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SELECTBIO Conferences 3D-Printing and Biofabrication 2020

3D-Printing and Biofabrication 2020 Agenda



Co-Located Conference Agendas

Innovations in Microfluidics 2020 | 3D-Printing and Biofabrication 2020 | 

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Monday, 23 March 2020

08:00

Conference Registration, Materials Pick-Up, Morning Coffee and Pastries


Session Title: Conference Plenary Session -- Innovations in Microfluidics, 3D-Bioprinting and BioFab 2020

08:45

Leanna LevineConference Chair

Welcome and Introduction to the Conference by Conference Chairperson
Leanna Levine, President & CEO, ALine, Inc., United States of America

09:00

Amy  ShenKeynote Presentation

Nanoplasmonic Platforms For Biosensing Applications
Amy Shen, Professor, Okinawa Institute of Science and Technology, Japan

Fabricating large-scale bioplasmonic materials at high-throughput is important for the development of bio/chemical sensors and high resolution nanomaterial based bioimaging tools. However, techniques specific to large-scale synthesis of biocompatible nanoplasmonic materials have found limited acceptance in industry due to their time-consuming and complex fabrication procedures. Here, by exploiting properties of reactive ions in a SF6 plasma environment, we assemble nanoplasmonic substrates containing mushroom-like structures with SiO2 (insulator) stems and metal caps of gold (45-60 nm in total height, ~20 nm in width), evenly distributed with ~10 nm spacing on a glass substrate. We demonstrate that our developed gold nanomushroom (Au NM) substrate is biocompatible and sensitive for localized surface plasmon resonance (LSPR) based biosensing applications. This nanoplasmonic platform (coupled with microfluidics) is used for monitoring mitosis of fibroblasts for 7 days, E. coli biofilm formation, protein/DNA based immunoassays , and DNA polymerase activity in real-time.

09:30

David WeitzKeynote Presentation

Drop-based Microfluidics For Single-Cell Analysis
David Weitz, Mallinckrodt Professor of Physics and Applied Physics, Director of the Materials Research Science and Engineering Center, Harvard University, United States of America

This talk will describe the use of microfluidic technology to control and manipulate drops whose volume is about one picoliter.  These can serve as reaction vessels for biological assays.  These drops can be manipulated with very high precision using an inert carrier oil to control the fluidics, ensuring the samples never contact the walls of the fluidic channels.  Small quantities of other reagents can be injected with a high degree of control.  The drops can also encapsulate cells, enabling cell-based assays to be carried out.  The use of these devices for cell analysis will be described.

10:00

Roger KammKeynote Presentation

Emergent Engineering of Human Neurological Disease Models
Roger Kamm, Cecil and Ida Green Distinguished Professor of Biological and Mechanical Engineering, Massachusetts Institute of Technology (MIT), United States of America

Microphysiological models have now been developed for a variety of single organs, as well as multi-organ systems.  These models are also beginning to find useful applications in the pharmaceutical and biotech industry as disease models and for intermediate throughput drug screening.  The current models range from those that are generated by precisely seeding in a device populations of fully differentiated or primary cells that then assemble into functional monolayers or simple 3D structures on one extreme, to ones that are fully emergent, forming by self-assembly often within a single cluster of pluripotent cells on the other.  We refer to these two approaches as ‘top-down engineering’ and ‘emergent engineering’.  In this presentation, the full range of techniques will be discussed, with examples derived from applications in the context of neurological function and disease.

10:30

Morning Coffee Break and Networking in the Exhibit Hall

11:00

Gabor ForgacsKeynote Presentation

Tissue Engineering Beyond Regenerative Medicine: Biofabricating Leather
Gabor Forgacs, Professor, University of Missouri-Columbia; Scientific Founder, Organovo; CSO, Modern Meadow, United States of America

Most tissue engineering efforts are focused on applications in regenerative medicine to improve the quality of life of patients. Despite spectacular progress in the last 20 years the expected breakthrough to replace dysfunctional tissues in the organism or mitigate the chronic shortage of donor organs has not yet been achieved. This is not surprising given the enormous challenge facing the biofabrication of complex living structures in vitro and the associated astronomical expenditures. Here we propose a more modest, but more realistic utilization of the knowledge accumulated in tissue engineering and associated biofabrication technologies over the years. As an example we detail specific efforts to engineer a particular compartment of a complex tissue, the skin that gives rise to a commercially useful leather-like material. We compare our process with that followed by the leather industry to point out the advantages and disadvantages of both. We conclude by speculating more broadly on the significant potential social benefits of our approach.

