2232 results about "Saline solutions" patented technology

According to the present invention, a catheter having at least one multi-purpose lumen formed through the catheter terminates proximal a relatively complex-shaped distal portion thereof. In one form of this embodiment, the relatively complex-shaped distal portion comprises a looped portion having diagnostic- and / or ablation-type electrodes coupled thereto and an elongated diameter-adjusting member coupled proximal the distal end of the looped portion. The multi-purpose lumen may be used to alternately accommodate a variety of dedicated materials; such as, (i) a guide wire for initial deployment or later repositioning of the catheter, (ii) a volume or flow of a contrast media and the like, (iii) a deployable hollow needle or tube and the like used to biopsy adjacent tissue or dispense a therapeutic agent into a volume of tissue, and (iv) a cooling fluid, such as saline solution and the like dispensed at least during therapeutic tissue ablation procedures.

A method and system for shrinking dilatations of a body, removing excess, weak or diseased tissue, and strengthening remaining tissues of the lumen walls. A catheter is disposed near the dilatation and fixed in position by inflatable occlusion balloons. Body fluids present in the occluded dilatation are evacuated and treatment fluid is exuded under pressure into the dilatation. Pressure is maintained by the treatment fluid while energy is applied by the catheter to heat the treatment fluid, causing the lumen walls to absorb the treatment fluid. Additional energy is then applied so as to preferentially heat the lumen wall tissues which have absorbed the treatment fluid, while at the same time treatment fluid is circulated to cool the inner surface of the lumen walls. The dilatation is occluded, a saline solution is introduced and absorbed into the lumen-wall tissue in the occluded region of the dilatation and then heated by application of radio frequency (“RF”) or other energy in order to soften only the lumen-wall tissue of the dilatation, the dilatation is shrunk by application of a chilled saline solution and a vacuum, and additional RF or other energy is emitted to ablate, further shrink, and harden only the lumen-wall tissue of the dilatation, without destroying the inner surface of the lumen or other tissues of the body beyond the lumen walls, thereby promoting growth of epithelial cells.

Adjustable gastric band implants contain a hollow elastomeric balloon with fixed end points encircling a patient's stomach just inferior to the esophago-gastric junction. These balloons can expand and contract through the introduction of saline solution into the balloon. In current bands, this saline solution must be injected into a subcutaneous port with a needle to reach the port located below the skin surface. The port communicates hydraulically with the band via a catheter. As an alternative to using a percutaneously accessed injection port, a system for regulating the flow of saline that is totally implanted may rely upon bi-directionally pumping fluid from an implant device. This system instead transfers AC magnetic flux energy from an external primary coil to a secondary coil that powers the pump in the implanted reservoir. A magnetically permeable rod centered within the primary coil increases power coupled to the secondary coil.

A protective, biocompatible coating or encapsulation material protects and insulates a component or device intended to be implanted in living tissue. The coating or encapsulation material comprises a thin layer or layers of alumina, zirconia or other ceramic, less than 25 microns thick, e.g., 5-10 microns thick. The alumina layer(s) may be applied at relatively low temperature. Once applied, the layer provides excellent hermeticity, and prevents electrical leakage. Even though very thin, the alumina layer retains excellent insulating characteristics. In one embodiment, an alumina layer less than about 6 microns thick provides an insulative coating that exhibits less than 10 pA of leakage current over an area 75 mils by 25 mils area while soaking in a saline solution at temperatures up to 80° C. over a three month period.

Heat exchanger-equipped catheters and related methods that are useable for changing or maintaining at least a portion of the body of a human or veterinary patient at a desired temperature and for the measurement of cardiac output or blood flow rate within a blood vessel, without the need for introduction of saline solution or any other foreign substance into the patient's blood.

An absorbent article having a distribution member comprising non-biopersistent inorganic vitreous microfibers. The microfibers have an average effective diameter between about 0.1 micron and about 6 microns and are arranged in a fibrous assembly having a basis weight between about 40 g / m2 and about 350 g / m2 and a density between about 0.04 g / m3 and about 0,25 g / m3. In preferred embodiments, the fibrous assembly can vertically wick a 0.9% saline solution to a height of 5 cm in less than about 5 minutes.

