Abstract: A method of sterilizing a material, said method comprising the steps of: (a) introducing a solution comprising peroxyacetic acid into a hot gaseous stream to produce a peroxyacetic acid vapor; and (b) contacting such peroxyacetic acid vapor with the material to be sterilized.

Abstract: A plasma sterilizing device has a container for a long tubule to be sterilized, having an adjustable internal pressure, and an electrode provided at at least one end of the long tubule. The device is configured so that plasma is generated inside the long tubule by applying an alternating current voltage to the electrode in such a state that the pressure inside and outside of the long tubule can be adjusted, so that there is a predetermined difference in pressure between the inside and the outside of the long tubule.

Abstract: To provide an efficient sterilization method for inexpensively sterilizing a medical article having a complex shape such as a body fluid treatment device of a generally-called dry or semi-dry type by so applying an electron beam that the overall absorbed dose distribution is small and to provide its application package form. [MEANS FOR SOLVING PROBLEMS] A method for sterilizing tubular body fluid treatment devices of a dry or semi-dry type contained in an electron beam-transmitting case with an electron beam. The method is characterized in that a stack structure which includes a gap layer having an average density of 0.010 to 0.180 g/cm3 and two body fluid treatment device layers having an average density of 0.050 to 0.200 g/cm3 and sandwiching the gap layer is contained in the electron beam-transmitting case, and the case is irradiated with the electron beam.

Abstract: The invention relates to a method of extending the production time of a pasteuriser. The pasteuriser is of the type which includes a plate heat exchanger with a number of sections, of which at least one section consists of regenerative section. The method comprises raising the temperature in the downstream part of the regenerative section to a temperature above 50° C., during a certain predetermined period of time and at regular intervals. During normal production, a part quantity of the product which passes downstream of the regenerative section is shunted past the regenerative section. At the regular intervals and during the predetermined period of time, a part quantity of the product which passes upstream of the regenerative section is shunted past the regenerative section. At the same time, all product passes the downstream part of the regenerative section during the predetermined period of time.

Abstract: The present invention relates to an air filtration system and a method for making a photocatalytic oxidation substrate by powder coating a photocatalyst onto a metal substrate.

Abstract: Shock waves are applied to clean and sterilize fluids in containers and conveyances. Shock waves destroy pathogens and pollutants in blood, water, food liquids and other fluids.

Abstract: In order to remove a pathogenic effect of a microorganism in a room or a work space in a short period of time, an ion diffusing apparatus, which includes an ion generator (17, 18) for generating positive ions each including H+(H2O)m and negative ions each including O2?(H2O)n, where m and n are arbitrary integers, and a blower for delivering the positive ions and the negative ions, which are generated from the ion generator (17), from a blowout opening, is operated to widely distribute, with a high concentration, the positive ions and the negative ions in the room.

Abstract: An apparatus for sanitizing oral appliances is provided. The apparatus includes a housing movable between open and closed positions, at least one ultraviolet light source for emitting one or more sanitization means within the sanitizing chamber, and at least one power source for powering the ultraviolet light source. In the open position the housing allows insertion of the appliance, and in the closed position the housing defines a sanitizing chamber. The apparatus may include an appliance suspension system. The apparatus may include a reflective interior surface provided on at least a portion of the sanitizing chamber. The ultraviolet light source may be adapted to generate ozone within the sanitizing chamber. The apparatus may include control circuitry connecting the ultraviolet light source to the power source for the purpose of activating and deactivating the ultraviolet light source.

Abstract: The present invention provides an allergen inhibitor which effectively prevents allergens from reacting with specific antibodies, mitigates the allergic symptoms or prevents appearance thereof, and is less likely to cause unpredictable discoloration and discoloration under usual conditions. The allergen inhibitor of the present invention comprises an allergen-inhibiting compound including a linear polymer having at least one of substituents represented by the formulas (1) to (3) at a side chain. Thus, the allergen inhibitor of the present invention shows excellent allergen-inhibiting effects.

Abstract: The invention provides a sterilization indicator (17), characterized in that it comprises: a compound (21) that is of the heating type when put into contact with atoms of oxygen O and/or nitrogen N; and a thermochromic dye (19), in thermal contact with the compound (21).

