INCUBATOR
20230265370 · 2023-08-24
Inventors
Cpc classification
C12M1/02
CHEMISTRY; METALLURGY
C12M29/00
CHEMISTRY; METALLURGY
C12M23/36
CHEMISTRY; METALLURGY
C12M1/12
CHEMISTRY; METALLURGY
International classification
C12M1/12
CHEMISTRY; METALLURGY
C12M1/02
CHEMISTRY; METALLURGY
Abstract
Provided in the present invention is an incubator capable of producing pressure fluctuations. The incubator comprises an incubator body and a variable pressure apparatus, the incubator body having a variable pressure interface, the variable pressure apparatus being connected to the incubator body by means of the variable pressure interface, and the variable pressure apparatus being used for inputting fluctuating or constant air pressure into the incubator body.
Claims
1. An incubator comprising an incubator body, wherein said incubator further comprises a variable pressure apparatus, said incubator body has a variable pressure interface, said variable pressure apparatus is connected to said incubator body via said variable pressure interface, and said variable pressure apparatus is configured to input fluctuating or constant gas pressure into said incubator body.
2. The incubator according to claim 1, wherein said variable pressure apparatus comprises a cylinder body and a piston, said cylinder body is communicated to said incubator body via said variable pressure interface, and said piston is movably disposed in said cylinder body so as to input said gas pressure by means of the movement of said piston.
3. The incubator according to claim 2, wherein said cylinder body is connected to said variable pressure interface directly or via a pipe.
4. The incubator according to claim 2, wherein said cylinder body is directly connected to said variable pressure interface, and said variable pressure interface is large enough to allow said cylinder body and said incubator body to synchronously change in gas pressure along with the movement of said piston.
5. The incubator according to claim 2, wherein said cylinder body is fixedly connected to said incubator body, and preferably, said cylinder body is fixedly connected to the top of said incubator body.
6. The incubator according to claim 2, wherein said variable pressure apparatus further comprises one of an electric cylinder, a pneumatic cylinder, and a hydraulic cylinder; preferably, the electric cylinder comprises a servo motor and a transmission mechanism, and the transmission mechanism connects the servo motor and the piston to convert the rotation of the servo motor into the movement of the piston; and preferably, the electric cylinder is an electric push rod, which can drive the piston to move.
7. The incubator according to claim 1, wherein said variable pressure apparatus comprises a gas storage tank, which is communicated to said incubator body via a pressurization gas circuit and a decompression gas circuit; the pressurization gas circuit is provided with a pressurization pump and a pressurization control valve, the pressurization pump is configured to transport a gas in the gas storage tank to the incubator body, and the pressurization control valve is configured to control the on-off of the pressurization gas circuit; and the decompression gas circuit is provided with a decompression pump and a decompression control valve, the decompression pump is configured to transport a gas in the incubator body to the gas storage tank, and the decompression control valve is configured to control the on-off of the decompression gas circuit.
8. The incubator according to claim 1, wherein said incubator body is further provided with a safety valve, which is opened after the pressure in said incubator body exceeds a safety threshold.
9. The incubator according to claim 1, wherein said incubator body further comprises an openable/closable gas inlet and an openable/closable gas outlet, independent of said variable pressure interface.
10. The incubator according to claim 1, wherein a sterilization apparatus or/and a humidification apparatus or/and an electric heating apparatus is/are disposed in said incubator body.
11. The incubator according to claim 10, wherein said sterilization apparatus is an ultraviolet light emitter or a steam sterilization apparatus.
12. The incubator according to claim 1, wherein one or more types of gases are present in said incubator, preferably a three-gas incubator; and more preferably, said gases comprise carbon dioxide, nitrogen, and oxygen.
13. The incubator according to claim 1, wherein said incubator further comprises a gas replenishing system, which comprises: a pressure relief apparatus for releasing the gas in said incubator body; and a gas supply system for supplying a gas with stable process parameters to said incubator body while said pressure relief apparatus performs releasing.
14. The incubator according to claim 13, wherein a gas mixing apparatus is disposed within said incubator body and is configured to keep the gas in said incubator body in a turbulent state so as to maintain the uniformity of the gas.
15. The incubator according to claim 13, wherein said gas supply system comprises a premixing tank, which receives said one or more types of gases via an input pipeline and is connected to said incubator body via an output pipeline; a gas mixing apparatus is disposed within said premixing tank; said input pipeline is provided with a gas source control apparatus for a gas source; and said output pipeline is provided with an incoming gas control apparatus for said incubator body.
