This method for producing fine particles includes: a step for forming a polyion complex by ion-bonding an ionic active material and an ionic polymer; and a step for forming fine particles which contain the polyion complex and at least one polymer (P) that is selected from among a polylactic acid and a lactic acid-glycolic acid copolymer. The step for forming fine particles includes: a step for mixing the polyion complex and the polymer (P) in an organic solvent; a step for forming an o/w emulsion by adding the organic solvent after mixing, the organic solvent containing the polyion complex and the polymer (P), to an aqueous solution in which a dispersant for preventing bonding between emulsions is dissolved; and a step for removing the organic solvent from the aqueous solution that contains the o/w emulsion.
The present disclosure provides a method to determine whether or not a patient has received administration of a direct oral anticoagulant (DOAC). The present disclosure provides a method comprising allowing magnetic particles in a reagent to move after the addition of a sample to a dry reagent containing magnetic particles, monitoring the movement signal of the magnetic particles, analyzing the monitored movement signal of the magnetic particles, and comparing the results of analysis with a threshold, and a program and an apparatus used for such method.
A draw solution contains a polymeric compound produced using, as starting materials, a compound represented by general formula (a) and a compound represented by general formula (b) as a draw solute.
A draw solution contains a polymeric compound produced using, as starting materials, a compound represented by general formula (a) and a compound represented by general formula (b) as a draw solute.
[In formula (a) and formula (b), R1 and R2 each independently represent a hydrogen atom or a methyl group.]
B01D 61/00 - Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltrationApparatus, accessories or auxiliary operations specially adapted therefor
C02F 1/44 - Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis
C08F 226/02 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
4.
MUCOSAL ADJUVANT AND METHOD FOR MANUFACTURING MUCOSAL ADJUVANT
[Problem] To provide a highly efficient mucosal adjuvant that can be safely administered to humans. [Solution] A mucosal adjuvant comprises bioapatite and is characterized in that low-sulfate bioapatite using calcined eggshells is included and that the antigenicity of solid membrane vesicles secreted by Streptococcus mutans is enhanced by the low-sulfate bioapatite. With this configuration, the low-sulfate bioapatite, being a component of bones and teeth, can be safely administered to humans and is easily taken up by dendritic cells, which are antigen-presenting cells, due to the very small particle size of approximately 20 nm, thereby providing a highly efficient mucosal adjuvant.
The present invention provides an ultrasonic vibration generation device the total length of which can be freely adjusted. An ultrasonic vibration body (3) comprises: a vibrator connection part (4) to which a vibrator unit (2) is connected; a conical horn (5) for converting at least a part of vertical vibration transmitted via the vibrator connection part 4 into lateral vibration having mutually different directions and sizes; and a columnar vibration part (6) which is provided so as to protrude from the conical horn (5) with the root thereof connected to the conical horn (5), and in which the tip is ultrasonically vibrated in a plane orthogonal to the traveling direction of the vertical vibration as the lateral vibration is transmitted.
An ultrasonic projection device for projecting ultrasonic waves includes a first block body, a second block body, and a piezoelectric unit sandwiched between the first block body and the second block body. A vibration plate is provided at one end on the first block body side in the axial direction of the first block body, the second block body, and the piezoelectric unit. The dimension from the one end to the other end on the second block body side in the axial direction approximately coincides with half of the wavelength of vibration generated by the piezoelectric unit. A connection portion having a groove with a smooth inner wall surface which connects the vibration plate and a base portion is provided between the vibration plate and the base portion which supports the vibration plate.
G10K 9/122 - Devices in which sound is produced by vibrating a diaphragm or analogous element, e.g. fog horns, vehicle hooters or buzzers electrically operated using piezoelectric driving means
A composition for absorbing carbon dioxide including an ionic liquid (A) containing a cation and an anion, and a protic compound (B) having a relative permittivity at 25° C. of 20 or more, wherein the cation at least includes a cation represented by the formula (1), the anion includes an anion where an acid dissociation constant (pKa) at 25° C. of its conjugate acid in water is 4.5 or more, and the ratio of a value obtained by multiplying the number of hydroxyl groups of the protic compound (B) by the number of moles of the protic compound (B) to the number of moles of the ionic liquid (A) [number of moles of protic compound (B)/number of moles of ionic liquid (A)] is 0.2 to 1.0:
A composition for absorbing carbon dioxide including an ionic liquid (A) containing a cation and an anion, and a protic compound (B) having a relative permittivity at 25° C. of 20 or more, wherein the cation at least includes a cation represented by the formula (1), the anion includes an anion where an acid dissociation constant (pKa) at 25° C. of its conjugate acid in water is 4.5 or more, and the ratio of a value obtained by multiplying the number of hydroxyl groups of the protic compound (B) by the number of moles of the protic compound (B) to the number of moles of the ionic liquid (A) [number of moles of protic compound (B)/number of moles of ionic liquid (A)] is 0.2 to 1.0:
A composition for absorbing carbon dioxide including an ionic liquid (A) containing a cation and an anion, and a protic compound (B) having a relative permittivity at 25° C. of 20 or more, wherein the cation at least includes a cation represented by the formula (1), the anion includes an anion where an acid dissociation constant (pKa) at 25° C. of its conjugate acid in water is 4.5 or more, and the ratio of a value obtained by multiplying the number of hydroxyl groups of the protic compound (B) by the number of moles of the protic compound (B) to the number of moles of the ionic liquid (A) [number of moles of protic compound (B)/number of moles of ionic liquid (A)] is 0.2 to 1.0:
wherein R1 and R2 each independently represent a hydrogen or a C1-C6 linear alkyl group.
B01D 53/14 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by absorption
8.
EYEDROPS FOR AMELIORATING OR PREVENTING RETINAL CIRCULATION DISORDER AND RETINAL NEUROVASCULAR COUPLING DISORDER
This pain determination device comprises: a first response data acquisition unit that acquires first response data including a combination of responses by a first patient to first questions about at least one of the type of sensation of a pain which is somatic pain, the intensity of the pain, the frequency of the pain, or triggers of the pain, and responses about the first patient to second questions about at least one of psychological factors, social factors, health status, or lifestyle; and a determination unit that, on the basis of a trained model trained on the relationship between second response data, including a combination of responses by a second patient to the first questions and responses about the second patient to the second questions, and the type of cause of the pain of the second patient, determines at least one of the type of the cause of the pain of the first patient from the first response data acquired by the first response data acquisition unit, or the degree of importance of each explanatory variable, included in the first response data, to the type of the cause of the pain of the first patient.
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
10.
METHOD AND KIT FOR PREDICTING EFFICACY OF TREATMENT WITH IMMUNOTHERAPEUTIC AGENT ON PATIENT WITH MUCOSAL LESION
The present invention provides a novel method and kit for predicting the efficacy of treatment with an immunotherapeutic agent on a patient with a mucosal lesion. The present invention is a method for predicting the efficacy of treatment with an immunotherapeutic agent on a patient with a mucosal lesion, the method comprising a step for measuring the expression level of CD86 in a biological sample derived from a patient with a mucosal lesion. The present invention is a kit for use in the above method, the kit comprising a substance that binds specifically to CD86, or forward and reverse primers for amplifying nucleic acids encoding CD86.
The present invention addresses the problem of providing a novel pharmaceutical composition for preventing proliferative vitreoretinopathy. The present invention solves the problem by providing a pharmaceutical composition for preventing proliferative vitreoretinopathy, comprising an autotaxin aptamer or a salt thereof.
A61K 31/7088 - Compounds having three or more nucleosides or nucleotides
A61K 31/712 - Nucleic acids or oligonucleotides having modified sugars, i.e. other than ribose or 2'-deoxyribose
A61K 31/7125 - Nucleic acids or oligonucleotides having modified internucleoside linkage, i.e. other than 3'-5' phosphodiesters
A61K 47/60 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
B01D 53/14 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by absorption
C25B 9/00 - Cells or assemblies of cellsConstructional parts of cellsAssemblies of constructional parts, e.g. electrode-diaphragm assembliesProcess-related cell features
C25B 15/08 - Supplying or removing reactants or electrolytesRegeneration of electrolytes
13.