Method and apparatus for monitoring a patient having a tumor to determine perfusion tumor heterogeneity wherein a solution containing a tracer, preferably a <2>H-saline solution is infused into the patient's bloodstream at a predetermined slow rate to effect perfusion into the tumor. An MRI machine is adjusted to acquire a set of dynamic <2>H magnetic resonance images of the tumor. The <2>H-images are obtained before infusion, during infusion and post infusion. First, the obtained images are processed to quantitatively determine perfusion per voxel of the images. Next, maps of perfusion parameters are generated to indicate spatial distribution of tumor perfusion. The maps are displayed in color code and analyzed.

Adjustable gastric band implants contain a hollow elastomeric balloon with fixed end points encircling a patient's stomach just inferior to the esophago-gastric junction. These balloons can expand and contract through the introduction of saline solution into the balloon. In current bands, this saline solution must be injected into a subcutaneous port with a needle to reach the port located below the skin surface. The port communicates hydraulically with the band via a catheter. As an alternative to using a percutaneously accessed injection port, a system for regulating the flow of saline that is totally implanted may rely upon bi-directionally pumping fluid from an implant device. This system instead transfers AC magnetic flux energy from an external primary coil to a secondary coil that powers the pump in the implanted reservoir. A magnetically permeable rod centered within the primary coil increases power coupled to the secondary coil.

A composition for promoting repair of damaged tissues, being a cross-linked alginate solution, which can be maintained in liquid form indefinitely (under constant conditions) and only gels in vivo. This cross-linked alginate solution is an ideal material to be used for tissue repair. Injection of said material into cardiac tissue post-myocardial infarct induced tissue regeneration. The invention provides such injectable solution, as well as compositions and method of preparation thereof. The invention also provides various methods and uses of the cross-linked alginate solution, for cardiac tissue regeneration, induction of neo-vascularization, enhancing SDF-1 expression and guiding stem cell chemotaxis, among others. A kit for tissue repair is also provided.

Super-oxidized water based on hypochlorous acid, such as is obtained by the electrochemical treatment of a saline solution, may be used in the treatment of leg ulcers or other open wounds. Preferably, the pH of the super-oxidized water is in a range of 4 to 7, and the water has a redox potential of >950 mV. Medicaments based on the super-oxidized water may be in liquid or gel form. The super-oxidized water is able to control the microbial population within the wound and at the same time permit cell proliferation.

The present invention discloses an electrode for an electric operation device including a hollow electrode being formed in a hollow tube shape extended long from a closed tip, and having an insulation-coating on the outside surface except a predetermined length of the closed tip side, a refrigerant tube having a smaller diameter than a diameter of the hollow electrode, and being inserted into the hollow electrode, the refrigerant tube supplying refrigerants for cooling a living tissue contacting the closed tip and the hollow electrode into the hollow electrode, and externally discharging the heat-exchanged refrigerants from the living tissue through the gap between the refrigerant tube and the hollow electrode, at least one first hole formed on the outside surface of the hollow electrode where the insulation coating has not been formed, for externally discharging some of the refrigerants supplied through the refrigerant tube from the hollow electrode, and a flow control means formed on the outside surface of the hollow electrode where the insulation coating has not been formed, and operated as a discharge resistance to the refrigerants discharged from the first hole, for controlling a flow of the refrigerants, whereby supplying an electrode structure using both a method for water-cooling the inside of the electrode and a method for discharging the saline solution.

An apparatus and method are described for quickly inducing therapeutic hypothermia of the heart by perfusing the myocardium with hypothermic fluid in alternatingly antegrade and retrograde directions. The apparatus and method provide rapid cooling of the affected myocardium to achieve optimal myocardial salvage in a patient experiencing acute myocardial infarction. The therapeutic hypothermia system includes one or more coronary artery perfusion catheters, a coronary sinus perfusion catheter and a fluid source for delivering a hypothermically-cooled physiologically-acceptable fluid, such as saline solution, oxygenated venous blood, autologously-oxygenated arterial blood and / or an oxygenated blood substitute. The system may also include one or more guidewires, subselective catheters and / or interventional catheters introduced through a lumen in one or more of the perfusion catheters.

A thrombectomy catheter deployment system which greatly simplifies setup procedures and operation of a thrombectomy catheter includes a stand alone drive unit and a disposable pump / catheter assembly which is manually placed into a carriage assembly in the drive unit. The pump / catheter assembly has a plurality of preconnected components including tubular structure and a thrombectomy catheter connected thereto and is transported into or out of the interior of the drive unit for automatic high pressure pump piston head engagement or disengagement with a reciprocating linear actuator and for automatic engagement or disengagement of an effluent waste tube with a roller pump. A barcode reader senses specific operational data pertaining to an individual pump and provides an interface for operation of the reciprocating linear actuator. A bubble trap incorporated for effective debubbling of saline solution is closely coupled to an insert molded pump having an improved valve arrangement. A spiked bag with large tubing is incorporated for bubble-free transfer of saline.

