Hemmrich Karsten, Salber Jochen, Meersch Melanie, Wiesemann Ute, Gries Thomas, Pallua Norbert, Klee Doris
Department of Plastic Surgery and Hand Surgery--Burn Centre, University Hospital of the RWTH Aachen University, Pauwelsstr. 30, 52057 Aachen, Germany.
J Mater Sci Mater Med. 2008 Jan;19(1):257-67. doi: 10.1007/s10856-006-0048-3. Epub 2007 Jun 28.
Biodegradable polyesters are established biomaterials in medicine due to their chemical characteristics and options for material processing. A main problem, however, is the release of acid degradation products during biodegradation with severe local pH-drops and inflammatory reactions. Polyesteramides, in contrast, show a less prominent pH-drop during degradation. In this study, we developed a simple, reproducible synthesis of the poly(ester amide) (PEA) type C starting from epsilon-caprolactame, 1,4-butanediol, and adipic acid in a one-batch two-step reaction and conducted the manufacturing of PEA-derived 3D textile scaffolds applicable for tissue engineering purposes. The thermal and mechanical properties of PEA-type C were analysed and the structural conformity of different batches was confirmed by NMR spectroscopy and size exclusion chromatography. The polymer was formed into nonwovens by textile manufacturing. Cytotoxicity tests and X-ray photoelectron spectroscopy (XPS) were used to analyze the effect of scaffold extraction before cell seeding. The manufactured carriers were seeded with human preadipocytes and examined for cellular proliferation and differentiation. The production of PEA type C successfully occurred via simultaneous ring-opening polymerization of epsilon-caprolactame and polycondensation with 1,4-butanediol and adipic acid at 250 degrees C under high-vacuum. Soxhlet extraction allowed optimal cleaning of nonwoven scaffolds. Extracted PEA-derived matrices were capable of allowing good adherence, proliferation, and differentiation of preadipocytes. These results are encouraging and guidance towards an optimally prepared nonwoven carrier applicable for clinical use.
由于其化学特性和材料加工的选择,可生物降解聚酯是医学领域公认的生物材料。然而,一个主要问题是在生物降解过程中会释放酸性降解产物,导致局部pH值急剧下降并引发炎症反应。相比之下,聚酯酰胺在降解过程中pH值下降不太明显。在本研究中,我们从ε-己内酰胺、1,4-丁二醇和己二酸出发,通过一步两步反应开发了一种简单、可重复的聚(酯酰胺)(PEA)C型合成方法,并进行了适用于组织工程目的的PEA衍生3D纺织支架的制造。分析了PEA-C型的热性能和力学性能,并通过核磁共振光谱和尺寸排阻色谱法确认了不同批次的结构一致性。通过纺织制造将聚合物制成无纺布。细胞毒性测试和X射线光电子能谱(XPS)用于分析接种细胞前支架提取物的效果。将制造的载体接种人前脂肪细胞,并检测细胞增殖和分化情况。PEA C型的生产通过在250℃高真空下ε-己内酰胺的同时开环聚合以及与1,4-丁二醇和己二酸的缩聚反应成功实现。索氏提取可实现无纺布支架的最佳清洁。提取的PEA衍生基质能够使前脂肪细胞良好地黏附、增殖和分化。这些结果令人鼓舞,并为制备适用于临床的最佳无纺布载体提供了指导。