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      Patient‐Specific 3‐Dimensional–Bioprinted Model for In Vitro Analysis and Treatment Planning of Pulmonary Artery Atresia in Tetralogy of Fallot and Major Aortopulmonary Collateral Arteries

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          Abstract

          Background

          Tetralogy of Fallot with major aortopulmonary collateral arteries is a heterogeneous form of pulmonary artery (PA) stenosis that requires multiple forms of intervention. We present a patient‐specific in vitro platform capable of sustained flow that can be used to train proceduralists and surgical teams in current interventions, as well as in developing novel therapeutic approaches to treat various vascular anomalies. Our objective is to develop an in vitro model of PA stenosis based on patient data that can be used as an in vitro phantom to model cardiovascular disease and explore potential interventions.

          Methods and Results

          From patient‐specific scans obtained via computer tomography or 3‐dimensional (3D) rotational angiography, we generated digital 3D models of the arteries. Subsequently, in vitro models of tetralogy of Fallot with major aortopulmonary collateral arteries were first 3D printed using biocompatible resins and next bioprinted using gelatin methacrylate hydrogel to simulate neonatal vasculature or second‐order branches of an older patient with tetralogy of Fallot with major aortopulmonary collateral arteries. Printed models were used to study creation of extraluminal connection between an atretic PA and a major aortopulmonary collateral artery using a catheter‐based interventional method. Following the recanalization, engineered PA constructs were perfused and flow was visualized using contrast agents and x‐ray angiography. Further, computational fluid dynamics modeling was used to analyze flow in the recanalized model.

          Conclusions

          New 3D‐printed and computational fluid dynamics models for vascular atresia were successfully created. We demonstrated the unique capability of a printed model to develop a novel technique for establishing blood flow in atretic vessels using clinical imaging, together with 3D bioprinting–based tissue engineering techniques. Additive biomanufacturing technologies can enable fabrication of functional vascular phantoms to model PA stenosis conditions that can help develop novel clinical applications.

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          Most cited references45

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          Epicardial FSTL1 reconstitution regenerates the adult mammalian heart.

          The elucidation of factors that activate the regeneration of the adult mammalian heart is of major scientific and therapeutic importance. Here we found that epicardial cells contain a potent cardiogenic activity identified as follistatin-like 1 (Fstl1). Epicardial Fstl1 declines following myocardial infarction and is replaced by myocardial expression. Myocardial Fstl1 does not promote regeneration, either basally or upon transgenic overexpression. Application of the human Fstl1 protein (FSTL1) via an epicardial patch stimulates cell cycle entry and division of pre-existing cardiomyocytes, improving cardiac function and survival in mouse and swine models of myocardial infarction. The data suggest that the loss of epicardial FSTL1 is a maladaptive response to injury, and that its restoration would be an effective way to reverse myocardial death and remodelling following myocardial infarction in humans.
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            Cardiac 3D Printing and its Future Directions.

            Three-dimensional (3D) printing is at the crossroads of printer and materials engineering, noninvasive diagnostic imaging, computer-aided design, and structural heart intervention. Cardiovascular applications of this technology development include the use of patient-specific 3D models for medical teaching, exploration of valve and vessel function, surgical and catheter-based procedural planning, and early work in designing and refining the latest innovations in percutaneous structural devices. In this review, we discuss the methods and materials being used for 3D printing today. We discuss the basic principles of clinical image segmentation, including coregistration of multiple imaging datasets to create an anatomic model of interest. With applications in congenital heart disease, coronary artery disease, and surgical and catheter-based structural disease, 3D printing is a new tool that is challenging how we image, plan, and carry out cardiovascular interventions.
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              Precise Tuning of Facile One-Pot Gelatin Methacryloyl (GelMA) Synthesis

              Gelatin-methacryloyl (GelMA) is one of the most commonly used photopolymerizable biomaterials in bio-applications. However, GelMA synthesis remains suboptimal, as its reaction parameters have not been fully investigated. The goal of this study is to establish an optimal route for effective and controllable GelMA synthesis by systematically examining reaction parameters including carbonate-bicarbonate (CB) buffer molarity, initial pH adjustment, MAA concentration, gelatin concentration, reaction temperature, and reaction time. We employed several analytical techniques in order to determine the degree of substitution (DS) and conducted detailed structural analysis of the synthesized polymer. The results enabled us to optimize GelMA synthesis, showing the optimal conditions to balance the deprotonation of amino groups with minimizing MAA hydrolysis, which led to nearly complete substitution. The optimized conditions (low feed ratio of MAA to gelatin (0.1 mL/g), 0.25 M CB buffer at pH 9, and a gelatin concentration of 10–20%) enable a simplified reaction scheme that produces GelMA with high substitution with just one-step addition of MAA in one pot. Looking forward, these optimal conditions not only enable facile one-pot GelMA synthesis but can also guide researchers to explore the efficient, high methacrylation of other biomacromolecules.
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                Author and article information

                Contributors
                bauserh@kidsheart.com
                Vahid.serpooshan@bme.gatech.edu
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                10 December 2019
                17 December 2019
                : 8
                : 24 ( doiID: 10.1002/jah3.v8.24 )
                : e014490
                Affiliations
                [ 1 ] Department of Biomedical Engineering Emory University School of Medicine and Georgia Institute of Technology Atlanta GA
                [ 2 ] Department of Pediatrics Emory University School of Medicine Atlanta GA
                [ 3 ] Children's Healthcare of Atlanta Atlanta GA
                [ 4 ] Sibley Heart Center at Children's Healthcare of Atlanta Atlanta GA
                Author notes
                [*] [* ] Correspondence to: Vahid Serpooshan, PhD, 1760 Haygood Drive, NE, HSRB Building, Suite E480, Atlanta, GA 30322. Email: Vahid.serpooshan@ 123456bme.gatech.edu

                and Holly Bauser‐Heaton, MD, PhD, 1405 Clifton Road NE, Atlanta, GA 30322. Email: bauserh@ 123456kidsheart.com

                [†]

                Dr Bauser‐Heaton and Dr Serpooshan contributed equally to this work.

                Article
                JAH34671
                10.1161/JAHA.119.014490
                6951056
                31818221
                5b0f7421-c8fb-4f9f-8737-c5be456f6aac
                © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 30 August 2019
                : 07 November 2019
                Page count
                Figures: 2, Tables: 0, Pages: 10, Words: 7716
                Funding
                Funded by: Emory University School of Medicine
                Funded by: National Institute of Health (NIH) ‐ NHLBI
                Award ID: R00HL127295
                Funded by: Emory University School of Medicine, Pediatric Research Alliance Pilot Grant
                Funded by: Emory University School of Medicine, the Dean'\s Imagine, Innovate and Impact (I3) Research Award
                Categories
                Original Research
                Original Research
                Congenital Heart Disease
                Custom metadata
                2.0
                jah34671
                17 December 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.7.2 mode:remove_FC converted:16.12.2019

                Cardiovascular Medicine
                cardiovascular disease,cardiovascular research,catheterization,pulmonary artery stenosis,tissue engineering,basic science research,translational studies,vascular biology,congenital heart disease,catheter-based coronary and valvular interventions

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