The invention relates to a synthesis method of fine grain ZSM-5 zeolite molecular sieve with high silicon aluminium ratio, which comprises using a surface active agent, charging it into acidified aluminium salt solution, then slowly dropping alkaline solution formed from sodium silicate, template agent and seed crystal into aluminium saline solution, the overall composition of the obtained reaction mixture being Na2O:Al2O3:SiO2:H2O=1.5-4.0:1:20-280:500-2000 by mol ratio, then subjecting the reaction mixture to thermal crystallization through the conventional method.

A method of controlling an 82Sr / 82Rb elution system having a generator valve for proportioning a flow of saline solution between an 82Sr / 82Rb generator and a bypass line coupled to an outlet of the generator such that saline solution traversing the bypass line will merge with eluted saline solution emerging from the generator to provide an active saline solution. During each elution run, a plurality of successive concentration parameter values are obtained at predetermined intervals. Each concentration parameter value is indicative of a respective instantaneous activity concentration of the active saline solution. Respective error values between each concentration parameter value and a target activity concentration value of the elution run are computed. Error data based on a plurality of the computed error values is accumulated. Between successive elution runs, at least one performance parameter of the elution system is adjusted based on the accumulated error data.

A method and apparatus utilizing an exothermic reaction to generate a heated gas that warms a baby bottle, providing a baby bottle warmer that is portable, convenient to use, simple, and lightweight. In one embodiment, a heating vessel holds the baby bottle and a vessel top removably attaches to an upper section of the heating vessel. A solution release mechanism situated in a lower section of said heating vessel includes a solution container having an activating liquid disposed therein, and a device for puncturing the solution container responsive to pressure supplied by insertion of the baby bottle. A heating element situated below the solution release mechanism includes a material for exothermically reacting with the activating liquid to generate the heated gas. In one embodiment, when a baby bottle is inserted into the bottle warmer, an upper and lower unit are pressured together to release a saline solution onto a magnesium wafer. Some embodiments of the baby bottle warmer comprise a system for spacing apart the lower and upper units, which is useful for storage and / or travel. Upon insertion of the baby bottle and application of pressure, the system disengages, thereby allowing the upper and lower units to move together.

The field of colonic diagnostic and surgical procedures is hampered by the lack of optimal means available to cleanse the colon. A compromise between convenient, distasteful, solid or low volume, hyperosmotic solutions which cause considerable fluid and electrolyte imbalances in patients and large volume, difficult to consume, iso-osmotic solutions has had to be made heretofore. This invention describes a low volume, hyper-osmotic solution consisting of sulfate salts with and with out polyethylene glycol. Unlike prior art, this composition is useful for the cleansing of the bowel and, in lower volumes, as a laxative, without producing clinically significant changes in bodily function.

The invention discloses an acrylamide modified graft copolymer and a preparation method and usage thereof. The invention is characterized in that 20 parts of acrylamide, 1-20 anionic monomer and / or cationic monomer, 0.1-15 macromonomer, 0.05-10 ionic lyophobic monomer and 50-1000 deionized water are added into a three-necked reaction bottle, the pH value is adjusted to be 3-9, N2 is introduced for 30min, then 0.002-0.5 part of initiator persulfate is added at 30-75 DEG C, the reaction lasts 8-36h, then copolymer PAB is obtained, and finally water is used for dilution to obtain strong PAB solution. During polymerization, no surfactant is used, and the macromonomer with a long chain and the ionic lyophobic monomer with intermolecular association function are introduced into the copolymer PAB, so the capabilities of cooperative tackification and salt-resistance between the rigid conformation of a molecular chain and the intermolecular association can be played optimally, the PAB exhibits unique solution property and has higher colloidal viscosity in high saline solution than in fresh water, and the PAB obtains the capabilities of tackification, salt resistance, low surface tension and strong molecular association and can be used for the oil-displacing acrylamide modified graft copolymer. The copolymer is prepared into water solution with mass concentration of 0.2-3.0g / L and surfactant concentration of 0.01-2 mmol / L, then the water solution is added into a mixing vessel by a stirring device, and then a polymer oil-displacing agent with tackification, salt resistance and cutting resistance is obtained. The PAB has the functions of both a tackifier and a macromolecule surfactant. The copolymer PAB is prepared into water solution which has mass concentration of 0.05-7%, so the macromolecule surfactant with excellent surface activeness can be obtained and then applicable to an emulsifier, an emulsion splitter, a solubilizer and a wetting agent.