DIAGNOSIS ASSISTANCE DEVICE, LEARNING MODEL CREATION DEVICE, DIAGNOSIS ASSISTANCE METHOD, LEARNING MODEL CREATION METHOD, AND PROGRAM
This diagnosis assistance device accepts myocardial ischemia automatic quantitative values, and cardiac function information and phase information acquired by implementing cardiac stress scintigraphy; and, on the basis of the myocardial ischemia automatic quantitative values, the cardiac function information, the phase information, and a trained model, the diagnosis assistance device acquires and outputs at least one from among a reperfusion therapy prediction result, a heart failure onset prediction result, a cardiac death prediction result, a total mortality prediction result, and a coronary artery disease prediction result. The trained model is obtained by training the model with the relationship between: a combination of myocardial ischemia automatic quantitative values, cardiac function information, and phase information; and at least one from among the reperfusion therapy result, the heart failure onset prediction result, the cardiac death prediction result, the total mortality prediction result, and the coronary artery disease prediction result.
A stable isotope-labeled indole carboxylic acid compound represented by Formula (I) is provided. In Formula (I), X1 to X8 are each independently C or 13C; Y is N or 15N; M is H, Na, K, Li, CH3, or C2H5; R1 is H or D; R2 is H, CH3, 13CH3, C2H5, or 13C2H5; R3 is H, CH3, 13CH3, C2H5, or 13C2H5; R4 is H or D; and R5 is H or D.
A stable isotope-labeled indole carboxylic acid compound represented by Formula (I) is provided. In Formula (I), X1 to X8 are each independently C or 13C; Y is N or 15N; M is H, Na, K, Li, CH3, or C2H5; R1 is H or D; R2 is H, CH3, 13CH3, C2H5, or 13C2H5; R3 is H, CH3, 13CH3, C2H5, or 13C2H5; R4 is H or D; and R5 is H or D.
G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
C07D 209/42 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
G01N 33/96 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving blood or serum control standard
15.
SAMPLE TEST METHOD, TEST KIT FOR GYNECOLOGICAL CANCER AND PRECANCEROUS LESION THEREOF, AND MEDICINE
Provided are: a simple and highly accurate sample test method which can be applied to the evaluation of the presence or absence of at least one selected from the group consisting of a gynecological cancer and a precancerous lesion thereof, the evaluation of the prognosis of a gynecological cancer patient, or the evaluation of the degree of malignancy of a gynecological cancer; a test kit which can be used for the test method; and a medicine for treating or preventing a gynecological cancer, which is intended to be administered to a subject detected by the test method. A sample test method is employed, the method comprising a step (A) for measuring the concentration of a free fatty acid in a sample from a subject and a step (B) for evaluating the possibility that the subject would have a of gynecological cancer on the basis of the concentration of the free fatty acid obtained in the step (A).
In this three-dimensional printing apparatus, a print material (F) supplied from a nozzle (64) is arranged along a print path to form a sheet-like material layer (FL) composed of a single layer or a plurality of layers. The material layer (FL) is compressed by a heating member (81) as a table (3) and the heating member (81) move relative to each other.
B33Y 30/00 - Apparatus for additive manufacturingDetails thereof or accessories therefor
B33Y 50/02 - Data acquisition or data processing for additive manufacturing for controlling or regulating additive manufacturing processes
B29C 64/118 - Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using filamentary material being melted, e.g. fused deposition modelling [FDM]
B29C 64/188 - Processes of additive manufacturing involving additional operations performed on the added layers, e.g. smoothing, grinding or thickness control
A method for producing an acidic gas absorbent containing a compound represented by general formula (1), the method comprising a step for mixing: a composition mixture of an acidic gas and a compound represented by general formula (1); and at least one protic solvent selected from the group consisting of water and alcohols having 1-3 carbon atoms and optionally having a substituent group. [In general formula (1), R1-R4each independently represent a hydrogen atom or an alkyl group having 1-6 carbon atoms, and X- represents an anion of a saturated aliphatic monocarboxylic acid having 2-6 carbon atoms.]
B01D 53/14 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by absorption
This method for producing human dedifferentiated fat cells comprises a step for culturing human mature fat cells using a culture medium containing human platelet lysate. This culture medium for producing human dedifferentiated fat cells from human mature fat cells contains human platelet lysate.
This quantum tomographic imaging device, which uses an optical element having a quantum pulse gate characteristic to acquire tomographic image information at a desired depth in a biological sample: emits a probe light pulse onto the biological sample and acquires a reflected light pulse thereof; includes a delay unit for imparting a delay to a pulse for pump light, and a waveform shaping unit for performing waveform shaping of the pulse for pump light; generates a pump light pulse as a result of the delay and the waveform shaping; combines the reflected light pulse and the pump light pulse to generate a combined light pulse thereof; inputs the combined light pulse into the optical element; and, by utilizing a quantum pulse gate characteristic of the optical element, employs a single-photon detector to detect an upward converted signal light pulse obtained as a result of an upward conversion of a frequency of a desired signal light pulse contained in the combined light pulse.
G01N 21/17 - Systems in which incident light is modified in accordance with the properties of the material investigated
A61B 10/00 - Instruments for taking body samples for diagnostic purposesOther methods or instruments for diagnosis, e.g. for vaccination diagnosis, sex determination or ovulation-period determinationThroat striking implements
G01B 11/24 - Measuring arrangements characterised by the use of optical techniques for measuring contours or curvatures
G01J 11/00 - Measuring the characteristics of individual optical pulses or of optical pulse trains
This ultrasonic projection device 1 for projecting ultrasonic waves comprises a first block body 2, a second block body 3, and a piezoelectric unit 4 clamped by the first block body 2 and the second block body 3. A vibration plate 6b is provided on one end on the first block body 2 side in the axial direction of the first block body 2, the second block body 3, and the piezoelectric unit 4. The dimension from the one end in the axial direction to the other end on the second block body 3 side is formed so as to approximately equal to a half wavelength of the vibration generated by the piezoelectric unit 4. A connection part 6c, in which a groove part 6e having a smooth inner wall surface 6e1 that connects the vibration plate 6b and the base part 6a is formed, is provided between the vibration plate 6b and a base part 6a that supports the vibration plate 6b.
H04R 17/10 - Resonant transducers, i.e. adapted to produce maximum output at a predetermined frequency
B06B 1/06 - Processes or apparatus for generating mechanical vibrations of infrasonic, sonic or ultrasonic frequency making use of electrical energy operating with piezoelectric effect or with electrostriction
21.
DRAW SOLUTION, WATER TREATMENT METHOD, AND WATER TREATMENT APPARATUS
For the purpose of providing a draw solution containing an UCST-type polymeric compound useful as a draw solute in a forward osmosis membrane separation method for performing the membrane separation of water using a forward osmosis membrane, a water treatment method and a water treatment apparatus, the draw solution contains a polymeric compound produced using, as starting materials, a compound represented by general formula (a) and a compound represented by general formula (b) as a draw solute. [In formula (a) and formula (b), R1and R2 each independently represent a hydrogen atom or a methyl group.]
B01D 61/00 - Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltrationApparatus, accessories or auxiliary operations specially adapted therefor
The purpose of the present invention is to provide a means for inhibiting intestinal absorption of β-alanine. This problem can be solved by the β-alanine absorption inhibitor of the present invention that comprises, as an active ingredient, a compound selected from the group consisting of γ-aminobutyric acid, taurine, glycine, lysophosphatidylcholine and α-glycerophosphocholine, or a salt thereof.
A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
A61K 31/185 - AcidsAnhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
A61K 31/198 - Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
A61K 31/661 - Phosphorus acids or esters thereof not having P—C bonds, e.g. fosfosal, dichlorvos, malathion
A61P 43/00 - Drugs for specific purposes, not provided for in groups
23.
