Chemical and Biomolecular Engineering - Research Publications

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    Photophysical and Fluorescence Anisotropic Behavior of Polyfluorene β-Conformation Films
    Yu, M-N ; Soleimaninejad, H ; Lin, J-Y ; Zuo, Z-Y ; Liu, B ; Bo, Y-F ; Bai, L-B ; Han, Y-M ; Smith, TA ; Xu, M ; Wu, X-P ; Dunstan, DE ; Xia, R-D ; Xie, L-H ; Bradley, DDC ; Huang, W (AMER CHEMICAL SOC, 2018-01-18)
    We demonstrate a systematic visualization of the unique photophysical and fluorescence anisotropic properties of polyfluorene coplanar conformation (β-conformation) using time-resolved scanning confocal fluorescence imaging (FLIM) and fluorescence anisotropy imaging microscopy (FAIM) measurements. We observe inhomogeneous morphologies and fluorescence decay profiles at various micrometer-sized regions within all types of polyfluorene β-conformational spin-coated films. Poly(9,9-dioctylfluorene-2,7-diyl) (PFO) and poly[4-(octyloxy)-9,9-diphenylfluoren-2,7-diyl]-co-[5-(octyloxy)-9,9-diphenylfluoren-2,7-diyl] (PODPF) β-domains both have shorter lifetime than those of the glassy conformation for the longer effective conjugated length and rigid chain structures. Besides, β-conformational regions have larger fluorescence anisotropy for the low molecular rotational motion and high chain orientation, while the low anisotropy in glassy conformational regions shows more rotational freedom of the chain and efficient energy migration from amorphous regions to β-conformation as a whole. Finally, ultrastable ASE threshold in the PODPF β-conformational films also confirms its potential application in organic lasers. In this regard, FLIM and FAIM measurements provide an effective platform to explore the fundamental photophysical process of conformational transitions in conjugated polymer.
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    Remote Control in Formation of 3D Multicellular Assemblies Using Magnetic Forces
    Jafari, J ; Han, X-L ; Palmer, J ; Tran, PA ; O'Connor, AJ (AMER CHEMICAL SOC, 2019-05)
    Cell constructs have been utilized as building blocks in tissue engineering to closely mimic the natural tissue and also overcome some of the limitations caused by two-dimensional cultures or using scaffolds. External forces can be used to enhance the cells' adhesion and interaction and thus provide better control over production of these structures compared to methods like cell seeding and migration. In this paper, we demonstrate an efficient method to generate uniform, three-dimensional cell constructs using magnetic forces. This method produced spheroids with higher densities and more symmetrical structures than the commonly used centrifugation method for production of cell spheroids. It was also shown that shape of the cell constructs could be changed readily by using different patterns of magnetic field. The application of magnetic fields to impart forces on the cells enhanced the fusion of these spheroids, which could be used to produce larger and more complicated structures for future tissue engineering applications.
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    Thiol-Reactive Star Polymers Functionalized with Short Ethoxy-Containing Moieties Exhibit Enhanced Uptake in Acute Lymphoblastic Leukemia Cells
    Bayat, N ; McOrist, N ; Ariotti, N ; Lai, M ; Sia, KCS ; Li, Y ; Grace, JL ; Quinn, JF ; Whittaker, MR ; Kavallaris, M ; Davis, TP ; Lock, RB (DOVE MEDICAL PRESS LTD, 2019)
    PURPOSE: Directing nanoparticles to cancer cells without using antibodies is of great interest. Subtle changes to the surface chemistry of nanoparticles can significantly affect their biological fate, including their propensity to associate with different cell populations. For instance, nanoparticles functionalized with thiol-reactive groups can potentially enhance association with cells that over-express cell-surface thiol groups. The potential of such an approach for enhancing drug delivery for childhood acute lymphoblastic leukemia (ALL) cells has not been investigated. Herein, we investigate the impact of thiol-reactive star polymers on the cellular association and the mechanisms of uptake of the nanoparticles. METHODS: We prepared fluorescently labeled star polymers functionalized with an mPEG brush corona and pyridyl disulfide to examine how reactivity to exofacial thiols impacts cellular association with ALL cells. We also studied how variations to the mPEG brush composition could potentially be used as a secondary method for controlling the extent of cell association. Specifically, we examined how the inclusion of shorter diethylene glycol brush moieties into the nanoparticle corona could be used to further influence cell association. RESULTS: Star polymers incorporating both thiol-reactive and diethylene glycol brush moieties exhibited the highest cellular association, followed by those functionalized solely with thiol reactive groups compared to control nanoparticles in T and B pediatric ALL patient-derived xenografts harvested from the spleens and bone marrow of immunodeficient mice. Transfection of cells with an early endosomal marker and imaging with correlative light and electron microscopy confirmed cellular uptake. Endocytosis inhibitors revealed dynamin-dependent clathrin-mediated endocytosis as the main uptake pathway for all the star polymers. CONCLUSION: Thiol-reactive star polymers having an mPEG brush corona that includes a proportion of diethylene glycol brush moieties represent a potential strategy for improved leukemia cell delivery.
