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    Predictive Modeling of Droplet Formation Processes in Inkjet-Based Bioprinting

    Source: Journal of Manufacturing Science and Engineering:;2018:;volume( 140 ):;issue: 010::page 101007
    Author:
    Wu, Dazhong
    ,
    Xu, Changxue
    DOI: 10.1115/1.4040619
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Additive manufacturing is driving major innovations in many areas such as biomedical engineering. Recent advances have enabled three-dimensional (3D) printing of biocompatible materials and cells into complex 3D functional living tissues and organs using bio-printable materials (i.e., bioink). Inkjet-based bioprinting fabricates the tissue and organ constructs by ejecting droplets onto a substrate. Compared with microextrusion-based and laser-assisted bioprinting, it is very difficult to predict and control the droplet formation process (e.g., droplet velocity and volume). To address this issue, this paper presents a new data-driven approach to predicting droplet velocity and volume in the inkjet-based bioprinting process. An imaging system was used to monitor the droplet formation process. To investigate the effects of polymer concentration, excitation voltage, dwell time, and rise time on droplet velocity and volume, a full factorial design of experiments (DOE) was conducted. Two predictive models were developed to predict droplet velocity and volume using ensemble learning. The accuracy of the two predictive models was measured using the root-mean-square error (RMSE), relative error (RE), and coefficient of determination (R2). Experimental results have shown that the predictive models are capable of predicting droplet velocity and volume with sufficient accuracy.
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      Predictive Modeling of Droplet Formation Processes in Inkjet-Based Bioprinting

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4252114
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    contributor authorWu, Dazhong
    contributor authorXu, Changxue
    date accessioned2019-02-28T11:03:03Z
    date available2019-02-28T11:03:03Z
    date copyright7/9/2018 12:00:00 AM
    date issued2018
    identifier issn1087-1357
    identifier othermanu_140_10_101007.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4252114
    description abstractAdditive manufacturing is driving major innovations in many areas such as biomedical engineering. Recent advances have enabled three-dimensional (3D) printing of biocompatible materials and cells into complex 3D functional living tissues and organs using bio-printable materials (i.e., bioink). Inkjet-based bioprinting fabricates the tissue and organ constructs by ejecting droplets onto a substrate. Compared with microextrusion-based and laser-assisted bioprinting, it is very difficult to predict and control the droplet formation process (e.g., droplet velocity and volume). To address this issue, this paper presents a new data-driven approach to predicting droplet velocity and volume in the inkjet-based bioprinting process. An imaging system was used to monitor the droplet formation process. To investigate the effects of polymer concentration, excitation voltage, dwell time, and rise time on droplet velocity and volume, a full factorial design of experiments (DOE) was conducted. Two predictive models were developed to predict droplet velocity and volume using ensemble learning. The accuracy of the two predictive models was measured using the root-mean-square error (RMSE), relative error (RE), and coefficient of determination (R2). Experimental results have shown that the predictive models are capable of predicting droplet velocity and volume with sufficient accuracy.
    publisherThe American Society of Mechanical Engineers (ASME)
    titlePredictive Modeling of Droplet Formation Processes in Inkjet-Based Bioprinting
    typeJournal Paper
    journal volume140
    journal issue10
    journal titleJournal of Manufacturing Science and Engineering
    identifier doi10.1115/1.4040619
    journal fristpage101007
    journal lastpage101007-9
    treeJournal of Manufacturing Science and Engineering:;2018:;volume( 140 ):;issue: 010
    contenttypeFulltext
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