METHOD FOR MANUFACTURING MOLDED ARTICLE WITH MOLDING DIE PRODUCED BY 3D PRINTER AND MOLDED ARTICLE
[Problem] To provide: a fabric-reinforced thermoplastic resin sheet molded article in which a corner part is not extremely thinned or bored, a curved part has a beautiful finished feeling without a disorder of fabric arrangement appearing on a surface of the molded article, and a fabric-reinforced thermoplastic resin sheet does not cause interlayer delamination during molding; and a manufacturing method for efficiently manufacturing the molded article. [Solution] Provided are: a method for manufacturing a fabric-reinforced thermoplastic resin sheet molded article characterized in that a fabric-reinforced thermoplastic resin sheet is vacuum-molded using a molding die having countless micropores produced by a thermally melting lamination method (3D printer) as a female die or a male die or as a female die and a male die; and a fabric-reinforced thermoplastic resin sheet molded article obtained by vacuum-molding a fabric-reinforced thermoplastic resin sheet and characterized by using a molding die having countless micropores produced by a thermally melting lamination method that is one of molding dies for vacuum molding as a female die or a male die or as a female die and a male die.
B29C 51/08 - Deep-drawing or matched-mould forming, i.e. using mechanical means only
B29C 51/14 - Shaping by thermoforming, e.g. shaping sheets in matched moulds or by deep-drawingApparatus therefor using multilayered preforms or sheets
B29K 105/08 - Condition, form or state of moulded material containing reinforcements, fillers or inserts of continuous length, e.g. cords, rovings, mats, fabrics, strands or yarns
B29C 64/118 - Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using filamentary material being melted, e.g. fused deposition modelling [FDM]
B29C 33/38 - Moulds or coresDetails thereof or accessories therefor characterised by the material or the manufacturing process
B29C 70/22 - Fibrous reinforcements only characterised by the structure of fibrous reinforcements using fibres of substantial or continuous length oriented in at least two directions forming a two dimensional structure
B29C 70/42 - Shaping or impregnating by compression for producing articles of definite length, i.e. discrete articles
A composition for carbon dioxide absorption comprising an ionic liquid (A) comprising one or more cations and an anion and a protonic compound (B) having a relative permittivity at 25°C of 20 or greater, wherein at least one of the cations is represented by general formula (1), the anion is one, the conjugate acid of which has an acid dissociation constant (pKa) in water at 25 degrees of 4.5 or greater, and the proportion of the number of moles of the protonic compound (B) multiplied by the number of hydroxyl groups of the protonic compound (B) to the number of moles of the ionic liquid (A), (number of moles of the protonic compound (B))/(number of moles of the ionic liquid (A)), is 0.2-1.0. [In general formula (1), R1and R2 each independently represent a hydrogen atom or a C1-C6 chain alkyl group.]
B01D 53/14 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by absorption
NATIONAL AGENCY FOR AUTOMOBILE AND LAND TRANSPORT TECHNOLOGY (Japan)
Inventor
Tsunashima Hitoshi
Takata Tetsuya
Ogino Masayuki
Sato Yasuhiro
Ogata Seigo
Abstract
An information processing device comprising: a first generation unit that uses waveforms for waves indicating changes in track displacement between a start point on a first track traveled by rolling stock to an end point on the first track, using the waveforms as track displacement waveforms, and generates a plurality of track displacement waveforms that are different from each other; a second generation unit that generates a vibration waveform, being a waveform for a wave that indicates the change in vibration expected to be generated between the start point and the end point, in a rolling stock that travels virtually along the first track, when the shape of a waveform indicating track displacement on the first track from the start point to the end point does not match the waveform indicated by the track displacement waveform, generating same for each of the plurality of track displacement waveforms generated by the first generation unit; and a third generation unit that generates correspondence information that indicates the correlation between the size of the track displacement and the size of the vibration, on the basis of the plurality of track displacement waveforms generated by the first generation unit and the vibration waveforms generated by the second generation unit for each of the plurality of track displacements.
Provided are novel determination techniques and systems enabling an AI process in which decisions are made from the viewpoint of allowing an expert to make a decision, and capable of providing a valid answer, even with a small amount of learning data, by adjusting errors in both the answer of the expert and the answer of AI. A system is configured to cause an AI process to be performed on subject teacher data for AI learning in which events of objects identified by identifying codes are divided into classes, and data pertaining to an object for which class determination of an event is required, and to receive class determination data obtained by the AI process. The system is configured to: cause teacher data for learning to be randomly input to, and learned by, each of a plurality of AI processes; input data pertaining to the object into each of the plurality of AI processes; receive from each AI process class determination data corresponding to each learning; and store the class determination data in a storage device. In this way, the class of an event of an object identified by each identifying code is determined on the basis of each class determination data item corresponding to the identifying code.
A plasmid transfection agent that comprises a peptide containing an amino acid sequence represented by SEQ ID NO: 1. SEQ ID NO: 1: CXDXXXXYXC (wherein: X represents an arbitrary amino acid residue; C represents cysteine; D represents aspartic acid; and Y represents tyrosine.)
C12N 1/00 - Microorganisms, e.g. protozoaCompositions thereofProcesses of propagating, maintaining or preserving microorganisms or compositions thereofProcesses of preparing or isolating a composition containing a microorganismCulture media therefor
C12N 15/62 - DNA sequences coding for fusion proteins
C12N 15/63 - Introduction of foreign genetic material using vectorsVectorsUse of hosts thereforRegulation of expression
The present invention has an object of providing a composition that is effective for the treatment of a prototheca disease. According to the present invention, a composition containing ravuconazole as an active ingredient, which is administered to an animal suffering from a prototheca disease caused by Prototheca wickerhamii or Prototheca zopfii, is provided.
A panoramic X-ray imaging apparatus includes: an X-ray generating unit; an X-ray detecting unit; a support that supports the X-ray generating unit and the X-ray detecting unit; a drive mechanism that turns at least the X-ray generating unit and the X-ray detecting unit by driving the support; a displacement mechanism that adds movement including a displacement component in a direction different from the turning to the X-ray detecting unit; a subject holding unit that holds an imaging subject; a turning controller that controls the turning by a drive mechanism and the displacement mechanism. The turning controller controls the drive mechanism and the displacement mechanism so as to add the movement avoiding the contact with the shoulder of the imaging subject during the turning of the X-ray generating unit and the X-ray detecting unit by the drive mechanism during the panoramic X-ray imaging.
The problem to be solved is to provide a new method and system for appropriately detecting a joint state from an acoustic of a joint. The present method comprises the step of obtaining, using a bio-acoustic sensor, an acoustic signal emitted by a joint during a time period that at least includes a first motion period wherein the joint changes from a first state to a second state, a pause period of the joint and a second motion period wherein the joint changes from the second state to the first state, the step of converting the obtained acoustic signal into time trend data that at least shows a relationship between an acoustic signal intensity and time, and the step of setting, from the time trend data, a basic threshold value regarding the acoustic signal intensity to calculate first acoustic information based on the basic threshold value, characterized in that the first acoustic information is an indicator of the joint state.
A jaw movement analysis system includes circuitry that is configured to acquire chewing information including time-series information that represents a jaw movement of a user chewing a bite of food, and to determine an attribute of the food having been chewed by the user based on the chewing information acquired and based on an analysis model. The analysis model is generated by machine learning based on training data including first information that includes time-series information indicating a past jaw movement during a chewing of a bite of food, and second information that indicates an attribute of the food chewed during the past jaw movement associated with the first information.
The purpose of the present invention is to provide a modified milk protein that has high solubility in an acidic region, excellent foaming properties and high safety, and a method for producing the milk protein while minimizing the risk of exposure to hydrolysis. This purpose can be solved by, for example, a method for producing deamidated casein that comprises a step for subjecting a casein-containing suspension to a deamidation reaction using a weakly acidic cation exchange resin, which has an alkali metal salt-type ion exchange group, for 4-50 hours at 40-90°C to thereby give deamidated casein having a deamidation ratio of 14% or more and less than 32%.
C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
A method of producing induced pluripotent stem cells including a step for introducing an initialization factor into somatic cells of a mammal, and culturing in a neural stem cell culture medium to obtain induced neural stem cell-like cells, and a step for cultivating said induced neural stem cell-like cells in a growth medium to obtain induced pluripotent stem cells, wherein the initialization factor contains an OCT family, a SOX family, a KLF family, a MYC family, a LIN28 family and a P53 function inhibitor.