Abstract: The method of the invention comprises the following steps: during the disinfection (A) of the apparatus, recording (1) with an acquisition and processing system the disinfection date and data relative to the apparatus disinfection type and level together with identification information of said apparatus; during the use (C) of the apparatus on a patient, recording (5) with said system the date and information concerning the apparatus type of use and the patient together with identification information of said apparatus; sequencing with the acquisition and processing system the information on the disinfection and use on a patient together with identification information of said apparatus; before each use, developing using the acquisition and processing system an instruction allowing or forbidding (6) the use of the apparatus based on the sequencing.

Abstract: A neutral pH aqueous ready-to-use cleaning and disinfectant compositions include hydrogen peroxide as an active disinfecting constituent including a C1-C6 monohydric alcohol, and a surfactant or surfactant mixture. Methods of cleaning and disinfecting surfaces are also disclosed.

Abstract: The present invention relates to a novel pharmaceutical composition with milk of immunized camelid, particularly Camelus dromedarius as the main component (i.e. active ingredient) and a method for the treatment or prevention of skin or mucus membrane infections, particularly Acne vulgaris. The present invention also discloses a process of preparing said composition.

Abstract: Methods and systems for selection radiation exposure in sterilization of medical devices are disclosed.

Abstract: The invention relates to the saturation of different gaseous, liquid, gel-like, solid and mixed media with ingredients emitted by vegetative plants. The method for treating a medium by saturating it with useful substances emitted by plants involves supplying a gaseous medium to a chamber containing vegetative or cut plants and passing the gaseous medium saturated with plant excreta through the medium undergoing treatment. Furthermore, a low pressure or a low and a high pressure is generated in the above-mentioned gaseous medium in the chamber containing the vegetative or cut plants. The medium treating device comprises a means for pumping the gaseous medium, at least one chamber for plants emitting plant excreta, which chamber is connected by a pipe to the above-mentioned means on the intake side and to the pumping means on the discharge side; furthermore, the above-mentioned means is connected on the discharge side to at least one container for the medium undergoing treatment.

Abstract: [Problem to be solved] To provide a method for sterilizing powder or grain by which the heating time is a minimum required time to reduce thermal degradation of the quality of the powder or grain while securing sufficient sterilization effect, and a sterilizing apparatus employing the method. [Means to solve the problem] The problem is solved by a method for sterilizing powder or grain, and a sterilizing apparatus employing the method, and the method includes applying heat and pressure in which powder or grain is supplied into a heated gas flow pipe kept under heated and pressurized conditions, and the powder or grain is transferred while coming into direct contact with a heated condensable gas in the heated gas flow pipe for 0.

Abstract: Method for controlling the sterilization of products in an autoclave, in which products are placed in at least one closed, unsealed and confined container of any type, and according to which inside this same container there is a loaded and autonomous device for measuring in the container at least one sterilization parameter wherein during at least one part of the duration of the sterilization cycle and according to a predefined frequency, at least one representative value of the measurement of the at least one parameter is recorded in the loaded device and at least one of these representative values is transmitted directly through the container that remains closed, through wireless transmission by electromagnetic rays of waves with a frequency of less than 250,000 GHz.

Abstract: A battery autoclaving system is provided including a battery pack having a housing, a battery cell disposed within the housing, and an isolation region disposed between the housing and the battery cell. The isolation region may be formed at least partially from at least one of a thermal insulating material, a phase change material or any combination thereof. The system may include a temperature sensor adapted to sense at least one of a temperature of the battery cell temperature of the isolation region. The system may include and an autoclave configured to receive a temperature indication from the temperature sensor and to inhibit autoclaving when the temperature indication exceeds a predetermined value.

Abstract: Collection devices and kits for biological sample collection include a biologic sample collection device having a hydrophilic swab matrix that includes a modified polycaprolactone (PCL). Methods of production and use thereof are also described herein. The biologic sample collection devices, kits and methods described herein are used to collect a biologic sample (e.g., blood, buccal cells, etc.) and to enable extraction of nucleic acids (e.g., DNA) from that biologic sample so that the nucleic acids can be analyzed (e.g., sequencing and subsequent analyses of DNA).

