Patent Application
20190017909
The present invention relates to the technical field of medical engineering, and in particular, to a mitochondria extraction apparatus.
Mitochondria are powerhouses of human cells and provide energy for cells. Mitochondrial diseases are caused by dysfunctional mitochondria. So far more than fifty related diseases have been found in Taiwan. Clinically, patients may suffer from abnormalities in organs such as brains, muscles, and hearts.
Therefore, it is urgent to develop treatments for mitochondrial diseases in the medical field. In mitochondrial replacement treatment, damaged mitochondria of a patient are replaced with healthy mitochondria to promote the proliferation of healthy mitochondria in the body of the patient, and at the same time the oxidative stress in cells is reduced to slow down the disease process. Therefore, a large quantity of intact mitochondria having desirable structure and activity are needed.
Conventional mitochondrial extraction using physical or chemical methods involves high-speed centrifugation, repeated freezing and thawing or reagent extraction. As a result, a small quantity of mitochondria with impaired structures and functions are obtained. Therefore, the technical content is still underdeveloped.
Therefore, the main objective of the present invention is to provide a mitochondria extraction apparatus. A mitochondria-containing mixture fluid may be filled in the mitochondria extraction apparatus, and the mitochondria extraction apparatus makes a circular mot ion about a moving axis. The mitochondria-containing mixture fluid flows through the mitochondria extraction apparatus at an increased speed under a centrifugal force, to obtain a large quantity of mitochondria with desirable quality for the application to treatment of mitochondrial diseases.
In view of this, to achieve the foregoing objective, a mitochondria extraction apparatus provided in the present invention includes a container used for holding a mixture fluid and a diafiltration assembly disposed in the container and used for isolating mitochondria. During a circular motion of the mitochondria extraction apparatus, a centrifugal force in the mitochondria extraction apparatus acts on the mixture fluid in a hole-shaped microfluidic channel included in the diafiltration assembly, so as to provide a pushing force for the mixture fluid, enabling the mixture fluid to rapidly flow in the microfluidic channel for diafiltration.
Both the effect of a centrifugal force and the flowing of a mixture fluid that undergoes diafiltration in a microfluidic channel are directional. Therefore, to ensure that a centrifugal force acts in a correct direction of pushing the mixture fluid to flow for diafiltration, the diafiltration assembly further includes a basement positioned in the container and used for arranging the microfluidic channel, so that the microfluidic channel is positioned by using the basement and the container, thereby ensuring that the centrifugal force acts in the correct direction of enabling the mixture fluid to flow for diafiltration.
The container has a first receiving chamber and a second receiving chamber that are not connected to each other, the first receiving chamber receives the mixture fluid that waits for diafiltration by the diafiltration assembly, and the second receiving chamber receives mitochondria obtained after diafiltration by the diafiltration assembly. Accordingly, the diafiltration assembly should be located between the first receiving chamber and the second receiving chamber, so that the first receiving chamber and the second receiving chamber can be connected only via the microfluidic channel.
When the first receiving chamber, the basement, and the second receiving chamber are sequentially arranged in an axial direction parallel to the moving axis, the basement has a plate form, and the microfluidic channel forms a flow inlet for entry of the mixture fluid on one side of the basement and forms a flow outlet for discharge of mitochondria obtained after diafiltration on the other side of the basement. The flow inlet of the microfluidic channel may be directly or indirectly connected to the first receiving chamber, and the flow outlet of the microfluidic channel is also directly or indirectly connected to the second receiving chamber.
The flow inlet of the microfluidic channel may be indirectly connected to the first receiving chamber via a flow inlet space, and the flow outlet of the microfluidic channel may be indirectly connected to the second receiving chamber via a flow outlet space.
To form the flow inlet space, the basement may have a first plate and a second plate stacked with each other and a hole penetrating the first plate, a hole opening at an end of the hole is closed by the second plate, and the hole forms a part of the flow inlet space.
The microfluidic channel is located between the first plate and the second plate, and the flow inlet of the microfluidic channel is connected to the flow inlet space.
The flow outlet space is disposed between the first plate and the second plate and extends to an outside end, away from the hole, of the basement. Furthermore, the outer diameter of the second plate may further be less than the outer diameter of the first plate, so that an open space between a circumferential side of the second plate and a side plate surface of the first plate forms a part of the flow outlet space.
To facilitate use and save users the trouble of aligning an effect direction of a centrifugal force with a flowing direction of the mixture fluid for diafiltration, a plurality of microfluidic channels are provided in the diafiltration assembly, and are distributed on the basement radially with a hole axis of the hole provided on the first plate being the center.
The container further includes a fixing space used for accommodating the diafiltration assembly, so that the diafiltration assembly is positioned in the container.
To provide the fixing space, the container may have a tube member that is open at two ends of a tube axis, a first baffle bar and a second baffle bar separated from each other are distributed in the tube member, and the fixing space is located between the first baffle bar and the second baffle bar.
The tube member has a tube body and an end ring, the end ring is fixedly disposed at an end of the tube axis of the tube body, and the first baffle bar and the second baffle bar are distributed on the tube body and the end ring.