11:30

Shulamit LevenbergKeynote Presentation

Engineering Printable 3D Vascularized Tissue Constructs
Shulamit Levenberg, Professor and Dean, Faculty of Biomedical Engineering, Technion Israel Institute of Technology, Israel

Living tissues require a vascular network to supply nutrients and gases and remove cellular waste. Fabricating vascularized constructs represents a key challenge in tissue engineering. Several methods have been proposed to create in vitro pre-vascularized tissues, including co-culturing of endothelial cells, support cells and cells specific to the tissue of interest. This approach supports formation of endothelial vessels and promotes endothelial and tissue-specific cell interactions. In addition, we have shown that in vitro pre-vascularization of engineered tissue can promote its survival and perfusion upon implantation.  Implanted vascular networks, can anastomose with host vasculature and form functional blood vessels in vivo. Sufficient vascularization in engineered tissues can be achieved through coordinated application of improved biomaterial systems with proper cell types. We have shown that vessel network maturity levels and morphology are highly regulated by matrix composition. We also explored the effect of mechanical forces on vessels organization and analyzed the vasculogenic dynamics within the constructs. We demonstrated that morphogenesis of 3D vascular networks is highly regulated by tensile forces.  Creating complex vascular networks with varying vessel sizes is the next challenge in engineering vascularized tissue constructs. 3D bioprinting, the controlled and automatized deposition of biomaterials and cells, represents a very attractive approach to solve this issue. This technique allows for combining different bioinks (biocompatible printable materials) in an organized fashion to attain native-tissue mimicking structures.

12:00

David L. KaplanKeynote Presentation

Title to be Confirmed.
David L. Kaplan, Stern Family Endowed Professor of Engineering, Professor & Chair -- Dept of Biomedical Engineering, Tufts University, United States of America

12:30

Mehmet TonerKeynote Presentation

“More is More”: Precision Microfluidics of Large Volumes
Mehmet Toner, Helen Andrus Benedict Professor of Biomedical Engineering, Massachusetts General Hospital (MGH), Harvard Medical School, and Harvard-MIT Division of Health Sciences and Technology, United States of America

Microfluidics gained prominence with the application of microelectromechanical systems (MEMS) to biology in an attempt to benefit from the miniaturization of devices for handling of minute samples of fluids under precisely controlled conditions. Microfluidics exploits the differences between micro- and macro-scale flows, for example, the absence of turbulence, electro-osmotic flow, surface and interfacial effects, capillary forces in order to develop scaled-down biochemical analytical processes. The field also takes advantage of MEMS and silicon micromachining by integrating micro-sensors, micro-valves, and micro-pumps as well as physical, electrical, and optical detection schemes into microfluidics to develop the so-called “micro-total analysis systems (µTAS)” or “lab-on-a-chip” devices. However, the ability to process ‘real world-sized’ volumes efficiently has been a major challenge since the beginning of the field of microfluidics. This begs the question whether it is possible to take advantage of microfluidic precision without the limitation on throughput required for large-volume processing? The challenge is further compounded by the fact that physiological fluids are non-Newtonian, heterogeneous, and contain viscoelastic living cells that continuously responds to the smallest changes in their microenvironment. Our efforts towards moving the field of microfluidics to process large-volumes of fluids was counterintuitive and not anticipated by the conventional wisdom at the inception of the field. We metaphorically called this “hooking garden hose to microfluidic chips.” We are motivated by a broad range of applications enabled by precise manipulation of extremely large-volumes of complex fluids, especially those containing living cells or bioparticles. This presentation will provide a summary of our efforts in bringing microfluidics to large volumes and complex fluids as well as various applications such as the isolation of extremely rare circulating tumor cells from whole blood. The use of high-throughput microfluidics to process large-volumes of complex fluids (e.g., whole blood, bone marrow, bronchoalveolar fluid) has found broad interest in both academia and industry due to its broad range of utility in medical applications.

