Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Apr 6;8(15):13492-13508.
doi: 10.1021/acsomega.3c00110. eCollection 2023 Apr 18.

Perspectives on Usage of Functional Nanomaterials in Antimicrobial Therapy for Antibiotic-Resistant Bacterial Infections

Affiliations
Review

Perspectives on Usage of Functional Nanomaterials in Antimicrobial Therapy for Antibiotic-Resistant Bacterial Infections

Arun Karnwal et al. ACS Omega. .

Abstract

The clinical applications of nanotechnology are emerging as widely popular, particularly as a potential treatment approach for infectious diseases. Diseases associated with multiple drug-resistant organisms (MDROs) are a global concern of morbidity and mortality. The prevalence of infections caused by antibiotic-resistant bacterial strains has increased the urgency associated with researching and developing novel bactericidal medicines or unorthodox methods capable of combating antimicrobial resistance. Nanomaterial-based treatments are promising for treating severe bacterial infections because they bypass antibiotic resistance mechanisms. Nanomaterial-based approaches, especially those that do not rely on small-molecule antimicrobials, display potential since they can bypass drug-resistant bacteria systems. Nanoparticles (NPs) are small enough to pass through the cell membranes of pathogenic bacteria and interfere with essential molecular pathways. They can also target biofilms and eliminate infections that have proven difficult to treat. In this review, we described the antibacterial mechanisms of NPs against bacteria and the parameters involved in targeting established antibiotic resistance and biofilms. Finally, yet importantly, we talked about NPs and the various ways they can be utilized, including as delivery methods, intrinsic antimicrobials, or a mixture.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing financial interest.

Figures

Figure 1
Figure 1
Different approaches used for the synthesis of nanoparticles.
Figure 2
Figure 2
Different approaches used for antibacterial activity by nanoparticles.
Figure 3
Figure 3
Pictorial presentation of nanoparticles’ cytotoxity effect on bacterial cell membrane and cell wall.

Similar articles

Cited by

References

    1. Bankier C.; Matharu R. K.; Cheong Y. K.; Ren G. G.; Cloutman-Green E.; Ciric L. Synergistic Antibacterial Effects of Metallic Nanoparticle Combinations. Sci. Rep. 2019, 9 (1), 16074.10.1038/s41598-019-52473-2. - DOI - PMC - PubMed
    1. Christensen S. B. Drugs That Changed Society: History and Current Status of the Early Antibiotics: Salvarsan, Sulfonamides, and beta-Lactams. Molecules. 2021, 26 (19), 6057.10.3390/molecules26196057. - DOI - PMC - PubMed
    1. Rutten A.; Kirchner T.; Musiol-Kroll E. M. Overview on Strategies and Assays for Antibiotic Discovery. Pharmaceuticals (Basel). 2022, 15 (10), 1302.10.3390/ph15101302. - DOI - PMC - PubMed
    1. Lam S. J.; O’Brien-Simpson N. M.; Pantarat N.; Sulistio A.; Wong E. H. H.; Chen Y. Y.; Lenzo J. C.; Holden J. A.; Blencowe A.; Reynolds E. C.; Qiao G. G. Combating multidrug-resistant Gram-negative bacteria with structurally nanoengineered antimicrobial peptide polymers. Nature. Microbiology 2016, 1, 16162.10.1038/nmicrobiol.2016.162. - DOI - PubMed
    1. Pushparaj Selvadoss P.; Nellore J.; Balaraman Ravindrran M.; Sekar U.; Tippabathani J. Enhancement of antimicrobial activity by liposomal oleic acid-loaded antibiotics for the treatment of multidrug-resistant Pseudomonas aeruginosa. Artificial Cells, Nanomedicine and Biotechnology. 2018, 46 (2), 268–73. 10.1080/21691401.2017.1307209. - DOI - PubMed