摘要:
The present invention relates to a culture device for tissue cell suspension. The culture device includes a tissue cell culture body. The tissue cell culture body is a porous material. The porous material is formed by cavities classified into different levels according to the pore size of material and cavity walls surrounding to form the cavities. A lower level of small cavities is provided to surround the cavity wall which forms the upper level of large cavity. Cavities of each level are in communication with each other, and cavities between respective levels are also in communication with each other. The culture device further includes a swirler device. Such culture device can particularly facilitate normal and unrestricted growth of the suspension of cells in three-dimensional space, obstructing the formation of over-dense cell region or nutrient-rich region during the cell culturing, enabling a uniform cell distribution, and facilitating normal growth of cells.
摘要:
A cell culture system disclosed herein comprises a culture medium container (10) to supply a culture medium to a culture container, two culture containers (20, 30) for use in cell culture, and a transfer tube (40) to connect these containers, whereby liquid delivery can be performed by use of only one pump (41). The containers in the cell culture system are connected to the transfer tube (40) in the order of the culture medium container (10), the second culture container (30) and the first culture container (20); the only one pump (41) is attached to the transfer tube; the second culture container is connected to the transfer tube on both sides of the pump by culture container connecting tubes (42) to connect the second culture container and the transfer tube, to inject cells into the first culture container; the culture medium is transferred from the culture medium container to the first culture container by the pump; after the cell culture in the first culture container, a cell suspension is transferred from the first culture container to the second culture container; and the culture medium is transferred from the culture medium container to the second culture container.
摘要:
The present invention provides a method of producing a photosynthetic product, the method comprising maintaining a photosynthetic plant or algal cell suspension culture, in the presence of water, light and a carbonic acid-enriched growth medium. The carbonic acid may, for example be provided by feeding the photosynthetic plant cell suspension culture with a carbonic acid solution, a solid or liquid precursor thereof, or a gaseous mixture of carbon dioxide and one or more other gases. The invention also provides a method for producing a photosynthetic product, the method comprising maintaining a photosynthetic plant or algal cell suspension culture, in the presence of water, light and a carbon source selected from carbon dioxide and carbonic acid, wherein the culture is maintained at a pH of less than 7.0, preferably 4.5 to 5.5.
摘要:
Provided is an apparatus to produce cultured cell products including: an isolator 3 configured to maintain its inside in aseptic conditions and process cell culture vessels 1 therein; and at least one robot arm 6, 7, and 10 to 12 located within the isolator 3, wherein a taking-out step of taking out cells cultured in the cell culture vessels 1, a cell density-adjusting step of adjusting density of the cells in a cell-containing liquid containing the taken-out cells, and a subdividing step of subdividing and placing the cell-containing liquid with its density adjusted into a plurality of product containers 9 are performed within the isolator 3 by the at least one robot arm 6, 7, and 10 to 12.
摘要:
One or more embodiments are described directed to a method and system for loading and distributing cells in a bioreactor of a cell expansion system. Accordingly, embodiments include methods and systems that may provide for adding a plurality of cells to a fluid within a bioreactor of the cell expansion system. A first percentage of the plurality of cells is allowed to settle in the bioreactor and a second percentage of the plurality of cells is allowed to settle outside of the bioreactor. The first percentage of cells is then expanded in the bioreactor. The second percentage of cells is wasted.
摘要:
A cell dissociation solution is used in dissociation of, from a substrate, a cell disposed on the substrate, by application of ultrasonic vibration to the cell and the cell dissociation solution contains a polymer including a polyalkylene glycol structure.
摘要:
[Object] To provide a compact culture device 10 capable of performing large-scale culture in an aseptic state. [Solution] The culture device 10 has a culture bag 70 which has ports 73 and 74 through which a liquid flows and enables cell culture, a bag holding portion 31 having holding plates 42 and 43 holding the culture bag 70 and rotating shafts 48 and 49, a rotation mechanism 34 supporting and rotating the rotating shaft 48, a liquid supply/discharge mechanism 37 supplying and discharging a liquid to/from the culture bag 70, and a rotation control portion 20 controlling the rotation of the rotation mechanism 34. The rotation control portion 20 brings the bag holding portion 31 into a first position in parallel with the approximately horizontal direction according to a first information, brings the bag holding portion 31 into a second position when a culture medium in the culture bag 70 is caused to flow out of the port 74 according to a second information, and brings the bag holding portion 31 into a third position in parallel with the approximately vertical direction at least when a cell suspension in the culture bag 70 is caused to flow out of the port 74 according to a third information.
摘要:
An object of the invention is to provide an electroporation method for treating vesicles with exogenous material for insertion of the exogenous material into the vesicles which includes the steps of: a. retaining a suspension of the vesicles and the exogenous material in a treatment volume in a chamber which includes electrodes, wherein the chamber has a geometric factor (cm -1 ) defined by the quotient of the electrode gap squared (cm 2 ) divided by the chamber volume (cm 3 ), wherein the geometric factor is less than or equal to 0.1 cm -1 , wherein the suspension of the vesicles and the exogenous material is in a medium which is adjusted such that the medium has conductivity in a range spanning 0.01 to 1.0 milliSiemens, wherein the suspension is enclosed in the chamber during treatment, and h. treating the suspension enclosed in the chamber with one or more pulsed electric fields. With the method, the treatment volume of the suspension is scalable, and the time of treatment of the vesicles in the chamber is substantially uniform.
摘要:
The present invention addresses the problem of providing a method for producing cell aggregates using suspension culture, wherein it is easy to control the size of the cell aggregates so as to be appropriate for culturing, and the likelihood of damaging the cells is low. The present invention pertains to a method for producing cell aggregates, the method comprising the step of culturing cells while suspended in a liquid culture medium containing a lysophospholipid.
摘要:
A cell culture system disclosed herein comprises a culture medium container (10) to supply a culture medium to a culture container, two culture containers (20, 30) for use in cell culture, and a transfer tube (40) to connect these containers, whereby liquid delivery can be performed by use of only one pump (41). The containers in the cell culture system are connected to the transfer tube (40) in the order of the culture medium container (10), the second culture container (30) and the first culture container (20); the only one pump (41) is attached to the transfer tube; the second culture container is connected to the transfer tube on both sides of the pump by culture container connecting tubes (42) to connect the second culture container and the transfer tube, to inject cells into the first culture container; the culture medium is transferred from the culture medium container to the first culture container by the pump; after the cell culture in the first culture container, a cell suspension is transferred from the first culture container to the second culture container; and the culture medium is transferred from the culture medium container to the second culture container.