13:00

Networking Lunch in the Exhibit Hall, Exhibits and Poster Viewing


Session Title: Emerging Themes in 3D-Bioprinting, circa 2020


Conference Chairperson: Y. Shrike Zhang, Brigham and Women's Hospital/Harvard Medical School

14:00

John FisherKeynote Presentation

3D Printing for the Engineering of Complex Tissues
John Fisher, Fischell Family Distinguished Professor & Department Chair; Director, NIH Center for Engineering Complex Tissues, University of Maryland, United States of America

14:30

Photocrosslinkable Biomaterials For Tissue Regeneration
Xin Zhao, Assistant Professor, Department of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong

The emphasis of this talk is placed on how photocrosslinkable materials (materials which are initially liquid and solidified upon light exposure), can be used to achieve regeneration of diseased or damaged tissues, for example, to be fabricated into various scaffolds (electrospun fibers, microspheres) to reconstruct hard tissues such as bone as well as soft tissues such as skin.

15:00

Tal DvirKeynote Presentation

Engineering Personalized Tissue Implants: From 3D Printing to Bionic Organs
Tal Dvir, Professor, Director, Laboratory for Tissue Engineering and Regenerating Medicine, Tel Aviv University, Israel

In this talk I will describe cutting-edge technologies for engineering functional tissues and organs, including the heart, brain, spinal cord and retina. I will focus on the design of new biomaterials, mimicking the natural microenvironment, or releasing biofactors to promote stem cell recruitment and tissue protection. In addition, I will discuss the development of patient-specific materials and 3D-printing of personalized vascularized tissues and organs. Finally, I will show a new direction in tissue engineering, where, micro and nanoelectronics are integrated within engineered tissues to form cyborg tissues.

15:30

Afternoon Coffee and Tea Break and Networking

16:15

Biomaterial Free 3D Cardiac Tissue Creation
Narutoshi Hibino, Associate Professor, University of Chicago, United States of America

16:45

Additive Manufacturing of 3D Bone Tissue Model
Jungwoo Lee, Assistant Professor, University of Massachusetts-Amherst, United States of America

Creating functional bone tissue analogs outside of the body represents a unique opportunity to understand bone biology better. Various biomaterials and engineering strategies have been developed, but a realistic bone tissue model that reproduces both surface and subsurface cellular and extracellular matrix complexity remain unsuccessful. Mature bone consists of multiple lamellar bones interfaced with osteocytes that are primary mechanosensory cells. In this presentation, I will introduce a new approach to create bone tissue replica by additive manufacturing of the lamellar structure of bone. We first developed a process to generate a thin section of demineralized compact bone that supports the aligned adhesion of osteoblasts and structural mineral deposition. We then exploited tissue-engineering strategies to induce osteoblast-to-osteocyte differentiation via stacking multiple layers of osteoblasts pre-seeded demineralized bone paper and subsequently applying cyclic mechanical compression under hypoxic milieu. Our additive manufacturing of bone tissue demonstrated precise control of the thickness and both surface and subsurface cellular complexity. We envision that the presented additive manufacturing bone tissue models is expected to greatly advance bioengineering trabecular bone for basic and applied researches.

17:15

Y. Shrike ZhangConference Chair

Formulating Bioinks for Tissue Bioprinting
Y. Shrike Zhang, Assistant Professor of Medicine and Associate Bioenginering, Harvard Medical School, Associate Bioengineer, Division of Engineering in Medicine, Brigham and Women’s Hospital, United States of America

Over the last decade, three-dimensional (3D) bioprinting has offered great versatility to fabricate biomimetic volumetric tissues that are both structurally and functionally relevant. It enables precise control over the composition, spatial distribution, and architecture of the bioprinted constructs, facilitating recapitulation of the delicate shapes and structures of targeted organs and tissues. This talk will discuss our recent efforts on developing various cytocompatible and cell-instructive bioink formulations for the fabrication of engineered tissue constructs, using a series of established or customized bioprinting strategies.

