“…To overcome such challenges, much effort has been pursued to engineer the surface geometry, surface chemistry, DNA conformation, and DNA packing density on a microarray chip. − Among these strategies, the creation of hydrogel-based DNA microarrays has attracted particular interest, given the multiple beneficial properties of hydrogels , in addressing the key drawbacks associated with conventional DNA microarrays. , The hydrated microenvironment of a hydrogel minimizes both conformational changes of the sensing DNA upon drying and nonspecific protein adsorption on the sensor surface . The porosity of a hydrogel can be tuned to enable stable physical entrapment of the sensing DNA, avoiding the need for expensive chemically modified oligonucleotides that are required for covalent − or high-affinity noncovalent DNA immobilization while facilitating improved sensor stability relative to DNA immobilization via physical adsorption. , Concurrently, the three-dimensional (3D) (or at least “2.5D”) dimensionality of a hydrogel enables the immobilization of two to three orders of magnitude higher DNA loadings per unit surface area than are achievable with 2D systems, , in most cases more than offsetting any enhanced mass transfer resistance associated with transport of the probe (i.e., the target to be detected) into the hydrogel .…”