Literature DB >> 34315189

Antibiotic-cell-penetrating peptide conjugates targeting challenging drug-resistant and intracellular pathogenic bacteria.

Samantha M Zeiders1, Jean Chmielewski1.   

Abstract

The failure to treat everyday bacterial infections is a current threat as pathogens are finding new ways to thwart antibiotics through mechanisms of resistance and intracellular refuge, thus rendering current antibiotic strategies ineffective. Cell-penetrating peptides (CPPs) are providing a means to improve antibiotics that are already approved for use. Through coadministration and conjugation of antibiotics with CPPs, improved accumulation and selectivity with alternative and/or additional modes of action against infections have been observed. Herein, we review the recent progress of this antibiotic-cell-penetrating peptide strategy in combatting sensitive and drug-resistant pathogens. We take a closer look into the specific antibiotics that have been enhanced, and in some cases repurposed as broad-spectrum drugs. Through the addition and conjugation of cell-penetrating peptides to antibiotics, increased permeation across mammalian and/or bacterial membranes and a broader range in bacterial selectivity have been achieved.
© 2021 John Wiley & Sons Ltd.

Entities:  

Keywords:  antibacterials; antimicrobial peptides; cell-penetrating peptides; conjugates; drug resistance

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Year:  2021        PMID: 34315189     DOI: 10.1111/cbdd.13930

Source DB:  PubMed          Journal:  Chem Biol Drug Des        ISSN: 1747-0277            Impact factor:   2.817


  1 in total

1.  Combination of Amphiphilic Cyclic Peptide [R4W4] and Levofloxacin against Multidrug-Resistant Bacteria.

Authors:  Muhammad Imran Sajid; Sandeep Lohan; Shun Kato; Rakesh Kumar Tiwari
Journal:  Antibiotics (Basel)       Date:  2022-03-20
  1 in total

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