Abstract: This disinfection system for medical instruments of the type comprising a disinfection chamber adapted to implement a cycle for disinfecting instruments, is characterized in that each instrument is associated with a radiofrequency label containing identification information and in that the chamber is associated with radiofrequency means for acquiring identification information about the or each instrument when put in place and removed from the chamber at the start and end of a disinfection cycle, with means of acquiring information characterizing the disinfection cycle and with means for combining identification information about the or each instrument with information characterizing the disinfection cycle in order to generate traceability information on the disinfection of the or each instrument.

Abstract: A flamer may be used to sterilize poultry litter, soil, concrete, etc. The stationary or mobile flamer disclosed comprises a hood to contain the heat, an external frame, and burners. A fuel tank may be carried on the flamer or on a tractor. An additional embodiment provides for mounting the flamer on wheels, permitting the unit to be towed by a truck, four-wheeler, tractor, etc. The burners are adjustable as to angle, and fueling rate. A pressure in the fuel system is controlled by selectively switching between the liquid and vaporous components of the fuel. By limiting how low the pressure may fall, the flow of fuel from the tank to the torches is more consistent.

Abstract: Disclosed herein are methods of preventing or reducing scale formation or corrosion by combining at least one scale-forming fluid comprising at least one scaling compound with at least one anti-scale material chosen from at least one scale-adsorbent agent. The methods may reduce or prevent the formation of scale on surfaces of liquid-related process equipment, such as boilers and heat exchangers.

Abstract: The present disclosure relates to the use of a split and single electrical cells in industrial applications, and particularly in aseptic packaging applications.

Abstract: The invention relates to the use of a polyolefin composition comprising a propylene-ethylene random copolymer having an ethylene content of 0.5-10 wt % and a randomness R of the ethylene distribution in the polymer chain of ?0.945 for the production of articles having high sterilization resistance.

Abstract: The present invention relates to a method for disinfecting a room and the objects that may be contained therein, or surfaces in general, including the following steps: (a) determining the volume of the room to be disinfected; (b) as a function of the value determined in step a) above, determining a volumetric concentration of an aqueous disinfecting solution delivered into the room in the form of a dry mist required for obtaining a predefined level of disinfection, said disinfecting solution comprising hydrogen peroxide and silver ions (Ag+); (c) delivering into the room said aqueous disinfecting solution in the form of a dry mist until the desired volumetric concentration is achieved; (d) keeping said aqueous disinfecting solution in the form of a dry mist in contact with the room and with the objects that may be contained therein for a predefined time, so as to achieve a desired level of disinfection.

Abstract: Disclosed are surgical kits and methods of making a surgical device for proximation of body parts. An exemplary method comprises receiving a ferrule defining a ferrule axis, the ferrule being received a room temperature; sterilizing the ferrule received in the previous step; receiving a sleeve defining a sleeve axis. The sleeve includes a projection configured to exert a force, parallel to the sleeve axis, against the ferrule, the sleeve being received at room temperature; and sterilizing the sleeve.

Abstract: A device and method for disinfecting a needleless connector, the device including a housing comprising a hub rotationally coupled to a motor, the motor being operably connected to a power source, the hub further comprising a receptacle configured to receive a cleaning head, wherein the device is configured to detect achievement of one or more minimum thresholds which are recommended to achieve proper disinfection of the needleless connector. Various devices and methods are further provided to permit tracking and reporting of disinfection events.

Abstract: Trays comprising a base have a plurality of axial slots adapted to receive buffer or other medical solution containers within the slots. A spring or other compression element at the bottom of the slot is configured to engage a plunger at the bottom of the solution container when present in the slot so that pressure is applied to the contents of the container in order to stabilize the contents while the containers are sterilized at an elevated temperature.

Abstract: Transport scheduling and transport processes for low microbial (“LM”) bulk products are described. The transport scheduling and processes facilitate low microbial activity in a LM bulk product during the transport of the LM bulk product.