The present invention employs the following method for determining the tolerance of a Trichophyton fungus to a squalene epoxidase inhibitor. This method comprises: step (a) for, using genomic DNA of a target Trichophyton fungus as a template, conducting a nucleic acid amplification reaction with the use of a primer comprising the base sequence represented by SEQ ID NO: 1 and a primer comprising the base sequence represented by SEQ ID NO: 2 to obtain a squalene epoxidase gene fragment; step (b) for analyzing the base sequence of the squalene epoxidase gene fragment; and step (c) for, when a deduced amino acid sequence of the squalene epoxidase of the target Trichophyton fungus has a Leu393Phe mutation and/or a Phe397Leu mutation, then determining that the target Trichophyton fungus has tolerance to a squalene epoxidase inhibitor.
C12Q 1/6895 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for plants, fungi or algae
C12N 15/31 - Genes encoding microbial proteins, e.g. enterotoxins
A nucleic acid detection kit including: (i) a first single-stranded circular DNA; (ii) a first oligonucleotide primer; (iii) a second single-stranded circular DNA; and (iv) a second oligonucleotide primer; wherein the first oligonucleotide primer is hound to a carrier through the 5′-end thereof, and the second oligonucleotide primer is bound, through the 5′-end thereof, to the carrier to which the first oligonucleotide primer is hound.
C12Q 1/70 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving virus or bacteriophage
C12Q 1/6853 - Nucleic acid amplification reactions using modified primers or templates
C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
C12Q 1/6834 - Enzymatic or biochemical coupling of nucleic acids to a solid phase
C07D 277/66 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
36.
METHOD FOR FIXING CARBON DIOXIDE TO CONCRETE, AND CONCRETE STRUCTURE INCLUDING CONCRETE
Provided is a method for efficiently fixing carbon dioxide to concrete. The method includes: forming a gas injection hole in concrete included in a concrete structure; introducing a gas containing carbon dioxide into the gas injection hole; and after introducing the gas containing carbon dioxide, capping one end of the gas injection hole to seal the gas including carbon dioxide in the gas injection hole. The method may further include decompressing the gas injection hole before the introduction of the gas including carbon dioxide. The gas including carbon dioxide may further include water.
E04C 3/20 - JoistsGirders, trusses, or truss-like structures, e.g. prefabricatedLintelsTransoms of concrete or other stone-like material, e.g. with reinforcements or tensioning members
E04C 3/34 - ColumnsPillarsStruts of concrete or other stone-like material, with or without permanent form elements, with or without internal or external reinforcement, e.g. metal coverings
E21D 11/10 - Lining with building materials with concrete cast in situShuttering or other equipment adapted therefor
E04G 21/02 - Conveying or working-up concrete or similar masses able to be heaped or cast
B28B 11/24 - Apparatus or processes for treating or working the shaped articles for curing, setting or hardening
C04B 28/02 - Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
C04B 40/02 - Selection of the hardening environment
Eyedrops for ameliorating retinal circulatory disturbance and disorders associated with retinal nerve blood vessels, which contains fibrate-containing nanoparticles.
The present invention addresses the problem of providing a novel method and system for appropriately detecting joint status from joint acoustics. The present method is characterized by comprising: a step for acquiring, from a biological acoustics sensor, acoustic signals generated by a joint during periods including at least a first movement period when the joint changes from a first state to a second state, a joint resting period, and a second movement period when the joint changes from the second state to the first state; a step for converting the acquired acoustic signals to time trend data that at least shows the correlation between the acoustic signal intensity and time; and a step for setting the basic threshold value of the acoustic signal intensity from the time trend data, and calculating the first audio information on the basis of the basic threshold value.
An antibody or an antigen-binding fragment thereof that binds specifically to a stabilon variant. A nucleic acid that encodes the antibody or antigen-binding fragment thereof. A vector containing the nucleic acid. A peptide capable of dissociating a stabilon variant tag fusion protein from the antibody or antigen-binding fragment. A transformant containing the nucleic acid. A kit containing the antibody or antigen-binding fragment.
Provided is a pyrrole-imidazole polyamide that binds to the promoters of two or more genes and simultaneously controls transcription of the two or more genes. Also provided is a pharmaceutical composition comprising the pyrrole-imidazole polyamide. Also provided are: a pyrrole-imidazole polyamide that simultaneously controls transcription of HGF gene and TGF-β gene; a TGF-β gene expression inhibitor comprising the pyrrole-imidazole polyamide; and a pharmaceutical composition for treating a TGF-β-associated disease or a fibrous disease.
C07D 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
A61K 31/787 - Polymers containing nitrogen containing heterocyclic rings having nitrogen as a ring hetero atom
A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
A61P 1/18 - Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
A61P 5/00 - Drugs for disorders of the endocrine system
A61P 9/00 - Drugs for disorders of the cardiovascular system
A61P 13/12 - Drugs for disorders of the urinary system of the kidneys
The present invention addresses the problem of providing a device for more efficiently performing a nucleic acid amplification reaction using a primer fixed to a magnetic bead. The present invention provides a device for performing a nucleic acid amplification reaction in a reactor vessel accommodating a reaction reagent containing a primer oligonucleotide fixed to a magnetic bead, the device comprising: a coil that can be connected to an AC power source; and a support which is installed inside the coil and made of a thermally conductive magnetic material on which the reaction vessel can be placed, wherein the device further comprises a heater that heats the support.
A magnetized plasmoid injection device including a cylindrical external electrode, a cylindrical internal electrode coaxially disposed inside the external electrode, a plasma generating gas supply unit that supplies plasma generating gas in a pulse shape between the external electrode and the internal electrode, a magnetic field generation unit that applies a magnetic field that generates magnetized plasmoid between the external electrode and the internal electrode, a power supply control unit that applies a discharge voltage between the external electrode and the internal electrode, and an impurity generation unit that contains an impurity in the magnetized plasmoid, the impurity generation unit having a cover electrode that opens to the external electrode, a thin-rod electrode that is located inside the cover electrode and is formed of an impurity, and an impurity generation power supply that applies a voltage to the cover electrode and the thin-rod electrode.
SCHOOL CORPORATION, AZABU VETERINARY MEDICINE EDUCATIONAL INSTITUTION (Japan)
Inventor
Sahara, Hiroeki
Nakayama, Tomohiro
Maruo, Takuya
Abstract
There is provided with a method of treating cancer. A set of administration of a compound represented by General Formula (I) or a pharmaceutically acceptable salt thereof to a patient, at a dose such that 8 mg/kg or less of the compound represented by General Formula (I) is administered, and irradiation to the patient immediately following the administration is repeated. A total dosage of the irradiation to a cancer is 10 Gy or more.
A61K 31/7032 - Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a polyol, i.e. compounds having two or more free or esterified hydroxy groups, including the hydroxy group involved in the glycosidic linkage, e.g. monoglucosyl-diacylglycerides, lactobionic acid, gangliosides
The present invention addresses the problem of providing: a premix reagent for nucleic acid amplification reactions, which makes it possible to perform a nucleic acid amplification reaction in a simple manner merely by mixing the premix reagent with a specimen; and a ready-to-use nucleic acid amplification reaction kit including the premix reagent for nucleic acid amplification reactions. A nucleic acid amplification reaction kit is provided, which comprises a reaction container and a nucleic acid amplification reaction reagent contained in the reaction container, the kit being characterized in that the reagent is a multi-layered reagent premix which is cryopreserved in a layered form comprising a first reagent layer that contains a nucleic acid polymerase, a second reagent layer that contains a primer oligonucleotide, and a film that separates the first reagent layer from the second reagent layer and is composed of a substance having a solid form at a temperature of lower than 0°C and capable of being dissolved in an aqueous solution at 0 to 35°C.
