posted on 2016-06-16, 00:00authored byFujian Huang, Wei-Ching Liao, Yang Sung Sohn, Rachel Nechushtai, Chun-Hua Lu, Itamar Willner
A method to assemble
light-responsive or pH-responsive microcapsules
loaded with different loads (tetramethylrhodamine-modified dextran,
TMR-D; microperoxidase-11, MP-11; CdSe/ZnS quantum dots; or doxorubicin-modified
dextran, DOX-D) is described. The method is based on the layer-by-layer
deposition of sequence-specific nucleic acids on poly(allylamine hydrochloride)-functionalized
CaCO3 core microparticles, loaded with the different loads,
that after the dissolution of the core particles with EDTA yields
the stimuli-responsive microcapsules that include the respective loads.
The light-responsive microcapsules are composed of photocleavable
o-nitrobenzyl-phosphate-modified DNA shells, and the pH-responsive
microcapsules are made of a cytosine-rich layer cross-linked by nucleic
acid bridges. Irradiating the o-nitrobenzyl phosphate-functionalized
microcapsules, λ = 365 nm, or subjecting the pH-responsive microcapsules
to pH = 5.0, results in the cleavage of the microcapsule shells and
the release of the loads. Preliminary studies address the cytotoxicity
of the DOX-D-loaded microcapsules toward MDA-MB-231 breast cancer
cells and normal MCF-10A breast epithelial cells. Selective cytotoxicity
of the DOX-D-loaded microcapsules toward cancer cells is demonstrated.