Abstract: Transport scheduling and transport processes for low microbial (“LM”) bulk products are described. The transport scheduling and processes facilitate low microbial activity in a LM bulk product during the transport of the LM bulk product.

Abstract: Transport scheduling and transport processes for low microbial (“LM”) bulk products are described. The transport scheduling and processes facilitate low microbial activity in a LM bulk product during the transport of the LM bulk product.

Abstract: Methods of reducing the capillary forces experienced by fragile high aspect ratio structures during drying to substantially prevent damage to said high aspect ratio structures during drying. They include modifying the surface of the high aspect ratio structures such that the forces are sufficiently minimized and as such less than 10% of the high aspect ratio features will have bent or collapsed during drying of the structure having said features thereon.

Abstract: The present invention relates to compositions and methods for protection against bacterial contamination. The invention provides bactericidal yeast expressing bacteriocin proteins and methods of using the bactericidal yeast.

Abstract: An incubator comprising: a culture chamber configured to accommodate culture; a dish structure configured to contain a liquid; an ultrasonic vibrator provided in a part of the dish structure, the ultrasonic vibrator configured to atomize the liquid; and a gas-liquid contact structure configured to bring the atomized liquid into contact with air in the chamber to be cultured.

Abstract: The disclosure relates to a transport container for accommodating products during a high-pressure treatment of these products. By means of the transport container, the products can be transported into and out of a chamber in which they are high-pressure treated. The transport container comprises a lower component and an upper component which are adapted to be connected to one another, the lower component as well as the upper component being configured for accommodating at least one product.

Abstract: Methods and compositions for detection of microbial contaminants in peritoneal dialysis solutions are provided. The methods and compositions employ modified bioburden testing and the detection of peptidoglycan. A novel cause of aseptic peritonitis is provided—aseptic peritonitis associated with gram positive microbial contamination of a dialysis solution. Peptidoglycan is a major component of a gram positive bacterial cell wall and thus can serve as a marker for gram positive bacteria. In this regard, testing for peptidoglycans can be utilized to effectively prevent peritonitis in patients that use the peritoneal dialysis solutions, such as peritoneal dialysis solutions that contain a glucose polymer including an icodextrin and the like.

Abstract: A device for separating blood into individual components and/or groups of components, in the form of a sterilizable system includes a filter arrangement forming inlet and outlet chambers using filter elements arranged therein, and respective receptacles for cellular blood components and for blood plasma. The inlet chamber can be connected to the blood source via a line on the inlet side to conduct the blood and is connected, on the outlet side, to the cellular blood components receptacle. The outlet chamber is connected to the blood plasma receptacle via a line on the outlet side. Thermal sterilization is used to sterilize the device by opening a respective line into the inlet-side line of the inlet chamber, into the inlet chamber and the outlet-side line of the outlet chamber, or into the outlet chamber, the line being connected to the exterior via a hydrophobic or hydrophilic filter.

Abstract: Continuous system and procedure of sterilization and physical stabilization of pumpable fluids, food, or other type of fluids, through ultra-high pressure homogenization (UHPH) includes a first heat exchanger 1 which preheats the fluid at temperature Tp between 40 and 90° C.; an ultra-homogenizer 3 through which fluid at temperature Tp is introduced at a pressure Pu between 200 and 600 MPa increasing its temperature up to a final value Tu. A second heat exchanger 4 has its cooling temperature adjusted at value Te. An aseptic tank 5 receives the cooled down fluid at value Te, from which it is pumped by sterile air pressure into an aseptic packaging machine, for the packaging of the final product.

Abstract: Methods and systems for sterilization of objects by gas-cluster ion-beam (GCIB) irradiation are disclosed. The sterilization may be in conjunction with other beneficial GCIB surface processing of the objects. The objects may be medical devices or surgically implantable medical prostheses.

