1052 results about "Saline" patented technology

A method for treating congestive heart failure (CHF) has been developed that restores kidney renal functions by artificial vasodilation of at least one kidney. A vasodilator drug is locally delivered to the kidney via a kidney perfusion catheter. The drug can be mixed with the patient's blood, saline or other suitable solvent and the mixture directly applied to the kidney through the catheter. The restoration of kidney function assists the heart by removing excess fluid, urine and toxin from the patient, and by normalizing the patient's renin-angiotensin system and other neurohormonal substances. The method is applicable to treat chronic and acute CHF.

A waste collection and disposal system for use in health care facilities is provided. The system includes a mobile waste collection unit for moving between use areas in the health care facility to collect waste material generated during medical procedures including body fluids, body tissues, saline, etc. The waste collection unit includes stacked upper and lower waste containers for receiving the waste material. During use, the upper waste container can be emptied into the lower waste container for temporary storage. In addition, different vacuum levels can be provided in the waste containers during complex procedures. Once a user desires to empty the waste collection unit, the waste collection unit is wheeled to a docking station. At the docking station, the waste material is off-loaded to a waste drain and the waste collection unit is cleaned and rinsed for further use.

An injectable and moldable putty comprising biodegradable calcium-based compounds including calcium sulfate, hydroxyapatite, and tricalcium phosphate is invented. The putty hardens into a solid body when mixed with water, saline, serum, or other neutral aqueous solutions. The hardening time of the putty can be tailored in order to meet the specific requirements of various dental or orthopedic applications. The pH of the putty is neutral during and after mixing. The invented putty may be used as bone graft, bone implant, or implantable drug delivery device.

An IV pole mountable, therapeutic infusate processing device is incorporated into a hypothermia system to receive therapeutic fluid(s), such as normal saline, peritioneal dialysis solution, or other crystalloid solution, to heat such therapeutic fluid(s) a few degrees centigrade above normal body temperature and to direct the resulting heated infusate to and through a selected anatomical portion of a patients body to raise the temperature of that body portion so as to affect any cancerous or other tumors that may be located therein. The processing device is provided with touch screen controls and visual indicators to facilitate its proper use; while the system further includes temperature and pressure sensors to monitor the hyperthermia processing to insure patient safety.

The invention relates to a method and device intelligently identifying characteristics of images collected by a colposcope. Automatic extraction and identification are conducted on a normal saline test colposcope original image red characteristic, an original image green light image blood vessel distribution characteristic and an acetic acid test image white epithelium distribution characteristic; the central position of a cervical opening is positioned through an identifier shape easy to identify, the identifier shape and the position can be automatically identified, and therefore the characteristic images are distributed in four quadrants , the identifiability of the images is improved, the extracted characteristics are presented in a direct and visible mode on this basis. According to the method and device intelligently identifying characteristics of the images collected by the colposcope, a method of the combination of automatic image characteristic identification and automatic image characteristic display is adopted, the complexity of judging and reading of the images is simplified, the amount of information of judging and reading of the images is enriched, the image characteristics which are direct, visible and easy to identify are provided for a doctor, the precision, the uniformity and the repeatability of an image judgment, reading and assessing method are improved, and the dependence on subjective experience is reduced.

The invention discloses a water-in-oil-in-water adjuvant vaccine and a preparation method thereof. The adjuvant vaccine is composed of an internal water phase, a middle oil phase used for cladding the internal water phase, and an external water phase for cladding the middle oil phase. The external water phase comprises: a composite surfactant, a hydrophilic surfactant and mormal saline. The middle oil phase consists of: a lipophilic surfactant, a stabilizer and mineral oil. The internal water phase comprises: an immunopotentiator solution, the hydrophilic surfactant, and an inactivated antigen solution. The W/O/W (water-in-oil-in-water) type adjuvant vaccine provided in the invention can induce an immunoreaction earlier than traditional W/O (water-in-oil) type adjuvant vaccines, and can make experimental animals obtain earlier protective antibodies. The vaccine has good absorption, and causes a small inflammatory response at an inoculation site. The adjuvant vaccine disclosed in the invention has better stability than existing W/O/W type vaccines, and the antibody generation speed is fast.

The present invention discloses one kind of folic acid acceptor targeting liposome as medicine carrier and its preparation process and application. The liposome has components including synthetic phospholipid, cholesterol, folic acid acceptor targeting anchor point and polyglycol hydrating anchor point. The present invention has relatively simple preparation process, and can prepare liposome of size smaller than 200 nm in large scale and prepare freeze dried powder of weak alkali medicine, including leurocristine, etc. carried on the liposome with greatly raised use convenience and stability. The medicine is re-constructed with bacteria-free water or brine before use, and the medicine leakage rate is lower than 10 %.

The present invention provides compositions and formulations of micronized Wharton's jelly having a controlled viscosity such that when delivered to the injured region of a subject, it remains substantially localized with little or no migration out of the injured region for the repair and/or regeneration thereof. Micronized Wharton's Jelly can be suspended in a pharmaceutically acceptable aqueous carrier, such as saline, sterile water, or any suitable buffer, to form a suspension or a gelatinous gel composition, or it can be in the form of a paste, suitable for delivery into the space adjacent the articular surface cartilage injured region of a subject. The micronized Wharton's jelly when employed at sufficient concentrations can be hydrated into a gel or paste and administered topically, or it can be injected into the body through the use of a needle and syringe. Accordingly, micronized Wharton's Jelly, compositions, or formulations thereof, can be delivered in a manner that is more convenient than Wharton's jelly that has not been micronized in accordance with the present invention.

