Journal
ACS APPLIED POLYMER MATERIALS
Volume 4, Issue 8, Pages 5287-5297Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsapm.2c00163
Keywords
cyclic olefin polymer; microfabrication; polymer micropillar arrays; solid-phase immunoassays; surface modification; wicking
Funding
- National Research Council (NRC)
- Canadian Space Agency (CSA) [19MOUNRC]
- NRC's Pandemic Response Challenge Program
- Microfluidic Sample Preparation (MFSP) initiative
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In this study, we investigated the use of periodic micropillar arrays for solid-phase immunoassays. These three-dimensional templates offer higher surface-to-volume ratios compared to two-dimensional substrates, resulting in increased signal intensity. Micropillar arrays also have the ability to induce wicking, allowing for spatial control of antibody distribution on the surface. Our findings suggest that the signal intensity scales proportionally with the 3D surface area available for performing solid-phase immunoassays, even at high aspect ratios and pillar densities.
We investigate the use of periodic micropillar arrays produced by high-fidelity microfabrication with cyclic olefin polymers for solid-phase immunoassays. These three-dimensional (3D) templates offer higher surface-to-volume ratios than two-dimensional substrates, making it possible to attach more antibodies and so increase the signal obtained by the assay. Micropillar arrays also provide the capacity to induce wicking, which is used to distribute and confine antibodies on the surface with spatial control. Micropillar array substrates are modified by using oxygen plasma treatment, followed by grafting of (3-aminopropyl)triethoxysilane for binding proteins covalently using glutaraldehyde as a cross-linker. The relationship between microstructure and fluorescence signal was investigated through variation of pitch (10-50 mu m), pillar diameter (5-40 mu m), and pillar height (5-57 mu m). Our findings suggest that signal intensity scales proportionally with the 3D surface area available for performing solid-phase immunoassays. A linear relationship between fluorescence intensity and microscale structure can be maintained even when the aspect ratio and pillar density both become very high, opening the possibility of tuning assay response by design such that desired signal intensity is obtained over a wide dynamic range compatible with different assays, analyte concentrations, and readout instruments. We demonstrate the versatility of the approach by performing the most common immunoassay formats.direct, indirect, and sandwich.in a qualitative fashion by using colorimetric and fluorescence-based detection for a number of clinically relevant protein markers, such as tumor necrosis factor alpha, interferon gamma (IFN-.), and spike protein of severe acute respiratory syndrome coronavirus 2. We also show quantitative detection of IFN-. in serum using a fluorescence-based sandwich immunoassay and calibrated samples with spike-in concentrations ranging from 50 pg/mL to 5 mu g/mL, yielding an estimated limit of detection of similar to 1 pg/mL for arrays with high micropillar density (11561 per mm(2)) and aspect ratio (1:11.35).
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