A photocleavable linker for the chemoselective functionalization of biomaterials


O'Donovan, L. and De Bank, P. A., 2012. A photocleavable linker for the chemoselective functionalization of biomaterials. Journal of Materials Chemistry, 22 (41), pp. 21878-21884.

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    The functionalization of matrices with ‘‘caged’’ functional groups and their subsequent selective uncaging is a promising approach for generating patterns of bioactive molecules to guide cell growth or recreate in vivo microarchitectures. To date, this has been limited to caged carboxylic acids, amines and thiols, functional groups found within biological systems. We present a bifunctional caged carbonyl linker as an alternative approach for the chemoselective functionalization of biomaterials. This linker was readily coupled to collagen, employed as a model biomaterial, and underwent rapid uncaging in aqueous media upon irradiation with ultraviolet light to yield free carbonyl groups. Modified surfaces proved to be non- adhesive to cells until the chemoselective reintroduction of adhesion following incubation of uncaged carbonyls with gelatin hydrazide, with native gelatin failing to elicit a cellular response.


    Item Type Articles
    CreatorsO'Donovan, L.and De Bank, P. A.
    Uncontrolled Keywordschemoselective ligation,photolabile protecting groups,cell patterning,tissue engineering,caged aldehyde
    DepartmentsFaculty of Science > Pharmacy & Pharmacology
    Research CentresCentre for Regenerative Medicine
    ID Code32432
    Additional InformationThis work was supported by the Engineering and Physical Sciences Research Council [grant number EP/G049572/1].


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