Murakami Yoshihiro, Endo Tatsuro, Yamamura Shouhei, Nagatani Naoki, Takamura Yuzuru, Tamiya Eiichi
Department of Chemical Materials Science, School of Materials Science, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Tatsunokuchi, Nomigun, Ishikawa 923-1292, Japan.
Anal Biochem. 2004 Nov 1;334(1):111-6. doi: 10.1016/j.ab.2004.07.029.
Tacrolimus (FK506) is a widely used immunosuppressant for preventing allograft rejection and the treatment of atopic dermatitis. FK506 necessitates therapeutic drug monitoring because of inter- and intrapatient variability and the lack of correlation between the administered dose and the blood concentration. Previous immunoassay-based methods required a relatively long assay time and troublesome liquid-handling procedures. In the present study, we aimed to establish a rapid monitoring method for FK506 determination by using a poly(dimethylsiloxane) (PDMS)-based microfluidic device. Polystyrene beads were coated with mouse anti-FK506 antibody and placed in the flow channel. As a competitive assay, sample solution was allowed to react in the flow channel. After the addition of the fluorogenic substrate, the fluorescent signal was observed under a microscope. As a result, the developed assay allowed a short detection time of approximately 15 min per each sample and a high sensitivity even by using only a single bead. The feasibility of performing a competitive assay using a PDMS-based antibody chip gives promising results over the existing immunoassay-based methods.
他克莫司(FK506)是一种广泛用于预防同种异体移植排斥反应和治疗特应性皮炎的免疫抑制剂。由于患者间和患者内的变异性以及给药剂量与血药浓度之间缺乏相关性,FK506需要进行治疗药物监测。以前基于免疫测定的方法需要相对较长的测定时间和繁琐的液体处理程序。在本研究中,我们旨在通过使用基于聚二甲基硅氧烷(PDMS)的微流控装置建立一种快速监测FK506的方法。将聚苯乙烯珠粒用小鼠抗FK506抗体包被并置于流动通道中。作为竞争性测定,使样品溶液在流动通道中反应。加入荧光底物后,在显微镜下观察荧光信号。结果,所开发的测定方法每个样品的检测时间约为15分钟,即使仅使用单个珠粒也具有高灵敏度。使用基于PDMS的抗体芯片进行竞争性测定的可行性比现有的基于免疫测定的方法给出了更有前景的结果。