摘要:
The application of microfluidics in the field of surface-based assays and more specifically, the spatial molecular profiling of tumor tissues has gained a lot of interest, especially with the increased interest in personalized medicine and targeted therapy. During a static incubation of the immunoreaction reagents with the tissue section, the reagents begin to adsorb and bind to the target epitopes on the tissue sample. However, the laminar fluid flow associated with the small dimensions of microfluidic systems and the domination of the diffusional mass transport of reagents can limit their transport to the tissue. Furthermore, during the reaction time, a depletion region is formed around the target area with a much lower abundance of the reagent. At this point, the reaction rate becomes limited due to the scarcity of the detection reagents and their diffusion-limited transport, which can lead to very lengthy experiments. Moreover, uniform staining of the tissue plays an important role in the analysis, since it ensures that all relevant antigen epitopes on the tissue are equally exposed to the detection reagents, thereby enhancing the signal contrast and facilitating quantifiable *** the current work, we have investigated and integrated two microfluidic mixing techniques, including AC electrothermal flow (ACET), and acoustofluidic mixing (AF). First, we report a novel ACET electrode design concept for generating in-plane microfluidic mixing vortices that act over a large volume and close to the reaction surface of interest. This is different from the traditional ACET parallel electrode design that provides rather local vertical mixing vortices directly above the electrodes. As a proof of concept, the new design has been used in ACET-enhanced immunoassays to improve the immunostaining signal of the HER2 cancer biomarker (Human epidermal growth factor receptor 2) on breast cancer cells. We have achieved a 6-times enhancement in the assay signal with a 75% red