Tuuminen T, Palomäki P, Rakkolainen A, Welin M G, Weber T, Käpyaho K
Labsystems Oy, Helsinki, Finland.
J Immunoassay. 1991;12(1):29-46. doi: 10.1080/01971529108055055.
The application of 3-p-hydroxyphenylpropionic acid (HPPA), a fluorogenic substrate of horseradish peroxidase (HRP) to an automated microplate fluorometric enzyme immunoassay is described. Fluorescence intensity of the end product was highly dependent on the pH of the buffer and on the concentrations of the substrate mixture ingredients. The determination of human thyrotropin (TSH) and recombinant hepatitis B surface antigen (rHBsAg) were performed using a fluorometric enzyme immunoassay (FEIA) with HPPA as the substrate, and a colorimetric one with tetramethylbenzidine (TMB) as the chromogenic substrate. The sensitivity of both types of assays proved comparable. The distinct advantage of a fluorometric assay is the possibility to perform a quantitative detection of analyte over a very wide dynamic range. Clinical evaluation of both assays showed good correlation between the FEIA and conventional methods.
描述了辣根过氧化物酶(HRP)的荧光底物3 - 对羟基苯丙酸(HPPA)在自动微孔板荧光酶免疫分析中的应用。终产物的荧光强度高度依赖于缓冲液的pH值和底物混合物成分的浓度。使用以HPPA为底物的荧光酶免疫分析(FEIA)以及以四甲基联苯胺(TMB)为显色底物的比色法对人促甲状腺激素(TSH)和重组乙型肝炎表面抗原(rHBsAg)进行了测定。两种类型的分析方法的灵敏度证明相当。荧光分析的明显优势在于能够在非常宽的动态范围内对分析物进行定量检测。两种分析方法的临床评估表明,FEIA与传统方法之间具有良好的相关性。