Rössler A
Department of Physiology, School of Medicine, Karl-Franzens University, Graz, Austria.
Clin Chim Acta. 1998 Feb 23;270(2):101-14. doi: 10.1016/s0009-8981(97)00211-8.
A time-resolved fluoroimmunoassay for measuring hyaluronan concentrations in plasma and several biological fluids is described. The solid-phase immunoassay is based on the competition between aggregation of hyaluronan with the cartilage proteoglycan monomer, followed by binding of a monoclonal antibody to keratan sulfate of the proteoglycan and a biotinylated anti-mouse IgG. Fluorescence can be measured by a time-resolved fluorometer after binding of Eu(3+)-labelled streptavidin to the biotinylated IgG. The assay is precise and correlates well (r = 0.986) with the only established radioimmunoassay known. The results show that it is essential to perform a blank run without addition of proteoglycan, as endogenous proteoglycan disturbs the measurement and causes underestimation of plasma hyaluronan. The distinguishing feature of this assay is its extreme sensitivity (< 0.24 microgram/l of plasma). The mean analytical recovery after serial dilutions and addition was 100.3 and 101.3%, the within-assay and between-assay coefficients of variation were 3.67% and 7.02%, respectively.
本文描述了一种用于测量血浆和多种生物体液中透明质酸浓度的时间分辨荧光免疫测定法。该固相免疫测定法基于透明质酸与软骨蛋白聚糖单体聚集之间的竞争,随后单克隆抗体与蛋白聚糖的硫酸角质素以及生物素化的抗小鼠IgG结合。在铕(Eu(3+))标记的链霉亲和素与生物素化的IgG结合后,可用时间分辨荧光计测量荧光。该测定法精确,与唯一已知的已确立的放射免疫测定法相关性良好(r = 0.986)。结果表明,不添加蛋白聚糖进行空白测定至关重要,因为内源性蛋白聚糖会干扰测量并导致血浆透明质酸的低估。该测定法的显著特点是其极高的灵敏度(< 0.24微克/升血浆)。连续稀释并添加后的平均分析回收率分别为100.3%和101.3%,批内和批间变异系数分别为3.67%和7.02%。