| Literature DB >> 27874260 |
Robert M Hughes1,2, Christina M Marvin1, Zachary L Rodgers1,3, Song Ding1, Nathan P Oien1,4, Weston J Smith1,5, David S Lawrence1.
Abstract
A strategy for the light-activated release of bioactive compounds (BODIPY, colchicine, paclitaxel, and methotrexate) from membrane-enclosed depots is described. We have found that membrane-permeable bioagents can be rendered membrane impermeable by covalent attachment to cobalamin (Cbl) through a photocleavable linker. These Cbl-bioagent conjugates are imprisoned within lipid-enclosed compartments in the dark, as exemplified by their retention in the interior of erythrocytes. Subsequent illumination drives the secretion of the bioactive species from red blood cells. Photorelease is triggered by wavelengths in the red, far-red, and near-IR regions, which can be pre-assigned by affixing a fluorophore with the desired excitation wavelength to the Cbl-bioagent conjugate. Pre-assigned wavelengths allow different biologically active compounds to be specifically and unambiguously photoreleased from common carriers.Entities:
Keywords: cobalamines; drug delivery; membranes; photolysis; prodrugs
Mesh:
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Year: 2016 PMID: 27874260 PMCID: PMC5177521 DOI: 10.1002/anie.201609731
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336