8 research outputs found
<English Paper Original Paper>Spectral Analysis of Surface EMG to Evaluation of Extraocular Muscles
<英文原著>外眼筋の表面筋電図と周波数分析
A new designed surface electrode for electromyogram (EMG) of extraocular muscle and spectral analysis is described. Electrode was made of a pair of silver-silver cloride wires which were embedded in both end of sclero-corneal shell which was made by silicone rubber to bring them closer to the medial and lateral rectus muscles. Power spectrum was computed of interference EMG during static and acting conditions. EMG of extraocular muscles demonstrated higher power spectrum than those of facial muscles. These enable us to pick up electrical activity of extraocular muscles and distinguish them from that of facial muscles
Controlling Surface Segregation of a Polymer To Display Carboxy Groups on an Outermost Surface Using Perfluoroacyl Groups
Controlling
the surface properties of solid polymers is important
for practical applications. We here succeeded in controlling the surface
segregation of polymers to display carboxy groups on an outermost
surface, which allowed the covalent immobilization of functional molecules
via the carboxy groups on a substrate surface. Random methacrylate-based
copolymers containing carboxy groups, which were protected with perfluoroacyl
(R<sub>f</sub>) groups, were dip-coated on acrylic substrate surfaces.
X-ray photoelectron spectroscopy and contact-angle measurements revealed
that the R<sub>f</sub> groups were segregated to the outermost surface
of the dip-coated substrates. The R<sub>f</sub> groups were removed
by hydrolysis of the R<sub>f</sub> esters in the copolymers, resulting
in the display of carboxy groups on the surface. The quantification
of carboxy groups on a surface revealed that the carboxy groups were
reactive to a water-soluble solute in an aqueous solution. The surface
segregation was affected by the molecular structure of the copolymer
used for dip-coating
Correction: Surface-functionalization of isotactic polypropylene via dip-coating with a methacrylate-based terpolymer containing perfluoroalkyl groups and poly(ethylene glycol)
Surfactant-Induced Polymer Segregation To Produce Antifouling Surfaces via Dip-Coating with an Amphiphilic Polymer
We
propose a rational strategy to control the surface segregation
of an amphiphilic copolymer in its dip-coating with a low-molecular-weight
surfactant. We synthesized a water-insoluble methacrylate-based copolymer
containing oligo(ethylene glycol) (OEG) (copolymer <b>1</b>)
and a perfluoroalkylated surfactant (surfactant <b>1</b>) containing
OEG. The dip-coating of copolymer <b>1</b> with surfactant <b>1</b> resulted in the segregation of surfactant <b>1</b> on the top surface of the dip-coated layer due to the high hydrophobicity
of its perfluoroalkyl group. OEG moieties of surfactant <b>1</b> were accompanied by those of copolymer <b>1</b> in its segregation,
allowing the OEG moieties of copolymer <b>1</b> to be located
just below the top surface of the dip-coated layer. The removal of
surfactant <b>1</b> produced the surface covered by the OEG
moieties of the copolymer that exhibited antifouling properties. Using
this strategy, we also succeeded in the introduction of carboxy groups
on the dip-coated surface and demonstrated that the carboxy groups
were available for the immobilization of functional molecules on the
surface