Responsive DNA-Based Hydrogels and Their Applications
The term hydrogel describes a type of soft and wet material formed by cross‐linked hydrophilic polymers. The distinct feature of hydrogels is their ability to absorb a large amount of water and swell. The properties of a hydrogel are usually determined by the chemical properties of their constituent...
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Veröffentlicht in: | Macromolecular rapid communications. 2013-08, Vol.34 (16), p.1271-1283 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The term hydrogel describes a type of soft and wet material formed by cross‐linked hydrophilic polymers. The distinct feature of hydrogels is their ability to absorb a large amount of water and swell. The properties of a hydrogel are usually determined by the chemical properties of their constituent polymer(s). However, a group of hydrogels, called “smart hydrogels,” changes properties in response to environmental changes or external stimuli. Recently, DNA or DNA‐inspired responsive hydrogels have attracted considerable attention in construction of smart hydrogels because of the intrinsic advantages of DNA. As a biological polymer, DNA is hydrophilic, biocompatible, and highly programmable by Watson‐Crick base pairing. DNA can form a hydrogel by itself under certain conditions, and it can also be incorporated into synthetic polymers to form DNA‐hybrid hydrogels. Functional DNAs, such as aptamers and DNAzymes, provide additional molecular recognition capabilities and versatility. In this Review, DNA‐based hydrogels are discussed in terms of their stimulus response, as well as their applications.
DNA as a type of biopolymer has attracted considerable attention in the construction of smart hydrogels. In addition to its intrinsic advantages, DNA can form functional structures that provide additional molecular recognition capabilities and versatility. This review discusses recent progress in DNA‐based hydrogels in terms of their stimulus response, as well as their applications. |
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ISSN: | 1022-1336 1521-3927 |
DOI: | 10.1002/marc.201300411 |