Synthesis
of Poly(2-(methylsulfinyl)ethyl methacrylate)
via Oxidation of Poly(2-(methylthio)ethyl methacrylate): Evaluation
of the Sulfoxide Side Chain on Cryopreservation
posted on 2022-08-05, 19:40authored byToru Ishibe, Natalia Gonzalez-Martinez, Panagiotis G. Georgiou, Kathryn A. Murray, Matthew I. Gibson
Conventional cryopreservation solutions rely on the addition
of
organic solvents such as DMSO or glycerol, but these do not give full
recovery for all cell types, and innovative cryoprotectants may address
damage pathways which these solvents do not protect against. Macromolecular
cryoprotectants are emerging, but there is a need to understand their
structure–property relationships and mechanisms of action.
Here we synthesized and investigated the cryoprotective behavior of
sulfoxide (i.e., “DMSO-like”) side-chain polymers, which
have been reported to be cryoprotective using poly(ethylene glycol)-based
polymers. We also wanted to determine if the polarized sulfoxide bond
(S+O– character) introduces cryoprotective
effects, as this has been seen for mixed-charge cryoprotective polyampholytes,
whose mechanism of action is not yet understood. Poly(2-(methylsulfinyl)ethyl
methacrylate) was synthesized by RAFT polymerization of 2-(methylthio)ethyl
methacrylate and subsequent oxidation to sulfoxide. A corresponding N-oxide polymer was also prepared and characterized: (poly(2-(dimethylamineoxide)ethyl
methacrylate). Ice recrystallization inhibition assays and differential
scanning calorimetry analysis show that the sulfoxide side chains
do not modulate the frozen components during cryopreservation. In
cytotoxicity assays, it was found that long-term (24 h) exposure of
the polymers was not tolerated by cells, but shorter (30 min) incubation
times, which are relevant for cryopreservation, were tolerated. It
was also observed that overoxidation to the sulfone significantly
increased the cytotoxicity, and hence, these materials require a precision
oxidation step to be deployed. In suspension cell cryopreservation
investigations, the polysulfoxides did not increase cell recovery
24 h post-thaw. These results show that unlike hydrophilic backboned
polysulfides, which can aid cryopreservation, the installation of
the sulfoxide group onto a polymer does not necessarily bring cryoprotective
properties, highlighting the challenges of developing and discovering
macromolecular cryoprotectants.