Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, TWIns, 8-1 Kawadacho, Shinjuku, Tokyo, 162-8666, Japan.
Macromol Rapid Commun. 2021 Aug;42(15):e2100208. doi: 10.1002/marc.202100208. Epub 2021 Jun 18.
In this study, poly(N-acryloyl-nipecotamide) (PNANAm), poly(N-acryloyl-isonipecotamide) (PNAiNAm), and poly(N-acryloyl-N,N-diethylnipecotamide) (PNADNAm) are synthesized as novel temperature-responsive polymers using reversible addition-fragmentation chain-transfer polymerization. Aqueous solutions of these three polymers are examined via temperature-dependent optical transmittance measurements. The PNANAm sample with a hydrophilic terminal group shows an upper critical solution temperature (UCST) in phosphate-buffered saline (PBS) when its molecular weight (M ) is 7600 or higher, whereas PNANAm (M < 7600) is soluble. The UCST is influenced by molecular weight and the polymer concentration. In contrast, PNANAm sample with nonionic terminal group shows UCST, when M is below 7600, suggesting that the terminal nonionic group possibly increases UCST of PNANAm. The urea addition experiment suggests that the driving force for expression of UCST of PNANAm is the formation of inter-and intramolecular hydrogen bonds among the polymer chains. PNAiNAm is soluble in PBS but exhibits an UCST in an appropriate concentration of ammonium sulfate. In contrast, PNADNAm exhibits a lower critical solution temperature. Comparing the chemical structure of these polymers and their phase transition behaviors suggests that the carboxamide group position in the piperidine ring could determine the UCST expression. These results could help design temperature-responsive polymers with a desired the cloud point temperature.
在这项研究中,使用可逆加成-断裂链转移聚合合成了三种新型温敏聚合物:聚(N-丙烯酰基-烟酰胺)(PNANAm)、聚(N-丙烯酰基-异烟酰胺)(PNAiNAm)和聚(N-丙烯酰基-N,N-二乙基烟酰胺)(PNADNAm)。通过温度依赖的光透过率测量来研究这三种聚合物的水溶液。具有亲水性末端基团的 PNANAm 样品在其分子量(M)为 7600 或更高时在磷酸盐缓冲盐水(PBS)中表现出上临界溶解温度(UCST),而分子量低于 7600 的 PNANAm 是可溶的。UCST 受分子量和聚合物浓度的影响。相比之下,具有非离子末端基团的 PNANAm 样品在 M 低于 7600 时表现出 UCST,这表明末端非离子基团可能会增加 PNANAm 的 UCST。尿素添加实验表明,PNANAm 表达 UCST 的驱动力是聚合物链之间形成的分子内和分子间氢键。PNAiNAm 可溶于 PBS,但在适当浓度的硫酸铵中表现出 UCST。相反,PNADNAm 表现出较低的临界溶解温度。比较这些聚合物的化学结构及其相转变行为表明,哌啶环中酰胺基团的位置可以决定 UCST 的表达。这些结果有助于设计具有所需浊点温度的温敏聚合物。