University of Utah Research Foundation

Other

Joseph D Andrade

Philip M Triolo

Richard A Van Wagenen

Lee Morgan Smith

Dwayne Ronald Westenskow

James N Herron

Jindrich Henry Kopecek

Robert E Benner

A Bruno Frazier

John David Brazzle

Vladimir Hlady

Frank J Miller

Jinn-Nan Lin

Robert J Scheer

I-Nan Chang

Daniel A Bartholomeusz

Chung-Yih Wang

Jin H Lee

An active needle device for fluid injection or extraction includes at least one hollow elongated shaft defining at least one channel. The channel provides communication between at least one input port and at least one output port of the needle device. At least one active component such as a sensor or actuator is placed or integrated into the elongated shaft. The needle device can include a macroneedle, a microneedle, or an array of macroneedles or microneedles. The microneedles can be fabricated on a substrate which can remain attached to the microneedles or be subsequently removed. The active component can facilitate biochemical, optical, electrical, or physical measurements of a fluid injected or extracted by the needle device.

Active needle devices with integrated functionality

A method and associated apparatus for measuring chemical concentration in a liquid sample based on spatial separation and resolution of light is disclosed. The method is preferably applied to sensitive, quantitative, luminescence-based biosensors which reads the analyte concentration via spatial distribution of the emitted light. The detection of light is used to assess the spatial position, rather than the intensity or wavelength, of emitted light. A bioluminescent or chemiluminescent reaction requiring, for example, ATP, NADPH or NADH as a specific, and sensitive co-factor is used. ATP or NADH concentration is modulated, &ldquo;tuned,&rdquo; and/or regulated via, for example, an enzyme which consumes (&ldquo;consumase&rdquo;) ATP, NADPH, or NADH, thereby producing a spatial distribution of ATP or NADH and a spatial distribution in the emitted light. By appropriate control of the consumase or &ldquo;synthase&rdquo; activity and kinetics, a sensitive, specific, and easily readable luminescent pattern is produced, permitting detection.

Method of measuring chemical concentration based on spatial separation and resolution of luminescence

The antigen-binding activity of an antibody immobilized on a siliceous support can be increased by pretreatment of the antibody with acid prior to its immobilization.

Immobilization of acid-treated antibodies on siliceous support

A reusable biosensor is disclosed. A molecule containing a moiety of an antibody-antigen complex and photosensitive polymers are bonded to an optical conduit. When placed in a solution, the presence or absence of a second complementary moiety of an antibody-antigen complex can be determined by sensing whether or not the first moiety is complexed. The first moiety of an antibody-antigen complex can then be regenerated by transmitting light through the optical conduit which alters the structure of the photosensitive polymers to cause interference with said complex, thereby dissociating the second complementary moiety from the first moiety. The ability to regulate and control specific binding has applications can be useful in information storage devices, bioorganic electronic devices, and optical devices.

Method and apparatus for the regulation of complex binding

The invention discloses the processes and materials for treating materials to minimize the deposition of proteins and other molecules, and for removing proteins and other molecules from materials. New copolymers containing polyethylene oxide sidechains called supersurfactants have the ability to bind themselves to interfaces to provide a stable protein-resistant interface. A process is presented to treat and modify interfaces with the new copolymers.

Polymer supersurfactants for protein resistance and protein removal

The concentration of multiple polyatomic gases are determined almost simultaneously by Raman scattering. The gas sample is placed in a sampling cell located in the resonance cavity of a laser and a polarized laser beam having sufficient intensity to produce detectable signals of Raman scattered light is passed through the cell. The scattered light is captured and redirected by means of a reflection mirror located parallel to the axis of the laser beam adjacent to and outside of the cell. Signals of both inelastic Raman scattered light and elastic laser scattered light are collected by a collection lens means opposite the reflection mirror and outside the gas cell. The collection lens is also parallel to the axis of the laser beam. The collected scattered signals are directed onto a laser line rejection filter where the scattered elastic laser signals are filtered out and the inelastic Raman scattered signals are transmitted to come in contact with a rotating filter wheel containing a series of interference filters with each filter being specific to the transmission of one Raman line. The Raman lines passing through the rotating filters are sensed sequentially by a single detector means and amplified and converted into digital electrical pulses which are processed and converted into visual readouts indicative of the concentration of each of the polyatomic molecules in the gas being determined.

Molecular gas analysis by Raman scattering in intracavity laser

Surfaces of hydrophobic polymers are treated to reduce their friction resistance characteristics when in contact with an aqueous environment by exposing the surfaces to an oxidation treatment, preferably by use of radio frequency glow discharge. This oxidation is followed by exposure to atmospheric air, until there is a substantial reduction in the air-water contact angle of the surfaces. The reduced friction resistance characteristics are important in aqueous applications where there is movement between the surfaces of two polymeric materials, such as in double slideable catheters and similar medical products. This process also provides lower coefficients of friction for general polymeric products in contact with water and aqueous solutions.

Process for treating polymer surfaces to reduce their friction

A process is presented for conducting fluorescence immunoassays without the use of added labels by utilizing ultraviolet radiation and internal reflection optics to activate fluorescent groups present in the molecules of interest. The assay is accomplished by directing a beam of light having wavelengths in the ultraviolet region to a solid liquid interface which (1) has a material X immobilized thereon, and (2) is contacted with an assay solution containing in unknown Y which contains intrinsic tyrosine, tryptophan, nucleic acid or related fluorescence groups which are activated by wavelengths in the ultraviolet region; X and Y may be in the relationship of antibody and antigen in that one had the ability of recognizing the particular spatial and polar configuration of the other and is attracted to and bound to such configuration, said beam of ultraviolet light being projected under such conditions that there is internal reflection at the interface, and then measuring the amount of fluorescence emitted from the surface of the interface, the amount of the fluorescence emission being a function of the amount of the unknown Y being detected. In the event that Y is not fluorescent, the X-Y sandwich can be further exposed to a solution containing X, to form XYX sandwich. The observed fluorescence of X is proportional to the amount of bound Y which is in turn related to the solution concentration of Y.

Growing community of inventors

Salt Lake City, UT, United States of America

Joseph D Andrade