Referring to
The container (20) has a tubular tube member (21) that is open at two ends of a tube axis. A first receiving chamber (22) is defined by a space in a hollow tube of the tube member (21). Two first baffle bars (23) and two second baffle bars (24) that respectively intersect in a cross form are distributed separately from each other on a tube wall at an end of the tube axis of the tube member (21), and are respectively perpendicular to the tube axis of the tube member (21). A fixing space (25) is located between the first baffle bars (23) and the second baffle bars (24), and is connected to the first receiving chamber (22). A generally cylindrical hollow sleeve member (26) is coaxially sleeved over the tube member (21). A second receiving chamber (27) is defined by the hollow inside of the sleeve member (26). The tube member (21) is located in the second receiving chamber (27), and the first receiving chamber (22) and the second receiving chamber (27) are not directly connected to each other. A filter (28) is fixedly disposed in the second receiving chamber (27), and is located between the tube member (21) and the cylindrical bottom the sleeve member (26).
Specifically, the tube member (21) has a tube body (211) and an end ring (212) coaxially threaded to an end of the tube axis of the tube body (211), and the first baffle bars (23) and the second baffle bars (24) are distributed at the end of the tube axis of the tube body (211) and the end ring (212).
The diafiltration assembly (30) is accommodated in the fixing space (25) and combined with the tube member (21), and structurally has a circular plate-form basement (31) inserted in the fixing space (25) with the center being coaxial with the tube axis of the tube member (21), so as to block the connection between the first receiving chamber (22) and the second receiving chamber (27). A plurality of hole-shaped microfluidic channels (32) are distributed on the basement (31), and the first receiving chamber (22) and the second receiving chamber (27) are connected via the microfluidic channels (32).
Furthermore, the basement (31) has a circular first plate (311) and a circular second plate (312) that are coaxially stacked with each other. A hole (313) penetrates through the center of the first plate (311), and a hole opening at an end is closed by the second plate (312), so that a hole space of the hole (313) defines a flow inlet space (314). The outer diameter of the second plate (312) is less than the outer diameter of the first plate (311), so that an annular flow outlet space (315) is defined between a circumferential side of the second plate (312) and a side plate surface of the first plate (311). The flow inlet space (314) is connected to the first receiving chamber (22), and the flow outlet space (315) is connected to the second receiving chamber (27).
The microfluidic channels (32) are distributed between the first plate (311) and the second plate (312) radially with a hole axis of the hole (313) being the center, and are respectively connected to the flow inlet space (314) through a flow inlet hole opening (321) and connected to the flow outlet space (315) through flow outlet hole openings (322).
In this way, the mitochondria extraction apparatus (10) receives a mitochondria-containing mixture fluid by using the first receiving chamber (22), and enabling the mitochondria-containing mixture fluid to enter the microfluidic channels (32) via the flow inlet space (314) and the connected flow inlet hole opening (321). After the mitochondria-containing mixture fluid flows in the microfluidic channels (32) and diafiltration is performed, mitochondria obtained after diafiltration flow out respectively through the flow outlet hole openings (322) of the microfluidic channels (32) and flow into the second receiving chamber (27) through the flow outlet space (315), and may be filtered by the filter (28) in the second receiving chamber (27), to achieve a mitochondria extraction effect.
Moreover, when the mitochondria extraction apparatus (10) makes a circular motion, an effect direction of a centrifugal force in the mitochondria extraction apparatus (10) is close to a flowing direction in which the mixture fluid flows in the microfluidic channels (32) for diafiltration, that is, is correspondingly the same as a direction from the flow inlet hole opening (321) to the flow outlet hole openings (322) of the microfluidic channels (32), so that the centrifugal force pushes the mixture fluid to flow in the microfluidic channels (32), to achieve better extraction efficacy.
Moreover, the following content should be further described:
First, when the mitochondria extraction apparatus (10) makes a circular motion, the mixture fluid in the flow inlet space (314) moves in a centrifugal direction and can only enter a microfluidic channel located on a centrifugal side, and a microfluidic channel on a centripetal side naturally does not achieve a mitochondria extraction effect with no mixture fluid entering. However, the microfluidic channels (32) are radially disposed, so that during the use of the mitochondria extraction apparatus (10), the direction of a centrifugal force does not need to be aligned with the flowing direction of the mixture fluid for diafiltration. Some microfluidic channels are always located on a centrifugal side to implement mitochondria extraction.
Second, the end ring (212) is threaded to the tube body (211) to facilitate the positioning and replacement of the diafiltration assembly (30), thereby achieving convenient use.
Third, the mixture fluid and extracted mitochondria are located in different receiving chambers. Therefore, after an extraction procedure is completed, the diafiltration assembly (30) can be separated from the sleeve member (26) at the same time when the tube member (21) is directly removed, so that only the extracted mitochondria are left in the second receiving chamber (27), thereby further achieving convenient use.
Four, the microfluidic channels (32) may form grooves on a side plate surface, facing the first plate (311), of the second plate (312) by using a manufacturing method of chemical etching or molding, and the first plate (311) and the second plate (312) are stacked with each other to close openings of the grooves, thereby defining the microfluidic channels.
In addition, the flow outlet space is not limited to the foregoing embodiments, and may alternatively be disposed between the first plate and the second plate and extend to a side of a basement, thereby connecting flow outlet hole openings of the microfluidic channels and a space outside the basement. The first plate and the second plate are plate-form bodies having the same outer diameter.
| Number | Date | Country | Kind |
|---|---|---|---|
| 106123558 | Jul 2017 | TW | national |
