Supramolecular Hydrogels Based on Minimalist Amphiphilic Squaramide–Squaramates for Controlled Release of Zwitterionic Biomolecules. Issue 31 (15th May 2017)
- Record Type:
- Journal Article
- Title:
- Supramolecular Hydrogels Based on Minimalist Amphiphilic Squaramide–Squaramates for Controlled Release of Zwitterionic Biomolecules. Issue 31 (15th May 2017)
- Main Title:
- Supramolecular Hydrogels Based on Minimalist Amphiphilic Squaramide–Squaramates for Controlled Release of Zwitterionic Biomolecules
- Authors:
- López, Carlos
Ximenis, Marta
Orvay, Francisca
Rotger, Carmen
Costa, Antonio - Abstract:
- Abstract: Supramolecular hydrogels with tunable properties have innovative applications in biomedicine, catalysis, and materials chemistry. Minimalist low‐molecular‐weight hydrogelators based on squaramide and squaramic acid motifs have been designed. This approach benefits from the high acidity of squaramic acids and the aromaticity of squaramides. Moreover, substituents on the aryl ring tune the π density of the arylsquaramide motif. Thus, materials featuring distinct thermal and mechanical properties have been successfully prepared. The hydrogel ( G ′≈400 Pa, G ′′≈57 Pa; at 1.0 % w/v; 1 Hz) obtained from 4‐nitrophenylsquaramide motif1 is thermoreversible ( T =57 °C at 0.2 % w/v), thixotropic, self‐healable, and undergoes irreversible shrinking in response to saline stress. Furthermore, the hydrogel is injectable and can be loaded with substantial amounts (5:1 excess molar ratio) of zwitterionic biomolecules, such asl ‐carnitine, γ‐aminobutyric acid (GABA), ord, l ‐Ala‐d, l ‐Ala, without any loss of structural integrity. Then, the release of these molecules can be modulated by saline solutions. Abstract : Drop the payload ! Smart supramolecular hydrogels based on squaramides and squaramate synthons are thermoreversible, thixotropic, and injectable. These hydrogels can be loaded with zwitterions and display ion‐stimulated shrinking and release of the payload (see figure). This combination of properties is unusual in supramolecular hydrogels derived from low‐molecular‐weightAbstract: Supramolecular hydrogels with tunable properties have innovative applications in biomedicine, catalysis, and materials chemistry. Minimalist low‐molecular‐weight hydrogelators based on squaramide and squaramic acid motifs have been designed. This approach benefits from the high acidity of squaramic acids and the aromaticity of squaramides. Moreover, substituents on the aryl ring tune the π density of the arylsquaramide motif. Thus, materials featuring distinct thermal and mechanical properties have been successfully prepared. The hydrogel ( G ′≈400 Pa, G ′′≈57 Pa; at 1.0 % w/v; 1 Hz) obtained from 4‐nitrophenylsquaramide motif1 is thermoreversible ( T =57 °C at 0.2 % w/v), thixotropic, self‐healable, and undergoes irreversible shrinking in response to saline stress. Furthermore, the hydrogel is injectable and can be loaded with substantial amounts (5:1 excess molar ratio) of zwitterionic biomolecules, such asl ‐carnitine, γ‐aminobutyric acid (GABA), ord, l ‐Ala‐d, l ‐Ala, without any loss of structural integrity. Then, the release of these molecules can be modulated by saline solutions. Abstract : Drop the payload ! Smart supramolecular hydrogels based on squaramides and squaramate synthons are thermoreversible, thixotropic, and injectable. These hydrogels can be loaded with zwitterions and display ion‐stimulated shrinking and release of the payload (see figure). This combination of properties is unusual in supramolecular hydrogels derived from low‐molecular‐weight hydrogelators. … (more)
- Is Part Of:
- Chemistry. Volume 23:Issue 31(2017)
- Journal:
- Chemistry
- Issue:
- Volume 23:Issue 31(2017)
- Issue Display:
- Volume 23, Issue 31 (2017)
- Year:
- 2017
- Volume:
- 23
- Issue:
- 31
- Issue Sort Value:
- 2017-0023-0031-0000
- Page Start:
- 7590
- Page End:
- 7594
- Publication Date:
- 2017-05-15
- Subjects:
- gels -- noncovalent interactions -- squaramides -- supramolecular chemistry -- zwitterions
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201701029 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2171.xml