Department of Chemistry, Government College University Faisalabad, Faisalabad 38000, Pakistan.
Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Molecules. 2023 Oct 22;28(20):7218. doi: 10.3390/molecules28207218.
The progressive trend of utilizing bioactive materials constitutes diverse materials exhibiting biocompatibility. The innovative aspect of this research is the tuning of the thermo-mechanical behavior of polyurethane (PU) composites with improved biocompatibility for vibrant applications. Polycaprolactone (CAPA) Mn = 2000 g-mol was used as a macrodiol, along with toluene diisocyanate (TDI) and hexamethylene diisocyanate (HMDI), to develop prepolymer chains, which were terminated with 1,4 butane diol (BD). The matrix was reinforced with various concentrations of chitosan (1-5 wt %). Two series of PU composites (PUT/PUH) based on aromatic and aliphatic diisocyanate were prepared by varying the hard segment (HS) ratio from 5 to 30 (wt %). The Fourier-transformed infrared (FTIR) spectroscopy showed the absence of an NCO peak at 1730 cm in order to confirm polymer chain termination. Thermal gravimetric analysis (TGA) showed optimum weight loss up to 500 °C. Dynamic mechanical analysis (DMA) showed the complex modulus (E*) ≥ 200 MPa. The scanning electron microscope (SEM) proved the ordered structure and uniform distribution of chain extender in PU. The hemolytic activities were recorded up to 15.8 ± 1.5% for the PUH series. The optimum values for the inhibition of biofilm formation were recorded as 46.3 ± 1.8% against and (%), which was supported by phase contrast microscopy.
利用生物活性材料的渐进趋势构成了具有生物相容性的多种材料。本研究的创新之处在于通过调整具有改善的生物相容性的聚氨酯 (PU) 复合材料的热机械性能,为充满活力的应用提供支持。使用聚己内酯 (CAPA) Mn = 2000 g/mol 作为大二醇,与甲苯二异氰酸酯 (TDI) 和六亚甲基二异氰酸酯 (HMDI) 一起开发预聚物链,并用 1,4-丁二醇 (BD) 终止。该基质用不同浓度的壳聚糖 (1-5wt%) 进行增强。通过改变硬段 (HS) 比例从 5 到 30(wt%),制备了基于芳香族和脂肪族二异氰酸酯的两种 PU 复合材料 (PUT/PUH) 系列。傅里叶变换红外 (FTIR) 光谱显示在 1730 cm 处没有 NCO 峰,以确认聚合物链的终止。热重分析 (TGA) 显示在高达 500°C 时的最佳失重。动态力学分析 (DMA) 显示复合模量 (E*)≥200 MPa。扫描电子显微镜 (SEM) 证明了在 PU 中链扩展剂的有序结构和均匀分布。溶血活性记录高达 15.8±1.5%的 PUH 系列。对生物膜形成的抑制的最佳值记录为 46.3±1.8%(%),这得到相差显微镜的支持。