The invention discloses a culture method, application and a combined preparation of a hypoxia mesenchymal stem cell. By adopting an umbilical or placenta mesenchymal stem cell and combining the means of transfusing compound amino acid injection and the like, the vitality, the implantation survival rate and the treating effect of the mesenchymal stem cell in vivo can be improved; and in order to avoid the possibility of conglutination, conglomerating and cell mass embolism of the mesenchymal stem cell in blood vessel, the matching of saline containing heparin during treatment can be carried out by a mode of intravenous injection or intravenous drip. With more than three times of treatment, physical conditions of curee can be remarkably improved and objective indicators such as immunity, blood fat, blood sugar and the like can be remarkably improved.

The invention provides a deer spleen extract preparation and a preparation method thereof. The preparation method comprises the following steps of: adding water or normal saline or buffer solution into deer spleen, mashing with a colloid mill, performing enzymolysis, centrifuging, taking supernate, concentrating, and performing spray drying to obtain dry powder, wherein the dry powder can be mixed with other one or more Chinese medicaments to prepare a compound preparation, and the dry powder is prepared by the same method; and adding accessories acceptable in health-care food into the dry powder, and thus obtaining the oral preparation facilitating oral administration. The preparation has health-care functions of assisting in improving human immunity and the like; and the waste deer spleen is changed into valuable, so that the utilization rate of the deer spleen is improved.

A reverse-osmosis polyamide member is prepared through providing the aqueous solution of lentine and piperazine, immersing the porous carrier in it to have a liquid layer on it, and single-surface contacting with the organic solution of symphenyl triformyl chloride for interface polymerizing reaction. Said reverse osmosis membrane can be used to treat the saline for removing either impurity (SO4 ions) or NaCl in different condition, having high selectivity.

A water-preserving agent resisting to saline and alkali is prepared from acrylic acid, acrylamide and attapulgite through graft copolymerizing under existance of trigger, cross-linking, washing, drying and pulverizing.

The invention provides an injectable mineralized collagen bone repair material and a preparing method. The bone repair material is prepared from mineralized collagen, collagen, calcium phosphate particles and an antiwashout agent. The preparing method for the material comprises the steps of preparing mineralized collagen powder; dissolving the antiwashout agent; swelling the collagen; carrying out blending; carrying out mould filling and freeze drying; carrying out cross-linking; carrying out grinding and screening. The bone material can be mixed with autoblood, marrow, normal saline and the like, has a good shape after being kneaded, is formed into dough, and has good cohesiveness, injectability and an antiwashout property. The material can be transplanted into a bone defect part in an injected or open operation mode, has good biocompatibility, promotes new bone generation, and can be used in the bone defect of a non-bearing part, path nailing, tooth fossa pulling, interbody fusion cage interior filling, autogenous bone fragment bonding and prefabricated and formed bone material gap supplementing materials. The bone material can carry antibiotic drugs and has a slow-release effect.

The invention provides a scale and corrosion inhibitor and application of the scale and corrosion inhibitor in a salt draining closed conduit of a saline and alkaline land. The scale and corrosion inhibitor comprises the components in parts by weight: 26-29 parts of ursolic acid, 15-18 parts of rosmarinic acid, 4-6 parts of trifluoroacetic acid, 6-8 parts of bis-1,6-hexylidenetriamine pentamethylene sodium phosphonate, 3-5 parts of thionothiolic acid, 1-3 parts of mannitol, 8-12 parts of polyepoxysuccinic acid, 6-9 parts of sodium benzotriazole, 2-4 parts of propyl hydroxybenzoate and 50-60 parts of water, wherein the purity of ursolic acid is 98%; the purity of rosmarinic acid is 95%; and the solid content of sodium benzotriazole is 40%. By using the scale and corrosion inhibitor provided by the invention, the corrosion rate, which is 0.0006-0.0009 mm/a, of the salt draining closed conduit is obviously reduced, and the service life of the salt draining closed conduit can be prolonged by 10 years.

The invention discloses a water-absorbing acrylate foam material and a preparation method and application thereof. The prepared water-absorbing acrylate foam material has a certain toughness and is small in foam hole size and suitable for dispersing and storing waterborne fluid, the average deionized water absorption rate, average saline water absorption rate, average artificial urine absorption rate and average artificial blood absorption rate are larger than 15g/g, and the water retention rate within half an hour is over 80 percent. Therefore, the massive soft water-absorbing material is applied to the field of hygienic products.

The invention relates to a nasal spray preparation for resisting respiratory virus infection. The preparation comprises liposome-loaded angiotensin converting enzyme 2 (ACE2) recombinant protein, sialic acid, natural polysaccharide and normal saline. The nasal spray preparation is mainly prepared from the liposome-loaded ACE2 extracellular domain recombinant protein, can competitively inhibit thecombination of viruses and host cells, prevents and treats respiratory tract infection caused by various viruses, and enhances the antiviral range and clinical indications of the nasal spray preparation for resisting respiratory tract virus infection. In addition, the nasal spray preparation can be used for directly spraying medicines to virus propagation parts, and is convenient and simple to use.