Hemocompatible Surfaces Through Surface-attached Hydrogel Coatings and their Functional Stability in a Medical Environment.

Blood compatible materials are a well-researched scientific field as such materials are required in a wide range of applications, for example, in heart-lung machines or ventricular assist devices. Surfaces coated with certain surface-bound neutral, water-swellable polymer networks have the ability to repel cells such as platelets and exhibit a significantly improved hemocompatibility. In this study, we investigate the interaction of platelets from whole blood with surfaces coated with photochemically generated surface-attached polymer networks based on polydimethyl acrylamide. As substrates medical-grade polyurethanes are used, and the networks are formed and attached to the substrate surfaces through C-H insertion reactions. The hydrogel-coated substrates are perfused with blood for extended periods of time. We show that the polymer coating prevents the adhesion of cells even at longer times of blood contact, regardless of the thickness of the coating employed. The surfaces can be sterilized following a standard autoclave procedure without any loss of function. Additionally, it is shown that the samples can be stored at least for 3 months under varying ambient conditions while retaining their functionality. The excellent blood compatibility, the possibility to coat even rather inert polymeric materials and the ability to handle the materials in an environment typical for a medical application make such coatings a promising candidate for future hemocompatible devices.

Platelet repellent properties of hydrogel coatings on polyurethane-coated glass surfaces.

Thromboembolism is a severe complication in patients with ventricular assist devices. Interactions of platelets with the artificial surface and pathological blood flow conditions could contribute to thrombus formation. Previous studies suggested that strongly swellable polymer coatings prepared from various poly(N-alkyl acrylamides) are bioinert as they repel proteins and cells. In this study, we tested structurally similar polymer coatings with varying degrees of crosslinking and swelling to explore if the bioinert character of such coatings is also valid under whole blood perfusion and shear stress. Glass substrates coated with medical grade polyurethane (PU) were modified with surface-attached poly(N-alkyl acrylamide) layers, which differed in crosslinking and in swelling. Slides were perfused with human blood containing fluoresceinated platelets at a shear rate of 1500 s for 3 minutes. Noncoated and PU-coated glass slides served as a reference for thrombogenic surfaces. We detected severe platelet adhesion on the reference surfaces. There was no platelet adhesion on poly(N-alkyl acrylamide) coatings with a swelling factor above 1.5-2 (p < 0.001 compared with PU). A lower swelling factor resulted in severe platelet adhesion. Different degrees of crosslinking ranging from 1% to 10% did not reverse platelet repellent properties of the representative polymer tested (p < 0.001 compared with PU).

Fast and efficient MCR-based synthesis of clickable rhodamine tags for protein profiling.

Protein profiling probes are important tools for studying the composition of the proteome and as such have contributed greatly to the understanding of various complex biological processes in higher organisms. For this purpose the application of fluorescently labeled activity or affinity probes is highly desirable. Especially for in vivo detection of low abundant target proteins, otherwise difficult to analyse by standard blotting techniques, fluorescently labeled profiling probes are of high value. Here, a one-pot protocol for the synthesis of activated fluorescent labels (i.e. azide, alkynyl or NHS), based on the Ugi-4-component reaction (Ugi-4CR), is presented. As a result of the peptoidic structure formed, the fluorescent properties of the products are pH insensitive. Moreover, the applicability of these probes, as exemplified by the labeling of model protein BSA, will be discussed.