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IC:C12M

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1 / 28,286
1.20250207079SYSTEMS AND METHODS FOR CYANOBACTERIA INDOOR AIR BIOFILTRATION TO REDUCE AIR HANDLING ENERGY CONSUMPTION
US - 26.06.2025
Int.Class C12M 1/34
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY
1Apparatus for enzymology or microbiology
34Measuring or testing with condition measuring or sensing means, e.g. colony counters
 Appl.No 18984125 Applicant VerdeTerra LLC Inventor Mark SNYDER

Systems and methods for cyanobacteria indoor air biofiltration to reduce air handling energy consumption are disclosed. A system may include: a heating, ventilation, and air conditioning (HVAC) system comprising an air valve that controls a flow of conditioned, untreated air from an enclosed area; and a biofiltration device comprising: a controller that interfaces with the air valve and controls the air valve to open or close; an air inlet that receives the untreated air from the air valve when the air valve is in an open position; a bioreactor comprising a bio-organism; an air bubble mixing system that receives the untreated air and diffuses the untreated air into the bioreactor, wherein the bio-organism is configured to consume CO2 via photosynthesis and to release treated air; and an air outlet that receives the treated air from the bioreactor and expels the treated air to enclosed area.

2.WO/2025/134419CELL CULTURE APPARATUS
WO - 26.06.2025
Int.Class C12M 1/00
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY
1Apparatus for enzymology or microbiology
 Appl.No PCT/JP2024/027994 Applicant NIKKISO CO., LTD. Inventor NASU Keita
Provided is a cell culture apparatus that enables operation units having different functions to operate in a more optimized environment. The cell culture apparatus is provided with: a first space (such as the internal space of a culture medium exchange section 22) that satisfies first criteria according to air cleanliness standards (such as ISO class 5); a second space (such as the internal space of a section other than the culture medium exchange section 22) that satisfies second criteria lower than the first criteria according to the air cleanliness standards (such as ISO class 6-7); a culture medium exchange robot (42) that is arranged in the first space and can perform an operation relating to medium exchange; a transfer robot (40) that is arranged in the second space and can perform an operation of moving a well plate (52) containing a culture medium; and a control unit that sets the movable range of the culture medium exchange robot (42) to the first space when the culture medium exchange robot (42) performs the operation relating to medium exchange, and sets the movable range of the transfer robot (40) to the second space and the first space when the transfer robot (40) moves the well plate (52).
3.WO/2025/129382POROUS MEMBRANE-BASED MULTI-STAGE DRUG METABOLISM ORGAN-ON-CHIP AND APPLICATION THEREOF
WO - 26.06.2025
Int.Class C12M 3/00
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY
3Tissue, human, animal or plant cell, or virus culture apparatus
 Appl.No PCT/CN2023/139418 Applicant SHANGHAI BIOCHIP CO., LTD. Inventor XU, Yichun
The present invention provides a porous membrane-based multi-stage metabolism organ-on-chip, comprising a porous membrane layer, and upper and lower chip layers, wherein a number N of non-intersected upper fluid channels are provided in the lower surface of the upper chip layer. A number N-1 of metabolic chambers are provided on the upper surface of the lower chip layer, projections of the metabolic chambers on the upper chip layer respectively overlap with two upper fluid channels adjacent thereto, and each metabolic chamber is in communication with the two upper fluid channels adjacent thereto by means of the porous membrane layer. The porous membrane layer is made of a material which is impermeable to cells but permeable to cellular metabolic secretions, wherein N is an integer greater than or equal to 2. By means of providing the porous membrane layer allowing the transfer of metabolites, the metabolites generated by the cells and test drugs in the first upper fluid channels enter the metabolic chambers on the lower chip layer, and then the metabolites in the metabolic chambers enter the next fluid channel of the upper chip layer, the cells in the next fluid channel can continue to interact with the metabolites generated in the previous stage, and the influences of multi-stage drug-cell metabolism can thus be researched.
4.WO/2025/131467BIOPROCESS ASSEMBLY WITH INTEGRATED FILTRATION AND SAMPLING SYSTEMS
WO - 26.06.2025
Int.Class C12M 1/34
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY
1Apparatus for enzymology or microbiology
34Measuring or testing with condition measuring or sensing means, e.g. colony counters
 Appl.No PCT/EP2024/082436 Applicant SARTORIUS STEDIM BIOTECH GMBH Inventor GRIMM, Christian
A bioprocess assembly (10) comprises a separation system (12) and a sampling system (14). The sampling system (14) is fluidically connected to the separation system (12) and comprises a sampling membrane (32) such that the separation system (12) and the sampling membrane (32) provide a separate sampling channel (30). The sampling channel (30) comprises at least one fluidic connection (36) to receive a buffer and at least one fluidic connection (51) to a sampling station (50). Further, the sampling channel (30) comprises a counter pressure generating unit (48) and at least one sensor (40), wherein the counter pressure generating unit (48) is configured to adjust the pressure within the sampling channel (30) based on data collected by the at least one sensor (40).
5.WO/2025/134917CULTURE MEDIUM MONITORING DEVICE, CULTURE MEDIUM MONITORING METHOD, AND PROGRAM
WO - 26.06.2025
Int.Class C12M 1/00
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY
1Apparatus for enzymology or microbiology
 Appl.No PCT/JP2024/044013 Applicant OMRON CORPORATION Inventor SAKAMOTO, Yuki
Provided are a culture medium monitoring device, a culture medium monitoring method, and a program, that assist efficient management of cell culture.　This culture medium monitoring device comprises: an acquisition unit that acquires, in cell culture using a culture medium, at least one of, first information on a measurement value obtained through sensing for the culture medium, second information on an environment of the cell culture, and third information on a facility of the cell culture; and an estimation unit that estimates the condition of the culture medium and/or a method for improving the condition of the culture medium on the basis of the information acquired by the acquisition unit.
6.3030032DEVICE FOR IN-VITRO MODELLING IN-VIVO TISSUES OF ORGANS
ES - 26.06.2025
Int.Class C12M 1/24
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY
1Apparatus for enzymology or microbiology
24tube or bottle type
 Appl.No 20152403 Applicant Universität Bern Inventor GUENAT, Olivier Thierry
7.WO/2025/135053CLOCKING DEVICE, CLOCKING METHOD, FLUID CONTROL DEVICE, DILUTION DEVICE, AND INSPECTION DEVICE
WO - 26.06.2025
Int.Class G01N 1/38
GPHYSICS
01MEASURING; TESTING
NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
1Sampling; Preparing specimens for investigation
28Preparing specimens for investigation
38Diluting, dispersing or mixing samples
 Appl.No PCT/JP2024/044704 Applicant SUMITOMO BAKELITE CO., LTD. Inventor TSUCHIDA Yuhei
A clocking device 10 comprises: a flow path groove 12 that is formed on at least one surface of a substrate 11; a coating material that covers the flow path groove 12; and a fluid introduction port 14 that communicates with the flow path groove 12. The flow path groove 12 has a section with a width of 0.8-2.0 mm and a depth of 70-100 μm. The clocking device can measure a prescribed time by a required time until a fluid that is introduced into the introduction port 14 reaches a prescribed end point G that is located downstream of the flow path groove 12.
8.20250207098METHOD FOR CULTIVATING MESENCHYMAL STEM CELL
US - 26.06.2025
Int.Class C12N 5/0775
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
5Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
07Animal cells or tissues
071Vertebrate cells or tissues, e.g. human cells or tissues
077Mesenchymal cells, e.g. bone cells, cartilage cells, marrow stromal cells, fat cells or muscle cells
0775Mesenchymal stem cells; Adipose-tissue derived stem cells
 Appl.No 18851462 Applicant NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM Inventor Kazuhiro FURUHASHI

