Gulliksen Anja, Solli Lars Anders, Drese Klaus Stefan, Sörensen Olaf, Karlsen Frank, Rogne Henrik, Hovig Eivind, Sirevåg Reidun
NorChip AS, Industriveien 8, 3490 Klokkarstua, Norway.
Lab Chip. 2005 Apr;5(4):416-20. doi: 10.1039/b415525d. Epub 2005 Jan 28.
A general multipurpose microchip technology platform for point-of-care diagnostics has been developed. Real-time nucleic acid sequence-based amplification (NASBA) for detection of artificial human papilloma virus (HPV) 16 sequences and SiHa cell line samples was successfully performed in cyclic olefin copolymer (COC) microchips, incorporating supply channels and parallel reaction channels. Samples were distributed into 10 parallel reaction channels, and signals were simultaneously detected in 80 nl volumes. With a custom-made optical detection unit, the system reached a sensitivity limit of 10(-6) microM for artificial HPV 16 sequences, and 20 cells microl(-1) for the SiHa cell line. This is comparable to the detection limit of conventional readers, and clinical testing of biological samples in polymer microchips using NASBA is therefore possible.
已开发出一种用于即时诊断的通用多功能微芯片技术平台。在包含供应通道和平行反应通道的环烯烃共聚物(COC)微芯片中,成功进行了基于实时核酸序列扩增(NASBA)的人工人乳头瘤病毒(HPV)16序列和SiHa细胞系样本的检测。样本被分配到10个平行反应通道中,并在80 nl体积中同时检测信号。使用定制的光学检测单元,该系统对人工HPV 16序列的灵敏度极限达到10(-6) microM,对SiHa细胞系的灵敏度极限达到20个细胞/微升。这与传统读数器的检测极限相当,因此使用NASBA在聚合物微芯片中对生物样本进行临床检测是可行的。