Hydrogels: Coordination driven gelation
Hydrogels: Coordination driven gelation
复制标题
DOI:
10.1038/nchem.2339
复制
发表时间:
2015-09
期刊:
影响因子:
21.8
通讯作者:
T. B. Faust
中科院分区:
文献类型:
--
作者:
T. B. Faust
However in this instance, since the formylpyridines used are already prefunctionalized by substantial polyethylene glycol chains (Mn= 1000 g mol–1), the complexation into a cage upon addition of metal ions simultaneously enforces polymer aggregation, and thus drives gelation. By controlled mixing of precursor solutions within a microfiuidic reactor, Nitschke and colleagues are also able to fabricate regularly sized microparticles of their cage-crosslinked hydrogels. Within the hydrogel, the cages retain their ability to selectively host guestmolecules with complementary steric and electronic properties. Since the imine bond formation is reversible, disassembly of the cage can be triggered by the introduction of competitive amines or aldehydes, which releases the payload and ultimately causes dissolution of the entire hydrogel. These properties may render these materials practically useful, perhaps as drug delivery vehicles. For example, a similar supramolecular cage could selectively host a therapeutic payload within a biocompatible hydrogel. The application of an external stimulus, or indeed a change in local environment (such as pH) could then trigger payload release. TF