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154 results about "Intracellular ferritin" patented technology

Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. The protein is produced by almost all living organisms, including algae, bacteria, higher plants, and animals.

High throughput multi-antigen microfluidic fluorescence immunoassays

The development of a high-throughput multi-antigen microfluidic fluorescence immunoassay system is illustrated in a 100-chamber PDMS (polydimethylsiloxane) chip which performs up to 5 tests for each of 10 samples. Specificity of detection is demonstrated and calibration curves produced for C-Reactive Protein (CRP), Prostate Specific Antigen (PSA), ferritin, and Vascular Endothelial Growth Factor (VEGF). The measurements show sensitivity at and below levels that are significant in current clinical laboratory practice (with SIN>8 at as low as 10 pM antigen concentration). The chip uses 100 nL per sample for all four tests and provides an improved instrument for use in scientific research and “point-of-care” testing in medicine.
Owner:SCHERER AXEL +3

Method of forming iron oxide core metal shell nanoparticles

A method of forming mono-disperse iron-oxide core metal shell nanoparticles is disclosed. Particle size of the oxide core seeds is controlled and capped seeds are formed. The capping layer is desorbed by a thermally activated process and metal such as gold is chemically deposited on the core seeds in situ. This process can be repeated to produce multi-metal or different metal shells. A second capping layer is applied on the core / shell composite nanoparticles. In another step, the particles are sized by centrifuging to obtain a tightly controlled and narrow particle size distribution. The water-dispersibility of the particles is achieved by a thiol exchange reaction on the gold shell of the core / shell nanoparticles or by deposition of gold on ferritin-derived iron oxide cores in aqueous solution. Mono and multilayer thin films are assembled on different substrates using the core / shell particles and linking molecules.
Owner:THE RES FOUND OF STATE UNIV OF NEW YORK

Drug carrier capable of realizing drug delivery specifically targeting tumor and application thereof

The invention discloses a tumor-targeting drug delivery system, and the system comprises a tumor-targeting drug carrier and a tumor-treating drug, wherein the tumor-targeting drug carrier comprises full heavy-chain human ferritin. The invention also discloses a preparation method for the tumor-treating drug delivery system. The method comprises: depolymerizing polymerized full heavy-chain human ferritin; adding the tumor-treating drug into the depolymerized full heavy-chain human ferritin, so as to enable depolymerized full heavy-chain human ferritin to be combined with the tumor-treating drug; and polymerizing the depolymerized full heavy-chain human ferritin combined with the tumor-treating drug again to form nano-particles.
Owner:CHINA SCI XINYUN BIOTECH BEIJING CO LTD

Reporter genes for magentic resonance imaging and methods of use thereof

The invention provides a fusion ferritin protein wherein a ferritin heavy chain polypeptide is fused to a peptide, wherein the peptide is fused to the C-terminal end of the ferritin heavy chain; and the peptide includes at least a portion of a Mms6 protein sequence and at least one heterologous amino acid at its N-terminal end. The invention further provides methods of use of the ferritin fusion protein for Magnetic Resonance Imaging.
Owner:YEDA RES & DEV CO LTD +1

Ferritin-loaded antitumor drug and preparation method thereof

The present invention provides an antineoplastic drug with ferritin as a carrier and a preparation method thereof, the method comprising the following steps: preparing ferritin; performing high pressure treatment on a mixed solution of ferritin and antineoplastic drug at a pressure of 200-800MPa6 ‑20h; the product after high pressure treatment is separated and purified to obtain an anti-tumor drug with ferritin as a carrier. The method of the present invention can not only increase the loading ratio of drugs, the yield of drug-loaded ferritin is close to 100%, but also can completely recover free unloaded anti-tumor drugs, improve production efficiency, reduce production costs, and is suitable for large-scale industrial production .
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

Preparation method of FER (Ferritin) zeolite molecular sieve with high silica-alumina ratio