17:45

Networking Reception with Beer and Wine in the Exhibit Hall -- Meet Exhibitors and Network with Colleagues

18:45

Close of Day 1 of the Conference

Tuesday, 24 March 2020

08:00

Morning Coffee, Tea and Pastries in the Exhibit Hall


Session Title: Challenges and Opportunities in the 3D-Bioprinting Field


Conference Chairperson: Y. Shrike Zhang, Brigham and Women's Hospital/Harvard Medical School

08:30

Xuanhe ZhaoKeynote Presentation

Merging Human-Machine Intelligence with Soft Materials Technology
Xuanhe Zhao, Associate Professor, Massachusetts Institute of Technology (MIT), United States of America

While human tissues and organs are mostly soft, wet and bioactive; machines are commonly hard, dry and biologically inert. Merging humans and machines and their intelligence is of imminent importance in addressing grand societal challenges in health, sustainability, security, education and joy of living. However, interfacing humans and machines is extremely challenging due to their fundamentally contradictory properties. At MIT Zhao Lab, we exploit soft materials technology to form long-term, high-efficacy, compatible and seamless interfaces and convergence between humans and machines.  In this talk, I will first discuss the mechanics to design extreme properties including tough, resilient, adhesive, strong, fatigue-resistant and conductive for hydrogels, which are new yet ideal materials for human-machine interfaces. Then I will discuss a set of soft materials technology platforms including i). bioadhesives for instant strong adhesion of diverse wet dynamic tissues and machines; ii). hydrogel bioelectronics and biophotonics for long-term multimodal interfaces; iii). ferromagnetic soft robots for teleoperated or autonomous navigations and operations in previously inaccessible lesions. I will conclude the talk with a perspective on future human-machine convergence enabled by soft materials technology.

09:00

Engineering Cryogel Scaffolds to Reconstruct Aspects of the Tumor Microenvironment
Sidi Bencherif, Assistant Professor, Department of Chemical Engineering, Northeastern University, United States of America

Hypoxia, defined as low oxygen tension, is a characteristic feature of solid tumors and a hallmark of aggressive cancers. Metabolic adaptation to hypoxia leads to tumor cell growth and invasion, resistance to apoptosis, and multi-drug resistance. For decades, a number of solid tumor models have been engineered to emulate key aspects of tumor biology such as hypoxia. However, challenges with tumor formation and reproducibility, inadequate biomechanical cues and 3D microenvironmental features provided to cells, and uncontrolled oxygen depletion among other limitations led to non-physiological tumor cell responses and inaccurate clinical predictions to anti-cancer drugs. To model solid tumors more accurately, we have recently developed an innovative approach using macroporous cryogel scaffolds to induce rapid oxygen depletion while enabling cellular rearrangement into spherical-like cell aggregates within a 3D polymer network. Our preliminary data suggest that our engineered cryogel scaffolds are capable of inducing local hypoxia while promoting tumor cell remodeling and aggressiveness, leading to anti-cancer drug resistance. Tumor-laden cryogels may mimic key aspects of the native tumor microenvironment, making these advanced cellularized scaffolds a promising platform for drug screening and potentially advancing drug development and discovery.