A thrombectomy catheter deployment system which greatly simplifies setup procedures and operation of a thrombectomy catheter includes a stand alone drive unit and a disposable pump / catheter assembly which is manually placed into a carriage assembly in the drive unit. The pump / catheter assembly has a plurality of preconnected components including tubular structure and a thrombectomy catheter connected thereto and is transported into or out of the interior of the drive unit for automatic high pressure pump piston head engagement or disengagement with a reciprocating linear actuator and for automatic engagement or disengagement of an effluent waste tube with a roller pump. A barcode reader senses specific operational data pertaining to an individual pump and provides an interface for operation of the reciprocating linear actuator. A bubble trap incorporated for effective debubbling of saline solution is closely coupled to an insert molded pump having an improved valve arrangement. A spiked bag with large tubing is incorporated for bubble-free transfer of saline.

A system for cryoablating target tissue at a treatment site includes a cryo-element mounted at the distal end of a cryo-catheter. A balloon catheter is provided having a U-shaped balloon attached thereon. The cryo-element is threaded onto a pre-positioned guidewire and advanced within the patient's vasculature until the cryo-element is positioned at the treatment site. Next, the balloon is threaded onto the guidewire and advanced within the patient's vasculature using the balloon catheter. At the treatment site, the U-shaped balloon is interposed between the cryo-element and the target tissue. Saline solution is pumped into the balloon causing the U-shaped balloon to expand and contact both the cryo-element and the surrounding target tissue. Next, a refrigerant is expanded to cool the cryo-element, which in turn, freezes the saline solution. The resulting “ice ball” extracts heat from surrounding tissue resulting in the cryoablation of a substantially circumferential portion of tissue.

A process for fabricating a medical assembly having a medical device at least a portion of which is formed of inorganic material is provided. The medical assembly is suitable for substantially long-term implantation in a host animal. The process includes modifying a surface of the medical device to form a hydrophilic adhesion-promoting surface. The hydrophilic adhesion-promoting surface is coated with an alginate solution comprising alginate and the alginate is reacted with alkaline earth metal cations.

The present invention relates to an electrode for an electrosurgical unit for the use in ablating and necrosing a living tissue by RF electric energy. The present invention provides an electrode for an electrosurgical unit, including: a hollow electrode formed in an elongated hollow tube shape, a non-insulating region of a predetermined length being formed on one side of which, an insulating region being formed on an outer surface of which other than the non-insulating region; a saline solution circulation structure that supplies pressurized saline solution for cooling a living tissue which is in contact with the hollow electrode from the outside of the living tissue to the inside of the hollow electrode, and discharges the pressurized saline solution from the inside of the hollow electrode to the outside of the living tissue; and one or more saline solution discharge holes formed in the non-insulating region of the hollow electrode to discharge some of the circulating pressurized saline solution to the living tissue which is in contact with the hollow electrode.

Carbon Dioxide capture processes utilizing ammonia, or ammonia in water as the capture fluid for carbon dioxide generate concentrated solutions of ammonium carbonate species in water, which are subsequently decomposed to capture the carbon dioxide and recycle the ammonia. Forward osmosis processes utilize ammonium carbonate species as draw solutions to pull water from saline solutions such as seawater in the ammonium carbonate solution. The ammonium carbonate solution is then heated to decompose the ammonium carbonate to ammonia and CO2 which are both reused, while a portion of the aqueous stream is recovered as pure water. Combination of carbon capture process with an integrated forward osmosis process provide great economies over standalone operations. Furthermore, the very high concentrations of ammonium carbonate provide a further opportunity to include osmotic power recovery cycles with the integrated forward osmosis and carbon capture process.

