Blackwell Catherine J, Haernvall Karolina, Guebitz Georg M, Groombridge Michael, Gonzales Denis, Khosravi Ezat
Department of Chemistry, Durham University, Durham DH1 3LE, UK.
Austrian Centre of Industrial Biotechnology GmbH, Konrad Lorenz Strasse 20, 3430 Tulln an der Donau, Austria.
Polymers (Basel). 2018 Nov 14;10(11):1266. doi: 10.3390/polym10111266.
Four-arm star poly(ε-caprolactone) with a central poly(ethylene glycol) PEG unit bridged with 2,2-(methyl) propionic acid, (PCL)₂--PEG--(PCL)₂, and six-arm star PCL homopolymer with a central dipentaerythritol units were hydrolysed using a lipase from and the cutinase Thc_Cut1. For comparative analysis, Y-shaped copolymers containing methylated PEG bridged with bisMPA, MePEG-(PCL)₂, and linear triblock copolymers PCL--PEG--PCL were also subjected to enzymatic hydrolysis. The hydrophilic nature of the polymers was determined using contact angle analysis, showing that a higher PEG content exhibited a lower contact angle and higher surface wettability. Enzymatic hydrolysis was monitored by % mass loss, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). A higher rate of mass loss was found for lipase catalysed hydrolysis of those polymers with the highest PEG content, leading to significant surface erosion and increase in crystallinity within the first two days. Liquid chromatography (LC) and size exclusion chromatography (SEC) of samples incubated with the cutinase showed a significant decrease in molecular weight, increase in dispersity, and release of -CL monomer units after 6 h of incubation.
一种中心聚乙二醇(PEG)单元通过2,2-(甲基)丙酸桥连的四臂星形聚(ε-己内酯),即(PCL)₂--PEG--(PCL)₂,以及一种中心为二季戊四醇单元的六臂星形聚己内酯均聚物,使用来自[具体来源未给出]的脂肪酶和角质酶Thc_Cut1进行水解。为了进行对比分析,还对含有通过双甲基丙烯酸丙酯桥连的甲基化PEG的Y形共聚物MePEG-(PCL)₂以及线性三嵌段共聚物PCL--PEG--PCL进行了酶促水解。通过接触角分析测定聚合物的亲水性,结果表明PEG含量越高,接触角越低,表面润湿性越高。通过质量损失百分比、扫描电子显微镜(SEM)和差示扫描量热法(DSC)监测酶促水解过程。发现脂肪酶催化水解那些PEG含量最高的聚合物时质量损失速率更高,在前两天导致显著的表面侵蚀和结晶度增加。用角质酶孵育后的样品进行液相色谱(LC)和尺寸排阻色谱(SEC)分析表明,孵育6小时后分子量显著降低、分散度增加且有ε-己内酯单体单元释放。