09:30

3D Bioprinted Vascularized Glioblastoma Model
Guohao Dai, Associate Professor, Department of Bioengineering, Northeastern University, United States of America

Glioblastoma (GBM), the most malignant brain cancer, remains deadly despite wide-margin surgical resection and concurrent chemo- & radiation therapies. Two pathological hallmarks of GBM are diffusive invasion along brain vasculature, and presence of therapy-resistant tumor initiating stem cells. Deconstructing the underlying mechanisms of GBM-vascular interaction may add a new therapeutic direction to curtail GBM progression. However, the lack of proper 3D models that recapitulate GBM hallmarks restricts investigating cell-cell/cell-molecular interactions in tumor microenvironments. In this study, we created GBM-vascular niche models through 3D bioprinting containing patient-derived glioma stem cells (GSCs), human brain microvascular endothelial cells (hBMVECs) cells, pericytes, astrocytes and various hydrogels to model glioma/endothelial cell-cell interactions in 3D. In summary we have created GBM-vascular niche models that can recapitulate various GBM characteristics such as cancer stemness, tumor type-specific invasion patterns, and drug responses with therapeutic resistance. Our models have a great potential in investigating patient-specific tumor behaviors under chemo-/radio-therapy conditions and consequentially helping to tailor personalized treatment strategy. The model platform is capable of modifying multiples variables including ECMs, cell types, vascular structures, and dynamic culture condition. Thus, it can be adapted to other biological systems and serve as a valuable tool for generating customized tumor microenvironments.

10:00

GE Healthcare Life SciencesThe Biologicalisation of Medicine and Manufacturing
William G Whitford, Strategic Solutions Leader Bioprocess, GE Healthcare Life Sciences

The biologicalization (or the biological transformation) of manufacturing is essentially the use of digital manufacturing approaches (Industry 4.0) with biological and bio-inspired principles to support more efficient and sustainable manufacturing.  It creates a biomimetic  design – from reactions, equipment, and assemblies to materials, processes, and facilities.  For example, Nobel Prize winner Frances H. Arnold invented systems directing the evolution of enzymes now routinely used in development catalysts in manufacturing.  This approach to biologicalisation of processes is dependent upon advances in biochemistry, many of the ‘omics, as well as genetic engineering.  From another direction, advances in fermentation and cell-culture technologies is supplying a cell-based biologicalisation of processes.  Harmonization of digital principals with bio-integrated systems supports processes composed not only of biological chemistries, but of engineered organoids, tissues and cells. As supported by nano/micro-technology, cell-based systems can enable the goals of sustainability, economy and efficiency in research and therapeutics.

10:30

Morning Coffee Break and Networking in the Exhibit Hall

11:15

A 3D Bioprinted Human Neurovascular Unit as a Tissue-in-a-well Platform For Brain Disease Modeling and Drug Screening
Yen-Ting Tung, Research Fellow, National Center for Advancing Translational Sciences (NCATS), United States of America

A 3D bioprinted human neurovascular unit (NVU) was developed in a 96-multiwell plate format for using as a tissue-in-a-well assay platform for high through-put screening.

11:45

Origami Microfluidics for Biomimetic Liver on a Chip
Carol Livermore, Associate Professor, Department of Mechanical and Industrial Engineering, Northeastern University, United States of America

Fluid mechanics at the shortest length scales enable many functions of life, including the human body’s microcirculation. Ideally, we would be able to translate the body’s fluid mechanics directly into engineered tissues and organ on a chip systems, but conventional microfluidics still lag behind much of what our bodies can do. A good example is the liver; conventional organs on a chip can struggle to replicate the liver’s massively parallel flow and perfusion architecture. Origami-based microfluidics offer a new paradigm for addressing these challenges. Folding offers a low-cost, rapid means of creating flow structures that mimic vasculature. Multi-material architectures enable additional transport via diffusion, and directed assembly of cells can offer hierarchical structure at the smallest length scales. This talk will present the enabling tools of origami tissue engineering, including the use of folding to create multi-material, flow/perfusion microfluidic devices as a platform for scalable tissue engineering. In particular, the presentation will focus on the design, fabrication, and characterization of liver tissue units made via this multi-functional, multi-material approach.