A SARS-CoV-2 detection kit comprising (i) first single-stranded cyclic DNA which comprises a sequence that is complementary to a first site in a nucleic acid derived from a novel coronavirus SARS-CoV-2 and is composed of 10 to 30 nucleotides, a first primer binding sequence that is contiguous to the 5'-side of the sequence and is composed of 7 to 8 nucleotides, and a second single-stranded cyclic DNA binding sequence; (ii) a first oligonucleotide primer which comprises a sequence that is complementary to a second site contiguous to the 3'-side of the first site in the nucleic acid derived from the SARS-CoV-2 and is composed of 8 to 15 nucleotides, and a sequence that is contiguous to the 3'-side of the sequence, is complementary to the first primer binding site in the first single-stranded cyclic DNA and is composed of 7 to 8 nucleotides; (iii) second single-stranded cyclic DNA which comprises a sequence that is identical to the second single-stranded cyclic DNA binding sequence in the first single-stranded cyclic DNA and a second primer binding sequence that is contiguous to the 5'-side of the sequence; and (iv) a second oligonucleotide primer which comprises a sequence that is identical to a site contiguous to the 5'-side of the second single-stranded cyclic DNA binding sequence in the first single-stranded cyclic DNA and a sequence that is contiguous to the 3'-side of the sequence and is complementary to the second primer binding sequence in the second single-stranded cyclic DNA, in which the first oligonucleotide primer is bonded to a support through the 5'-terminal thereof, and the second oligonucleotide primer is bonded, through the 5'-terminlal thereof, to the support having the first oligonucleotide primer bonded thereto.
C12Q 1/70 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving virus or bacteriophage
This bone augmentation structure comprises a collagen tube and a collagen structure stored within the collagen tube. The collagen tube has a porosity of 70-98%.
This shape-memory resin composition contains: a resin (A) having a constitutional unit (a1) represented by general formula (a-1) and a constitutional unit (a2) represented by general formula (a-2); titania nanoparticles (B); and a tetraalkylphosphonium salt (C), and can be thermally melted and molded. In formula (a-1), R1is a hydrogen atom or the like. Ra1is a C1-C5 alkyl group. In formula (a-2), R2is a hydrogen atom or the like. X2is a nitrogen-containing cyclic group, a group represented by formula (a-2-1), or a group represented by formula (a-2-2). In formula (a-2-2), Ya2 is a C1-C5 alkylene group.
C08F 226/06 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
Provided are novel determination techniques and systems enabling an AI process in which decisions are made from the viewpoint of allowing an expert to make a decision, and capable of providing a valid answer, even with a small amount of learning data, by adjusting errors in both the answer of the expert and the answer of AI. A system is configured to cause an AI process to be performed on subject training data for AI learning in which events of objects identified by identifying codes are divided into classes, and data pertaining to an object for which class determination of an event is required, and to receive class determination data obtained by the AI process. The system is configured to: cause training data for learning to be randomly input to, and learned by, each of a plurality of AI processes; input data pertaining to the object into each of the plurality of AI processes; receive from each AI process class determination data corresponding to each learning; and store the class determination data in a storage device. In this way, the class of an event of an object identified by each identifying code is determined on the basis of each class determination data item corresponding to the identifying code.
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
A user terminal 4 comprises: an analysis unit 42 (a chewing segment identification module 42a and a filtering/calculation module 42b) that obtains chewing information, which is chronological information indicating jaw movement for one mouthful when a user is eating; and an analysis unit 42 (analysis module 42c) that enters the chewing information to an analysis model M1 and obtains attributes for food estimated as having been chewed by a user by using jaw movement for one mouthful, output from the analysis model M1. The analysis model M1 is a trained model that has machine-learned from teaching data that includes: first information being chronological information indicating past jaw movement for one mouthful, obtained for the user; and second information indicating attributes of food chewed by the user, using past jaw movement for one mouthful.
G16H 20/00 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
A61B 5/11 - Measuring movement of the entire body or parts thereof, e.g. head or hand tremor or mobility of a limb
A learning model provided in a segmentation device is a learning model which is generated using training data such that segmentation data of a biologically important region is output when data of a constituent maxillofacial region is input.
A spectral image generation device comprising: a light source that outputs weak light including photons having different energy; a digital micro mirror device that reflects photons output from the light source and transmits the photons through an imaging subject, reflects photons that have passed through the imaging subject, reflects photons that have been reflected by the imaging subject, or reflects photons output from the light source towards the imaging subject; a photon detector that executes processing that detects photons that have passed through the imaging subject and processing that measures the energy of those photons or processing that detects photons reflected by the imaging subject and processing that measures the energy of those photons; and a spectral image generation unit that uses the results of the processing executed by the photon detector and generates a spectral image of the imaging subject.
G01N 21/01 - Arrangements or apparatus for facilitating the optical investigation
G01N 21/27 - ColourSpectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands using photo-electric detection
The purpose of the present invention is to provide a composition that is effective for the treatment of a prototheca disease. The present invention provides a composition characterized by containing ravuconazole as an active ingredient, and being administered to an animal suffering from a prototheca disease caused by Prototheca wickerhamii or Prototheca zopfii.
The purpose of the present invention is to provide a composition that is effective for the treatment of a prototheca disease. The present invention provides a composition characterized by containing ravuconazole as an active ingredient, and being administered to an animal suffering from a prototheca disease caused by Prototheca wickerhamii or Prototheca zopfii.
Provided is a method for producing a gelatinous composition, the method including: a step for mixing lecithin that has been dissolved or dispersed in water and an organic compound (excluding lecithin) having a molecular weight of 500 or more that has been dissolved or dispersed in water to obtain a mixed liquid containing the lecithin and the organic compound; a step for freeze-drying or heat-drying the mixed liquid to obtain a solid mixture containing the lecithin and the organic compound; and a step for mixing the solid mixture, an oil component and a polar liquid to obtain a gelatinous composition. Also provided is a gelatinous composition produced using the production method.
A61K 8/02 - Cosmetics or similar toiletry preparations characterised by special physical form
A61K 8/55 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing phosphorus
A61K 47/06 - Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
A61K 47/14 - Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
A61K 47/24 - Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing atoms other than carbon, hydrogen, oxygen, halogen, nitrogen or sulfur, e.g. cyclomethicone or phospholipids
57.
DRUG DELIVERY COMPOSITION AND PHARMACEUTICAL COMPOSITION
SHIZUOKA PREFECTURAL UNIVERSITY CORPORATION (Japan)
Inventor
Kanazawa Takanori
Kosuge Yasuhiro
Miyagishi Hiroko
Suzuki Naoto
Abstract
This drug delivery composition is for the delivery of a drug to the spinal cord; comprises a membrane-permeable peptide and a block copolymer in which a polyethylene glycol segment is linked to a hydrophobic polyester segment; and is administered nasally. This pharmaceutical composition comprises the drug delivery composition and a drug for the treatment of a spinal cord disease and is administered nasally for the treatment of a spinal cord disease.
A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups
A61P 25/04 - Centrally acting analgesics, e.g. opioids
A61K 47/34 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
A61K 47/42 - ProteinsPolypeptidesDegradation products thereofDerivatives thereof, e.g. albumin, gelatin or zein
58.
METHOD FOR DETERMINING SENSITIVITY TO SGLT2 INHIBITOR AND SENSITIVITY MARKER FOR SGLT2 INHIBITOR
The object of the present invention is to provide a method for determining the sensitivity of a subject to an SGLT2 inhibitor, and a sensitivity marker for the SGLT2 inhibitor. The present invention provides a method for determining the sensitivity of a subject to an SGLT2 inhibitor, comprising measuring a biomarker in the biological sample of a subject, and determining the sensitivity of the subject to the SGLT2 inhibitor using the measured biomarker value as an indicator.
C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
59.
PRODUCTION METHOD AND KIT OF INDUCED PLURIPOTENT STEM CELLS
This method of producing induced pluripotent stem cells involves a step for introducing an initialization factor into somatic cells of a mammal, and culturing in a neural stem cell culture medium to obtain induced neural stem cell-like cells, and a step for cultivating said induced neural stem cell-like cells in a growth medium to obtain induced pluripotent stem cells , wherein the initialization factor contains an OCT family, a SOX family, a KLF family, a MYC family, a LIN28 family and a P53 function inhibitor.
A nucleic acid detection kit comprising (i) a first single-stranded circular DNA, (ii) a first oligonucleotide primer, (iii) a second single-stranded circular DNA and (iv) a second oligonucleotide primer, wherein the first oligonucleotide primer is attached to a carrier via the 5'-terminus thereof, and the second oligonucleotide primer is attached to the carrier, to which the first oligonucleotide primer is attached, via the 5'-terminus thereof.