16. The incubator according to claim 15, wherein a gas control apparatus is further disposed within said premixing tank, and said gas control apparatus comprises a gas concentration detecting meter, a heating apparatus, a humidification apparatus and/or a temperature/humidity detection apparatus.
17. The incubator according to claim 16, wherein said gas source control apparatus and/or said incoming gas control apparatus comprises a heating apparatus, a humidification apparatus or/and a gas filter apparatus.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0023] The above and other features, properties and advantages of the present invention will become more obvious from the following description combined with the accompanying drawings and embodiments, in which:
[0024]
[0025]
[0026]
[0027]
[0028]
[0029]
[0030]
DETAILED DESCRIPTION OF THE INVENTION
[0031] As illustrated in
[0032]
[0033] The decompression gas circuit 95 is provided with a decompression pump 15 and a decompression control valve 18. The decompression pump 15 is configured to transport the gas in the incubator body 16 to the gas storage tank 96, and the decompression control valve 18 is configured to control the on-off of the decompression gas circuit.
[0034] When the pressure in the chamber 3 needs to be increased, the control valve 17 in front of the pressurization pump 14 is opened; the pressurization pump 14 starts to pump the gas from the gas storage tank 96 into the chamber 3; the control valve 18 in front of the decompression pump 15 is closed; and the pressure in the chamber 3 increases to a pressure value to end the pressurization. Then, the control valve 17 in front of the pressurizing pump 14 is closed; the control valve 18 in front of the decompression pump 15 is opened; the decompression pump 15 pumps the gas from the chamber 3 into the gas storage tank 96; and the pressure of the chamber 3 decreases to a specified value to end the decompression. The pressurization pump 14, the decompression pump 15, and the two control valves 17 and 18 may be connected to a controller, in which pressurization and decompression operations are controlled by means of a program, and the pressure in the chamber 3 fluctuates periodically over time.
[0035] More detailed configurations may also be implemented on the incubator body 16. As illustrated in
[0036] An embodiment of the application of an incubator is described below.
[0037] “Different conditions” or “different culture conditions” means that cell culture conditions involved in the comparison differ from each other only by the unique characteristics of a gas environment indicated below, and such a set of different culture conditions for comparison is referred to as “four conditions” for short:
normoxia (20%): the oxygen concentration is 20%, and no additional pressure is applied beyond one atmospheric pressure;
hypoxia (5%): the oxygen concentration is 5%, and no additional pressure is applied beyond one atmospheric pressure;
hypoxic static pressure (5%+static): the oxygen concentration is an additional constant pressure of 95 mmHg is applied at one atmospheric pressure, the incubator body 16 is pressurized by means of the variable pressure apparatus 9, when the additionally applied pressure reaches 95 mmHg, the incoming and outgoing gases of the incubator body 16 are allowed to reach a dynamic balance without stopping inflation and pressurization, and the gas in the incubator body 16 is maintained at one atmospheric pressure+95 mmHg; and
hypoxic dynamic pressure (5%+dynamic): the oxygen concentration is 5%, an additional pressure is applied at one atmospheric pressure, and the pressure in the incubator body 16 periodically fluctuates sinusoidally in the range of 1 atmospheric pressure+(75-115) mmHg, with the frequency of 14 times/min.
Embodiment: Comparison of Expansion Folds of Hair Follicle Mesenchymal Stem Cells Cultured Under Different Conditions
[0038] 1) To obtain intact human hair follicle tissues, the hair follicle tissues were carefully placed at the bottom of a 1.5 mL EP tube by using microforceps. 5 μL of enzymolysis solution TripLE (Gibco-12604021) was added to each hair follicle; the tube was then let stand in the incubator filled with 5% CO.sub.2 at 37° C. for 3 hours; the bottom of the tube was carefully flicked every hour; and the resulting mixture was gently mixed.
2) After 3 hours of enzymolysis, it could be seen under a microscope that an outer root sheath of each hair follicle was completely enzymolyzed, but the hair shaft could not be completely enzymolyzed. Without removing the unenzymolyzed part, the enzymolysis solution was blown 10 times by using a 100-1000 μL pipette to completely mix the enzymolysis solution. The enzymolysis solution was let stand for 1 minute until the unenzymolyzed hair shaft sunk to the bottom of the EP tube, and the upper enzymolysis suspension, i.e., the primary mesenchymal stem cells, was sucked.
