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Dipeptide and Tripeptide Conjugates as Low‐Molecular‐Weight Hydrogelators
Abstract
Dipeptide and tripeptide conjugates are receiving significant current interest as LMWG, driven by the accessibility of these materials, their relatively low cost and also the large number of examples that successfully form hydrogels. Their behaviour can easily modified by changes in the amino acids or the aromatic end groups chosen. The assembly process has been relatively well described for a small subset of these gelators, giving a good idea of the behaviour of these molecules and allowing an understanding of the conditions under which assembly will occur. Here, we critically review the literature in this area and consider the importance of gelator choice and method of assembly on the outcome of the gelation. We also discuss the applications of these hydrogels. magnified image
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Citations
Cites
Hydrogels for tissue engineering: scaffold design variables and applications
Drury, J. L., & Mooney, D. J. (2003) · Biomaterials · doi:10.1016/s0142-9612(03)00340-5 · Cited by 5,136
Cited by
Tao, K., Levin, A., Adler-Abramovich, L., & Gazit, E. (2016) · Chemical Society Reviews · doi:10.1039/c5cs00889a · Cited by 482
Multicomponent peptide assemblies
Raymond, D. M., & Nilsson, B. L. (2018) · Chemical Society Reviews · doi:10.1039/c8cs00115d · Cited by 346
Metadata
- Authors
- Adams, D. J.
- Venue
- Macromolecular Bioscience
- Publisher
- Wiley
- Published
- 2010-11-15
- Volume
- 11
- Issue
- 2
- Pages
- 160-173
- ISSN
- 1616-5187 (ISSN-L)
- 1616-5195
- OpenAlex
- W2165117362
- Cited by
- 185
- References
- 1
- FWCI
- 6.96
- Type
- journal article
- Language
- en
- Open access
- closed
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- Adams, D. J. (2011). Dipeptide and Tripeptide Conjugates as Low‐Molecular‐Weight Hydrogelators. Macromolecular Bioscience. https://doi.org/10.1002/mabi.201000316
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