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1917 results about "Glutaraldehyde" patented technology

Glutaraldehyde, sold under the brandname Cidex and Glutaral among others, is a disinfectant, medication, preservative, and fixative. As a disinfectant, it is used to sterilize surgical instruments and other areas of hospitals. As a medication, it is used to treat warts on the bottom of the feet. Glutaraldehyde is applied as a liquid.

Processes for removing cells and cell debris from tissue and tissue constructs used in transplantation and tissue reconstruction

Methods for decellularizing mammalian tissue for use in transplantation and tissue engineering. The invention includes methods for simultaneous application of an ionic detergent and a nonionic detergent for a long time period, which may exceed five days. One method utilizes SDS as the ionic detergent and Triton-X 100 as the nonionic detergent. A long rinse step follows, which may also exceed five days in length. This long duration, simultaneous extraction with two detergents produced tissue showing stress-strain curves and DSC data similar to that of fresh, unprocessed tissue. The processed tissue is largely devoid of cells, has the underlying structure essentially intact, and also shows a significantly improved inflammatory response relative to fresh tissue, even without glutaraldehyde fixation. Significantly reduced in situ calcification has also been demonstrated relative to glutaraldehyde fixed tissue. Applicants believe the ionic and non-ionic detergents may act synergistically to bind protein to the ionic detergent and may remove an ionic detergent-protein complex from the tissue using the non-ionic detergent. The present methods find one exemplary use in decellularizing porcine heart valve leaflet and wall tissue for use in transplantation.
Owner:UEDA YUICHIRO +1

Method for treatment of biological tissues to mitigate post-implantation calcification and thrombosis

A method of treating a biological tissue including contacting the biological tissue with an aqueous sterilizing solution, and maintaining the aqueous sterilizing solution at a temperature of about 50° C. for a time period of about 1 to 2 days. The method of treating a biological tissue may be utilized as a terminal sterilization step in a method for fixation of biological tissues, and bioprosthetic devices may be prepared by such fixation method. The fixation method may include the steps of A) fixing the tissue, B) treating the tissue with a mixture of i) a denaturant, ii) a surfactant and iii) a crosslinking agent, C) fabricating or forming the bioprosthesis (e.g., forming the tissue and attaching any non-biological components thereto) and D) subjecting the bioprosthesis to the terminal sterilization method. The aqueous sterilizing solution may be glutaraldehyde of about 0.625 weight percent buffered to a pH of about 7.4.
Owner:EDWARDS LIFESCIENCES CORP

Polyvinyl alcohol/chitosan nano fiber film dressing containing nano silver and preparation thereof

The invention relates to a polyvinyl alcohol / chitosan nano fiber film dressing containing nano silver and preparation thereof. The nano fiber film dressing is prepared by the following steps: taking a mixture of polyvinyl alcohol and chitosan as the base material, then mixing nano silver into the polyvinyl alcohol / chitosan nano fiber film through an electrostatic spinning technology, and finally adding glutaraldehyde to crosslink the nano fiber film so as to obtain the target product. The obtained dressing has the characteristics that the preparation technology is simple; a wet environment can be achieved for promoting wound healing; and the dressing has an antiseptic function.
Owner:WUYI UNIV

Method for preparing protein magnetic blotting nanospheres

InactiveCN101347721AAvoid complicated centrifugationSimplified centrifugation processOther chemical processesPolymerSerum protein
The invention relates to a preparation method of a protein magnetic imprinting nano sphere, in particular to a preparation method of a protein magnetic imprinting nano sphere which takes one of hemoglobin, muramidase or serum protein as template molecules; the preparation method includes the following steps: synthesizing magnetic nano particles which are Fe3O4 nano particles covered with silicon dioxide on the surfaces; carrying out silanization to the amino-groups on the surface of the magnetic sphere; using glutaric dialdehyde to connect protein; using silylation agent to fix the space structure of template protein; alkaline eluting the protein on the surface of the magnetic sphere to form imprinting sites. The hemoglobin, muramidase or serum protein magnetic nano imprinting polymer sphere prepared by the invention combines the precise and specific identification property of molecular imprinting and the quick separation property of the magnetic nano sphere under the action of an external magnetic field, integrates the advantages of molecular imprinting and the magnetic nano sphere, avoids complex centrifugation operation, plays vital roles in the separation of cells, protein and nucleic acid, the detection of biomolecules, tumor diagnosis and medicine targeting therapy and has promising application prospect in the field of isolation analysis.
Owner:NANKAI UNIV

Preparation method and application of magnetic silicon dioxide composite microsphere