25 μL of enzymolytic primary mesenchymal stem cell suspension obtained by combining the enzymolysis solutions of 5 hair follicles was added to one well of a six-well plate, and then 2 mL of amniotic fluid medium (purchased from Guangzhou Baiyunshan Baidi Biotechnology Co., Ltd.) was added for resuspension. The six-well plate was cultured under the four conditions including normoxia (20%), hypoxia (5%), hypoxic static pressure (5%+static), and hypoxic dynamic pressure (5%+dynamic) at 37° C., and the medium was changed every 3 days.
3) After culturing for 10-12 days, the culture medium could be discarded when the cell density in the six-well plate reached more than 80%; 0.5 mL of TryplE digestion solution was added to the bottom of the six-well plate, which was then placed in a 37° C. incubator for 3-minute digestion; then, 1 mL of amniotic fluid medium was added to the six-well plate to terminate the digestion; the supernatant was removed and placed in a 15 mL centrifuge tube; the well plate was rinsed once with 1 mL of amniotic fluid medium; the rinse solution was added to the centrifuge tube. The centrifuge tube was centrifuged at 1500 rpm for 5 minutes in a centrifuge; the supernatant was discarded; 1 mL of amniotic fluid medium was added for resuspension; the cells were counted and inoculated into a T25 culture flask, and cultured to obtain P1-generation hair follicle mesenchymal stem cells,
4) The cells were continuously subcultured to the P12 generation, and the cells under the four conditions were always maintained under their respective culture conditions. Expansion fold=count of cells harvested per passage/count of inoculated cells. In this embodiment, the cells were passaged strictly according to the density of 5000 cells/cm.sup.2. The area of a T25 culture flask was 25 cm.sup.2, that is, a T25 culture flask was inoculated with 1.25×10.sup.5 cells each time, and the calculation formula of the expansion fold is “expansion fold=count of cells per harvest/(1.25×10.sup.5)”.
[0039] The results were shown in
[0040]
[0041] In various embodiments, the incubator may further optionally comprise a gas replenishing system, which can be used in any of the preceding embodiments. The gas replenishing system comprises a gas supply system and a pressure relief apparatus. The pressure relief apparatus is configured to release the gas in the incubator body. The gas supply system is configured to supply a gas with stable process parameters to the incubator body while the gas in the incubator body is released, to ensure the stability of the process parameters of the gas in the incubator body. The gas supply system is also configured to reduce the fluctuation of a gas atmosphere in the incubator body, to ensure a more stable culture environment. The process parameters comprise, but are not limited to, gas concentration, gas temperature, and gas humidity.
[0042] In the embodiment illustrated in
[0043] The gas comes out from the gas source 19 and enters the premixing tank 21 after being adjusted by the gas source control apparatus 20. The gas passes through the gas mixing apparatus 22 to allow the gas in the premixing tank 21 to be mixed evenly. After the gas is adjusted to a set value by the gas control apparatus 23 in the premixing tank 21, the gas may be introduced into the incubator 16 by means of the incoming gas control apparatus 24. According to the flow direction of the gas in the incubator body 16, one or more gas outlet holes 161 are arranged in parts that are difficult to reach by the gas flow; automatic gas releasing is effected by means of the gas relief apparatus 27; and at the same time, the incoming gas control apparatus 24 is started for replenishing the gas. To further improve the uniformity and cleanliness of the gas inside the incubator body 16, one or more gas mixing apparatuses 25 are placed in the incubator 16 to keep the gas in the incubator body 16 in a turbulent state so as to maintain the gas uniformity. To precisely adjust the process parameters of the gas in the incubator body 16, the incubator body 16 is further provided therein with a gas control apparatus 26. The gas control apparatus 26 comprises, but is not limited to, various types of gas concentration detecting meters, heating apparatuses, humidification apparatuses, temperature/humidity detection apparatuses, etc.
[0044] Although the present invention is disclosed above with preferred embodiments, they are not intended to limit the present invention, and any person skilled in the art can make possible changes and alternations without departing from the spirit and scope of the present invention. Therefore, without departing from the content of the technical solutions of the present invention, any alternation, equivalent variation and modification made to the embodiments above based on the technical essence of the present invention shall be construed as falling within the protection scope defined by the claims of the present invention.