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Biocompatible Microvascular Networks for Tissue Engineering

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Title: Biocompatible Microvascular Networks for Tissue Engineering


1
ITG Forum Biocompatible Microvascular Networks
for Tissue Engineering
Taylor Simpson Autonomic Materials Group
2
Outline
  • Background
  • Network manufacturing
  • Current research at UIUC utilizing mvascular
    networks
  • mvascular networks as tissue scaffolds
  • Scaffold requirements
  • Current technologies
  • Substrate approach
  • Deposition ink approach
  • Conclusions/Future Work
  • Questions

3
Previous Work
  • Robotic Controlled Deposition
  • Substrate Infiltration

4
Previous Work
5
Key Issues for Tissue Scaffolds
  • Requirements
  • Fully connected, open pore system
  • Controlled pore size and location to optimize
    pore function (to diffuse nutrients and gasses
    and remove waste)
  • Multiple layers for large tissues
  • Degree of porosity should balance mechanical
    needs of the scaffold
  • Current Issues
  • Lack of control over porosity- location and size
  • mm scale
  • square channels vs. cylindrical channels

6
Current Technologies
7
Manufacturing Process

8
Biocompatible Substrate
Hydroxy ethylmethacrylate (HEMA) ethylene
glycol dimethacrylate (EGDMA)
  • Utilize existing ink
  • Biocompatible
  • Infiltrate at room temperature
  • Requires a surfactant
  • Tough (flexible)

9
Biocompatible Substrate
Micro-CT Images
Cone-beam reconstruct
Amira- Isosurface
10
Biocompatible Substrate
Micro-CT Images
Amira- Projection View
Amira- Isosurface
Amira-
Voltex View
Amira- Isosurface
11
Biocompatible/Biodegradable Deposition Inks
PEG (C2H4O)n
PCL (C6H10O2)n
  • Advantages
  • Biocompatible/biodegradable
  • Tm 43-46 0C
  • Tg -95- -15 0C (varying MW)
  • Cheap
  • Disadvantages
  • Stiff
  • Water soluble
  • Short degradation time (min)
  • Advantages
  • Biocompatible/biodegradable
  • Tm 59-64 0C
  • Tg -60 0C
  • Cheap
  • Long degradation time (yrs)
  • Disadvantages
  • Stiff
  • Low solubility
  • Requires heat for extrusion

72 layer PEG network
12
Conclusions/Future Work
  • Shown ability to manufacture a biocompatible 3-D
    mvascular network
  • Designate use
  • Manufacture a mvascular PCL network
  • Demonstrate manufacturability of PCL/PEG
    copolymer with predicted decomposition rate

13
References
Acknowledgements
Professor Scott White Katie Toohey Rob
Sheperd Ben Grosser Dan Webber
  • M.E. Gomes, J.S. Godinho, D. Tchalamov, A.M.
    Cunha, R.L. Reis. Alternative Tissue Engineering
    Scaffolds Based on Starch Processing
    Methodologies, Morphology, Degradation and
    Mechanical Properties. Materials Science and
    Engineering C 20 (2002) 1926.
  • Andreas Pfister, Rudiger Landers, Andres Laib,
    Ute Hubner, Rainer Schmelzeisen, Rolf Mulhaupt.
    Biofunctional Rapid Prototyping for
    Tissue-Engineering Applications 3D Bioplotting
    versus 3D Printing. 2003 Wiley Periodicals, Inc.
    J Polym Sci Part A Polym Chem 42 624638, 2004.
    Received 27 January 2003 accepted 9 June 2003.
  • Jeffery Borenstein, Wing Cheung, Lauren Hartman,
    Mohammad Kaazempur-Mofrad, Kevin King, Alec Sevy,
    Michael Shin, Eli Weinberg, Joseph Vacanti.
    Living 3-Dimensional Microfabricated Construct
    for the Replacement of Vital Organ. 2003 IEEE.
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