C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
C12Q 1/70 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving virus or bacteriophage
G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing
The purpose of the present invention is to provide an anti-fungal agent effective for cryptococcosis. The present invention provides an anti-fungal agent containing ravuconazole as an active ingredient, the anti-fungal agent being characterized by being administered to an animal with cryptococcosis. The present invention also provides an anti-fungal agent containing ravuconazole as an active ingredient, the anti-fungal agent being characterized by being administered to an animal infected by Cryptococcus neoformans having resistance against a triazole-based antibacterial agent selected from the group consisting of fluconazole, itraconazole, and voriconazole.
The purpose of the present invention is to provide an anti-fungal agent effective for cryptococcosis. The present invention provides an anti-fungal agent containing ravuconazole as an active ingredient, the anti-fungal agent being characterized by being administered to an animal with cryptococcosis. The present invention also provides an anti-fungal agent containing ravuconazole as an active ingredient, the anti-fungal agent being characterized by being administered to an animal infected by Cryptococcus neoformans having resistance against a triazole-based antibacterial agent selected from the group consisting of fluconazole, itraconazole, and voriconazole.
SCHOOL CORPORATION, AZABU VETERINARY MEDICINE EDUCATIONAL INSTITUTION (Japan)
Inventor
Sahara, Hiroeki
Nakayama, Tomohiro
Maruo, Takuya
Abstract
The present invention improves the effect of radiotherapy. This radiosensitizer for treating cancer contains a compound represented by general formula (I) or a pharmaceutically acceptable salt thereof, the radiosensitizer being characterized by being used so that a compound represented by general formula (I) is administered to a patient in an amount of 8 mg/kg or less per dose. This radiosensitizer is also characterized by being used to repeat a set of the administration of the radiosensitizer and the irradiation with radiation immediately after the administration so that the total irradiation dose of radiation with respect to cancer is 10 Gy or greater.
The present invention is to provide a tissue slice selection method and an embedded block-preparing cassette which are capable of suppressing occurrence of errors in inspection results. The present invention makes it possible to suppress the occurrence of errors in inspection results by including: an embedded block-preparing process of preparing an embedded block by embedding both a biological tissue fragment and a standard substance in the same embedding agent; an embedded tissue slice preparing step of slicing the embedded block to prepare a sheet-like embedded tissue slice having a tissue slice and standard substance slices appearing on a surface thereof; and a tissue slice selecting step of selecting the tissue slice to be inspected, based on a light signal from the standard substance slice.
A magnetized plasmoid injection device (10) which enables the precise control of the amount of impurities, and which is provided with: a cylindrical external electrode (11); an internal electrode (12) which is coaxially arranged within the external electrode; a plasma generating gas supply unit (13) which supplies a plasma generating gas in a pulse state between the external electrode and the internal electrode; a magnetic field generation unit (15) which applies a magnetic field that generates a magnetized plasmoid between the external electrode and the internal electrode; a power supply control unit (14) which applies a discharge voltage between the external electrode and the internal electrode; and an impurity generation unit (100) which has the magnetized plasmoid contain impurities. The impurity generation unit comprises: a cover electrode (102) which opens to the external electrode; a needle-like electrode (101) which is positioned within the cover electrode, while being composed of impurities; and an impurity generating power supply which applies a voltage to the cover electrode and the needle-like electrode.
C23C 14/22 - Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
A three-dimensional printing apparatus (1) allowing a linear filament (F) in which a fiber bundle (C) is impregnated with resin (P) to be continuously ejected includes twisting means (6) for allowing a total amount of twisting of the filament (F) or an amount of twisting of the fiber bundle (C) to be changed.
B33Y 30/00 - Apparatus for additive manufacturingDetails thereof or accessories therefor
B29C 64/118 - Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using filamentary material being melted, e.g. fused deposition modelling [FDM]
3 is, identically or differently in each occurrence, selected from hydrogen and an optionally substituted aliphatic hydrocarbon group; and n represents an integer of 1 or more.
The invention provides a novel polymer, a composition, and a molded article. The polymer contains a constitutional unit represented by the following formula (1):
11 is a hydrogen atom or an alkyl group optionally containing a fluorine atom; and a is an integer of 1 to 4.
C08G 77/52 - Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages containing aromatic rings
C08L 27/18 - Homopolymers or copolymers of tetrafluoroethene
C09K 3/10 - Materials not provided for elsewhere for sealing or packing joints or covers
69.
COMPOUND, DISPERSANT, COMPLEX, DISPERSION, AND METHOD FOR PRODUCING COMPLEX
B01J 13/00 - Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided forMaking microcapsules or microballoons
NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (Japan)
NIHON UNIVERSITY (Japan)
FUKUI FIBERTECH CO., LTD. (Japan)
AISIN SEIKI KABUSHIKI KAISHA (Japan)
KYOWA INDUSTRIAL CO., LTD. (Japan)
Inventor
Ishikawa Takashi
Ichiki Makoto
Fukui Eisuke
Hirayama Norio
Sakata Kazuhiro
Hirabayashi Akiko
Abstract
A production device 10 for fiber-reinforced thermoplastic resin comprising: an impregnation chamber for impregnating a thermoplastic resin monomer liquid or solution into a plurality of long fibers 20; a polymerization chamber 11 for polymerizing the monomer by heating the long fibers 20 that are impregnated with the monomer; and a moving unit 16 for drawing the long fibers 20 impregnated with the thermoplastic resin from the chamber.
B29K 77/00 - Use of polyamides, e.g. polyesteramides, as moulding material
B29K 105/08 - Condition, form or state of moulded material containing reinforcements, fillers or inserts of continuous length, e.g. cords, rovings, mats, fabrics, strands or yarns
A61B 1/24 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor for the mouth, i.e. stomatoscopes, e.g. with tongue depressorsInstruments for opening or keeping open the mouth
A61C 19/04 - Measuring instruments specially adapted for dentistry
A61B 1/07 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor with illuminating arrangements using light-conductive means, e.g. optical fibres
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61C 1/08 - Machine parts specially adapted for dentistry
72.
Medical x-ray CT imaging apparatus, medical x-ray ray CT imaging condition setting method, and non-transitory computer readable medium
A medical X-ray CT imaging apparatus includes an X-ray generator that generates a cone beam, an X-ray detector, a support that supports the X-ray generator and the X-ray detector while the X-ray generator and the X-ray detector are opposed to each other, a turning drive unit that turns the X-ray generator and the X-ray detector, which are supported by the support, an imaging information receiving unit, and an X-ray output condition setting unit. The imaging information receiving unit receives an imaging area setting relating to at least one of a size of an imaging area, an imaging purpose, and an imaging region. The X-ray output condition setting unit automatically sets an output condition of the X-ray generator according to at least one of the size of the imaging area, the imaging purpose, and the imaging region, which are received by the imaging information receiving unit.
A first position setting unit receives an operation to designate a position in a mesiodistal on a panoramic tomographic image displayed on a display, and sets a first position on a curved section based on the designation operation. The fluoroscopic imaging information providing unit provides information irradiating a subject with an X-ray beam along a direction having a component of a tangential direction at the first position of the curved section to execute fluoroscopic imaging acquiring a fluoroscopic image to a main body. A second position setting unit receives an operation to designate a position in a buccolingual direction on the fluoroscopic image displayed on the display, and sets a second position in the buccolingual direction based on the designation operation.
Provided are a tissue slice selection method and an embedded block preparing cassette with which it is possible to suppress the occurrence of errors in inspection results. This tissue slice selection method makes it possible to suppress the occurrence of errors in inspection results by comprising: an embedded block preparing step of preparing an embedded block 24 by embedding a biological tissue piece 22 and a reference material 21 in the same embedding agent 23; an embedded tissue slice preparing step of thinly cutting the embedded block 24 to prepare a sheet-like embedded tissue slice 44 in the surface of which a tissue slice 42 and a reference material slice 41a, 41b, 41c, 41d, 41e appear; and a tissue slice selecting step of selecting the tissue slice 42 to be inspected, on the basis of an optical signal from the reference material slice.
