TY - JOUR
T1 - Highly Branched Gradient Glycopolymer
T2 - Enzyme-Assisted Synthesis and Enhanced Bacteria-Binding Ability
AU - Zheng, Lifang
AU - Luo, Yan
AU - Chen, Kui
AU - Zhang, Zexin
AU - Chen, Gaojian
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/12/14
Y1 - 2020/12/14
N2 - A one-pot strategy was applied to synchronize enzymatic monomer transformation with reversible addition fragmentation chain transfer (RAFT) polymerization for the synthesis of glycopolymers with highly branched gradient architectures. Also, the linear analogues, block glycopolymers, and gradient glycopolymers were also synthesized for comparison. The binding ability of glycopolymers toward bacteria was then studied by optical density (OD) test, confocal laser scanning microscopy (CLSM), and quartz crystal microbalance with dissipation (QCM-D). The results show that the highly branched gradient glycopolymers have the most remarkable bacteria-binding ability compared with the two linear analogues, gradient glycopolymers, and block glycopolymers. The highly branched glycopolymers were further used as inhibitors in the anti-infection test, demonstrating a significant inhibitory effect on preventing bacteria from infecting the cells.s
AB - A one-pot strategy was applied to synchronize enzymatic monomer transformation with reversible addition fragmentation chain transfer (RAFT) polymerization for the synthesis of glycopolymers with highly branched gradient architectures. Also, the linear analogues, block glycopolymers, and gradient glycopolymers were also synthesized for comparison. The binding ability of glycopolymers toward bacteria was then studied by optical density (OD) test, confocal laser scanning microscopy (CLSM), and quartz crystal microbalance with dissipation (QCM-D). The results show that the highly branched gradient glycopolymers have the most remarkable bacteria-binding ability compared with the two linear analogues, gradient glycopolymers, and block glycopolymers. The highly branched glycopolymers were further used as inhibitors in the anti-infection test, demonstrating a significant inhibitory effect on preventing bacteria from infecting the cells.s
UR - http://www.scopus.com/inward/record.url?scp=85097757478&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.0c01311
DO - 10.1021/acs.biomac.0c01311
M3 - Article
C2 - 33258599
AN - SCOPUS:85097757478
SN - 1525-7797
VL - 21
SP - 5233
EP - 5240
JO - Biomacromolecules
JF - Biomacromolecules
IS - 12
ER -