A system for cryoablating target tissue at a treatment site includes a cryo-element that is attached to the distal end of a cryo-catheter. An annular shaped balloon is attached to a cylindrical shaped sleeve and the sleeve is slideably mounted over the cryo-catheter. The distal end of a fill tube is attached to the sleeve to place the lumen of the fill tube in fluid communication with the balloon. In use, the cryo-element is first positioned at the treatment site using the cryo-catheter. Next, the fill tube is used to advance the balloon and sleeve over the cryo-catheter until the balloon is interposed between the cryo-element and the target tissue. Saline solution is then pumped through the fill tube to expand the balloon between the cryo-element and target tissue. A refrigerant is then expanded in the cryo-element which freezes the saline solution and cryoablates the target tissue.

A human or animal implant device including a first, inner sealed silicone sheet sac, a second, intermediate sealed silicone sheet sac completely surrounding the first, inner sac, and a third, outer sealed silicone sheet sac completely surrounding the second sac. Each sac has a coating of beeswax on inner and outer walls thereof, and the first, inner sac is filled with a substantially sterile liquid material, preferably of viscosity at least 15 cp. The second, intermediate sac and the third, outer sac are filled with aqueous saline solution.

The invention relates to an electrode material of a lithium ion battery, in particular to a method for pre-lithiating a cathode material. The method comprises the steps that an electrolytic cell cathode cavity is made of the electrode material such as a lithium ion cathode material and arranged in a lithium ion conductive organic electrolyte; an anode cavity is an aqueous solution containing lithium salt or an organic solution; the anode cavity is separated from the cathode cavity by a lithium ion conductor ceramic membrane or a composite membrane of lithium ion conductor ceramic and a high molecular material; an electric potential and current density are controlled by external circuit charge and discharge equipment to allow lithium ions to migrate to a cathode from an anode through the membrane; and an SEI (Solid Electrolyte Interphase) membrane is formed on the surface of the material; or the electrode material is pre-lithiated. According to the method, a cheap and safe lithium ion saline solution serves as a source of the lithium ion; the SEI membrane is generated for the cathode of the lithium ion battery in advance; or lithium is supplemented to the electrode material; the coulombic efficiency and cycling stability of the cathode material can be improved; a formation process in production of the lithium ion battery in the prior art is simplified; the electrode material and cost are saved; and the method is safe and efficient and has a large-scale application prospect.

The invention discloses an image-text firework production method with users dyeing a partial preset part. The image-text firework production method is characterized in that an image-text firework carrier, dyeing articles and a dyeing image-text production method are adopted. The image-text firework carrier is provided with a lift-off rocket, a lattice structural body, preset image-text display flames, flame primary color powder, simultaneous propellant powder and a simultaneous ignition device, wherein the lift-off rocket is connected with the lattice structural body, and the simultaneous propellant powder, the preset image-text display flames and the flame primary color powder are filled in the lattice structural body. The dyeing articles include a dyeing saline solution and a dyeing device. The dyeing image-text production method includes image-text sample manuscript design, dyeing saline solution application, flame primary color powder penetrating staining, liquid component removing for sufficient drying and the like. According to the image-text firework production method, the displayed picture part of set off fireworks is preset and can be randomly combined according to free expressing of users, and accordingly the users can experience pleasure brought by personal participation and can directly express affection. In addition, the image-text firework production method is simple to implement, low in cost and suitable for volume production.

Disclosed are fiber optic assemblies having at least one optical fiber and a water-swellable powder within a tube and / or cavity and methods for making the same. Fiber optic assemblies of the present invention use relatively low-levels of water-swellable powder while still effectively blocking the migration of tap water and / or saline solutions of 3% by weight along the tube and / or cavity. Furthermore, cleaning of the optical fibers is not necessary before connectorization like with conventional fiber optic cables that use a gel or grease. Generally speaking, at least some of the water-swellable powder is transferred to the inside surface of the tube, cavity, optical fiber or the like; rather, than being a loose powder that is able to migrate within the tube or cavity. Moreover, the existence of water-swellable powder within the fiber optic assembly or cable is nearly transparent to the craft since relatively low-levels are possible.

A urinary catheter and companion packaging system for packaging sterile items utilized during a catheterization procedure are shown. A lightweight, flexible package contains a collection of ancillary materials and a catheter package. The catheter package houses a solution pouch, a protection sheath, and a catheter within the protection sheath. A saline solution is contained within the solution pouch, and is capable of being released from the solution pouch once external pressure breaks a weakened seam along one side of the solution pouch. A hydrophilic coating on the catheter activates once the saline solution contacts the exterior surface of the catheter. The catheter has an insertion tip that has been oven blasted and rounded in order to reduce the coefficient of friction. The overall length of the catheter is greater than about sixteen inches.