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396 results about "Succinimides" patented technology

A subclass of IMIDES with the general structure of pyrrolidinedione. They are prepared by the distillation of ammonium succinate. They are sweet-tasting compounds that are used as chemical intermediates and plant growth stimulants.

Crosslinked gels comprising polyalkyleneimines, and their uses as medical devices

One aspect of the present invention generally relates to methods of sealing a wound or tissue plane or filling a void splace. In a preferred embodiment, the wound is an ophthalmic, pleural or dural wound. In certain instances, the compositions used to seal the wound or tissue plane comprises a polyalkyleneamine. In a preferred embodiment, the polyalkyleneamine is polyethyleneimine. Treatment of the polyethyleneimine with a cross-linking reagent causes the polyethyleneimine polymers to polymerize forming a seal. In certain instances, the cross-linking reagent is a polyethylene glycol having reactive terminal groups. In certain instances, the reactive terminal groups are activated esters, such as N-hydroxy succinimide ester. In certain instances, the reactive terminal groups are isocyanates. In certain instances, the polyethyleneimine has a lysine, cysteine, isocysteine or other nucleophilic group attached to the periphery of the polymer. In certain instances, the polyethyleneimine is mixed with a second polymer, such as a polyethylene glycol containing nucleophilic groups. In certain instances, the compositions used to seal the wound or tissue plane are formed by reacting a polyalkyleneamine bearing electrophilic groups with a cross-linking reagent containing nucleophilic groups. In certain instances, the electrophilic groups on the polyalkyleneamine are activated esters, such as N-hydroxy succinimide ester. In certain instances, the compositions used to seal the wound or tissue plane are formed by reacting a polyalkyleneamine bearing photopolymerizable groups with ultraviolet or visibile light. Compositions used to seal the wound which contain PEI or a derivative of PEI are found to adhere tightly to the tissue. Other aspects of the present invention relate to methods of filling a void of a patient or adhering tissue. In certain instances, the methods use a polyalkyleneamine. In a preferred embodiment, the polyalkyleneamine is polyethyleneimine. Another aspect of the present invention relates to a polymeric composition formed by exposing a polyalkyleneamine to an activated polyalkylene glycol. In certain instances, the composition is attached to mammalian tissue.
Owner:SQUARE 1 BANK

Novel bio-medical adhesive and preparation method thereof

The invention discloses a bio-medical adhesive, which can be cross-linked with a wound in situ, and a preparation method of the bio-medical adhesive. The preparation method is characterized by comprising the steps of first, preparing oxidized sodium alginate by using sodium periodate to oxidize sodium alginate; dissolving the oxidized sodium alginate in an MES (Methyl Ester Sulfonate) buffer solution, dissolving 1-(3-dimethyl aminopropyl)-3-ethyl carbodiimide hydrochloride and N-hydroxyl succinimide in the MES buffer solution as well under nitrogen protection, continuously adding dopamine, carrying out dialyzing and freeze-drying after reacting for 8 to 24 hours, and obtaining A liquid by dissolving a reaction product in a PBS (Phosphate Buffer Solution) or a sodium borate solution; then, dissolving I-shaped collagen in an acid solution, and obtaining B liquid by neutralizing the solution pH (potential of Hydrogen) to be 5 to 8; firstly pre-treating the wound by using hydrogen peroxide or HRP (Horse Radish Peroxidase) before the bio-medical adhesive is used, then immediately coating the wound with the bio-medical adhesive after mixing the A liquid with the B liquid, and forming gel in 30 to 120 s, wherein the gel is firmly adhered to the surface of the wound. The bio-medical adhesive disclosed by the invention has a stronger adhesive force under a moist environment in vivo, integrates filling, sealing and bleeding stopping functions, is good in biocompatibility, is bio-degradable and can be used for promoting wound healing.
Owner:SICHUAN UNIV

Preparation of CT/MRI dual-modality imaging contrast agent based on dendrimer

The invention relates to a method for preparing a computed tomography (CT)/magnatic resonance imaging (MRI) bimodal imaging contrast agent based on dendrimers. The method comprises the following steps of: (1) adding DOTA-N-hydroxy succinimide (NHS) solution into the fifth generation of poly(amidoamine) (PAMAM) dendrimer solution, adding methoxy poly(ethylene glycol) (mPEG)-COOH solution which is subjected to 1-ethy 1-3-[3-dimethylaminopropyl] carbodiimide hydrochloride (EDC) activation, reacting with stirring, and thus obtaining functionalized dendrimer solution; (2) adding chloroauric acid solution and sodium borohydride solution into the functionalized dendrimer solution, reacting with stirring, adding gadolinium nitrate solution, stirring, adding triethylamine and acetic anhydride, andreacting with stirring for 8 to 24 hours; and (3) dialyzing the solution obtained in the step (2), performing freeze drying treatment, and thus obtaining the contrast agent. The method has a simple preparation process, and experimental conditions are realized at normal temperature and under normal pressure; and the CT/MRI bimodal imaging contrast agent prepared by the method has a good CT/MRI effect, and a favorable foundation is laid for the development of a novel multifunctional contrast agent.
Owner:DONGHUA UNIV

