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Dynamic Hydrogels from Host-Guest Supramolecular Interactions
被引:128
|作者:
Mantooth, Siena M.
[1
]
Munoz-Robles, Brizzia G.
[1
]
Webber, Matthew J.
[1
]
机构:
[1] Univ Notre Dame, Dept Chem & Biomol Engn, 205 McCourtney Hall, Notre Dame, IN 46556 USA
关键词:
drug delivery;
injectable biomaterials;
materials chemistry;
rheology;
SHEAR-THINNING HYDROGELS;
SUSTAINED-RELEASE SYSTEM;
POLYPSEUDOROTAXANE HYDROGELS;
DRUG-DELIVERY;
THERMORESPONSIVE HYDROGELS;
BIOMEDICAL APPLICATIONS;
INCLUSION COMPLEXATION;
MECHANICAL-PROPERTIES;
PEPTIDE AMPHIPHILES;
TRIBLOCK COPOLYMERS;
D O I:
10.1002/mabi.201800281
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Hydrogel biomaterials are pervasive in biomedical use. Applications of these soft materials range from contact lenses to drug depots to scaffolds for transplanted cells. A subset of hydrogels is prepared from physical cross-linking mediated by host-guest interactions. Host macrocycles, the most recognizable supramolecular motif, facilitate complex formation with an array of guests by inclusion in their portal. Commonly, an appended macrocycle forms a complex with appended guests on another polymer chain. The formation of poly(pseudo)rotaxanes is also demonstrated, wherein macrocycles are threaded by a polymer chain to give rise to physical cross-linking by secondary non-covalent interactions or polymer jamming. Host-guest supramolecular hydrogels lend themselves to a variety of applications resulting from their dynamic properties that arise from non-covalent supramolecular interactions, as well as engineered responsiveness to external stimuli. These are thus an exciting new class of materials.
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