Overproduction
of reactive oxygen species (ROS) in cells is a major
health concern as it may lead to various diseases through oxidative
damage of biomolecules. Commonly used traditional small molecular
antioxidants (polyphenols, carotenoids, vitamins, etc.) have inadequate
efficacy in lowering excessive levels of ROS due to their poor aqueous
solubility and bioavailability. In response to the widespread occurrence
of antioxidant polyphenols in various biorenewable resources, we aimed
to develop water-soluble antioxidant polymers with side chain phenolic
pendants. Four different types of copolymers (P1–P4) containing phenyl rings with different numbers of hydroxy
(−OH) substituents (0: phenylalanine, 1: tyrosyl, 2: catechol,
or 3: gallol) were synthesized via reversible addition–fragmentation
chain transfer (RAFT) polymerization with a desired molar mass (8500–10000
g/mol) and a narrow dispersity (Đ ≤
1.3). After successful characterizations of P1–P4, their in vitro antioxidant properties
were analyzed by different methods, including 2,2-diphenyl-1-picrylhydrazyl
(DPPH•), 2,2-azino-bis-3-ethylbenzothiazoline-6-sulfonic
acid (ABTS•+), 4,4′-diamino-3,3′,5,5′-tetramethylbiphenyl
(TMB), and β-carotene (βC) assays. Our results revealed
that the gallol pendant polymers can effectively scavenge ROS. Furthermore,
electron paramagnetic resonance (EPR) spectroscopy with DPPH• also confirmed the radical quenching ability of the synthesized
polymers. The gallol pendant polymers, at a well-tolerated concentration,
could effectively penetrate the macrophage cells and restore the H2O2-induced ROS to the basal level. Overall, the
present approach demonstrates the efficacy of water-soluble antioxidant
polymers with gallol pendants toward the mitigation of cellular oxidative
stress.