Chen Y H, Chen S H
Department of Chemistry, National Cheng Kung University, Tainan, Taiwan.
Electrophoresis. 2000 Jan;21(1):165-70. doi: 10.1002/(SICI)1522-2683(20000101)21:1<165::AID-ELPS165>3.0.CO;2-I.
Microfluidic devices were fabricated on poly(methyl methacrylate) (PMMA) substrate using two small-diameter (79 microm) wires to create a cross impression in plastics softened by low-temperature heating. The resulting channels had a rounded shape and 75 microm in depth. The variability of the channel dimensions was found to be less than 6% from different locations of the same channel and less than 10% between chips. Moreover, the fabricated PMMA chip appeared to sustain an electric field strength up to 300 V/cm without significant Joule heating. The function of resulting devices for electrophoretic injection and separation of a DNA size marker, HaeIII digest of (phiX174, was also characterized. Results indicated that all of the 11 DNA fragments of the size marker could be identified in less than 3 min with relative standard deviations less than 0.4% and 8% for migration time and peak area, respectively. Moreover, with the use of near infrared (IR) dye, fluorescence signals of the higher molecular weight fragments (> 603 bp in length) could be detected at total DNA concentrations as low as 0.1 microg/mL (S/N = 4.2). In conclusion, the performance of wire-imprinted devices on PMMA substrate were comparable to those fabricated by other professional means.
微流控装置是在聚甲基丙烯酸甲酯(PMMA)基板上制造的,使用两根小直径(79微米)的导线在通过低温加热软化的塑料中形成交叉印记。由此产生的通道呈圆形,深度为75微米。发现同一通道不同位置的通道尺寸变化小于6%,芯片之间的变化小于10%。此外,制造的PMMA芯片似乎能够承受高达300 V/cm的电场强度,而不会产生明显的焦耳热。还对所得装置用于DNA大小标记物(phiX174的HaeIII酶切产物)的电泳进样和分离的功能进行了表征。结果表明,大小标记物的所有11个DNA片段都可以在不到3分钟内被识别,迁移时间和峰面积的相对标准偏差分别小于0.4%和8%。此外,使用近红外(IR)染料时,在总DNA浓度低至0.1微克/毫升(信噪比=4.2)的情况下,可以检测到高分子量片段(长度>603 bp)的荧光信号。总之,PMMA基板上的线压印装置的性能与通过其他专业方法制造的装置相当。