Ftiti Sondes, Cifuentes Sandra C, Guidara Awatef, Rams Joaquín, Tounsi Hassib, Fernández-Blázquez Juan P
Laboratory of Advanced Materials (LR01ES26), National Engineering School of Sfax, University of Sfax, Sfax 3038, Tunisia.
Department of Applied Mathematics, Materials Science and Engineering and Electronic Technology, Universidad Rey Juan Carlos (URJC), 28933 Móstoles, Spain.
Polymers (Basel). 2024 Mar 6;16(5):719. doi: 10.3390/polym16050719.
Biocomposite films based on PLA reinforced with different β-TCP contents (10%, 20%, and 25%wt.) were fabricated via solvent casting and immersed in SBF for 7, 14, and 21 days. The bioactivity, morphological, and thermal behavior of composites with immersion were studied using scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) microanalysis, weight loss (W), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and gel permeation chromatography (GPC). This broad analysis leads to a deeper understanding of the evolution of the polymer-filler interaction with the degradation of the biocomposites. The results showed that β-TCP gradually evolved into carbonated hydroxyapatite as the immersion time increased. This evolution affected the interaction of β-TCP with PLA. PLA and β-TCP interactions differed from PLA and carbonated hydroxyapatite interactions. It was observed that β-TCP inhibited PLA hydrolysis but accelerated the thermal degradation of the polymer. β-TCP retarded the cold crystallization of PLA and hindered its crystallinity. However, after immersion in SBF, particles accelerated the cold crystallization of PLA. Therefore, considering the evolution of β-TCP with immersion in SBF is crucial for an accurate analysis of the biocomposites' degradation. These findings enhance the comprehension of the degradation mechanism in PLA/β-TCP, which is valuable for predicting the degradation performance of PLA/β-TCP in medical applications.
通过溶液浇铸法制备了基于聚乳酸(PLA)并添加不同含量(10%、20%和25%重量)β-磷酸三钙(β-TCP)的生物复合膜,并将其浸入模拟体液(SBF)中7天、14天和21天。采用扫描电子显微镜(SEM)、能量色散X射线(EDX)微分析、失重(W)、X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、热重分析(TGA)和凝胶渗透色谱法(GPC)研究了浸泡后复合材料的生物活性、形态和热行为。这种广泛的分析有助于更深入地了解聚合物-填料相互作用随生物复合材料降解的演变。结果表明,随着浸泡时间的增加,β-TCP逐渐演变成碳酸羟基磷灰石。这种演变影响了β-TCP与PLA的相互作用。PLA与β-TCP的相互作用不同于PLA与碳酸羟基磷灰石的相互作用。观察到β-TCP抑制PLA水解,但加速了聚合物的热降解。β-TCP延缓了PLA的冷结晶并阻碍了其结晶度。然而,在浸入SBF后,颗粒加速了PLA的冷结晶。因此,考虑β-TCP在SBF中的浸泡演变对于准确分析生物复合材料的降解至关重要。这些发现增强了对PLA/β-TCP降解机制的理解,这对于预测PLA/β-TCP在医学应用中的降解性能具有重要价值。