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1.
Langmuir ; 22(9): 4353-6, 2006 Apr 25.
Article in English | MEDLINE | ID: mdl-16618186

ABSTRACT

A photoresponsive hydrogel was prepared by radical copolymerization of N-isopropylacrylamide, a vinyl monomer having a spirobenzopyran residue and cross-linker. By the observation of photoresponsive shrinking and the conductance change, it was confirmed that the hydrogel in an acidic condition exhibited drastic and rapid volume shrinkage and proton dissociation when it was irradiated with blue light. Further, to examine its application to the mass transfer control, we prepared a photo- and thermoresponsive gate membrane by introducing this photoresponsive hydrogel to the surface of a porous membrane. As the first demonstration of the photocontrol of membrane permeation for liquid, it was observed that its permeability for 1 mM HCl aqueous solution increased by 2 times in response to the blue light irradiation, and this photoresponse of the permeability was confirmed to be repeatable.

2.
Biomacromolecules ; 6(2): 970-4, 2005.
Article in English | MEDLINE | ID: mdl-15762667

ABSTRACT

A photoresponsive culture surface (PRCS) allowing photocontrol of cell adhesion was prepared with a novel polymer material composed of poly(N-isopropylacrylamide) having spiropyran chromophores as side chains. Cell adhesion of the surface was drastically enhanced by the irradiation with ultraviolet (UV) light (wavelength: 365 nm); after subsequent cooling and washing on ice, many cells remained in the irradiated region, whereas most cells were removed from the nonirradiated region. The cell adhesion of the PRCS, which had been enhanced by previous UV irradiation, was reset by the visible light irradiation (wavelength 400-440 nm) and the annealing at 37 degrees C for 2 h. Also it was confirmed that the regional control of cell adhesion was induced several times by repeating the same series of operations. Further, living cell patterning with the 200 microm line width was produced readily by projecting UV light along a micropattern on the PRCS on which the living cells had been seeded uniformly in advance. By using a fluorescent probe that stains living cells only, it was confirmed that the cells maintained sufficient viability even after UV light irradiation followed by cooling and washing.


Subject(s)
Cell Adhesion , Cell Separation/methods , Photochemistry/methods , Acrylic Resins/radiation effects , Cell Culture Techniques , Cell Survival , Surface Properties , Ultraviolet Rays
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