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Chapter 1
Chemical Modification of Porous Scaffolds Using Plasma Polymers
| 1.1 |
 |
Introduction |
| 1.2 |
Experimental Design |
| 1.3 |
Materials |
| 1.4. |
Methods |
| 1.4.1 |
Scaffold preparation |
| 1.4.2 |
Deposition of plasma polymers |
| 1.4.3 |
Surface analysis |
| 1.4.4 |
Cell culture on scaffolds |
| 1.4.5 |
Alamar Blue assay |
| 1.4.6 |
Cell viability assay on scaffolds |
| 1.4.7 |
Scanning electron microscopy |
| 1.4.8 |
Microcomputed tomography of scaffolds |
| 1.5. |
Data Acquisition, Anticipated Results, and Interpretation |
| 1.5.1 |
Surface analysis |
| 1.5.2 |
Investigation of cell culture on modified scaffolds |
| 1.6. |
Discussion and Commentary |
| 1.7. |
Application Notes |
| 1.8. |
Summary Points, Acknowledgments,References |
|
Chapter 2
Three-Dimensional Cultures in Soft Self-Assembling Nanofibers
| 2.1. |
 |
Introduction |
| 2.2. |
Experimental Design |
| 2.3 |
Materials |
| 2.3.1 |
Reagents |
| 2.3.2 |
Equipment |
| 2.4 |
Methods |
| 2.4.1 |
Self-assembling peptide preparation |
| 2.4.2 |
Cell encapsulation into the self-assembling peptide |
| 2.4.3 |
Sandwich method |
| 2.4.4 |
Cell isolation and culture of isolated cells |
| 2.4.5 |
Cryosections of the 3D cultures |
| 2.4.6 |
Cell proliferation study using 5-bromodeoxyuridine (BrdU)
uptake analysis |
| 2.4.7 |
Cell viability |
| 2.4.8 |
Protein analysis |
| 2.4.9 |
Sample staining |
| 2.4.10 |
sGAG quantification |
| 2.4.11 |
Lysis of 3D cultures for RNA extraction |
| 2.5 |
Data Acquisition, Anticipated Results, and Interpretation |
| 2.6 |
Discussion and Commentary |
| 2.7 |
Troubleshooting |
| 2.8 |
Application Notes |
| 2.9 |
Summary points, Acknowledgments, References |
Previous Chapter | Next Chapter
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