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    The use of carbonic anhydrase to accelerate carbon dioxide capture processes
    Yong, JKJ ; Stevens, GW ; Caruso, F ; Kentish, SE (WILEY, 2015-01)
    The chemical absorption of CO2 into a monoethanolamine solvent is currently the most widely accepted commercial approach to carbon dioxide capture. However, the subsequent desorption of CO2 from the solvents is extremely energy intensive. Alternative solvents are more energy efficient, but their slow reaction kinetics in the CO2 absorption step limits application. The use of a carbonic anhydrase (CA) enzyme as a reaction promoter can potentially overcome this obstacle. Native, engineered and artificial CA enzymes have been investigated for this application. Immobilization of the enzyme within the gas absorber or in a membrane format can increase enzyme stability and avoid thermal denaturation in the stripper. However, immobilization is only effective if the mass transfer of carbon dioxide through the liquid phase to reach the immobilization substrate does not become rate controlling. Further research should also consider the process economics of large-scale enzyme production and the long-term performance of the enzyme under real flue gas conditions.
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    Self-template construction of nanoporous carbon nanorods from a metal-organic framework for supercapacitor electrodes
    Yang, Y-W ; Liu, X-H ; Gao, E-P ; Feng, T-T ; Jiang, W-J ; Wu, J ; Jiang, H ; Sun, B (ROYAL SOC CHEMISTRY, 2018)
    The morphologies and structures of nanostructured carbons generally influence their catalysis, electrochemical performance and adsorption properties. Metal-organic framework (MOF) nanocrystals usually have various morphologies, and can be considered as a template to construct nanostructured carbons with shaped nanocubes, nanorods, and hollow particles by thermal transformation. However, thermal carbonization of MOFs usually leads to collapse of MOF structures. Here, we report shape-preserved carbons (termed as CNRods) by thermal transformation of nickel catecholate framework (Ni-CAT) nanorods. Supercapacitors of CNRods treated at 800 °C were demonstrated to have enhanced performance due to their structural features that facilitate electron conduction and ion transport as well as abundant O content benefiting the wettability of the carbon materials. This may provide a potential way to explore novel carbon materials for supercapacitors with controllable morphologies and high capacitive performance.
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    A modelling approach to assess the long-term stability of a novel microbial/electrochemical system for the treatment of acid mine drainage.
    Brewster, ET ; Pozo, G ; Batstone, DJ ; Freguia, S ; Ledezma, P (Royal Society of Chemistry (RSC), 2018-05-17)
    Microbial electrochemical processes have potential to remediate acid mine drainage (AMD) wastewaters which are highly acidic and rich in sulfate and heavy metals, without the need for extensive chemical dosing. In this manuscript, a novel hybrid microbial/electrochemical remediation process which uses a 3-reactor system - a precipitation vessel, an electrochemical reactor and a microbial electrochemical reactor with a sulfate-reducing biocathode - was modelled. To evaluate the long-term operability of this system, a dynamic model for the fluxes of 140 different ionic species was developed and calibrated using laboratory-scale experimental data. The model identified that when the reactors are operating in the desired state, the coulombic efficiency of sulfate removal from AMD is high (91%). Modelling also identified that a periodic electrolyte purge is required to prevent the build-up of Cl- ions in the microbial electrochemical reactor. The model furthermore studied the fate of sulfate and carbon in the system. For sulfate, it was found that only 29% can be converted into elemental sulfur, with the rest complexating with metals in the precipitation vessel. Finally, the model shows that the flux of inorganic carbon under the current operational strategy is insufficient to maintain the autotrophic sulfate-reducing biomass. The modelling approach demonstrates that a change in system operational strategies plus close monitoring of overlooked ionic species (such as Cl- and HCO3 -) are key towards the scaling-up of this technology.
