Institute of Macromolecular Chemistry AS CR, Heyrovskeho Sq. 2, Prague 6, 162 06, Czech Republic.
Macromol Rapid Commun. 2011 Jul 1;32(13):958-65. doi: 10.1002/marc.201100176. Epub 2011 Jun 3.
Among the class of zwitterionic polymers poly(carboxybetaine)s (poly(CB)s) are unique, emerging as the only ultra-low fouling materials known allowing the preparation of biosensors, fouling resistant nanoparticles, and non-adhesive surfaces for bacteria. Poly(carboxybetaine methacrylate) and poly(carboxybetaine acrylamide) have been prepared via atom transfer radical polymerization (ATRP), however a polymerization with living characteristics has not been achieved yet. Herein, the first successful living/controlled reversible addition fragmentation transfer (RAFT) polymerization of (3-methacryloylamino-propyl)-(2-carboxy-ethyl)-dimethyl-ammonium (carboxybetaine methacrylamide) (CBMAA-3) in acetate buffer (pH 5.2) at 70 and 37 °C is reported. The polymerization afforded very high molecular weight polymers (determined by absolute size exclusion chromatography, close to 250,000 g·mol(-1) in less than 6 h) with low PDI (<1.3) at 70 °C. The polymerization was additionally carried out at 37 °C allowing to achieve yet lower PDIs (1.06 ≤ PDI ≤ 1.15) even at 90% conversion, demonstrating the suitability of the polymerization conditions for bioconjugate grafting. The living character of the polymerization is additionally evidenced by chain extending poly(CBMAA-3) at 70 and 37 °C. Block copolymerization from biologically relevant poly[N-(2-hydroxypropyl)methacrylamide] macroCTAs was additionally performed.
在两性离子聚合物中,聚(羧酸甜菜碱)(poly(CB)s)是独特的,是唯一已知的超低污染材料,可用于制备生物传感器、抗污染纳米粒子和非粘附细菌表面。聚(羧酸甜菜碱甲基丙烯酰胺)和聚(羧酸甜菜碱丙烯酰胺)已通过原子转移自由基聚合(ATRP)制备,但尚未实现具有活性特征的聚合。在此,首次成功地在 70 和 37°C 的乙酸盐缓冲液(pH 5.2)中进行了(3-甲基丙烯酰基氨基丙基)-(2-羧乙基)-二甲基-铵(羧酸甜菜碱甲基丙烯酰胺)(CBMAA-3)的活性/可控可逆加成-断裂链转移(RAFT)聚合。该聚合在 70°C 下可在不到 6 小时内提供非常高分子量的聚合物(通过绝对尺寸排阻色谱法确定,接近 250,000 g·mol(-1)),PDI 低(<1.3)。该聚合还在 37°C 下进行,即使在 90%转化率下,仍可实现更低的 PDI(1.06≤PDI≤1.15),证明聚合条件适用于生物缀合物接枝。聚合的活性特征还通过在 70 和 37°C 下延伸 poly(CBMAA-3)链得到证实。此外,还进行了来自生物相关的聚[N-(2-羟丙基)甲基丙烯酰胺]大分子引发剂的嵌段共聚。