The invention relates to a preparation method and application of a magnetic silicon dioxide composite microsphere. Superparamagnetic ferroferric oxide nano particles of which the diameter ranges from 4 nm to 30 nm are prepared through a high-temperature pyrolysis method, a silicon dioxide shell of which the thickness ranges from 5 nm to 20nm covers the outer surfaces of the magnetic ferroferric oxide nano particles through a reverse microemulsion method, amination modification is conducted on the silicon dioxide surface, glutaraldehyde is used as a crosslinking arm, ligand protein is connected into, and protein separation is conducted through specific binding of ligand protein and target protein. The prepared magnetic microsphere is small in particle diameter and good in monodispersity, the composite microsphere with amine is large in specific surface area, nucleophilic addition is utilized, after the crosslinking arm glutaraldehyde is connected into, multiple kinds of ligand protein can be connected into, and then multiple kinds of target protein can be separated. The method is suitable for rapid separation and application of protein in biological samples, and has wide application prospect and great application value in the biomedical field and other fields.
Owner:HARBIN YICAI NEW MATERIAL

Biological-degradable chitosan porous hemostasis material and its preparing method

The invention supplies a biodegradable nanometer channel multi orifice stanching material and manufacturing method which uses chitosan as raw material. It includes orifice making, forming, orifice making agent removing. The multi orifice structure can be gained by adding orifice making agent in preparation, removing it in forming, which emulsifies to form latex, solidifies to form hydrogel, removes the agent by alcohol or ketone solvent, dries the hydrogel, or processes cross linking for the formaldehyde, glutaraldehyde, solidifies chitosan aqueous solution to form hydrogel, removes the agent by water, dries the hydrogel. This material can fast adsorb the moisture in the blood to stanch.
Owner:南京零一新材料工程研究中心(普通合伙) +1

PVA hydrogel-based photo-thermal evaporation material and preparation and application thereof

The invention relates to a PVA hydrogel-based photo-thermal evaporation material and preparation and application thereof. The preparation method comprises the following steps: step 1, respectively preparing an aqueous polyvinyl alcohol (PVA) solution, an aqueous nanometer photo-thermal material dispersion solution, an aqueous glutaraldehyde solution and a low-concentration hydrochloric acid solution; 2, fully mixing and stirring the aqueous PVA solution, the aqueous nanometer photo-thermal material dispersion solution, the aqueous glutaraldehyde solution and the low-concentration hydrochloricacid solution in the step 1 according to a certain sequence under a certain temperature condition; and 3, transferring the mixed and stirred product into a forming mold when the mixed and stirred product is not cured, and carrying out standing until a cross-linking reaction is complete, thereby obtaining the hydrogel material. The preparation method disclosed by the invention has the beneficial effects that preparation process is environment-friendly, pollution-free, simple and feasible; preparation cost is low; the obtained hydrogel can be used as an ideal photo-thermal evaporation and solarseawater desalination material; and the prepared hydrogel has high light absorption efficiency, photo-thermal conversion efficiency and evaporation efficiency, and can be applied to the field of solarseawater desalination.
Owner:ZHEJIANG ZHENENG TECHN RES INST +1

Metal-organic framework supported heteropoly acid catalyst for synthesizing glutaraldehyde and production method of metal-organic framework supported heteropoly acid catalyst

The invention relates to a metal-organic framework supported heteropoly acid catalyst for synthesizing glutaraldehyde and a production method of the metal-organic framework supported heteropoly acid catalyst. The catalyst is prepared by a one-step synthesis method, namely a heteropoly acid component with catalytic oxidation activity is introduced into a duct of a metal-organic framework material UiO-66 in the process of synthesizing the metal-organic framework material UiO-66. The catalyst has the characteristics that the catalyst has a crystal framework structure, the active component is highly dispersed, and the heteropoly acid is over-high in load. The catalyst is applied to catalytic selective oxidation reaction of cyclopentene, so that the selectivity and the yield of the glutaraldehyde is greatly improved; the numerical value is much higher than the reported homogeneous catalysis level; and the metal-organic framework supported heteropoly acid catalyst has important industrial application value.
Owner:HENAN UNIVERSITY OF TECHNOLOGY

Composite type mercury ion adsorbent and preparation method thereof

The invention relates to a composite type mercury ion adsorbent and a preparation method thereof. The adsorbent consists of chitosan, polyvinyl alcohol and clay. A polyvinyl alcohol macromolecular chain and a chitosan macromolecular chain are penetrated and wound mutually by high-speed stirring, so that the inorganic clay is dispersed fully; and the release of the chitosan and the polyvinyl alcohol in the process of using the adsorbent is avoided effectively by a method of combining cross linking agent cross linking and freezing crossing linking of glutaraldehyde. The adsorbent has high adsorption capacity and high adsorptive selectivity on Hg(II) ions, hardly adsorbs Cd(II) and Pb(II) ions, and adsorbs a small amount of Cu(II) ions, and can be recycled, and adsorbability of the adsorbentis slightly influenced by the pH value of a solution. The integral preparation process is performed in an aqueous solution, the preparation method is simple and convenient, low in energy consumption,low in production cost, environment-friendly, and easy to industrialize, and special process equipment is avoided.
Owner:XINJIANG TECHN INST OF PHYSICS & CHEM CHINESE ACAD OF SCI

ECL (electrochemiluminescence) immunosensor for detecting tumor markers and preparation method and applications thereof