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    Flexible C-Mo2C fiber film with self-fused junctions as a long cyclability anode material for sodium-ion battery
    Zhang, W ; Guo, Z ; Liang, Q ; Lv, R ; Shen, W ; Kang, F ; Weng, Y ; Huang, Z-H (ROYAL SOC CHEMISTRY, 2018)
    Electrospun carbon fiber films have high contact resistance at the fiber junctions, which causes poor cycling stability and limits their further improvement in energy storage performances. To eliminate the contact resistance of the film, we provide a new strategy to fuse the fiber junctions by introducing MoO2 in the fibers, which replaces the C-C interface by a more active C-MoO2-C interface at the fiber junction to promote mass transfer. MoO2 reacts with C matrix to generate Mo2C and form self-fused junctions during the carbonization process. Due to much lower charge transfer and sodium diffusion resistance, the C-Mo2C fiber film with self-fused junctions shows much better cyclability with capacity retention of 90% after 2000 cycles at a constant current density of 1 A g-1. Moreover, the Mo2C particles provide many electrochemically active sites, leading to additional improvement in sodium storage. The C-Mo2C fiber film has a capacity of 134 mA h g-1 at 1 A g-1 and a high capacity of 99 mA h g-1 even at 5 A g-1.
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    Polysulfides made from re-purposed waste are sustainable materials for removing iron from water
    Lundquist, NA ; Worthington, MJH ; Adamson, N ; Gibson, CT ; Johnston, MR ; Ellis, AV ; Chalker, JM (ROYAL SOC CHEMISTRY, 2018)
    Water contaminated with Fe3+ is undesirable because it can result in discoloured plumbing fixtures, clogging, and a poor taste and aesthetic profile for drinking water. At high levels, Fe3+ can also promote the growth of unwanted bacteria, so environmental agencies and water authorities typically regulate the amount of Fe3+ in municipal water and wastewater. Here, polysulfide sorbents-prepared from elemental sulfur and unsaturated cooking oils-are used to remove Fe3+ contaminants from water. The sorbent is low-cost and sustainable, as it can be prepared entirely from waste. The preparation of this material using microwave heating and its application in iron capture are two important advances in the growing field of sulfur polymers.
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    Self-assembly of "patchy" nanoparticles: a versatile approach to functional hierarchical materials
    Lunn, DJ ; Finnegan, JR ; Manners, I (ROYAL SOC CHEMISTRY, 2015)
    The solution-phase self-assembly or "polymerization" of discrete colloidal building blocks, such as "patchy" nanoparticles and multicompartment micelles, is attracting growing attention with respect to the creation of complex hierarchical materials. This approach represents a versatile method with which to transfer functionality at the molecular level to the nano- and microscale, and is often accompanied by the emergence of new material properties. In this perspective we highlight selected recent examples of the self-assembly of anisotropic nanoparticles which exploit directional interactions introduced through their shape or surface chemistry to afford a variety of hierarchical materials. We focus in particular on the solution self-assembly of block copolymers as a means to prepare multicompartment or "patchy" micelles. Due to their potential for synthetic modification, these constructs represent highly tuneable building blocks for the fabrication of a wide variety of functional assemblies.
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    Enhancing dendritic cell activation and HIV vaccine effectiveness through nanoparticle vaccination
    Glass, JJ ; Kent, SJ ; De Rose, R (TAYLOR & FRANCIS LTD, 2016)
    Novel vaccination approaches are needed to prevent and control human immunodeficiency virus (HIV) infection. A growing body of literature demonstrates the potential of nanotechnology to modulate the human immune system and generate targeted, controlled immune responses. In this Review, we summarize important advances in how 'nanovaccinology' can be used to develop safe and effective vaccines for HIV. We highlight the central role of dendritic cells in the immune response to vaccination and describe how nanotechnology can be used to enhance delivery to and activation of these important antigen-presenting cells. Strategies employed to improve biodistribution are discussed, including improved lymph node delivery and mucosal penetration concepts, before detailing methods to enhance the humoral and/or cellular immune response to vaccines. We conclude with a commentary on the current state of nanovaccinology.