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• W2024872597 abstract "The erroneous and unpredictable behavior of percutaneous glucose sensors just days following implantation has limited their clinical utility for diabetes management. Recent research has implicated the presence of adherent inflammatory cells as the key mitigating factor limiting sensor functionality in this period of days post-implantation. Here we present a novel in vitro platform to mimic the cell-embedded provisional matrix that forms adjacent to the sensor immediately after implantation for the focused investigation of the effects of early stage tissue response on sensor function. This biomimetic surrogate is formed by imbibing fibrin-based gels with physiological densities of inflammatory RAW 264.7 macrophages. When surrounding functional sensors, macrophage-embedded fibrin gels contribute to sensor signal declines that are similar in both shape and magnitude to those observed in previous whole blood and small animal studies. Signal decline in the presence of gels is both metabolically-mediated and sensitive to cell type and activation. Computational modeling of the experimental setup is also presented to validate the design by showing that the cellular glucose uptake parameters necessary to achieve such experimental declines align well with literature values. Together, these data suggest this in vitro provisional matrix surrogate may serve as an effective screening tool for testing the biocompatibility of future glucose sensor designs." @default.
• W2024872597 created "2016-06-24" @default.
• W2024872597 creator A5033255876 @default.
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• W2024872597 date "2014-12-01" @default.
• W2024872597 modified "2023-10-10" @default.
• W2024872597 title "Macrophage embedded fibrin gels: An in vitro platform for assessing inflammation effects on implantable glucose sensors" @default.
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• W2024872597 doi "https://doi.org/10.1016/j.biomaterials.2014.08.002" @default.
• W2024872597 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4164605" @default.
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