Dynamic Hydrogels from Host-Guest Supramolecular Interactions

被引:137
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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页数:12
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