The invention discloses a preparation method of an FER (Ferritin) zeolite molecular sieve with high silica-alumina ratio. The method comprises the following steps of: first, dissolving an aluminum source in a mixed liquid of sodium hydroxide, alkali and alkaline earth salt of weak acid; after adding the aluminum source, stirring and dispersing for a period of time by strong magnetic force at room temperature; mixing uniformly dispersed aluminum source and aluminum source liquid at room temperature to form glue; adding the FER zeolite molecular sieve as crystal seeds; after uniformly stirring and mixing at room temperature by strong force, transferring to a reaction crystallization kettle; crystallizing for 0.5-3 days by 130-170 DEG C microwave; and conventionally, filtering, washing and drying to obtain the sieve. According to the preparation method provided by the invention, expensive organic amine is not used as a structure-directing agent, and the FER zeolite molecular sieve is used as a crystal seed for microwave crystallization in an inorganic system with low alkalinity and high salinity. The crystallization degree and purity of products prepared are high, the silica-alumina ratio is easy to regulate, the synthetic cost is low, the environmental-pollution less, and the method is convenient for industrial large-scale production.
Owner:EAST CHINA NORMAL UNIV

Methods and kits for the diagnosis of acute coronary syndrome

Provided are methods for the detection and diagnosis of acute coronary syndrome or ACS. The methods are based on the discovery that abnormal levels of selected analytes in sample fluid, typically blood samples, of patients who are at risk are supportive of a diagnosis of ACS. At least two new biomarkers for ACS are thus disclosed, MMP-3 and SGOT. Altogether the concentrations of twelve analytes provide a sensitive and selective picture of the patient's condition, namely, whether the patient is suffering a heart attack. Other important biomarkers for ACS are described, including but not limited to IL-18, Factor VII, ICAM-1, Creatine Kinase-MB, MCP-1, Myoglobin, C Reactive Protein, von Willebrand Factor, TIMP-1, Ferritin, Glutathione S-Transferase, Prostate Specific Antigen (free), IL-3, Tissue Factor, alpha-Fetoprotein, Prostatic Acid Phosphatase, Stem Cell Factor, MIP-1-beta, Carcinoembryonic Antigen, IL-13, TNF-alpha, IgE, Fatty Acid Binding Protein, ENA-78, IL-1-beta, Brain-Derived Nerotrophic Factor, Apolipoprotein A1, Serum Amyloid P, Growth Hormone, Beta-2 microglobulin, Lipoprotein (a), MMP-9, Thyroid Stimulating hormone, alpha-2 Macroglobulin, Complement 3, IL-7, Leptin, and IL-6. Kits containing reagents to assist in the analysis of fluid samples are also described.
Owner:RULES BASED MEDICINE

Technique for extracting fish protein ferritin peptide from low value sea water fish and leftover protein

The invention discloses a technology for extracting fish protein iron peptide from the a low value seawater fish and its processing tailings. The technology comprises the following steps: grinding the material and adding 2-5 times of water; milling into slurry and regulating the pH value of the slurry to 5-7; adding papain and flavor enzyme according to the vitality ratio 1:1 controlling the enzyme amount at 600-2400IU for hydrolyzing; filtering the enzymatic hydrolyzed liquid to obtain the hydrolysate and regulating its pH value to 6-8; adding 1-5% ferrous chloride solution according to the weight / volume ratio of ultra-filtered hydrolysate : ferrous chloride solution as 50:1 for chelating while stirring continuously; keeping for 15-60 minutes for killing the activity of enzyme; spray drying and obtaining the fish protein iron peptide. The invention can be used as organic iron intensifying agent for food or health product.
Owner:ZHEJIANG OCEAN UNIV +1

Transferrin glycans composition for the induction of immune tolerance

The invention pertains to a process for the production of a pharmaceutical composition effective for controlling in a recipient mammalian host, particularly man, immune reactions of the type that are involved in graft of foreign tissue or cells, particularly transplantation of foreign tissues, organs or cells, particularly of allogeneic or even xenogeneic origin, or in immunodeficiency-linked diseases, which pharmaceutical composition is characterized by an active principle consisting of pooled transferrin-derived glycans obtained from a number of donors sufficient to allow the pool to contain sufficient phenotypic information required to ensure an induction of tolerance against antigens in an immuno-depressed host grafted with said antigens, after that host had been administered an amount of such pooled transferrin glycans effective to induce said tolerance.
Owner:CELLENA CELL ENG