A method for efficiently culturing mesenchymal stem cells (MSCs) on hollow fiber membranes and an object for applying cultured MSCs on hollow fiber membranes to diseases. MSCs are cultured by a method that includes: a step of hydrophilizing the outer luminal surface of a hollow fiber membrane; a step of placing the hydrophilized hollow fiber membrane in a culture solution for seeding MSCs on the outer luminal surface; and a step of culturing MSCs under conditions of applying hydrodynamic loading into the hollow fiber membrane with the cells seeded thereon. A column cartridge containing MSCs and the hollow fiber membrane, wherein the MSCs are adhered in multiple layers to the outer luminal surface of the hollow fiber membrane are present for therapeutic devices.

9.20250205677POLYMER-COATED GLASS SUBSTRATE
US - 26.06.2025
Int.Class B01J 20/26
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
20Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
22comprising organic material
26Synthetic macromolecular compounds
 Appl.No 18967346 Applicant SUMITOMO RUBBER INDUSTRIES, LTD. Inventor Yasuhisa MINAGAWA

Provided is a polymer-coated glass substrate having a surface with controlled irregularities and a low elastic modulus. The polymer-coated glass substrate includes a glass substrate and a hydrophilic polymer layer including a blend of hydrophilic polymers with different molecular weights, the hydrophilic polymer layer being on a surface of the glass substrate.

10.WO/2025/131357CENTRIFUGE CONTAINER FOR CLARIFYING A LIQUID AND METHOD THEREOF
WO - 26.06.2025
Int.Class B04B 5/04
BPERFORMING OPERATIONS; TRANSPORTING
04CENTRIFUGAL APPARATUS OR MACHINES FOR CARRYING-OUT PHYSICAL OR CHEMICAL PROCESSES
BCENTRIFUGES
5Other centrifuges
04Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers
 Appl.No PCT/EP2024/077019 Applicant THERMO ELECTRON SAS Inventor LIMON, Benoit
A centrifuge container for clarifying a liquid containing suspended particles is provided. The centrifuge container comprises: a connection end for connection to a centrifuge rotor; and an outer end for concentration of particles. The outer end is spaced from the connection end in a first direction along a longitudinal axis of the centrifuge container. The centrifuge container further comprises: a first fluid port at the connection end for flowing a liquid containing suspended particles into the centrifuge container; a second fluid port at the connection end for flowing the liquid containing suspended particles from the centrifuge container; and a flushing tube extending from the connection end towards the outer end, the flushing tube for delivering a flushing fluid to flush concentrated particles from the outer end.
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