Abstract: Certain disclosed embodiments concern systems and methods of preparing dialysate for use in a home dialysis system that is compact and light-weight relative to existing systems and consumes relatively low amounts of energy. The method includes coupling a household water stream to a dialysis system; filtering the water stream; heating the water stream to at least about 138 degrees Celsius in a non-batch process to produce a heated water stream; maintaining the heated water stream at or above at least about 138 degrees Celsius for at least about two seconds; cooling the heated water stream to produce a cooled water stream; ultrafiltering the cooled water stream; and mixing dialysate components into the cooled water stream in a non-batch process.

Abstract: A system for sanitizing an enclosed structure has first and second sensors, a germicidal ultraviolet light source, a motor, and a controller. The first sensor detects humans within the enclosed structure. The second sensor detects the position of at least one door to the structure. The motor selectively moves the light source from an inactive position to an active position. The controller receives inputs from the first and second sensors and transmits outputs to the light source and the motor. When the controller receives signals that no humans or animals are present in the enclosed structure and that the door is in a closed position, the controller transmits a signal to the motor to move the light source from the inactive to the active position. If humans are detected in the structure or if the door is detected open, then the controller deactivates or repositions the light source.

Abstract: The disclosed subject matter relates to a mixture that can facilitate preservation of animal scent, such as, e.g., doe pee; as well as to an apparatus and method for creating the mixture.

Abstract: Disclosed are systems and methods of preparing dialysate for use in a home dialysis system that is compact and light-weight relative to existing systems and consumes relatively low amounts of energy. The method includes coupling a household water stream to a dialysis system; filtering the water stream; heating the water stream to at least about 138 degrees Celsius in a non-batch process to produce a heated water stream; maintaining the heated water stream at or above at least about 138 degrees Celsius for at least about two seconds; cooling the heated water stream to produce a cooled water stream; ultrafiltering the cooled water stream; and mixing dialysate components into the cooled water stream in a non-batch process.

Abstract: A method of controlling floating virus infection. The method includes the step of: supplying chlorine dioxide gas into a space where floating virus can be present by a gas concentration which allows the animal to live or stay, but deactivates the virus.

Abstract: According to embodiments of the invention, a selective ultraviolet disinfection method is provided. The method includes selecting operating parameters for an ultraviolet disinfection process of flowing liquid carrying first and second types of entities to affect the first type of entities while the second type of entities remains intact, illuminating the liquid with ultraviolet light according to the operating parameters and continuously adjusting the operating parameters based on real-time measurements of ultraviolet transmission and flow rate of the liquid.

Abstract: Methods and systems for reduced temperature radiation sterilization of stents are disclosed.

Abstract: An objective of the present invention is to provide an antifreeze protein which is capable of being efficiently produced on an industrial level at low cost and which is safe and has an excellent antifreezing activity for use on a practical level. Also, an objective of the present invention is to provide a polypeptide that corresponds to the active part of the antifreeze protein; a composition, a food, a biological sample protectant and a cosmetic containing the antifreeze protein or the polypeptide; and an antibody that specifically reacts with the antifreeze protein or the polypeptide. The antifreeze protein according to the present invention is characterized in being derived from a plant and having a specific amino acid sequence or being a plant seed protein.

Abstract: An apparatus for indicating biological content within a container is provided. The apparatus includes a medical sterilization container having a cover removably attached to the medical sterilization container. An enclosable, sterilizable interior compartment is formed by the medical sterilization container and the cover, wherein the interior compartment is sized to house at least one medical instrument. A biological indicator is located at least partially in communication with the interior compartment, wherein the biological indicator provides at least one indication of biological content within the interior compartment after the medical sterilization container and cover are subjected to a sterilization process.

Abstract: The invention relates to a technique of disinfecting household and industrial waste water used as the basis of organo-mineral fertilizers. The present method of disinfection is carried out by means of quick vacuum-pulse actions on sewage sludge using a receiver and quick response valves, with a pulse duration of less than 1.0 seconds at a pressure of not more than 20 mmHg to achieve the required degree of disinfection. Technical result of the use of the invention is to accelerate and simplify the process of disinfection method.

Abstract: The present application is directed to methods of sterilizing bendamustine and its pharmaceutically acceptable salt forms. Preferred sterilization methods include dry heat sterilization, gamma irradiation, and e beam radiation. Sterile pharmaceutical compositions are also described.