Magnetic molecules: a process utilizing functionalized magnetic ferritins for the selective removal of contaminants from solution by magnetic filtration

A decontamination system uses magnetic molecules having ferritin cores to selectively remove target contaminant ions from a solution. The magnetic molecules are based upon a ferritin protein structure and have a very small magnetic ferritin core and a selective ion exchange function attached to its surface. Various types of ion exchange functions can be attached to the magnetic molecules, each of which is designed to remove a specific contaminant such as radioactive ions. The ion exchange functions allow the magnetic molecules to selectively absorb the contaminant ions from a solution while being inert to other non-target ions. The magnetic properties of the magnetic molecule allow the magnetic molecules and the absorbed contaminant ions to be removed from solution by magnetic filtration.
Owner:ELECTRIC POWER RES INST INC

Method for separating purified ferritins from biological tissues or engineering bacteria

The invention discloses a method for separating purified ferritins from biological tissues or engineering bacteria. The method comprises the following steps of: performing mechanical lapping or ultrasonication by taking ferritin-enriched animal tissues or organs or engineering bacteria which are collected by fermenting and contain recombination ferritin genes as a raw material for extracting ferritins to obtain uniform serum, performing heat denaturation treatment on the filtered uniform serum in water with the temperature between 70 DEG C and 75 DEG C for 20 minutes, and centrifugally extracting supernatant to obtain a crude protein solution; performing dialysis equilibrium on the obtain crude protein solution, performing nickel column affinity chromatography and eluting by using 250 mM of competitive imidazole buffer solution to obtain electrophoretically pure ferritins; and further performing sepHarose 6B molecular sieve exclusion chromatography on the ferritins to obtain monomer ferritins and polymer ferritins which are separated from each other. By adopting the method, electrophoretically pure ferritins can be obtained by directly performing nickel column affinity chromatography in the absence of tag, so that purifying steps of the ferritins are greatly eliminated.
Owner:INST OF GEOLOGY & GEOPHYSICS CHINESE ACAD OF SCI

Ferritin fusion proteins for use in vaccines and other applications

An isolated ferritin fusion protein is provided in which ferritin is fused with a protein or peptide capable of being fused to ferritin without interfering with the polymeric self-assembly of the resulting fusion protein, and the protein may be of the endocapsid form when fused at the C terminus or an exocapsid form when fused at the N terminus. These fusion proteins may self-assemble into a variety of useful higher polymeric forms, e.g., capsid or other polymeric aggregate, and they are advantageous in that they are useful in a variety of applications, including human and veterinary vaccines and therapeutics, blood substitutes, image contrast agents, metal chelating agents, gelling agents, protein purification platforms, and therapeutic receptor-binding proteins.
Owner:NEW CENTURY PHARMA INC

Bionic binary cooperative nano-carrier as well as preparation method and application thereof

The invention provides a bionic binary cooperative nano-carrier as well as a preparation method and an application thereof. The bionic binary cooperative nano-carrier comprises an erythrocyte membrane, glucose oxidase, iron-supporting ferritin nano-particles and a photosensitizer, wherein the glucose oxidase and the iron-supporting ferritin nano-particles are coated with the erythrocyte membrane,and the photosensitizer is embedded into the surface of the erythrocyte membrane or entrapped by the erythrocyte membrane. Chain stimulative responsibility coordination of tumor hunger therapy and chemical kinetic therapy is realized, two enzymes are conveyed to a target site of an organism with the carrier on the basis of biocompatibility of the erythrocyte membrane and tumor targeting of targeting molecules, accurate administration is realized by membrane rupture based on 808 nm near-infrared light illumination in the tumors, the problem of drug resistance is solved effectively, furthermore,systemic toxicity caused by drug application is remarkably reduced, and damage to other normal tissue in an in-vivo circulation process is prevented effectively. The invention further provides the preparation method of the bionic binary cooperative nano-carrier. The bionic binary cooperative nano-carrier and the preparation method have good application prospect.
Owner:JINAN UNIVERSITY

