Low-Generation Cationic Phosphorus Dendrimers: Novel Approach to Tackle Drug-Resistant and .

Biomacromolecules

Division of Molecular Microbiology and Immunology, CSIR-Central Drug Research Institute, Sitapur Road, Sector 10, Janakipuram Extension, Lucknow-226031, Uttar Pradesh India.

Published: July 2023

AI Article Synopsis

  • * Methicillin-resistant Staphylococcus aureus (MRSA) causes higher mortality than drug-susceptible infections, and there is a shortage of effective treatments for these serious infections.
  • * AE4G0, a new cationic-phosphorus dendrimer, has shown strong antimicrobial effects against MRSA and works well with gentamicin, indicating its potential as a novel treatment for drug-resistant skin infections.

Article Abstract

The incessant, global increase in antimicrobial resistance (AMR) is a very big challenge for healthcare systems. AMR is predicted to grow at an alarming pace, with a dramatic increase in morbidity, mortality, and a 100 trillion US$ loss to the global economy by 2050. The mortality rate caused by methicillin-resistant . (MRSA) is much higher as compared to infections caused by drug-susceptible . . Additionally, there is a big paucity of therapeutics available for treatment of serious infections caused by MRSA. Thus, the discovery and development of novel therapies is an urgent, unmet medical need. In this context, we synthesized AE4G0, a low-generation cationic-phosphorus dendrimer expressing potent antimicrobial activity against . and sp., and demonstrating a broad selectivity index against eukaryotic cells. AE4G0 exhibits concentration-dependent, bactericidal activity and synergizes with gentamicin, especially against gentamicin-resistant MRSA NRS119. Fluorescence and scanning electron microscopy demonstrate that treatment with AE4G0 led to the utter destruction of . ATCC 29213 without inducing resistance, despite repeated exposure. When tested , AE4G0 demonstrates significant efficacy against . ATCC 29213, alone and in combination with gentamicin against gentamicin-resistant . NRS119 in the murine skin model of infection. Taken together, AE4G0 demonstrates the potential to be translated as a novel therapeutic option for the treatment of topical, drug-resistant . infections.

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Source
http://dx.doi.org/10.1021/acs.biomac.3c00266DOI Listing

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