Issue 10, 2016

Controlled antibody release from gelatin for on-chip sample preparation

Abstract

A practical way to realize on-chip sample preparation for point-of-care diagnostics is to store the required reagents on a microfluidic device and release them in a controlled manner upon contact with the sample. For the development of such diagnostic devices, a fundamental understanding of the release kinetics of reagents from suitable materials in microfluidic chips is therefore essential. Here, we study the release kinetics of fluorophore-conjugated antibodies from (sub-) μm thick gelatin layers and several ways to control the release time. The observed antibody release is well-described by a diffusion model. Release times ranging from ∼20 s to ∼650 s were determined for layers with thicknesses (in the dry state) between 0.25 μm and 1.5 μm, corresponding to a diffusivity of 0.65 μm2 s−1 (in the swollen state) for our standard layer preparation conditions. By modifying the preparation conditions, we can influence the properties of gelatin to realize faster or slower release. Faster drying at increased temperatures leads to shorter release times, whereas slower drying at increased humidity yields slower release. As expected in a diffusive process, the release time increases with the size of the antibody. Moreover, the ionic strength of the release medium has a significant impact on the release kinetics. Applying these findings to cell counting chambers with on-chip sample preparation, we can tune the release to control the antibody distribution after inflow of blood in order to achieve homogeneous cell staining.

Graphical abstract: Controlled antibody release from gelatin for on-chip sample preparation

Supplementary files

Article information

Article type
Paper
Submitted
09 Oct 2015
Accepted
30 Mar 2016
First published
30 Mar 2016

Analyst, 2016,141, 3068-3076

Author version available

Controlled antibody release from gelatin for on-chip sample preparation

X. Zhang, D. Wasserberg, C. Breukers, L. W. M. M. Terstappen and M. Beck, Analyst, 2016, 141, 3068 DOI: 10.1039/C5AN02090E

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