Serum ferritin content detection kit

The invention relates to a serum ferritin content detection kit. The serum ferritin content detection kit has the advantages of being high in accuracy, good in anti-jamming capability and the like. The serum ferritin content detection kit contains a reagent R1, a reagent R2 and a standard ferritin product. The reagent R1 is prepared from, by weight, 5-50 mM of buffer solution, 100-200 mM of electrolyte, 0.5-3% of sealing agent, 0.05-0.5% of surfactant, 0.05-0.5% of preservative and 0.5-5% of coagulant. The reagent R2 is prepared from, by weight, 5-50 mM of buffer solution, 100-200 mM of electrolyte, 0.5-3% of sealing agent, 3-10 mM of metal chelate agent, 0.05-0.5% of surfactant, 0.05-0.5 % preservative, 3-10% protective agent and 0.05-0.5% of ferritin monoclonal antibody F (ab') 2 fragment sensitized nano latex particles.
Owner:NINGBO RUI BIO TECH

Method for preparing gene recombinant human ferritin light chain

InactiveCN101921798ASolve the disadvantages of long-term dependence on importsImprove accuracyMicroorganism based processesFermentationEscherichia coliEnzyme digestion
The invention discloses a method for preparing a gene recombinant human ferritin light chain. The method comprises the following steps of: amplifying a coding genetic sequence of a ferritin light chain (Ferritin L) in human fresh complete blood cells by PCR, cloning the amplified coding genetic sequence into an expression vector pET-30a by enzyme digestion and connection, transforming E.coli BL21 (DE3), identifying a positive cloning colony, performing induction expression on the Ferritin L by IPTG, and analyzing the antigenicity of the Ferritin L by using Westernblot. The method successfully constructs the prokaryotic expression vector of the FTL, and obtains the pure ferritin light chain by induction expression and purification in colon bacillus. Proved by the Westernblot, the protein has good antigenicity.
Owner:张曼

Fusion protein and application thereof

The invention provides fusion protein, which comprises monomeric ferritin subunit protein connected to porcine epidemic diarrhea virus antigenic protein, which includes porcine epidemic diarrhea virus S protein and / or fragments thereof, and further includes S1 protein, M protein, N protein and / or fragments thereof. The invention further provides nanoparticles containing the fusion protein. The invention further provides a vaccine composition containing the nanoparticles and / or a carrier. The invention further discloses a preparation method of the vaccine composition and an application of the vaccine composition to prepare a medicine for preventing and / or treating porcine epidemic diarrhea virus. The vaccine composition made from the nanoparticles overcomes the technical problem that whole viruses are hard to separate and culture in a process of manufacturing a conventional inactivation vaccine from porcine epidemic diarrhea whole viruses. The nanoparticles can be subjected to massive recombinant expression via genetic engineering technology. The time consumption is short, and the fusion protein is convenient for massive production.
Owner:PU LIKE BIO ENG

Protein chip used for detecting human ferrum reserve and reagent kit thereof

InactiveCN102621330AImprove accuracyReduce harmBiological testingSoluble transferrin receptorNutrition
The invention discloses a protein chip used for detecting human ferrum reserve, which belongs to the field of human ferrum nutrition detection. The protein chip comprises a solid-phase carrier, antiserum ferritin monoclonal antibodies, antiserum transferrin receptor monoclonal antibodies and anti-C-reactive-protein monoclonal antibodies, wherein the antiserum ferritin monoclonal antibodies, the antiserum transferring receptor monoclonal antibodies and the anti-C-reactive-protein monoclonal antibodies are distributed on the solid-phase carrier in an array manner, wherein the monoclonal antibodies are fixed on the surface of the solid-phase carrier by covalent bonds, and the solid-phase carrier is finished by hydroformylation. The invention further discloses a detection reagent kit based on the protein chip. Compared with the prior art, the protein chip can detect three indexes of human ferrum reserve simultaneously, is accurate and reliable in results, high in detection specificity, sensitivity and detection speed and stable in detection results. Furthermore, by multi-sample microarray technology, the protein chip is applicable to screening and detecting of massive people, low in blood sample quantity, detection and cost and low in harms to examined people.
Owner:中国疾病预防控制中心营养与食品安全所

