Issue 12, 2006

Open-access microfluidic patch-clamp array with raised lateral cell trapping sites

Abstract

A novel open-access microfluidic patch-clamp array chip with lateral cell trapping sites raised above the bottom plane of the chip was developed by combining both a microscale soft-lithography and a macroscale polymer fabrication method. This paper demonstrates the capability of using such an open-access fluidic system for patch-clamp measurements. The surface of the open-access patch-clamp sites prepared by the macroscale hole patterning method of soft-state elastic polydimethylsiloxane (PDMS) is examined; the seal resistances are characterized and correlated with the aperture dimensions. Whole cell patch-clamp measurements are carried out with CHO cells expressing Kv2.1 ion channels. Kv2.1 ion channel blocker (TEA) dosage response is characterized and the binding activity is examined. The results demonstrate that the system is capable of performing whole cell measurements and drug profiling in a more efficient manner than the traditional patch-clamp set-up.

Graphical abstract: Open-access microfluidic patch-clamp array with raised lateral cell trapping sites

Article information

Article type
Paper
Submitted
14 Jun 2006
Accepted
07 Sep 2006
First published
27 Sep 2006

Lab Chip, 2006,6, 1510-1515

Open-access microfluidic patch-clamp array with raised lateral cell trapping sites

A. Y. Lau, P. J. Hung, A. R. Wu and L. P. Lee, Lab Chip, 2006, 6, 1510 DOI: 10.1039/B608439G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements