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  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2010
    In:  Microfluidics and Nanofluidics Vol. 9, No. 6 ( 2010-12), p. 1143-1149
    In: Microfluidics and Nanofluidics, Springer Science and Business Media LLC, Vol. 9, No. 6 ( 2010-12), p. 1143-1149
    Type of Medium: Online Resource
    ISSN: 1613-4982 , 1613-4990
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2010
    detail.hit.zdb_id: 2155772-X
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  • 2
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2016
    In:  Protein & Peptide Letters Vol. 23, No. 3 ( 2016-02-15), p. 273-282
    In: Protein & Peptide Letters, Bentham Science Publishers Ltd., Vol. 23, No. 3 ( 2016-02-15), p. 273-282
    Type of Medium: Online Resource
    ISSN: 0929-8665
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2016
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  • 3
    Online Resource
    Online Resource
    American Physical Society (APS) ; 2009
    In:  Physical Review Letters Vol. 102, No. 4 ( 2009-1-26)
    In: Physical Review Letters, American Physical Society (APS), Vol. 102, No. 4 ( 2009-1-26)
    Type of Medium: Online Resource
    ISSN: 0031-9007 , 1079-7114
    RVK:
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    Language: English
    Publisher: American Physical Society (APS)
    Publication Date: 2009
    detail.hit.zdb_id: 1472655-5
    detail.hit.zdb_id: 208853-8
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  • 4
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2008
    In:  Proceedings of the National Academy of Sciences Vol. 105, No. 21 ( 2008-05-27), p. 7434-7438
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 105, No. 21 ( 2008-05-27), p. 7434-7438
    Abstract: We show that it is possible to direct particles entrained in a fluid along trajectories much like rays of light in classical optics. A microstructured, asymmetric post array forms the core hydrodynamic element and is used as a building block to construct microfluidic metamaterials and to demonstrate refractive, focusing, and dispersive pathways for flowing beads and cells. The core element is based on the concept of deterministic lateral displacement where particles choose different paths through the asymmetric array based on their size: Particles larger than a critical size are displaced laterally at each row by a post and move along the asymmetric axis at an angle to the flow, while smaller particles move along streamline paths. We create compound elements with complex particle handling modes by tiling this core element using multiple transformation operations; we show that particle trajectories can be bent at an interface between two elements and that particles can be focused into hydrodynamic jets by using a single inlet port. Although particles propagate through these elements in a way that strongly resembles light rays propagating through optical elements, there are unique differences in the paths of our particles as compared with photons. The unusual aspects of these modular, microfluidic metamaterials form a rich design toolkit for mixing, separating, and analyzing cells and functional beads on-chip.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2008
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2008
    In:  Lab on a Chip Vol. 8, No. 9 ( 2008), p. 1448-
    In: Lab on a Chip, Royal Society of Chemistry (RSC), Vol. 8, No. 9 ( 2008), p. 1448-
    Type of Medium: Online Resource
    ISSN: 1473-0197 , 1473-0189
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2008
    detail.hit.zdb_id: 2056646-3
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    AIP Publishing ; 2012
    In:  AIP Advances Vol. 2, No. 4 ( 2012-12-01)
    In: AIP Advances, AIP Publishing, Vol. 2, No. 4 ( 2012-12-01)
    Abstract: Circulating tumor cells (CTCs) and circulating clusters of cancer and stromal cells have been identified in the blood of patients with malignant cancer and can be used as a diagnostic for disease severity, assess the efficacy of different treatment strategies and possibly determine the eventual location of metastatic invasions for possible treatment. There is thus a critical need to isolate, propagate and characterize viable CTCs and clusters of cancer cells with their associated stroma cells. Here, we present a microfluidic device for mL/min flow rate, continuous-flow capture of viable CTCs from blood using deterministic lateral displacement (DLD) arrays. We show here that a DLD array device can isolate CTCs from blood with capture efficiency greater than 85% CTCs at volumetric flow rates of up to 10 mL/min with no effect on cell viability.
    Type of Medium: Online Resource
    ISSN: 2158-3226
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2012
    detail.hit.zdb_id: 2583909-3
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  • 7
    Online Resource
    Online Resource
    AIP Publishing ; 2008
    In:  Applied Physics Letters Vol. 92, No. 8 ( 2008-02-25)
    In: Applied Physics Letters, AIP Publishing, Vol. 92, No. 8 ( 2008-02-25)
    Abstract: The effects of high temperature cycling on the resistance of metallic single-walled carbon nanotube (SWCNT) devices is measured in situ. Individual, small-diameter SWCNTs contacted by palladium or titanium electrodes were measured from room temperature up to 1000K in ultrahigh vacuum. Upon the first thermal cycling, the device resistances fluctuate and generally decrease. Pd-contacted devices typically become stable by 450K, whereas Ti-contacted devices require higher treatments above 600K. Once these temperatures have been exceeded, subsequent thermal cycling has minimal effects. Heat-treated devices exhibit linear temperature dependences, with Pd and Ti contacts producing average temperature coefficients of −3×10−4∕K and 1.1×10−3∕K, respectively.
    Type of Medium: Online Resource
    ISSN: 0003-6951 , 1077-3118
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    Language: English
    Publisher: AIP Publishing
    Publication Date: 2008
    detail.hit.zdb_id: 211245-0
    detail.hit.zdb_id: 1469436-0
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  • 8
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2013
    In:  Proceedings of the National Academy of Sciences Vol. 110, No. 40 ( 2013-10), p. 16103-16108
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 110, No. 40 ( 2013-10), p. 16103-16108
    Abstract: The emergence of resistance to chemotherapy by cancer cells, when combined with metastasis, is the primary driver of mortality in cancer and has proven to be refractory to many efforts. Theory and computer modeling suggest that the rate of emergence of resistance is driven by the strong selective pressure of mutagenic chemotherapy and enhanced by the motility of mutant cells in a chemotherapy gradient to areas of higher drug concentration and lower population competition. To test these models, we constructed a synthetic microecology which superposed a mutagenic doxorubicin gradient across a population of motile, metastatic breast cancer cells (MDA-MB-231). We observed the emergence of MDA-MB-231 cancer cells capable of proliferation at 200 nM doxorubicin in this complex microecology. Individual cell tracking showed both movement of the MDA-MB-231 cancer cells toward higher drug concentrations and proliferation of the cells at the highest doxorubicin concentrations within 72 h, showing the importance of both motility and drug gradients in the emergence of resistance.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2013
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    American Physiological Society ; 2020
    In:  American Journal of Physiology-Cell Physiology Vol. 319, No. 3 ( 2020-09-01), p. C552-C560
    In: American Journal of Physiology-Cell Physiology, American Physiological Society, Vol. 319, No. 3 ( 2020-09-01), p. C552-C560
    Abstract: A number of cell culture approaches have been described for maintenance of primary hepatocytes. Forming hepatocytes into three-dimensional (3-D) spheroids is one well-accepted method for extending epithelial phenotype of these cells. Our laboratory has previously observed enhanced function of two-dimensional (2-D, monolayer) hepatocyte cultures in microfluidic devices due to increased production of several hepato-inductive growth factors, including hepatocyte growth factor (HGF). In the present study, we wanted to test a hypothesis that culturing hepatocyte spheroids (3-D) in microfluidic devices will also result in enhanced phenotype and function. To test this hypothesis, we fabricated devices with small and large volumes. Both types of devices included a microstructured floor containing arrays of pyramidal wells to promote assembly of hepatocytes into spheroids with individual diameters of ~100 µm. The hepatocyte spheroids were found to be more functional, as evidenced by higher level of albumin synthesis, bile acid production, and hepatic enzyme expression, in low-volume compared with large-volume devices. Importantly, high functionality of spheroid cultures correlated with elevated levels of HGF secretion. Although decay of hepatic function (albumin secretion) was observed over the course 3 wk, this behavior could be abrogated by inhibiting TGF-β1 signaling. With TGF-β1 inhibitor, microfluidic hepatocyte spheroid cultures maintained high and stable levels of albumin synthesis over the course of 4 wk. To further highlight utility of this culture platform for liver disease modeling, we carried out alcohol injury experiments in microfluidic devices and tested protective effects of interleukin-22: a potential therapy for alcoholic hepatitis.
    Type of Medium: Online Resource
    ISSN: 0363-6143 , 1522-1563
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2020
    detail.hit.zdb_id: 1477334-X
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2022
    In:  Microfluidics and Nanofluidics Vol. 26, No. 8 ( 2022-08)
    In: Microfluidics and Nanofluidics, Springer Science and Business Media LLC, Vol. 26, No. 8 ( 2022-08)
    Abstract: Cell therapy is an emerging field that uses cells as living drugs to treat a broad array of acute and chronic diseases. Most cell therapies in clinical trials are made using standard bench methods, whose open processing require manufacturing in expensive GMP cleanrooms. As cell therapies progress, new methods are needed to enable scalable manufacturing while maintaining process integrity, reducing environmental exposure, and limiting critical cell and reagent use. Here, we introduce capture and reagent exchange (CARE) wells that allow critical processing steps to be integrated into a closed microfluidic device. The unique property of CARE wells is that they allow reagent exchange from an attached channel without cell loss from wells. We show through simulation and experiment that this feature is present in cylindrical wells whose depth is sufficient to generate multiple recirculating vortices and is independent of flow rate in the channel. We demonstrate that CARE wells can be used to perform cell separation, on-chip labeling, and characterization of monocytes as the first steps toward a closed microfluidic system for production of dendritic cell therapies. Immunomagnetic separation of CD14 + monocytes from peripheral blood mononuclear cells (PBMCs) into wells was performed with purity of 97 ± 2% and capture efficiency of 50 ± 17%. On-chip labeling, washing, and characterization were performed using two cell surface markers (CD14 and HLA-DR) on over 3000 cells captured in a 5193-well device. The combination of high purity separation and reagent exchange without cell loss with robust performance over wide range of input and operating conditions makes this technique a promising approach for scalable manufacturing and analysis of cell therapies.
    Type of Medium: Online Resource
    ISSN: 1613-4982 , 1613-4990
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2022
    detail.hit.zdb_id: 2155772-X
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