Provided is a preparation which has an effect of promoting the healing of a tissue wound. The wound healing promoter according to the present invention comprises, as an active ingredient, at least one member selected from among a compound represented by formula (1), a salt thereof and a hydrate of the same. In formula (1): R1 and R2 are either the same or different and represent a hydrogen atom or a hydrocarbon group optionally having one or more substituents selected from the group consisting of a halogen atom, -COOR3, -CONR32, -COR3, -CN, -NO2, -NHCOR3, -OR3, -SR3, -OCOR3, -SO3R3 and -SO2NR32 (wherein R3's are either the same or different and represent a hydrogen atom or an optionally substituted aliphatic hydrocarbon group); and n is an integer of 1 or greater.
This score determination device of a medical examination for biological function is provided with: a weight calculation unit which calculates a weight on the basis of first data including, among data about a first subject, at least one among data that includes a determination score of a medical examination based on the subject's own report and indicates an examination result of the medical examination, and data that indicates a physical feature; and a score determination unit which determines a determination score of a second subject on the basis of the weight calculated by the weight calculation unit, and second data including, among data about the second subject, at least one among data which indicates an examination result of a medical examination and data which indicates a physical feature.
A61B 10/00 - Instruments for taking body samples for diagnostic purposesOther methods or instruments for diagnosis, e.g. for vaccination diagnosis, sex determination or ovulation-period determinationThroat striking implements
A61B 5/1455 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value using optical sensors, e.g. spectral photometrical oximeters
78.
TEMPERATURE-RESPONSIVE HYDROGEL AND METHOD FOR PRODUCING SAME
[Problem] To provide a temperature-responsive hydrogel by means of a simple method (mixing), said temperature-responsive hydrogel having a feature such that the viscosity thereof is high at high temperatures but low at low temperatures. [Solution] It is found that a temperature-responsive hydrogel which has high viscosity at high temperatures and low viscosity at low temperatures, while having a high (viscosity at high temperatures)/(viscosity at low temperatures) ratio, is able to be obtained by a method for mixing an aqueous solution containing a polyalkylene glycol (A) that has a weight average molecular weight of from 20,000 to 10,000,000 and an aqueous solution containing a silicate (B) within a specific component composition range, specifically at a mass concentration of A of 0.01-1.5% by mass, preferably at a mass concentration of A of 0.1-0.4% by mass and at a mass concentration of B of 0.5-10% by mass, preferably at a mass concentration of B of 1-5% by mass, with the mass ratio R of A to B (R = (mass of A)/(mass of B)) being within the range of from 0.01 to 0.5; and this finding led to the completion of the present invention.
A61L 31/14 - Materials characterised by their function or physical properties
B01J 13/00 - Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided forMaking microcapsules or microballoons
A three-dimensional printing apparatus (1) capable of continuously ejecting a linear filament (F) in which a fiber bundle (C) is impregnated with resin (P) is provided with twisting means (6) capable of changing the overall amount of twisting of the filament (F) or a twisting amount of the fiber bundle (C).
B29C 64/118 - Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using filamentary material being melted, e.g. fused deposition modelling [FDM]
B33Y 30/00 - Apparatus for additive manufacturingDetails thereof or accessories therefor
D02G 3/44 - Yarns or threads characterised by the purpose for which they are designed
Conventional reverse photochromic compounds have difficulty in sensing light in a visible light region of 600 nm or more used in medical applications, etc. The present invention addresses the problem of providing a reverse photochromic compound and polymer which are highly sensitive even to light of 600 nm or more. The present invention pertains to a compound or the like represented by general formula (1) (wherein, R1 and R4 each independently represent a hydrogen atom or the like, R2, R3, and R5 each independently represent an alkyl group or the like, R6 represents a group having a polymerizable unsaturated group, a carboxy group, an alkoxycarbonyl group, or the like, R31 and R32 each independently represent an alkoxy group or the like, R33 and R34 each independently represent a hydrogen atom or the like, Y1 represents an oxygen atom or a sulfur atom, An- represents an anion, n1-n3 represent a specific integer, and R1 and R2, R3 and R4, and/or R33 and R34 may form an alkylene group.)
C07D 405/06 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
C08F 20/36 - Esters containing nitrogen containing oxygen in addition to the carboxy oxygen
The present invention provides a novel polymer, a composition, and a molded article. This polymer has a structural unit represented by general formula (1) (in the formula, X11 and X12 may be the same or different from each other, and each represent a hydrogen atom, an alkyl group optionally having a fluorine atom, or a phenyl group, Y11 represents an oxygen atom or a sulfur atom, Rf11 represents a hydrogen atom or an alkyl group optionally having a fluorine atom, and a represents an integer of 1-4).
C08G 77/52 - Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages containing aromatic rings
C08L 83/14 - Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon onlyCompositions of derivatives of such polymers in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
C08L 101/04 - Compositions of unspecified macromolecular compounds characterised by the presence of specified groups containing halogen atoms
C09K 3/10 - Materials not provided for elsewhere for sealing or packing joints or covers
The disease condition determination device according to the present invention is provided with: a first separation degree calculation unit for calculating a degree of separation on the basis of first load blood flow information which is blood flow information for a task state in which a first load for varying the blood flow state of a subject is imposed on the subject, and second load blood flow information which is blood flow information for a control state in which a second load different from the first load is imposed on the subject, from among blood flow information obtained by measuring blood flow in the brain of a subject by optical measurement using near-infrared rays; an oscillation detection unit for detecting oscillation in variation of the hemoglobin concentration of the blood flow of the subject on the basis of non-load blood flow information; a phase detection unit for detecting the phase of the variation in hemoglobin concentration of the blood flow of the subject on the basis of the non-load blood flow information; and a determination unit for determining the disease condition of the subject on the basis of the degree of separation calculated by the first separation degree calculation unit, the oscillation detected by the oscillation detection unit, and the phase detected by the phase detection unit.
A61B 5/1455 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value using optical sensors, e.g. spectral photometrical oximeters
A61B 10/00 - Instruments for taking body samples for diagnostic purposesOther methods or instruments for diagnosis, e.g. for vaccination diagnosis, sex determination or ovulation-period determinationThroat striking implements
83.
Device for calculating construction assistance information, system for calculating construction assistance information, and program
A device for calculating construction assistance information includes: an acquisition unit that acquires, from a vibratory hammer construction machine, information that contains at least values indicating a eccentricity force of a vibratory hammer which the vibratory hammer construction machine imparts to a construction object, the number of impacts, and a depth of penetration of the construction object; and a calculation unit that calculates a accumulated impact force indicating a work load of construction on the basis of the information acquired by the acquisition unit.
An oligonucleotide selected from the group consisting of the following oligonucleotides (i) to (iii): (i) an oligonucleotide which comprises the nucleotide sequence represented by SEQ ID NO: 15; (ii) an oligonucleotide which comprises a nucleotide sequence produced by deleting, substituting or adding one or several residues in the nucleotide sequence represented by SEQ ID NO: 15 and which has a binding ability specific to ITS2 of Aspergillus terreus; and (iii) an oligonucleotide which comprises a nucleotide sequence complementary to the nucleotide sequence for the oligonucleotide (i) or (ii).
A dental caries diagnosis device comprising a light source which emits examination light (R), and a light receiving unit (4f) which receives the examination light (R) with which a tooth has been irradiated comprises: a head-side casing (4a1) which is inserted into the mouth in a contactless manner with respect to the tooth or the gum, and which projects the examination light (R) toward the tooth; and a filter (4e) which is disposed in front of the light receiving unit (4f) and which removes a noise component from the received light, wherein the light receiving unit (4f) receives the examination light (R) that has been transmitted through the tooth.
A61B 1/24 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor for the mouth, i.e. stomatoscopes, e.g. with tongue depressorsInstruments for opening or keeping open the mouth
A61C 19/04 - Measuring instruments specially adapted for dentistry
87.
PERIODONTITIS TEST KIT USING MIRNA AS MARKER, AND TEST METHOD
Since a miRNA that serves as a diagnostic marker for periodontitis of the present invention displays a change specific to periodontitis, diagnosis of periodontitis can be performed accurately.
