Levinefitzpatrick1907

Cryopreservation is an essential part of tissue banking and effective cryopreservation methods are critical for the development of cost-effective cell therapy products. Cell sheets are an attractive subset of cell therapy types, and cryopreservation has the potential to further drive down costs of allogeneic cell sheet therapy. This is currently a challenge as adhered cell monolayers are more susceptible to membrane damage during the freezing process. In this article, we investigate the performance of a surface-modified dressing for the cryopreservation of cells and strategies to improve cell recovery. Cryopreservation of multipotent adult progenitor cells (MAPC®) was performed on cells following their attachment to a surface for different periods of time. MAPC cells, given just 1 h to attach, washed off and were not recovered on the surface following thawing. Cells attached for longer periods, elongated further, and were more susceptible to damage from cryopreservation. A temporal window was identified that could allow cryopreservation on adherent surfaces where cells had attached to a surface without full elongation. By functionalizing the surface with coupled hyaluronic acid, cell spreading was initially retarded, thereby widening this temporal window. This approach demonstrates a novel method for enhancing the recovery of cryopreserved cell sheets on surfaces.There are many different types of surfaces found in nature which can increase or reduce friction, such as the well-studied frog toe or lotus leaf. However, methods for replicating these surfaces on a large scale for use in industrial applications are needed in order to take advantage of this natural friction engineering. read more Most replication processes rely on molding that requires an input surface size comparable to the desired output surface. We present a novel approach of replicating large-scale biosurfaces using a laser scanning confocal microscope for surface digitization and 3D two-photon lithography for the fabrication of the digitized surface. Two different natural surfaces (banana skin and daffodil petal) were replicated. An intermediary tiling process was used to cover a target area of arbitrary size independent of the input texture size. The surfaces were coated with a thin layer of ZnO, and the frictional and wettability characteristics of the replicated surfaces were then examined, demonstrating significant friction reduction up to 42% and increased hydrophobicity due to the presence of texture.A key hurdle toward effective application of nanoparticles (NPs) in biomedicine is still the incomplete understanding of the biomolecular adsorption layer, the so-called protein corona, which inevitably forms around NPs when they are immersed in a biofluid. NP sizing techniques via the analysis of Brownian motions offer a powerful way to measure the thickness of the protein corona in situ. Here, the fundamentals of three techniques, dynamic light scattering, fluorescence correlation spectroscopy, and nanoparticle tracking analysis are briefly summarized. Then, experimental procedures for the determination of binding curves are presented in a tutorial fashion. Nanoparticle sizing experiments are illustrated with a selection of recent results on the interactions of transferrin with hydrophilic and hydrophobic polystyrene nanoparticles, and key insights gained from this work are discussed.Many natural surfaces, including the wings of cicada insects, have shown to display bactericidal properties as a result of surface topography. Moreover, the size and distribution of the surface features (on the nano- and microscale) are known to influence the efficacy of the surface at inhibiting bacterial cell growth. While these types of natural surfaces illustrate the effect of structure on the bactericidal activity, a deeper understanding can be achieved by creating surfaces of different feature sizes. This is essential in order to understand the effects of changes of surface topography on bacteria-surface interactions. To this end, we have performed a series of replica molding processes of the wings of the Megapomponia Intermedia cicada to prepare wing replicas in polyethylene glycol (PEG), which possess the topographical features of the wing surface, with a minimum loss of feature resolution. Atomic force microscopy characterization of these patterned surfaces in both air and aqueous environments shows that by controlling the swelling characteristics of the PEG, we can control the ultimate swollen dimensions of the nanopillar structures on the surface of PEG. As a result, by using a single wing with an average nanopillar height of 220 nm, different patterned PEG samples with nanopillar heights ranging from 180 to 307 nm were produced.Fluorescent dyes and nanoparticles (NPs) have been widely used together to make novel biosensors, taking advantage of their unique characteristics. It is crucial to have techniques that enable us to gain detailed and high-resolution information regarding the interaction between NPs and fluorescent dyes. In this work, we chose rhodamine B (RhB) and amidine- and carboxylate-modified polystyrene (CML) NPs as models and employed both NMR (1H and STD-NMR) and optical (UV-vis and fluorescence) techniques to investigate the interaction between NPs and fluorescent dyes. From UV-vis and fluorescence spectroscopy, we see that there are larger red shifts when rhodamine B binds to carboxylate-modified polystyrene NPs than amidine-modified NPs. Correspondingly, RhB has broader NMR peaks and a larger STD effect when binding to CML NPs than amidine NPs. Results from these two techniques validate each other. It is notable that the NMR techniques provide more reliable data than UV-vis and fluorescence methods. Moreover, we show that NMR techniques, especially STD-NMR, can provide more atomic-level binding geometry information. The higher STD effect of the smaller aromatic ring of RhB implies that this aromatic ring is closer to the surface of NPs when binding to polystyrene NPs.Mastering the magnetic response of molecular spin interfaces by tuning the occupancy of the molecular orbitals, which carry the spin magnetic moment, can be accomplished by electron doping. We propose a viable route to control the magnetization direction and magnitude of a molecular spin network, in a graphene-mediated architecture, achieved via alkali doping of manganese phthalocyanine (MnPc) molecules assembled on cobalt intercalated under a graphene membrane. The antiparallel magnetic alignment of the MnPc molecules with the underlying Co layer can be switched to a ferromagnetic state by electron doping. Multiplet calculations unveil an enhanced magnetic state of the Mn centers with a 3/2 to 5/2 spin transition induced by alkali doping, as confirmed by the steepening of the hysteresis loops, with higher saturation magnetization values. This new molecular spin configuration can be aligned by an external field, almost independently from the hard-magnet substrate effectively behaving as a free magnetic layer.