protein

  • Increase electrical conductivity and disruption of cell wall and cell membrane

Song et al. (2016)
18. Hybrid Tellurium−Lignin Nanoparticles (TeLigNPs) S. aureus (ATCC25923), E. coli (ATCC25922), and P. aeruginosa (ATCC10145), ROS generation and membrane disruption
  • Strong antibacterial activity due to interaction of lignin with hydrophilic surface of Gram – bacteria as compared to Gram +

  • Insertion of TeLig NPs into the outer membrane caused lipid peroxidation decomposing it into highly reactive short-chain aldehydes which further diffused into cytoplasm and oxidize thiol and amino groups of proteins leading to death

Morena et al. (2021)