The invention discloses an ECL (electrochemiluminescence) immunosensor for detecting tumor markers and a preparation method and applications thereof. The immunosensor comprises a working electrode, a reference electrode and a counter electrode, wherein the working electrode is a gold electrode, cysteamine, glutaraldehyde, a tumor marker first-antibody, a tumor marker, and a composite functionalized nanosphere are sequentially decorated on the surface of the gold electrode, the composite functionalized nanosphere is simultaneously marked by a tumor marker second-antibody and an ECL marker, and non-specific active sites are closed by using bovine serum albumins. The preparation method comprises the steps of preparing the gold electrode on which the tumor marker first-antibody is fixedly carried; synthesizing the composite functionalized nanosphere simultaneously marked by the tumor marker second-antibody and the ECL marker; and finally, assembling the obtained gold electrode and the composite functionalized nanosphere into an ECL immunosensor. The ECL immunosensor disclosed by the invention is high in sensitivity, rapid in analysis speed, strong in stability and selectivity, good in reproducibility, easy to operate, and flexible in method.
Owner:NINGBO UNIV

Formula and method for immobilizing tick sample for scanning electron microscopy

The invention relates to a formula and method for immobilizing a tick sample for scanning electron microscopy, which belongs to the technical field of methods for immobilizing samples for scanning electron microscopy. The immobilization formula comprises a PBS buffer solution, polysorbate and glutaraldehyde, and a glutaraldehyde immobilization liquid is prepared from the above-mentioned components. The method comprises the following steps: (1) observing whether host tissue is left in basis capituli of the tick sample and if so, removing the host tissue; (2) cleaning the surface of the tick sample; (3) immobilizing the tick sample at room temperature by using the glutaraldehyde immobilization liquid; (4) carrying out gradient dehydration with ethanol on the immobilized tick sample; (5) putting the tick sample into mixed liquor of absolute ethyl alcohol and acetone for displacement, and then putting the tick sample into acetone for displacement; and (6) drying the tick sample in a vacuum freeze drying instrument for drying and spraying gold on the tick sample. During scanning electron microscopic observation, the phenomenon of fuzzy and foggy images or incapable imaging due to ionization discharging of the sample as water vapor produced after electron beam bombardment of the sample encounters high-energy electron streams is prevented.
Owner:XINJIANG AGRI UNIV

Macroreticular polyvinyl alcohol bead carrier and preparation thereof

The invention provides a method for preparing a macroporous reticulated polyvinyl alcohol spherical vector. The method comprises the following steps: firstly, polyvinyl alcohol, calcium carbonate, sodium alginate and water are mixed in a certain mass proportion, and stirring is performed for full dissolution of the polyvinyl alcohol and uniform mixture, and then white PVA sol is obtained; secondly, the sol obtained is added into saturated boric acid solution containing 3 percent of calcium chloride by a peristaltic pump, and PVA gel beads are formed, cleaned by water and then placed into diluted hydrochloric acid solution for dipping until no air bubble is generated; thirdly, a spherical vector is thrown into glutaral pentanedial water solution and adjusted into acidity so as to generate crosslinking reaction to form a more stable crosslinking structure; and fourthly, the spherical vector is dipped into water and cleaned into neutrality, and then the white macroporous reticulated PVA spherical vector with elasticity is obtained. The macroporous reticulated polyvinyl alcohol vector prepared by the method has stable macroporous reticulated structure and good hydrophilicity, physical and chemical stability and anti-biological degradability, is suitable for immobilized enzymes and microorganisms so as to form a plurality of bed-shaped bioreactors, and is used in the modern bioengineering field such as sewage treatment and so on.
Owner:LANZHOU UNIVERSITY

Microcapsule sustained release agent and preparation method and application thereof

The invention provides a microcapsule sustained release agent and a preparation method and application thereof. The microcapsule sustained release agent is prepared by embedding essence with gelatin and Arabic gum, and is applied to sanitary towels or sanitary cushions or panty-shape diapers or pet cushions. The microcapsule sustained release agent consists of a core material and a wall material, wherein the wall material consists of natural high molecular gelatin, Arabic gum and a curing agent; the core material consists of essence and essential oil; the curing agent consists of tannic acid and glutaraldehyde; and microencapsulation is performed on the core material and the wall material in the ratio 1:2. The invention further provides a preparation method of the microcapsule sustained release agent. The preparation method comprises the following steps of: adding an emulsifier into Arabic gum for mixing; adding essence or essential oil into an emulsion for homogenizing and emulsifying; adding a gelatin solution into the emulsified emulsion; agglomerating into a capsule; curing with a curing agent; and drying to obtain a high-dispersity microcapsule sustained release agent. By adding the microcapsule sustained release agent into the space between a skin contact layer and a water-absorbing layer of a sanitary towel or sanitary cushion or panty-shape diaper or pet cushion, the effect of keeping fragrance for a long time can be achieved.
Owner:TIANJIN SINOSH NEW MATERIAL TECH
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