Method for diagnosing liver fibrosis

A method for the detection of the presence and / or the severity of a liver disease in a patient comprising measuring in an isolated sample TIMP-1 (tissue inhibitor of metalloproteinase I), ferritin, at least one additional parameter selected from the group consisting of A2M (alpha-2-macroglobulin) and PI (prothrombin index) and optionally measuring at least one additional biochemical or clinical parameter and diagnosing the presence and / or severity of a liver disease based on the presence or measured levels of these parameters. The method can be used for monitoring therapeutic treatment of liver fibrosis and staging of liver fibrosis.
Owner:ROCHE DIAGNOSTICS OPERATIONS INC

Method for detecting ferritin based on nanogold catalytic chemiluminescence analysis

The invention discloses a method for detecting ferritin based on nanogold catalytic chemiluminescence analysis. The method comprises the following steps that 1), a nanogold solution is prepared, 0.01% w / w of a HAuC14 solution of is heated to boiling, a sodium citrate solution of 1% is added under hard stirring, a heating source is removed after the mixed solution keeps boiling for fifteen minutes, the mixed solution is continuously stirred and cooled to the room temperature, and the obtained solution is stored in a refrigerator with the temperature of 4 DEG C for standby application; 2) nanogold is marked through ferritin antibodies, and the ferritin antibodies are utilized for modifying nanogold particles; 3), immunoreaction is carried out; 4), ferritin is detected through the chemiluminescence analysis, a nonogold / ferritin mixed solution modified by the ferritin antibodies after the immunoreaction is finished is moved into a chemiluminescence pool, a luminol-potassium periodate chemiluminescence reagent is injected into the solution, and the chemiluminescence intensity of the solution is measured and recorded through an IFFL-D chemiluminescencent analyzer to obtain the correlation between the chemiluminescence intensity and the ferritin to be measured.
Owner:FUJIAN UNIV OF TECH

Nano-drug carrier loading anticancer drugs, and preparation method and application of nano-drug carrier

The invention relates to a nano-drug carrier loading anticancer drugs, and a preparation method and application of the nano-drug carrier. The nano-drug carrier is a physiological polymer of pyrococcusfuriosus ferritin and a derivative thereof, wherein the derivative comprises fusion proteins modified based on the pyrococcus furiosus ferritin, and ferritin modified based on the amino acid sequenceof a protein shell inner cavity of the pyrococcus furiosus ferritin; and the anticancer drugs include but are not limited to small molecule drugs, oligonucleotides and functional peptide fragments.
Owner:INSITUTE OF BIOPHYSICS CHINESE ACADEMY OF SCIENCES

DNA sequence encoding oncofetal ferritin protein

A DNA sequence coding for oncofetal ferritin 1 (OFF1) as well as an amino acid sequence encoded by the DNA sequence. Pharmaceutical compositions may be prepared comprising the above-sequences for treating various diseases, for facilitating transplantations and for treating pathological pregnancies.
Owner:GARDINO INVESTMENT

Ferritin/chitosan-based natural pigment molecule embedding material preparation method

