Jungraithmayr Wolfgang, Laube Isabelle, Hild Nora, Stark Wendelin J, Mihic-Probst Daniela, Weder Walter, Buschmann Johanna
Division of Thoracic Surgery, University Hospital Zurich, Switzerland.
Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering, ETH Zurich, Zurich, Switzerland.
J Biomater Appl. 2014 Jul;29(1):36-45. doi: 10.1177/0885328213513621. Epub 2013 Nov 28.
Chest-wall invading malignancies usually necessitate the resection of the respective part of the thoracic wall. Gore-Tex® is the material of choice that is traditionally used to repair thoracic defects. This material is well accepted by the recipient; however, though not rejected, it is an inert material and behaves like a 'foreign body' within the thoracic wall. By contrast, there are materials that have the potential to physiologically integrate into the host, and these materials are currently under in vitro and also in vivo investigation. These materials offer a gradual but complete biodegradation over time, and severe adverse inflammatory responses can be avoided. Here, we present a novel material that is a biodegradable nanocomposite based on poly-lactic-co-glycolic acid and amorphous calcium phosphate nanoparticles in comparison to the traditionally employed Gore-Tex® being the standard for chest-wall replacement. On a mouse model of thoracic wall resection, that resembles the technique and localization applied in humans, poly-lactic-co-glycolic acid and amorphous calcium phosphate nanoparticles and Gore-Tex® were implanted subcutaneously and additionally tested in a separate series as a chest-wall graft. After 1, 2, 4 and 8 weeks cell infiltration into the respective materials, inflammatory reactions as well as neo-vascularization (endothelial cells) were determined in six different zones. While Gore-Tex® allowed for cell infiltration only at the outer surface, electrospun poly-lactic-co-glycolic acid and amorphous calcium phosphate nanoparticles were completely penetrated by infiltrating cells. These cells were composed mainly by macrophages, with only 4% of giant cells and lymphocytes. Total macrophage count increased by time while the number of IL1-β-expressing macrophages decreased, indicating a protective state towards the graft. As such, poly-lactic-co-glycolic acid and amorphous calcium phosphate nanoparticles seem to develop ideal characteristics as a material for chest-wall replacement by (a) having the advantage of full biodegradation, (b) displaying stable chest-wall structures and (c) adapting a physiological and integrating graft compared to Gore-Tex®.
侵犯胸壁的恶性肿瘤通常需要切除胸壁的相应部分。戈尔特斯(Gore-Tex®)是传统上用于修复胸壁缺损的首选材料。这种材料很容易被接受;然而,尽管它不会被排斥,但它是一种惰性材料,在胸壁内表现得像一个“异物”。相比之下,有些材料有可能在生理上与宿主整合,目前这些材料正在进行体外和体内研究。这些材料会随着时间的推移逐渐但完全地生物降解,并且可以避免严重的不良炎症反应。在这里,我们展示了一种新型材料,它是一种基于聚乳酸-乙醇酸共聚物和无定形磷酸钙纳米颗粒的可生物降解纳米复合材料,与传统使用的戈尔特斯(Gore-Tex®)作为胸壁置换的标准材料进行比较。在一个类似于人类应用的技术和定位的胸壁切除小鼠模型中,将聚乳酸-乙醇酸共聚物和无定形磷酸钙纳米颗粒以及戈尔特斯(Gore-Tex®)皮下植入,并在另一个单独的系列中作为胸壁移植物进行测试。在1、2、4和8周后,在六个不同区域测定细胞向各自材料的浸润情况、炎症反应以及新血管形成(内皮细胞)。虽然戈尔特斯(Gore-Tex®)仅允许细胞在外表面浸润,但电纺聚乳酸-乙醇酸共聚物和无定形磷酸钙纳米颗粒被浸润细胞完全穿透。这些细胞主要由巨噬细胞组成,只有4%的巨细胞和淋巴细胞。总巨噬细胞计数随时间增加,而表达白细胞介素-1β(IL1-β)的巨噬细胞数量减少,表明对移植物处于保护状态。因此,聚乳酸-乙醇酸共聚物和无定形磷酸钙纳米颗粒似乎具有作为胸壁置换材料的理想特性,即(a)具有完全生物降解的优势,(b)显示出稳定的胸壁结构,以及(c)与戈尔特斯(Gore-Tex®)相比,能适应生理并整合移植物。