110results about How to "Minimize migration" patented technology

A miniaturized brush particularly adapted for medical use formed at the distal end of an elongated brush drive shaft having a hollow lumen formed therein for introduction over a guidewire. The brush drive shaft is enclosed in the lumen of a brush delivery catheter and other components of a brush sub-assembly adapted to deliver infusate through the catheter lumen and to be coupled to a drive motor unit for rotating the brush drive shaft and brush. The brush bristles of the distal brush are adapted to be garaged in a distal end section of the brush delivery catheter lumen during introduction through a body lumen. The brush bristles are formed of a thin sheet of rigid plastic material that is shaped to have a plurality of fringe elements extending in parallel from a mounting web. The mounting web is wound about and attached to a distal end section of the drive shaft outer circumference so that the fringe elements extend outward from the drive shaft surface and obliquely of the drive shaft axis. Preferably, proximal and distal spiral brush sections are formed in this manner so that fluids are impelled distally and proximally, respectively, between the proximal and distal brush sections as infusate is delivered.

Disclosed are methods useful for treating vascular lesions wherein a non-particulate agent such as a metal coil is introduced into a vascular site (e.g., an aneurysm cavity) in conjunction with an embolizing composition comprising a biocompatible polymer and a biocompatible solvent. The biocompatible solvent is miscible or soluble in blood and also solubilizes the polymer during delivery. The biocompatible polymer is selected to be soluble in the biocompatible solvent but insoluble in blood. Upon contact with the blood, the biocompatible solvent dissipates from the embolic composition whereupon the biocompatible polymer precipitates. Precipitation of the polymer in the presence of the non-particulate agent permits the agent to act as a structural lattice for the growing polymer precipitate. In another embodiment, the biocompatible polymer composition can be replaced with a biocompatible prepolymer composition containing a biocompatible prepolymer.

A cavity wall system and a method of forming a cavity wall including: a wall structure (1); a plurality of outer wall cladding panels (2); and a plurality of discrete mounting elements (4, 5, 6) for mounting the cladding panels a predetermined distance away from the wall structure (1) so as to form a substantially flat exterior wall surface (7) and a substantially uninterrupted internal wall cavity (8) between the cladding panels (2) and the wall structure (1); the mounting elements (4, 5, 6) being sized and arranged so as to allow substantially uninterrupted fluid flow throughout the cavity (8); and the system further including moisture control means defining a moisture control plane to minimise migration of liquid moisture from the cavity (8) into the wall structure (1). The invention also provides a mounting member (4) and a termination member (5) for use as mounting elements in the cavity wall system and method.

Sensing devices and methods of implanting sensing devices within an anatomical vessel network of a patient are provided. In one method, a fixation element (e.g., a stent or coil) of the sensing device is expanded into firm contact with a wall of a main anatomical vessel (e.g., a right pulmonary artery), and a stabilization element of the sensing device is placed into contact with a wall of an anatomical vessel branch of the main anatomical vessel. In another method, a first fixation element of the sensing device is expanded into firm contact with the wall of the main anatomical vessel (e.g., a right pulmonary artery) at a longitudinal location proximal to the anatomical vessel branch, and a second fixation element of the sensing device is expanded into firm contact with the wall of the main anatomical vessel at a longitudinal location distal to the anatomical vessel branch.

The present invention is directed to devices, systems and methods for removing undesirable materials from a sample fluid by contact with a second fluid. The sample fluid flows as a thin layer adjacent to, or between, concurrently flowing layers of the second fluid, without an intervening membrane. In various embodiments, a secondary separator is used to restrict the removal of desirable substances and effect the removal of undesirable substances from blood. The invention is useful in a variety of situations where a sample fluid is to be purified via a diffusion mechanism against an extractor fluid. Moreover, the invention may be used for the removal of components from a sample fluid that vary in size. When blood is the sample fluid, for example, this may include the removal of ‘small’ molecules, ‘middle’ molecules, macromolecules, macromolecular aggregates, and cells, from the blood sample to the extractor fluid.

The present invention provides both a device and a method. The device is a human made replacement for the soft discs in the spine. A fabric pouch encloses a central hydraulic element made up of small soft beads. Two pouches with beads are implanted into a prepared disc space to function as an intervertebral disc. The method is conversion of the device into a fusion element.

This invention relates to methods and devices that improve cell culture efficiency. They include the use of gas permeable culture compartments that reduce the use of space while maintaining uniform culture conditions, and are more suitable for automated liquid handling. They include the integration of gas permeable materials into the traditional multiple shelf format to resolve the problem of non-uniform culture conditions. They include culture devices that use surfaces comprised of gas permeable, plasma charged silicone and can integrate traditional attachment surfaces, such as those comprised of traditional tissue culture treated polystyrene. They include culture devices that integrate gas permeable, liquid permeable membranes. A variety of benefits accrue, including more optimal culture conditions during scale up and more efficient use of inventory space, incubator space, and disposal space. Furthermore, labor and contamination risk are reduced.

A method of preventing damage to the shoots and foliage of a plant by a pest includes treating a seed having an exogenous gene that encodes for the production of a protein having activity against European corn borer or corn root worm with a composition comprising at least one pyrethrin or synthetic pyrethroid that is selected on the basis of having an activity against an insect other than European corn borer or corn root worm. Treated seeds are also provided.

The present invention relates to a radially-expandable stent for implantation in a bodily passageway, being expandable from an initial unexpanded state to an expanded state, having an outer surface with a geometric pattern covering said outer surface to minimize migration after implantation.

A medical lead includes a pitted, grooved or threaded electrode array tip and a flexible tube or sheath encompassing the electrode array located near the lead tip. In some embodiments, the electrode array adheres to tissue, the tube or sheath adheres to the electrode array at the distal end of the electrode array or the tube or sheath adheres to tissue at the proximal end of the tube or sheath. Embodiments of the tube or sheath may be made from biodegradable material and can include electrode windows spaced along the tube or sheath corresponding to placement of electrode contacts of the electrode array.

A UV screening composition comprising particles which are capable of absorbing UV light so that electrons and positively charged holes are formed within the particles, characterised in that the particles are adapted to minimise migration to the surface of the particles of the electrons and/or the positively charged holes when said particles are exposed to UV light in an aqueous environment.

A container defines an interior volume, an opening into the interior volume, and a sealing surface bordering the opening. A closure assembly may be attachable over the opening and includes at least one of an induction seal liner, an inner seal, and a sealable film. A radio frequency identification tag includes a microprocessor and an antenna for receiving, storing, and transmitting selected digitized information. The induction seal liner, inner seal, and sealable film minimizes migration of fluids between the interior volume and the container exterior when the closure assembly may be engaged with the sealing surface. The radio frequency identification tag may be included in the closure assembly, or within the interior volume, or on the container exterior, or may be incorporated into the induction seal liner, inner seal, or sealable film, without the closure assembly electromagnetically interfering with the receiving, storing, or transmitting of digitized information.

This invention relates to a photosensitive element for use as a flexographic printing plate and a process for preparing the plate from the element. The photosensitive element has at least one photopolymerizable elastomeric layer that comprises a binder, a monomer, a photoinitiator, an onium salt, and a leuco dye. Upon exposure to actinic radiation, the onium salt and leuco dye react resulting in a change of color in polymerized portions of the photopolymerizable layer. The color change provides enhanced image color contrast in the photosensitive element.