TY - JOUR
T1 - Effect of star topology versus linear polymers on antifungal activity and mammalian cell toxicity
AU - Schaefer, Sebastian
AU - Melodia, Daniele
AU - Corrigan, Nathaniel
AU - Lenardon, Megan Denise
AU - Boyer, Cyrille
PY - 2024/5
Y1 - 2024/5
N2 - The global increase in invasive fungal infections and the emergence of drug-resistant strains demand the urgent development of novel antifungal drugs. In this context, synthetic polymers with diverse compositions, mimicking natural antimicrobial peptides, have shown promising potential for combating fungal infections. This study investigates how altering polymer end-groups and topology from linear to branched star-like structures affects their efficacy against Candida spp., including clinical isolates. Additionally, the polymers’ biocompatibility is accessed with murine embryonic fibroblasts and red blood cells in vitro. Notably, a low-molecular weight star polymer outperforms both its linear polymeric counterparts and amphotericin B (AmpB) in terms of an improved therapeutic index and reduced haemolytic activity, despite a higher minimum inhibitory concentration against Candida albicans (C. albicans) SC5314 (16–32 µg mL−1 vs 1 µg mL−1 for AmpB). These findings demonstrate the potential of synthetic polymers with diverse topologies as promising candidates for antifungal applications.
AB - The global increase in invasive fungal infections and the emergence of drug-resistant strains demand the urgent development of novel antifungal drugs. In this context, synthetic polymers with diverse compositions, mimicking natural antimicrobial peptides, have shown promising potential for combating fungal infections. This study investigates how altering polymer end-groups and topology from linear to branched star-like structures affects their efficacy against Candida spp., including clinical isolates. Additionally, the polymers’ biocompatibility is accessed with murine embryonic fibroblasts and red blood cells in vitro. Notably, a low-molecular weight star polymer outperforms both its linear polymeric counterparts and amphotericin B (AmpB) in terms of an improved therapeutic index and reduced haemolytic activity, despite a higher minimum inhibitory concentration against Candida albicans (C. albicans) SC5314 (16–32 µg mL−1 vs 1 µg mL−1 for AmpB). These findings demonstrate the potential of synthetic polymers with diverse topologies as promising candidates for antifungal applications.
KW - antifungal agents
KW - antimicrobial polymers
KW - controlled/living radical polymerisation
KW - polymer topology
UR - http://www.scopus.com/inward/record.url?scp=85179371221&partnerID=8YFLogxK
U2 - 10.1002/mabi.202300452
DO - 10.1002/mabi.202300452
M3 - Article
C2 - 38009827
AN - SCOPUS:85179371221
SN - 1616-5187
VL - 24
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
IS - 5
M1 - 2300452
ER -