A three-dimensional printing apparatus (1) is provided with: a head (4) to which linear print material is to be fed; a driving unit that performs relative movement between the head (4) and a target surface (3a); a controller; and a pressing means (30) having a pressing surface (41) disposed to be capable of coming in contact with the print material on the target surface (3a). The pressing means (30) is configured to allow movement of the pressing surface (41) with respect to the head (4).
A three-dimensional printing system (1) includes: a head (2) to which a first continuous material (FL) including a resin and a second continuous material (FB) including fibers are fed; a platform (3) on which a printing material based on the first and second continuous materials from the head is stacked; a cutting device (10) which is capable of cutting at least fibers; and a controller (5) which controls an operation device including at least one of the head, the platform, and the cutting device.
B33Y 30/00 - Apparatus for additive manufacturingDetails thereof or accessories therefor
B29C 64/118 - Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using filamentary material being melted, e.g. fused deposition modelling [FDM]
B29C 70/38 - Automated lay-up, e.g. using robots, laying filaments according to predetermined patterns
B29K 105/08 - Condition, form or state of moulded material containing reinforcements, fillers or inserts of continuous length, e.g. cords, rovings, mats, fabrics, strands or yarns
A culture container 1 comprising a culture container body 11, a partition board 15 that is disposed in the vicinity of the bottom surface 11c of the culture container body 11 facing the bottom surface 11c and forms a culture area A1 as a culture area being positioned between the partition board 15 and the bottom surface 11c, and a sample inlet/outlet 19 that is formed in the culture container body 11, wherein the sample inlet/outlet 19 communicates with the culture area A1 via an opening formed on one end side of the partition board 15. By using the culture container 1 and a culture method using the same, a large amount of fat cells can be cultured at once by a simple operation. Thus, a large amount of fat cells can be efficiently dedifferentiated and non-dedifferentiated cells can be efficiently removed.
Seat members 31 are held in a state of being movable with respect to first slide members 21 or second slide members 22 correspondingly. By rotating screws 39 in directions to increase the distances d between surfaces A of the first slide members 21 or the second slide members 22 and surfaces B of the seat members 31, chucks 25 are moved in directions to increase the distance between the chucks to apply pretension to a test piece correspondingly. When backlash in a force transmission system from a support part to the respective chucks 25 is eliminated, a biaxial tensile test is started.
The present invention is a labeled peptide formed from a non-naturally occurring amino acid sequence that is represented by formula (1). (XFNXN)mXp(XFNXN)nXq (1) (In formula (1), each X is independently an aspartic acid residue or a glutamic acid residue, F is a phenylalanine residue, N is an asparagine residue, m is an integer of 0 to 5, n is an integer of 1 to 5, p is an integer of 1 to 20, and q is an integer of 1 to 4.)
The present invention addresses the problem of providing a cell for use in a vascular regeneration therapy, which has a superior blood flow-improving effect compared with a bone marrow-derived MSC, an ASC or the like that is a conventional cell for use in a therapy, and which can be obtained easily in an amount sufficient enough for transplantation, and which has stable quality. It is found that a human DFAT has a high neovascularization ability, can exhibit a high proliferation ability after being subcultured and therefore can be produced easily in an amount needed for transplantation, and does not undergo transformation. Therefore, it is found for the first time that a human DFAT is effective for a vascular regeneration therapy for a human body. These findings lead to the accomplishment of the present invention. That is, the present invention provides a blood flow-improving agent containing human dedifferentiated fat cells (human DFAT) as an active ingredient.
A61P 9/00 - Drugs for disorders of the cardiovascular system
A61P 9/04 - Inotropic agents, i.e. stimulants of cardiac contractionDrugs for heart failure
A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
C12N 5/077 - Mesenchymal cells, e.g. bone cells, cartilage cells, marrow stromal cells, fat cells or muscle cells
94.
METHOD FOR IDENTIFYING CELLS CAUSING PERIODONTITIS, METHOD FOR SCREENING PERIODONTITIS THERAPEUTICS, METHOD FOR TESTING PERIODONTITIS, AND TEST KIT
Established are an analysis of markers of aggressive fibroblasts which are cells that cause periodontitis, screening of novel periodontitis therapeutics, a test method, and a test kit. As a result of analyzing aggressive fibroblasts, it has become apparent that expression from the P1 promoter of RUNX2 and expression of DLX5 are decreased to a greater extent than in normal gingival fibroblasts. An increase in expression of FLT1 was also seen. Using these expressions characteristic of aggressive fibroblasts as markers makes possible the identification of aggressive fibroblasts, a method for screening therapeutics, and a test method.
A device for calculating construction assistance information comprises: an acquiring unit that acquires, from vibratory hammer construction machinery, information that contains at least values indicating the vibratory hammer vibrating force applied to the object of construction by the vibratory hammer construction machinery, the number of impacts, and the depth of penetration of the object of construction; and a calculating unit that calculates, on the basis of the information acquired by the acquiring unit, the cumulative impact force that indicates the amount of construction work.
A reverse ABO blood grouping test device (1) according to the present invention is provided with: a chip (2) which has a waveguide layer (6) formed therein; an antigen-immobilizing surface (10) which is formed on a first surface (2a) of the chip (2); an antigen (20) which has an immobilizing end (20a) that is immobilized onto the antigen-immobilizing surface (10) and an open end (20b) that is kept non-immobilized, and which can cause an antigen-antibody reaction with an anti-A antibody (PA) or an anti-B antibody (PB); and a determination section (40) in which it is determined whether or not an antigen-antibody reaction occurs at the antigen (20) on the basis of the wavelength distribution of the intensity of light that enters the chip (2) and is emitted through the chip (2).
G01N 33/80 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving blood groups or blood types
G01N 21/17 - Systems in which incident light is modified in accordance with the properties of the material investigated
G01N 21/27 - ColourSpectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands using photo-electric detection
Provided is a muon-plasmoid complex nuclear fusion reactor whereby muon reactivation can be performed in order to increase the efficiency of energy production. A muon-plasmoid nuclear fusion reactor for obtaining a nuclear fusion reaction comprises a target container 10, a solid hydrogen ice fog generating source 20, a plasmoid generating source 30, and a muon generating source 40. The solid hydrogen ice fog generating source 20 is connected to the target container 10, and injects solid hydrogen into the target container 10 and forms a solid hydrogen ice fog 21. The plasmoid generating source 30 is connected to the target container 10, and generates a magnetized plasmoid 31, transports the magnetized plasmoid into the solid hydrogen ice fog 21 in the target container 10, and forms a solid-plasma complex region 32. The muon generating source 40 is connected to the target container 10, and injects muons 41 into the solid-plasma complex region 32 to obtain a nuclear reaction.
This vaccine for activating CD8 T-cells has an active ingredient of bacillus Calmette–Guérin (BCG) in which a protein derived from pathogenic microorganisms is expressed. The vaccine is useful due to the ability of the vaccine to activate CD8+ T-cells that are specific to an antigen derived from pathogenic microorganisms.
CELLULAR-DISORDER INHIBITOR, MEDICINAL COMPOSITION CONTAINING SAID CELLULAR-DISORDER INHIBITOR FOR PREVENTION OR TREATMENT OF ORGAN DERANGEMENT CAUSED BY HYPOXEMIA, AND MEDICINAL COMPOSITION CONTAINING SAID CELLULAR-DISORDER INHIBITOR FOR PREVENTION OR TREATMENT OF ISCHEMIC CEREBROVASCULAR DISORDER
The present invention is a cellular-disorder inhibitor characterized by containing any one of peptides (a) to (g), a derivative thereof, or a salt or ester of these as an active ingredient.
A steam corrosion-resistant multilayered film formed on a base material containing a silicon carbide composite material, said steam corrosion-resistant multilayered film being characterized by comprising: an eutectic structure layer containing an eutectic structure of a plurality of metal oxides which is formed without any grain boundary glass phase existing therein; and a gradient composition layer which is interposed between the eutectic structure layer and the base material, which contains the metal oxides and metal carbides, and in which the compositional ratio of the metal carbides gradiently increases toward the base material.