TY - JOUR
T1 - Morphologic Design of Silver-Bearing Sugar-Based Polymer Nanoparticles for Uroepithelial Cell Binding and Antimicrobial Delivery
AU - Song, Yue
AU - Elsabahy, Mahmoud
AU - Collins, Christina A.
AU - Khan, Sarosh
AU - Li, Richen
AU - Hreha, Teri N.
AU - Shen, Yidan
AU - Lin, Yen Nan
AU - Letteri, Rachel A.
AU - Su, Lu
AU - Dong, Mei
AU - Zhang, Fuwu
AU - Hunstad, David A.
AU - Wooley, Karen L.
N1 - Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/6/23
Y1 - 2021/6/23
N2 - Platelet-like and cylindrical nanostructures from sugar-based polymers are designed to mimic the aspect ratio of bacteria and achieve uroepithelial cell binding and internalization, thereby improving their potential for local treatment of recurrent urinary tract infections. Polymer nanostructures, derived from amphiphilic block polymers composed of zwitterionic poly(d-glucose carbonate) and semicrystalline poly(l-lactide) segments, were constructed with morphologies that could be tuned to enhance uroepithelial cell binding. These nanoparticles exhibited negligible cytotoxicity, immunotoxicity, and cytokine adsorption, while also offering substantial silver cation loading capacity, extended release, and in vitro antimicrobial activity (as effective as free silver cations) against uropathogenic Escherichia coli. In comparison to spherical analogues, cylindrical and platelet-like nanostructures engaged in significantly higher association with uroepithelial cells, as measured by flow cytometry; despite their larger size, platelet-like nanostructures maintained the capacity for cell internalization. This work establishes initial evidence of degradable platelet-shaped nanostructures as versatile therapeutic carriers for treatment of epithelial infections.
AB - Platelet-like and cylindrical nanostructures from sugar-based polymers are designed to mimic the aspect ratio of bacteria and achieve uroepithelial cell binding and internalization, thereby improving their potential for local treatment of recurrent urinary tract infections. Polymer nanostructures, derived from amphiphilic block polymers composed of zwitterionic poly(d-glucose carbonate) and semicrystalline poly(l-lactide) segments, were constructed with morphologies that could be tuned to enhance uroepithelial cell binding. These nanoparticles exhibited negligible cytotoxicity, immunotoxicity, and cytokine adsorption, while also offering substantial silver cation loading capacity, extended release, and in vitro antimicrobial activity (as effective as free silver cations) against uropathogenic Escherichia coli. In comparison to spherical analogues, cylindrical and platelet-like nanostructures engaged in significantly higher association with uroepithelial cells, as measured by flow cytometry; despite their larger size, platelet-like nanostructures maintained the capacity for cell internalization. This work establishes initial evidence of degradable platelet-shaped nanostructures as versatile therapeutic carriers for treatment of epithelial infections.
KW - Silver-bearing polymer nanostructures
KW - antimicrobial
KW - cell-binding and internalization
KW - platelet-shaped nanostructures
KW - urinary tract infections
UR - http://www.scopus.com/inward/record.url?scp=85104347285&partnerID=8YFLogxK
U2 - 10.1021/acs.nanolett.1c00776
DO - 10.1021/acs.nanolett.1c00776
M3 - Article
C2 - 34115938
AN - SCOPUS:85104347285
SN - 1530-6984
VL - 21
SP - 4990
EP - 4998
JO - Nano Letters
JF - Nano Letters
IS - 12
ER -