Visible Genetics Inc.

University Health Network

Holland Bloorview Kids Rehabilitation Hospital

Holland Bloorview Kids Rehabilitation

Bruno C Maruzzo

John K Stevens

Alexandre M Izmailov

Paul Waterhouse

Marina T Larson

Thomas D Yager

Thomas T K Chau

Ervin Sejdic

Catriona Steele

In a method and apparatus for swallowing impairment detection, a candidate executes one or more swallowing events, and dual axis accelerometry data is acquired representative thereof. Upon feature extraction and classification, vibrational data acquired in respect of each swallowing event is classified as indicative of one of normal or possibly impaired swallowing.

Method and device for swallowing impairment detection

A method and an apparatus for swallowing impairment detection acquire dual axis accelerometry data representative of one or more swallowing events executed by a candidate. Upon feature extraction and classification, vibrational data acquired in respect of each swallowing event is classified as indicative of one of normal or possibly impaired swallowing. Computer-readable media comprising statements and instructions for implementation by a processing device are also described in facilitating swallowing impairment detection respective to candidate swallowing events.

A microelectrophoresis chip comprises a substrate in which there are formed one or more channels, one channel for each sample to be evaluated. The channels extend for the length of the chip, a distance of generally around 1 cm, and are about 1 to 10 &mgr;m wide and 1 to 10 &mgr;m in depth. The channels are filled with a homogeneous separation matrix which acts as an obstacle to the electrophoretic migration of the charged molecules. Microelectrodes disposed in the channels are used to induce an electric filed within the homogeneous separation medium. When a voltage is applied across two or more of the microelectrodes, the charged molecules are induced to move and separate according to the electric field density, the type of solvent film, and the charge, shape and size of the charged molecule. The chip may further comprise detectors, such as light polarization detectors, fluorescence emission detectors, biosensors, electrochemical sensors or other microcomponents which may include sites for enzymatic or chemical manipulation of the moved or separated charged molecules.

Micro-electrophoresis chip for moving and separating nucleic acids and other charged molecules

A microelectrophoresis chip comprises a substrate in which there are formed one or more channels, one channel for each sample to be evaluated. The channels extend for the length of the chip, a distance of generally around 1 cm, and are about 1 to 10 &mgr;m wide and 1 to 10 &mgr;m in depth. The channels are filled with a homogeneous separation matrix which acts as an obstacle to the electrophoretic migration of the charged molecules. Microelectrodes disposed in the channels are used to induce an electric field within the homogeneous separation medium. When a voltage is applied across two or more of the microelectrodes, the charged molecules are induced to move and separate according to the electric field density, the type of solvent film, and the charge, shape and size of the charged molecule. The chip may further comprise detectors, such as light polarization detectors, fluorescence emission detectors, biosensors, electrochemical sensors or other microcomponents which may include sites for enzymatic or chemical manipulation of the moved or separated charged molecules.

Nanofabricated separation matrix for analysis of biopolymers and methods

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Toronto, Canada

Bruno C Maruzzo