Kiviranta I, Jurvelin J, Tammi M, Säämänen A M, Helminen H J
Histochemistry. 1985;82(3):249-55. doi: 10.1007/BF00501401.
A new microspectrophotometric method was developed for quantitation of glycosaminoglycans with Safranin O dye in articular cartilage matrix. From histological sections molar extinction coefficient of Safranin O was determined and used to measure the dye content of the sections. The amount of glycosaminoglycans was determined with depth of bovine articular cartilage by both gas chromatography and thin layer chromatography to calculate the fixed negative charge content. Comparison between the results revealed that binding of Safranin O to glycosaminoglycan polyanions was stoichiometric and showed minimal nonspecific staining. The method provides an accurate technique for quantitation and localization of fixed negative charge content of glycosaminoglycans in the articular cartilage matrix. Specific enzyme digestions enable detection of separate glycosaminoglycans.
开发了一种新的显微分光光度法,用于定量分析关节软骨基质中与番红O染料结合的糖胺聚糖。通过组织学切片测定番红O的摩尔消光系数,并用于测量切片中的染料含量。采用气相色谱法和薄层色谱法测定牛关节软骨不同深度的糖胺聚糖含量,以计算固定负电荷含量。结果比较表明,番红O与糖胺聚糖多阴离子的结合是化学计量的,非特异性染色极少。该方法为定量分析和定位关节软骨基质中糖胺聚糖的固定负电荷含量提供了一种准确的技术。特异性酶消化能够检测出不同的糖胺聚糖。