The invention discloses a novel method for preparing embeddings, which comprises the following steps: placing ferritin solution in a centrifuge tube, adjusting the pH value with sodium hydroxide solution to denature, and stirring; taking natural pigments and dissolving them in ethanol Solution: mix the polyphenol ethanol solution with the above-mentioned ferritin solution, stir at room temperature, adjust the pH value for renaturation, stir in a chromatographic cabinet at 4°C, and dialyze the above-mentioned solution three times to obtain the ferritin natural pigment embedding. Then, the ferritin pigment embedding material and chitosan were mixed in a certain proportion, stirred, statically prepared, and dialyzed in a chromatographic cabinet at 4°C in the dark to obtain the final product. The final product is a new type of embedding material loaded with natural pigment molecules by ferritin / chitosan, which can be used as a new food additive, can also be used to improve medical efficacy, and can also be used as a component in cosmetics, embedding material Ferritin and natural pigments produced after decomposition also have certain biological activity. This product makes full use of the functions of ferritin and natural pigment, and has high practical application and promotion value.
Owner:TIANJIN UNIVERSITY OF SCIENCE AND TECHNOLOGY

Method of arrangement of titanium-binding ferritin and inorganic particles

A method for selectively arranging ferritin modified with a peptide, which specifically binds to titanium, to titanium formed on a substrate surface is provided. The method for arranging ferritin of the present invention is characterized in that ferritin is selectively bound on titanium on a substrate by modifying the N-terminal part of ferritin with a peptide which specifically binds to titanium. Also, the method for arranging ferritin of the present invention is characterized in that selectivity for titanium can be markedly improved by adding a nonionic surface activating agent.
Owner:PANASONIC CORP

Method for transdermal iontophoretic delivery of chelated agents

Embodiments provide devices, systems and methods for the transdermal delivery of chelated compounds. One embodiment provides a method for the iontophoretic transdermal delivery of a chelated iron complex for the treatment of anemia. A first patch comprising an active electrode and a chelated iron complex is applied to the skin; a second patch containing an electrode is also applied. An electrical current is then delivered to the skin from the active electrode. The chelated complex is transported across the skin via electromotive force from the current, with the iron being substantially chromogenically unreactive with the skin during transport so that there is little or no tattooing of the skin due to the formation of insoluble oxidative products. The complex is then dissociated by phagocytosis or related process to release the iron where it may be bound by transferrin or ferritin and carried to other sites for storage or metabolic use.
Owner:FE3 MEDICAL

Method of extracting lacto ferritin from transgene lactoferritin paddy rice

The present invention discloses a method for extracting lactoferrin from transgenic lactoferrin rice. Said method includes the following steps: 1), adding water or buffer solution in transgenic lactoferrin rice seed, mixing them, pulverizing to form wet powder; or directly pulverizing transgenic lactoferrin rice seed, then adding water or buffer solution to form wet powder; the buffer solution contains NaCl, whose concentration is less than 0.1 mol / L and whose pH value is 6-9, the temperature of the above-mentioned pulverization process is below 70deg.C, the material-adding ratio of water or buffer solution and transgenic lactoferrin rice seed is 1-10ml / g; and 2), mixing and shaking the above-mentioned wet powder, then making centrifugal separation for 10min, and separating precipitate and supernatant.
Owner:ZHEJIANG UNIV

Self-assembled nanoparticle vaccines

InactiveUS20150110825A1Effective vaccinePrevent stericSsRNA viruses negative-sensePowder deliveryF proteinNanoparticle
The present invention provides nanoparticles and compositions of various constructs that combine meta-stable viral proteins (e.g., RSV F protein) and self-assembling molecules (e.g., ferritin, HSPs) such that the pre-fusion conformational state of these key viral proteins is preserved (and locked) along with the protein self-assembling into a polyhedral shape, thereby creating nanoparticles that are effective vaccine agents. The invention also provides nanoparticles comprising a viral fusion protein, or fragment or variant thereof, and a self-assembling molecule, and immunogenic and vaccine compositions including the same.
Owner:MASSACHUSETTS INST OF TECH

GLP-1 infusion proteins, their preparation and use

The invention discloses a fusing protein and preparing method and application, which is combined of para-insanguinin peptide 1 repeating sequence and human serum albumin, immune globulin, ferritin, steroid connecting protein, transferrin, thyroid connecting protein, alpha-2 macroglobulin and haptoglobin. The invention also provides the coding sequence of fusing protein and carrier and host with the coding chain, which possesses better stability and internal half-life.
Owner:ZHEJIANG WOLWO BIOTECH
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