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THE UNIVERSITY OF AKRON DEPARTMENT OF POLYMER ENGINEERING PRESENTS The 2015 Bayer Lectureship Prof. Michael Rubner Department of Materials Science, Massachusetts Institute of Technology Lecture 1, April 16th 1:30 pm: “Stimuli-Responsive Polymer Assemblies for Biomedical Applications” Lecture 2, April 17th 11:00 am: “Hydrogen-Bonded Multilayers: from Zwitter-Wettable Surfaces to pH-Controlled Multi-Stage Dissolution” Lectures to be held in GDYR 229 SPONSORED BY BAYER MATERIALSCIENCE, PITTSBURGH BAYER LECTURESHIP IN POLYMER ENGINEERING Michael F. Rubner is the TDK Professor of Polymer Materials Science and Engineering in the Department of Materials Science and Engineering at MIT where he has been faculty since 1986. He has been the director of MIT’s NSF MRSEC since 2002. Prof. Rubner received his bachelor’s degree from the UMass Lowell (summa cum laude) in 1982 and his Ph.D from MIT in materials science in 1986. While pursuing these degrees, he also worked full time at GTE Laboratories. Prof. Rubner has won every major teaching award given at MIT and was named an MIT MacVicar Teaching Fellow in 1986. He has given approximately 200 invited lectures and published over 200 technical papers, including 5 book chapters. From 1995 to 1999 he was the U.S. Editor of Supramolecular Science for Elsevier and he has been on the board of directors for the Materials Research Society and the Advisory Boards of the Brookhaven National Lab and the ACS Chemistry of Materials Journal. He is an MRS Fellow as well as an ACS PMSE fellow. He is considered to be one of the founding fathers in the rapidly growing area of polyelectrolyte multilayers. His contributions have played a seminal role in defining and shaping the landscape of this area of polyelectrolyte processing. Thursday April 16th, 1:30 pm “Stimuli-Responsive Polymer Assemblies for Biomedical Applications” Recently, a number of new strategies have been developed for drug delivery and disease diagnostic applications that exploit the benefits of an active immune system modified with synthetic materials for added functionality. For example, we have demonstrated the successful functionalization of living cells with 7-10 μm diameter polymer patches, fabricated by using layer-bylayer (LbL) assembly. These patches, which are referred to as cell backpacks, can adhere to the surface of immune cells, such as T and B lymphocytes, through specifically engineered interactions, like antibody-antigen binding. Since immune cells (e.g. monocytes and T cells), are activated and recruited during an immunological response to diseases such as cancer, they can be used as vehicles to carry and deliver potent anticancer drugs for site-specific drug delivery. The use of non-cytotoxic, stimuli-responsive materials is a key enabling aspect of such systems. In this presentation, a variety of different stimuli-responsive systems that have utility in biomedical applications will be discussed. These include the use of echogenic liposomes (ELIPs) in polyelectrolyte multilayer (PEM) films for drug delivery applications (see image below). Also discussed will be the demonstration that bovine submaxillary mucin (BSM) and the lectin jacalin (JAC) can be successfully assembled into multilayer films using LbL assembly. This particular biocompatible multilayer system can be utilized as an “on-demand” release platform with the ability to disassemble by using added sugar molecules as opposed to potentially damaging pH or temperature changes. This novel release system is compatible with drug-loaded and cell adhesive multilayers at neutral pH, thus broadening the potential drug or protein payloads that can be incorporated into cell backpacks. Friday April 17th, 11:00 am “Hydrogen-Bonded Multilayers: from Zwitter-Wettable Surfaces to pH-Controlled Multi-Stage Dissolution” Imagine a coating that can simultaneously appear to be both hydrophobic and hydrophilic. We refer to this phenomenon as zwitter-wettabllity. In essence, it means that the coating exhibits hydrophobic qualities when exposed to water droplets (contact angle >110°), but, at the same time, is capable of imbibing a significant amount of water from the vapor phase, as would be the case for a hydrophilic coating. By adding a high enough concentration of polymers that strongly hydrogen bond with water, it is further possible to create an anti-frost coating. This ability to resist frost formation when the coating is first exposed to below freezing temperatures and then to room temperature and high humidity is a direct result of the coatings capacity for absorbing water molecules in a non-freezing state. In this talk, the design, characterization and properties of new zwitter-wettable coatings will be presented. In addition, it will be demonstrated that noncrosslinked, multi-zone heterostructures with similar compositions can be created that can undergo a pH-driven process involving the selective dissolution of specific, well defined compartments within the thin film.