Imamura H, Maruyama T, Okabe H, Shimada H, Otagiri M
Faculty of Pharmaceutical Sciences, Kumamoto University, Japan.
Pharm Res. 1994 Apr;11(4):566-70. doi: 10.1023/a:1018926902083.
We examined different fluorescent probes suitable for fluorometric determination of alpha 1-acid glycoprotein (AGP) in serum. Quinaldine red (QR) was shown to bind strongly and selectively to AGP. Taking advantage of the enhanced fluorescence of QR in the presence of AGP, we developed a direct method for the determination of serum AGP without removal of other serum proteins such as albumin. AGP concentrations in serum of healthy volunteers and patients correlated well with results from the conventional single radial immunodiffusion (SRID) method (r = 0.93, slope = 1). The newly developed method is faster and has a larger analytical concentration range than the SRID method. This method can also be used to determine AGP in serum of experimental animals, and it can serve to monitor AGP serum concentrations for pharmacokinetic evaluation of basic drugs.
我们研究了适用于荧光法测定血清中α1-酸性糖蛋白(AGP)的不同荧光探针。结果表明,喹哪啶红(QR)能与AGP强烈且选择性地结合。利用AGP存在时QR荧光增强的特性,我们开发了一种直接测定血清AGP的方法,无需去除白蛋白等其他血清蛋白。健康志愿者和患者血清中的AGP浓度与传统单向放射免疫扩散法(SRID)的结果具有良好的相关性(r = 0.93,斜率 = 1)。新开发的方法比SRID方法更快,且分析浓度范围更大。该方法还可用于测定实验动物血清中的AGP,并且可用于监测AGP血清浓度,以进行基础药物的药代动力学评估。