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Related Concept Videos

The Extracellular Matrix01:42

The Extracellular Matrix

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The Extracellular Matrix01:29

The Extracellular Matrix

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In order to maintain tissue organization, many animal cells are surrounded by structural molecules that make up the extracellular matrix (ECM). Together, the molecules in the ECM maintain the structural integrity of tissue as well as the remarkable specific properties of certain tissues.
Composition of the Extracellular Matrix
The extracellular matrix (ECM) is commonly composed of ground substance, a gel-like fluid, fibrous components, and many structurally and functionally diverse...

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Microengineering 3D Collagen Hydrogels with Long-Range Fiber Alignment
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Modified dendrimer cross-linked collagen-based matrices.

M A Princz1, H Sheardown

  • 1a Department of Chemical Engineering , McMaster University , 1280 Main Street W. , Hamilton , ON , Canada , L8S 4L8.

Journal of Biomaterials Science. Polymer Edition
|December 6, 2011
PubMed
Summary

Dendrimer cross-linking creates strong collagen hydrogels. Commercially sourced collagens (PureCol, human collagen, and ECM) were tested, showing potential for tissue engineering despite varying stability.

Keywords:
Collagendendrimersextracellular matrixheparin

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Area of Science:

  • Biomaterials Science
  • Tissue Engineering
  • Polymer Chemistry

Background:

  • Collagen hydrogels are crucial for tissue engineering.
  • Dendrimer cross-linking offers a method to enhance hydrogel properties.
  • Investigating commercial collagen sources is vital for practical applications.

Purpose of the Study:

  • To evaluate commercially available collagen products (PureCol, human collagen, human ECM) for dendrimer cross-linking.
  • To compare the stability and properties of these gels against a benchmark dendrimer-crosslinked collagen gel.
  • To assess the cell compatibility of the fabricated collagen-based hydrogels.

Main Methods:

  • Concentration of PureCol (PC), human collagen (HC), and human extracellular matrix (hECM).
  • Cross-linking using generation two polypropyleneimine octaamine dendrimers with EDC/NHS chemistry.
  • Fabrication of PC gels at 20 and 30 mg/ml concentrations.
  • Assessment of gel stability via collagenase digestion and swelling.
  • Evaluation of 3T3 fibroblast cell growth over four days.

Main Results:

  • PureCol (PC) gels exhibited increased swelling and reduced stability compared to benchmark dendrimer-crosslinked collagen gels (CG).
  • Highly purified bovine (PC) and human collagen (HC) gels showed similar performance but were less stable than CG gels.
  • Addition of hECM to PC created looser networks (PC-hECM gels) compared to heparinized dendrimer-crosslinked bovine collagen gels (CHG).
  • All tested collagen-based hydrogels supported 3T3 fibroblast cell proliferation.

Conclusions:

  • Commercially sourced collagens can be effectively cross-linked with dendrimers, but stability varies.
  • Purification and storage methods of commercial collagen products may influence hydrogel performance.
  • The developed collagen-based hydrogels demonstrate good cell compatibility, suggesting suitability for tissue engineering.