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Published April 15, 2010 | Accepted Version + Supplemental Material
Journal Article Open

SlipChip for immunoassays in nanoliter volumes

Abstract

This article describes a SlipChip-based approach to perform bead-based heterogeneous immunoassays with multiple nanoliter-volume samples. As a potential device to analyze the output of the chemistrode, the performance of this platform was tested using low concentrations of biomolecules. Two strategies to perform the immunoassay in the SlipChip were tested: (1) a unidirectional slipping method to combine the well containing a sample with a series of wells preloaded with reagents and (2) a back-and-forth slipping method to introduce a series of reagents to a well containing the sample by reloading and slipping the well containing the reagent. The SlipChips were fabricated with hydrophilic surfaces on the interior of the wells and with hydrophobic surfaces on the face of the SlipChip to enhance filling, transferring, and maintaining aqueous solutions in shallow wells. Nanopatterning was used to increase the hydrophobic nature of the SlipChip surface. Magnetic beads containing the capture antibody were efficiently transferred between wells and washed by serial dilution. An insulin immunoenzymatic assay showed a detection of limit of ∼13 pM. A total of 48 droplets of nanoliter volume were analyzed in parallel, including an on-chip calibration. The design of the SlipChip is flexible to accommodate other types of immunoassays, both heterogeneous and homogeneous. This work establishes the possibility of using SlipChip-based immunoassays in small volumes for a range of possible applications, including analysis of plugs from a chemistrode, detection of molecules from single cells, and diagnostic monitoring.

Additional Information

© 2010 American Chemical Society. Published In Issue: April 15, 2010. Article ASAP: March 24, 2010. Received: January 7, 2010. Accepted: March 5, 2010. This work was supported by the NSF CRC Grant CHE-0526693 and the NIH Director's Pioneer Award program, part of the NIH Roadmap for Medical Research (Grant 1 DP1 OD003584). We thank Heidi Park for contributions to writing and editing this manuscript.

Attached Files

Accepted Version - nihms191229.pdf

Supplemental Material - Ismagilov_Anal_Chem_2010_SlipChip_Immunoassays_WL_DC_WD_KP_supp_info.pdf

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