Gonzalez G, Cid-Amador A, Steele B, Castro A
Clin Chem. 1982 Jul;28(7):1494-6.
We describe the Ames Fluorescent Enzyme Immunoassay procedure for the detection of phenytoin in serum, and compare the results with it with those by enzyme immunoassay(EMIT), "high-pressure" liquid chromatography, and the Dupont aca. Sera from 48 patients who were receiving phenytoin were promptly analyzed in duplicate by EMIT, frozen, then assayed within four weeks by the other three methods. Correlation was good between results by the fluorescent immunoassay and the other methods. The fluorescent immunoassay procedure is sensitive and requires a small sample volume (100 microliters). Sample reading time can be shortened from 30 to 15 s as the technician becomes more proficient, with no sacrifice of accuracy. The procedure is fast, easy to perform, specific, sensitive, and inexpensive; involves no radioactivity; and requires no temperature control. It is the current method of choice for detection of phenytoin in serum, in terms of precision and accuracy.
我们描述了用于检测血清中苯妥英的艾姆斯荧光酶免疫分析方法,并将其结果与酶免疫分析(EMIT)、“高压”液相色谱法和杜邦aca的结果进行比较。对48例接受苯妥英治疗患者的血清,先用EMIT法立即进行一式两份分析,然后冷冻,在四周内用其他三种方法进行检测。荧光免疫分析结果与其他方法之间相关性良好。荧光免疫分析方法灵敏,所需样本量小(100微升)。随着技术人员操作更加熟练,样本读数时间可从30秒缩短至15秒,且不影响准确性。该方法快速、易于操作、特异、灵敏且成本低廉;不涉及放射性;无需温度控制。就精密度和准确性而言,它是目前检测血清中苯妥英的首选方法。