Synthesis of Poly(2-(methylsulfinyl)ethyl methacrylate) via Oxidation of Poly(2-(methylthio)ethyl methacrylate): Evaluation of the Sulfoxide Side Chain on Cryopreservation

IF 4.7 Q1 POLYMER SCIENCE
Toru Ishibe, Natalia Gonzalez-Martinez, Panagiotis G. Georgiou, Kathryn A. Murray and Matthew I. Gibson*, 
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引用次数: 2

Abstract

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.

Abstract Image

聚(2-(甲基硫代)甲基丙烯酸乙酯氧化合成聚(2-(甲基亚砜基)甲基丙烯酸乙酯):亚砜侧链对低温保存的评价
传统的冷冻保存溶液依赖于添加有机溶剂,如DMSO或甘油,但这些并不能完全恢复所有细胞类型,而创新的冷冻保护剂可以解决这些溶剂无法保护的损伤途径。大分子低温保护剂正在兴起,但有必要了解它们的结构-性能关系和作用机制。在这里,我们合成并研究了亚砜(即“类二甲基亚砜”)侧链聚合物的低温保护行为,该聚合物已被报道使用聚乙二醇基聚合物进行低温保护。我们还想确定极性亚砜键(S+O -特征)是否引入了低温保护作用,因为这已经在混合电荷低温保护多两性聚合物中看到,其作用机制尚不清楚。以2-(甲基硫代)甲基丙烯酸乙酯为原料,采用RAFT聚合法制备了聚(2-(甲基亚砜基)甲基丙烯酸乙酯)。制备了相应的n -氧化物聚合物,并对其进行了表征:聚(2-(二甲胺氧化物)甲基丙烯酸乙酯。冰重结晶抑制实验和差示扫描量热分析表明,亚砜侧链在冷冻保存过程中不调节冷冻组分。在细胞毒性试验中,发现细胞不能耐受长时间(24小时)暴露于聚合物中,但可以耐受较短的孵育时间(30分钟),这与低温保存有关。还观察到对砜的过度氧化显著增加了细胞毒性,因此,这些材料需要精确的氧化步骤来部署。在悬浮细胞冷冻保存研究中,聚亚砜在解冻后24 h没有增加细胞的恢复。这些结果表明,与可以帮助低温保存的亲水骨架型多硫化物不同,将亚砜基团安装到聚合物上并不一定具有低温保护性能,这突出了开发和发现大分子低温保护剂的挑战。
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CiteScore
2.50
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