Composite gold nanorod carrier having photo-thermal/photodynamic therapy treatment performance and preparation method thereof

The invention provides a composite gold nanorod carrier having photo-thermal/photodynamic therapy treatment performance and a preparation method thereof. The composite gold nanorod carrier uses a gold nanorod as a core and uses silicon dioxide as a shell layer, a near infrared fluorescent dye for photodynamic therapy is modified on the outer surface of the shell layer. The preparation method comprises the steps that a chloroauric acid solution and a cetyl trimethyl ammonium bromide solution are mixed, a sodium borohydride ice water mixed solution is added to obtain a nano gold seed solution A; a silver nitrate solution and a chloroauric acid solution are added to a binary surface active agent solution, a hydrochloric acid is added after reaction to obtain a solution B, then ascorbic acid and the solution A are added, and a gold nanorod is obtained after reaction; a tetraethoxysilane methanol solution and an aminopropyl trimethoxy silane methanol solution are added to a gold nanorod solution to obtain composite nanoparticles; 1-(3-dimethyl amino propyl)-3-ethyl carbodiimide hydrochloride is added to the near infrared fluorescent dye, then N-hydroxyl succinimide is added to obtain a solution C; the composite nanoparticle solution is mixed with the solution C to obtain a product.
Owner:XIAMEN UNIV

Magnetic biological probe and test strip for detecting hepatitis B virus (HBV) and preparation method and using method of biological probe

The invention discloses a magnetic nanoparticle biological probe and a test strip for detecting hepatitis B virus (HBV) and a preparation method and a using method of the biological probe. The method for preparing the biological probe comprises the following steps of: performing surface amino functionlization treatment on magnetic nanoparticles with the particle size of 50-300nm, performing carboxylation treatment, mixing and reacting the magnetic nanoparticles subjected to surface carboxylation, carbodiimide and N-hydroxy succinimide in a buffer solution, and washing to obtain a reactant A; mixing and reacting the reactant A and an antibody for a HBV marker in a coupled buffer solution to obtain a reactant B; mixing and reacting the reactant B and a solution of a compound containing amino, and washing to obtain the product. The biological probe is high in specificity, sensitive in signal and high in stability and is suitable for detecting multiple hepatitis B markers according to the selected targeting markers and matched antibodies. According to the test strip, an obtained magnetic signal can be subjected to secondary determination through visual inspection and MAR detection, the personal error can be greatly reduced, and the accuracy is high.
Owner:上海爱纳玛斯医药科技有限公司

Preparation method of in-tube solid-phase micro-extraction column

The invention discloses an in-tube solid-phase micro-extraction column and a preparation method thereof, and belongs to the technical field of analytic chemistry sample pretreatment. The in-tube solid-phase micro extraction column is composed of a quartz capillary tube and a graphene oxide coating layer, wherein the graphene oxide coating layer is fixed on the inner wall of the quartz capillary tube through chemical bonding. During preparation, the inner wall of the quartz capillary tube is successively washed with an acid, washed with an alkali and blown to dry by nitrogen, a toluene solution containing 3-aminopropyltriethoxysilane (APTES) is poured into the capillary tube, the capillary tube has both ends sealed and is placed in a water bath for reaction, then a graphene oxide aqueous solution activated by 1-ethyl-3-(3-dimethylaminopropyl)-carbide diimine/N-hydroxy succinimide (EDC/NHS) is poured into the capillary tube, the capillary tube has the both ends sealed and is subjected to a reaction in the water bath, the graphene oxide is allowed to be bonded to the quartz capillary tube wall, and the in-tube solid-phase micro-extraction column is obtained. The in-tube solid-phase micro-extraction column has simple and rapid preparation method, allows the graphene coating layer to have good chemical property, mechanical property and thermal stability, has high extraction capacity and long service life, and has broad application prospects in the analytic chemistry and environmental analysis fields.
Owner:DALIAN UNIV OF TECH
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