12:15

Orit ShefiKeynote Presentation

Title to be Confirmed.
Orit Shefi, Head of Neuroengineering Laboratory, Faculty of Engineering and Institute of Nanotechnologies and Advanced Materials, Bar-Ilan University Israel, Israel

12:45

Networking Lunch in the Exhibit Hall, Exhibits and Poster Viewing

13:45

Next-Generation Bioprinting For Manufacturing Tissue-Engineered Products
Fabien Guillemot, Chief Executive Officer, Poietis, France

Main challenges for the manufacturing of tissue engineered advanced therapy medicinal products (ATMPs) relate to the standardisation of manufacturing processes and the improvement of tissue functionality, and cost-effectiveness and profitability of related treatments. Producing advanced therapy medicinal products remains a cumbersome process with costs, reproducibility and scalability issues.

Poietis develops biomanufacturing solutions based on Next Generation Bioprinting (NGB). This new platform integrates automation and robotics technologies, and is coupled with numerous online sensors – including cell microscopy – and Artificial Intelligence processing. In addition, it integrates all bioprinting techniques (laser-assisted bioprinting, bioextrusion, micro-valve bioprinting), a world’s first in the bioprinting market.
 
Based on our experience on bioprinting full-thickness skin equivalents, we will discuss how next-gen bioprinting technology – should make it possible to overcome current tissue manufacturing bottlenecks and also provide new therapeutic opportunities.

14:15

Joyce WongKeynote Presentation

Extracellular Matrix Alloys For Vascular Tissue Engineering
Joyce Wong, Professor of Biomedical Engineering and Materials Science & Engineering, Boston University, United States of America

To engineer and build tissues, one requires an understanding of key relationships between cell behavior and the underlying substrate. In native tissues, extracellular matrix proteins are in the form of fibrous networks, sheets, and fibers. Over the past few years, we have been investigating the role of composition and processing conditions of various extracellular matrix fibers and alloy fibers on mechanical properties and biological properties. These fibers are also critical components of tissues such as blood vessels. We have also determined the role of mechanical strain on binding of different antibodies and peptide-functionalized contrast agents to these fibers. Importantly, we discovered that composition can be tuned to stabilize extracellular matrix proteins in fiber forms, which is especially useful with compositions where it is difficult to process the proteins into fibers. Through an integrated computational and experimental approach, we have discovered relationships between hydrophobicity and protein fiber forming capability and stability. Moreover, we have verified that the protein alloy fibers support cell adhesion and allow one to tune the mechanical properties of the fiber. This is of significance as the mechanical properties of the substrate play an important role in modulating cell behavior, e.g. cell migration and proliferation.

14:45

Bioinspired-Fabrication Towards Replicating Tissue Functions
Yan Yan Shery Huang, University Lecturer in Bioengineering, University of Cambridge, United Kingdom

Emerging devices created at the bio-abio interfaces calls for new fabrication processes that can integrate a wider choice of biological and synthetic materials, combined with delivery of complexity in feature sizes, structures and functionalities.

Herein, we explore various bioinspired fabrication approaches to replicate the cross-length scale, and multi-material nature of tissue functions. At the extracellular matrix (nano/ micro feature) length-scale, 3D fibre patterning was used to create fibrillar structures in multiple arrays with designable orientations. We demonstrate biological applications utilising the fibers’ topography to guide the assembly of cellular aggregates in a 3D culture context; and optoelectronic applications showing ‘floating’ fibre-array electronics. Spanning to the cellular and organ-scale, embedded printing is employed to structure soft materials, such as elastomers and hydrogels. By formulating the ‘supporting bath’ and ‘sacrificial ink’ compositions, we show that soft materials can be tailor-made for their external shapes and internal architectures (such as porosity). Applications in creating heterogeneous material integration to mimic the tissue microenvironments, and dissecting the impedance properties of human cochlea, are demonstrated.

15:15

Title to be Confirmed.
John Hundley Slater, Assistant Professor of Biomedical Engineering, University of Delaware, United States of America

15:45

Afternoon Coffee and Round-Table Discussions


Add to Calendar ▼2020-03-23 00:00:002020-03-24 00:00:00Europe/London3D-Printing and Biofabrication 20203D-Printing and Biofabrication 2020 in Boston, USABoston, USASELECTBIOenquiries@selectbiosciences.com