Oki Akio, Takamura Yuzuru, Ito Yoshitaka, Horiike Yasuhiro
Department of Materials Engineering, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan.
Electrophoresis. 2002 Sep;23(17):2860-4. doi: 10.1002/1522-2683(200209)23:17<2860::AID-ELPS2860>3.0.CO;2-J.
During the electrophoresis separation of B- and T-cells from lymphocytes employing a microcapillary chip, they were found to become inactive in the reservoir after a short time. This was caused by the buffer solution becoming alkaline due to electrolysis. This was considered to take place in chips with small reservoir volumes. The pH change was confirmed by the ISFET (ion-sensitive field effect transistor) embedded in the chip. To suppress the pH change, two methods were studied. One is the insertion of a salt bridge just in front of and behind the capillary, thus introducing an electric potential but stopping flow of the acid and alkaline solutions into the capillary. The other is neutralization of the alkaline solution in the reservoir by injecting the acid solution produced in another capillary with the same structure by employing an electroosmotic flow (EOF) pump. Both methods achieved no pH change during electrophoresis measurements in the microcapillary.
在用微毛细管芯片从淋巴细胞中电泳分离B细胞和T细胞的过程中,发现它们在储液器中短时间后就会变得不活跃。这是由于电解导致缓冲溶液变为碱性所致。这种情况被认为发生在储液器体积较小的芯片中。通过嵌入芯片的离子敏感场效应晶体管(ISFET)证实了pH值的变化。为了抑制pH值变化,研究了两种方法。一种是在毛细管前后插入盐桥,从而引入电势,但阻止酸碱溶液流入毛细管。另一种是通过使用电渗流(EOF)泵注入由具有相同结构的另一个毛细管产生的酸溶液来中和储液器中的碱性溶液。在微毛细管中的电泳测量过程中,两种方法都实现了pH值无变化。