Liu Songyun, Hall Deborah J, McCarthy Stephanie M, Jacobs Joshua J, Urban Robert M, Pourzal Robin
Department of Bioengineering, University of Illinois at Chicago, 851 S Morgan St, Chicago, IL 60607, USA.
Department of Orthopedic Surgery, Rush University Medical Center, 1611W Harrison Street, Suite 200, Chicago, IL 60612, USA.
J Biomed Mater Res B Appl Biomater. 2020 Feb;108(2):513-526. doi: 10.1002/jbm.b.34408. Epub 2019 May 17.
Implant debris generated by wear and corrosion is a prominent cause of joint replacement failure. This study utilized Fourier transform infrared spectroscopic imaging (FTIR-I) to gain a better understanding of the chemical structure of implant debris and its impact on the surrounding biological environment. Therefore, retrieved joint capsule tissue from five total hip replacement patients was analyzed. All five cases presented different implant designs and histopathological patterns. All tissue samples were formalin-fixed and paraffin-embedded. Unstained, 5 μm thick sections were prepared. The unstained sections were placed on BaF windows and deparaffinized with xylene prior to analysis. FTIR-I data were collected at a spectral resolution of 4 cm using an Agilent Cary 670 spectrometer coupled with Cary 620 FTIR microscope. The results of study demonstrated that FTIR-I is a powerful tool that can be used complimentary to the existing histopathological evaluation of tissue. FTIR-I was able to distinguish areas with different cell types (macrophages, lymphocytes). Small, but distinct differences could be detected depending on the state of cells (viable, necrotic) and depending on what type of debris was present (polyethylene [PE], suture material, and metal oxides). Although, metal oxides were mainly below the measurable range of FTIR-I, the infrared spectra of tissues exhibited noticeable difference in their presence. Tens of micrometer sized polyethylene particles could be easily imaged, but also accumulations of submicron particles could be detected within macrophages. FTIR-I was also able to distinguish between PE debris, and other birefringent materials such as suture. Chromium-phosphate particles originating from corrosion processes within modular taper junctions of hip implants could be identified and easily distinguished from other phosphorous materials such as bone. In conclusion, this study successfully demonstrated that FTIR-I is a useful tool that can image and determine the biochemical information of retrieved tissue samples over tens of square millimeters in a completely label free, nondestructive, and objective manner. The resulting chemical images provide a deeper understanding of the chemical nature of implant debris and their impact on chemical changes of the tissue within which they are embedded.
磨损和腐蚀产生的植入物碎片是关节置换失败的一个主要原因。本研究利用傅里叶变换红外光谱成像(FTIR-I)来更好地了解植入物碎片的化学结构及其对周围生物环境的影响。因此,对五例全髋关节置换患者取出的关节囊组织进行了分析。所有五例病例均呈现不同的植入物设计和组织病理学模式。所有组织样本均用福尔马林固定并石蜡包埋。制备了未染色的5μm厚切片。在分析之前,将未染色的切片放置在氟化钡窗口上,并用二甲苯脱蜡。使用与Cary 620 FTIR显微镜联用的安捷伦Cary 670光谱仪,以4 cm的光谱分辨率收集FTIR-I数据。研究结果表明,FTIR-I是一种强大的工具,可作为对现有组织病理学评估的补充。FTIR-I能够区分不同细胞类型(巨噬细胞、淋巴细胞)的区域。根据细胞状态(存活、坏死)以及存在何种类型的碎片(聚乙烯[PE]、缝合材料和金属氧化物),可以检测到微小但明显的差异。尽管金属氧化物主要低于FTIR-I的可测量范围,但组织的红外光谱在其存在时表现出明显差异。几十微米大小的聚乙烯颗粒很容易成像,而且在巨噬细胞内也能检测到亚微米颗粒的聚集。FTIR-I还能够区分PE碎片和其他双折射材料,如缝合线。源自髋关节植入物模块化锥度连接处腐蚀过程的铬磷酸盐颗粒可以被识别,并很容易与其他磷材料(如骨)区分开来。总之,本研究成功证明FTIR-I是一种有用的工具,它可以以完全无标记、无损和客观的方式对数十平方毫米的取出组织样本进行成像并确定其生化信息。所得的化学图像能更深入地了解植入物碎片的化学性质及其对其所嵌入组织化学变化的影响。