A novel method for the generation of surface-attached hydrogel coatings and their use in biomedical applications is discussed. This short review concentrates on surface architectures that are prepared from prepolymers carrying reactive groups suitable for crosslinking via C,H insertion reactions [C,H insertion crosslinking (CHic)]. Upon photochemical or thermal activation these groups do not only induce the crosslinking of the system, but also connect the forming gel to the surface as long as the surface itself consists of an organic material. C,H groups as the reaction partner are available in abundance at practically all types of organic surfaces such as biomaterials or polymers, rendering the technique almost universally applicable. Surface-attached gels prepared this way show unique swelling properties due to the confinement of the chains, as the obtained essentially two-dimensional gels can only swell in one dimension. This anisotropic swelling does not permit penetration of the layers by macromolecules so that the surfaces become bioinert, i.e., are strongly protein and cell repellent. It is discussed how this property can be used to control the interaction of surfaces with biological species ranging from the level of biomolecules to living cells. A combination of the CHic chemistry and microstructuring techniques opens further avenues for the study of the behavior of cells to the generation of novel bioanalytical devices.

For the miniaturization of biological assays, especially for the fabrication of microarrays, immobilization of biomolecules at the surfaces of the chips is the decisive factor. Accordingly, a variety of binding techniques have been developed over the years to immobilize DNA or proteins onto such substrates. Most of them require rather complex fabrication processes and sophisticated surface chemistry. Here, a comparatively simple immobilization technique is presented, which is based on the local generation of small spots of surface attached polymer networks. Immobilization is achieved in a one-step procedure: probe molecules are mixed with a photoactive copolymer in aqueous buffer, spotted onto a solid support, and cross-linked as well as bound to the substrate during brief flood exposure to UV light. The described procedure permits spatially confined surface functionalization and allows reliable binding of biological species to conventional substrates such as glass microscope slides as well as various types of plastic substrates with comparable performance. The latter also permits immobilization on structured, thermoformed substrates resulting in an all-plastic biochip platform, which is simple and cheap and seems to be promising for a variety of microdiagnostic applications.

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