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通过同步辐射傅里叶变换红外光谱法对关节含钙质晶体进行表征

Characterization of articular calcium-containing crystals by synchrotron FTIR.

作者信息

Rosenthal A K, Mattson E, Gohr C M, Hirschmugl C J

机构信息

Department of Medicine, Division of Rheumatology, Medical College of Wisconsin, Milwaukee, WI, USA.

出版信息

Osteoarthritis Cartilage. 2008 Nov;16(11):1395-402. doi: 10.1016/j.joca.2008.03.019. Epub 2008 May 12.

Abstract

OBJECTIVE

Sixty percent of synovial fluids from patients with severe osteoarthritis (OA) contain calcium pyrophosphate dihydrate (CPPD) or basic calcium phosphate (BCP) crystals. These bioactive crystals can be particularly difficult to accurately identify in complex biologic systems, such as in vitro models of crystal formation. We sought to determine if synchrotron Fourier Transform Infrared spectroscopy (sFTIR) could be used to identify and characterize calcium-containing crystals in mineralization models.

METHODS

CPPD and BCP crystals from porcine models of crystal formation were examined with an FTIR Microscope attached to a synchrotron light source. As a comparison, crystals from human synovial fluids were also examined. The sFTIR spectra generated were compared with known spectra of multiple forms of BCP and CPPD crystals, as well as spectra generated by synthetic CPPD and BCP crystals and cartilage proteoglycans, alone and in mixtures.

RESULTS

sFTIR readily identified CPPD and BCP crystals in porcine models as well as in fresh synovial fluids. Brushite was also present in human and porcine samples, and whitlockite was seen in some porcine samples. Mixtures of minerals were commonly found in a single crystal aggregate in both human and porcine samples. In spectra from many CPPD crystals, the peak at the 1134 cm(-1) found on the standard spectrum for CPPD was diminished. Addition of spectra from cartilage proteoglycans to those of synthetic CPPD crystals dampened the peak at this frequency region, much as this peak was diminished in biologically derived CPPD crystals.

CONCLUSION

sFTIR analysis allows for accurate identification of CPPD and BCP crystals generated in vitro and will be a useful research tool to study articular crystals.

摘要

目的

重度骨关节炎(OA)患者60%的滑液含有二水焦磷酸钙(CPPD)或碱性磷酸钙(BCP)晶体。在复杂的生物系统中,如晶体形成的体外模型中,这些生物活性晶体可能特别难以准确识别。我们试图确定同步加速器傅里叶变换红外光谱(sFTIR)是否可用于识别矿化模型中含钙晶体并对其进行表征。

方法

使用连接到同步加速器光源的傅里叶变换红外显微镜对猪晶体形成模型中的CPPD和BCP晶体进行检查。作为对照,也对人滑液中的晶体进行了检查。将生成的sFTIR光谱与多种形式的BCP和CPPD晶体的已知光谱,以及合成CPPD和BCP晶体及软骨蛋白聚糖单独和混合产生的光谱进行比较。

结果

sFTIR很容易在猪模型以及新鲜滑液中识别出CPPD和BCP晶体。透钙磷石也存在于人和猪的样本中,并且在一些猪样本中发现了白磷钙矿。在人和猪的样本中,通常在单个晶体聚集体中发现矿物质混合物。在许多CPPD晶体的光谱中,CPPD标准光谱上在1134 cm(-1)处的峰减弱。将软骨蛋白聚糖的光谱添加到合成CPPD晶体的光谱中,会使该频率区域的峰减弱,就像在生物来源的CPPD晶体中该峰减弱一样。

结论

sFTIR分析能够准确识别体外生成的CPPD和BCP晶体,将成为研究关节晶体的有用研究工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f995/2574906/d200ff199374/nihms70576f1.jpg

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