Patent classifications
A61L2/0023
TREATING CATALYTICALLY OXIDIZED NANOFIBRILLAR CELLULOSE HYDROGEL
The invention relates to a method for treating a nanofibrillar cellulose hydrogel, wherein the method comprises the steps of: providing a nanofibrillar cellulose hydrogel, wherein the nanofibrillar cellulose is oxidized nanofibrillar cellulose, wherein the oxidation has been carried out through N-oxyl mediated catalytic oxidation of cellulose-based raw material, and has at most 50 μmol of aldehyde groups per gram of dry nanofibrillar cellulose; and subjecting the nanofibrillar cellulose hydrogel to a heat treatment.
DEVICES FOR APPLYING A TOPICAL TREATMENT
A device comprising a housing having a handle end and a treatment end. The treatment end is configured to provide an antimicrobial treatment and a heat treatment. The treatment end comprises an applicator having an applicator surface for providing at least the heat treatment. The device includes a heat generation unit configured to heat the applicator surface in use, a source of antimicrobial agent, and a control unit operatively connected to at least the heat generation unit for controlling the heat generation unit. The device can be a hand-held device and used to apply topical treatment to a treatment area of a subject.
HEAT-STERILIZED FORMULATION COMPRISING CHITOSAN AND PROCESS OF PREPARATION THEREOF
The present invention relates to a heat-sterilized aqueous composition comprising a solubilized chitosan and glycerol. It also relates to a process of preparation of the same, as well as the use thereof, including compositions useful for the prevention and treatment of dry eye syndrome and arthritic diseases or disorders.
Method for Filtering Fibrinogen
Disclosed is a method for filtering a fibrinogen composition, comprising the following steps: a) purifying the fibrinogen composition by chromatographic purification using an elution buffer comprising arginine; b) optionally, at least one step of filtering the fibrinogen composition obtained by chromatographic elution in step a), on a filter having a pore size of between 0.08 μm and 0.22 μm, c) filtering the fibrinogen composition obtained by chromatographic elution in step a), or optionally obtained in step b), on a symmetrical filter having a pore size of between 15 nm and 25 nm, and preferably between 18 nm and 22 nm, and d) recovering the resulting fibrinogen solution, the filtering method being carried out without adding arginine after step a), at a high capacity and without a prior freezing and/or thawing step.
Waste destruction device
A device for converting harmful waste products into environmentally friendly discharge is provided. The discharge, as a result of the waste destruction process, meets or exceeds the Environmental Protection Agency (EPA) standards. The device includes a waste disposal chamber where a crucible is positioned. The crucible is configured to retain a removable basket that is heated via induction heating. The waste residing within the removable basket is then vaporized and ionized within a vacuum to form a waste gas that is drawn through an accelerated jet of thermal plasma via vacuum suction. Once the waste gas passes through the plasma, it passes through a discharge duct where it is condensed by a heat exchanger and exhausted into the environment surrounding the device.
PERITONEAL DIALYSATE FLUID GENERATION SYSTEM
Systems and methods of generating peritoneal dialysate are provided. The systems and methods use a water purification module, a sterilization module and concentrates to prepare a bolus of peritoneal dialysate from source water for use with an non-integrated cycler.
STERILIZATION COMPOSITIONS AND METHODS
A biological indicator is provided for measuring the effectiveness of a sterilization procedure. The biological indicator comprises a carrier having a microorganism and at least one of a humectant, anti-agglomerating agent or surfactant disposed thereon, the carrier having a solidity of greater than 5%. Various embodiments of a device, kits and methods are disclosed.
Process and unit for harvesting and processing water hyacinths
Method for harvesting and processing water hyacinths, characterized in that the following steps are performed: a) the water hyacinths growing in an aquatic medium are cut; b) the water hyacinths are collected on board a barge at berth (1); c) the collected water hyacinths are transferred onto draining racks (2) near the quayside; d) the drained hyacinths are washed with clean water; e) the washed water hyacinths are drained on vibrating belts (7) in order to remove some of the excess water; f) the water hyacinths are dried on a dryer (8) at a temperature of between 50 and 100° C. for 5 to 17 h; g) the water hyacinths and their seeds are steam-sterilised at a temperature of between 80 and 100° C. in order to sterilise them; h) the sterilised water hyacinths and seeds are ground in order to make profitable use thereof.
Heat sterilization techniques for chlorhexidine based antiseptic formulations
Techniques for sterilizing chlorhexidine based antiseptic formulations include exposing a sealed container containing the formulation to heat at a temperature and heating time sufficient to sterilize the chlorhexidine based antiseptic formulation and the hermetically sealed interior of the container, which may be an applicator, a bottle, a swab stick, or a pad-containing pouch.
STEAM STERILIZATION OF HYDROGELS CROSSLINKED BY BETA-ELIMINATIVE LINKERS
Methods for the steam sterilization of hydrogels crosslinked with a beta-eliminative linker without the drawback of significant degradation are provided.