University of South Florida

Telebyte, Inc.

Joel A Strom

Elizabeth Hood

Michael VanAuker

John J Murray

Joseph Allen Knight

Kenneth S Schneider

Leo E Ondrovic

Karl Muffly

Donald E McMillan

Michael Breneisen

Michael D Van Auker

A device and a system, based upon Deep Optical Scanning (DEOS), for the detection of certain cancers such as breast cancer and the determination of their response to therapy. DEOS is based upon the nonlinear optical interaction of incident laser generated light with tissue. The cancers may either be subsurface or on the surface. The system includes hardware and software components that form subsystems including: an Optical Electronic Subsystem, a Digitization Subsystem, a Parameter Computation Subsystem, an Archive, an Artificial Intelligence Subsystem, and a Presentation Subsystem. The device can be made portable and is non-invasive in its application to a patient. The system can be integrated into a hybrid architecture with other imaging techniques used for the detection of cancers.

Optical cancer detector using deep optical scanning and multi layer neural network

A method of targeted drug delivery and imaging using nonionic surfactant vesicles (niosomes) in combination with ultrasound is presented. Niosomes have potential applications in targeted drug delivery and imaging because of their ability to encapsulate therapeutic agents and their enhanced uptake by physiological membranes. The niosomes may be administered to the subject via catheter. Ultrasound may be used to mediate delivery non-invasively by altering the niosome membrane structure. Niosomes composed of polyoxyethylene sorbitan monostearate (Tween 61), cholesterol, and dicetyl phosphate were synthesized via a thin film hydration technique and used for encapsulation studies. Carboxyfluorescein dye (CF) was used as a drug model to demonstrate delivery. The amount of dye in the niosomes, the concentration of the vesicles, and their mean particle size after each 5 minute incremental exposure to ultrasound was monitored. It was found that ultrasound at specific frequencies can reversibly permeabilize the lipid membrane of niosomes to allow the controlled release of a compound without destroying the niosome structure.

Ultrasound enhancement of drug release across non-ionic surfactant membranes

The subject invention concerns vascular prosthetic devices and methods for ascending aorta and/or valve replacement in humans and animals. In one embodiment, a device of the invention includes a vessel-like structure having a first end adapted for surgical attachment to a left ventricle, a second end adapted for surgical attachment to an aorta, and, interposed between the first and second ends, a sinus portion configured in the shape of the sinuses of Valsalva in a human aortic valve.

Vascular prosthesis

A method of targeted drug delivery and imaging using nonionic surfactant vesicles (niosomes) in combination with ultrasound. Niosomes have potential applications in targeted drug delivery and imaging because of their ability to encapsulate therapeutic agents and their enhanced uptake by physiological membranes. Ultrasound may be used to mediate delivery non-invasively by altering the niosome membrane structure. Niosomes composed of polyoxyethylene sorbitan monostearate (Tween 61), cholesterol, and dicetyl phosphate were synthesized via a thin film hydration technique and used for encapsulation studies. Carboxyfluorescein dye (CF) was used as a drug model to demonstrate delivery. The amount of dye in the niosomes, the concentration of the vesicles, and their mean particle size after each 5 minute incremental exposure to ultrasound was monitored. Dye concentration in niosome samples decreased while the population and size distribution of the niosome remained largely unchanged. Ultrasound is demonstrated to enhance the rate of dye diffusion across the niosome membrane non-destructively.

Growing community of inventors

Tampa, FL, United States of America

Joel A Strom