1,984 research outputs found

    IP Restoration vs. WDM Protection: Is There an Optimal choice?

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    On Energy Reduction and Green Networking Enhancement due to In-Network Caching

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    In-network caching in information centric networking (ICN) is considered as a promising approach to reducing energy consumption of an entire network. However, it is also considered as an energy consuming technique. These contradictory claims lead to one research question: Does caching really reduce the energy consumption of the entire network? To answer the question, we formulate an ICN network as an optimization problem with a realistic energy consumption model for an ICN router. By solving the formulation assuming that ICN forwarding software currently under development is used as a forwarding engine of an ICN router, we reveal that in-network caching alone does not reduce much energy but it enhances a currently developed green networking technique even though the forwarding engine is not fully optimized

    On Energy Reduction and Green Networking Enhancement due to In-Network Caching

    Get PDF
    In-network caching in information centric networking (ICN) is considered as a promising approach to reducing energy consumption of an entire network. However, it is also considered as an energy consuming technique. These contradictory claims lead to one research question: Does caching really reduce the energy consumption of the entire network? To answer the question, we formulate an ICN network as an optimization problem with a realistic energy consumption model for an ICN router. By solving the formulation assuming that ICN forwarding software currently under development is used as a forwarding engine of an ICN router, we reveal that in-network caching alone does not reduce much energy but it enhances a currently developed green networking technique even though the forwarding engine is not fully optimized

    BIOMIMETIC ORAL MUCIN FROM POLYMER MICELLE NETWORKS

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    Mucin networks are formed by the complexation of bottlebrush-like mucin glycoprotein with other small molecule glycoproteins. These glycoproteins create nanoscale strands that then arrange into a nanoporous mesh. These networks play an important role in ensuring surface hydration, lubricity and barrier protection. In order to understand the functional behavior in mucin networks, it is important to decouple their chemical and physical effects responsible for generating the fundamental property-function relationship. To achieve this goal, we propose to develop a synthetic biomimetic mucin using a layer-by-layer (LBL) deposition approach. In this work, a hierarchical 3-dimensional structures resembling natural mucin networks was generated using affinity-based interactions on synthetic and biological surfaces. Unlike conventional polyelectrolyte-based LBL methods, pre-assembled biotin-functionalized filamentous (worm-like) micelles was utilized as the network building block, which from complementary additions of streptavidin generated synthetic networks of desired thickness. The biomimetic nature in those synthetic networks are studied by evaluating its structural and bio-functional properties. Structurally, synthetic networks formed a nanoporous mesh. The networks demonstrated excellent surface hydration property and were able capable of microbial capture. Those functional properties are akin to that of natural mucin networks. Further, the role of synthetic mucin as a drug delivery vehicle, capable of providing localized and tunable release was demonstrated. By incorporating antibacterial curcumin drug loading within synthetic networks, bacterial growth inhibition was also demonstrated. Thus, such bioactive interfaces can serve as a model for independently characterizing mucin network properties and through its role as a drug carrier vehicle it presents exciting future opportunities for localized drug delivery, in regenerative applications and as bio-functional implant coats

    Poroelastic osmoregulation of living cell volume

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    Cells maintain their volume through fine intracellular osmolarity regulation. Osmotic challenges drive fluid into or out of cells causing swelling or shrinkage, respectively. The dynamics of cell volume changes depending on the rheology of the cellular constituents and on how fast the fluid permeates through the membrane and cytoplasm. We investigated whether and how poroelasticity can describe volume dynamics in response to osmotic shocks. We exposed cells to osmotic perturbations and used defocusing epifluorescence microscopy on membrane-attached fluorescent nanospheres to track volume dynamics with high spatiotemporal resolution. We found that a poroelastic model that considers both geometrical and pressurization rates captures fluid-cytoskeleton interactions, which are rate-limiting factors in controlling volume changes at short timescales. Linking cellular responses to osmotic shocks and cell mechanics through poroelasticity can predict the cell state in health, disease, or in response to novel therapeutics.Peer ReviewedPostprint (published version
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