KR20180120024A - Apparatus for extraction and separation of intracellular substance - Google Patents

Abstract

To an apparatus for separating and extracting an intracellular substance from an extracellular endoplasmic reticulum. The intracellular material separation and extraction apparatus includes a first input channel, an electric field generating unit, a second input channel, a connection channel, and a plurality of output channels. The input channel is a buffer and a cell containing a plurality of intracellular materials of varying sizes. The electric field generator applies an electric field to cells flowing along the first input channel to form perforations, and to separate intracellular substances from the perforations. The second input channel is connected to the first input channel, and a buffer is introduced. The connection channel is once connected to the first input channel and the second input channel. The output channel extends at different angles at the other end of the connection channel and at least one of the intracellular material or buffer introduced into the first input channel is discharged and the intracellular material is classified by size.

Description

[0001] APPARATUS FOR EXTRACELLULAR MATERIALS [0002]

The present invention relates to a device for separating and extracting substances in cells used for diagnosing and treating diseases, and more particularly, to an intracellular material separating and extracting device for separating extracellular endoplasmic reticulum from cells through an electroporation method and a pinched flow classification method Separation and extraction apparatus.

It is difficult to rapidly process biological information, which is soaring at present, with conventional laboratory analysis systems. Biological detection systems for the identification of life phenomena and drug development and diagnosis are based on microfluidics, and a micro total analysis system (μ -TAS: micro-Total Analysis System) and lab-on-a-chip.

Since most of the biochemical samples to be analyzed are present in solution, the technique of delivering liquid samples is the most important factor. Microfluidics is a research field for controlling the flow of such microfluidics, and is a field for research and development of core technologies that are based on commercialization of the microcomputer analysis system and lab-on-a-chip.

The micro total analysis system is a system that comprehensively implements chemical and biological experiments and analyzes, which are subjected to a plurality of experimental steps and reactions, on one unit existing on one laboratory. Such a micro total analysis system is composed of a sampling region, a microfluidic circuit, a detector, and a controller for controlling them.

On the other hand, in vivo extracellular endoplasmic reticulum, which is one of the elements acquired through the microintegration analysis system, is a small vesicle of membrane structure that exists in various kinds of cells or is secreted from cells. The microvesicles secreted out of the cell are (i) exosomes: membranous vesicles of 30-100 nm in diameter originated from the origin of the bacteria, (ii) shedding microvesicles (SMVs): flowing directly from the plasma membrane (Iii) Apoptotic blebs: vesicles of 50-5000 nm in diameter, which are released by dying cells.

The in vivo extracellular endoplasmic reticulum, such as exosomes, includes microRNAs (miRNAs), which can be used as useful markers in molecular diagnostics such as early diagnosis of diseases such as cancer. Although the significance and value of in vivo micro-endoplasmic reticulum as described above have been revealed, it is difficult to obtain micro-endoplasmic reticulum.

Trapping-on porous system, membrane separation method, and iron oxide nanoparticle separation method are widely used for obtaining the above-mentioned micro-vesicles.

However, the trapping on porous system method creates a mimic nanosphere that is used for releasing cells to destroy all the cells pushed out on the chip to separate the extracellular endoplasmic reticulum, It is necessary to further process such as ultracentrifugation after extraction.

Membrane separation method is used because the polymer of the membrane recognizes only a specific function of a molecule and functions as a filter only for a specific molecule.

However, since the extracellular endoplasmic reticulum recovered by such a method is a method of extracting extracellular endoplasmic reticulum from a solution containing only cells, a large amount of cells are contained in order to recover the extracellular endoplasmic reticulum with low recovery rate of extracellular endoplasmic reticulum And therefore the purification rate is low.

The separation method using iron oxide nanoparticles uses a phenomenon in which the extracellular endoplasmic reticulum is negatively charged. In this method, the iron oxide particles adhere to the extracellular endoplasmic reticulum, and the extracellular endoplasmic reticulum is elicited by electrical attraction to separate the extracellular endoplasmic reticulum.

This method has a merit that the extracellular endoplasmic reticulum changes little and the centrifugation process is performed little, but it is not clearly confirmed whether or not the nanoparticles are correctly attached only to the extracellular endoplasmic reticulum which is the target. And the purchase cost is large. Further, since the iron oxide particles are used, there is a problem that the bioavailability after the recovery is lowered.

Published Japanese Patent Application No. 10-2016-0133837 (published Nov. 23, 2016)

Disclosure of the Invention The object of the present invention is to provide a method for separating extracellular endoplasmic reticulum and intracellular material from a cell using an electroporation method and then separating the extracellular endoplasmic reticulum by a pinched flow classification method, And a device for separating and extracting substances.

According to an aspect of the present invention, there is provided an intracellular material separation and extraction apparatus including a first input channel, an electric field generating unit, a second input channel, a connection channel, and a plurality of output channels. The input channel is a buffer and a cell containing a plurality of intracellular materials of varying sizes. The electric field generator applies an electric field to cells flowing along the first input channel to form perforations, and to separate intracellular substances from the perforations. The second input channel is connected to the first input channel, and a buffer is introduced. The connection channel is once connected to the first input channel and the second input channel. The output channel extends at different angles at the other end of the connection channel and at least one of the intracellular material or buffer introduced into the first input channel is discharged and the intracellular material is classified by size.

Also, the intracellular material separation and extraction apparatus according to the present invention includes a first input channel, a pulse voltage generating unit, a second input channel, a connection channel, a first output channel, and a second output channel. The first input channel is a cell in which a first buffer is introduced with cells containing a plurality of intracellular substances larger in size than the extracellular endoplasmic reticulum and the extracellular endoplasmic reticulum to be separated. The pulse voltage generator generates a perforation by applying a pulse voltage to cells flowing along the first input channel, and separates extracellular endoplasmic reticulum and intracellular material from the perforation. The second input channel is connected to the first input channel, and the second buffer is input. The connection channel is once connected to the first input channel and the second input channel. The first output channel is connected to the other end of the connection channel, and the extracellular endoplasmic reticulum isolated by the pulse voltage generator is discharged. A plurality of second output channels are provided and connected to the connection channel and the first output channel, respectively, and the cells separated by the pulse voltage generator and the cells formed with perforations are respectively discharged. The intracellular material separation and extraction apparatus is characterized in that the width of the connection channel is smaller than the widths of the first input channel, the second input channel, the first output channel, and the second output channel.

According to the present invention, since the extracellular endoplasmic reticulum and the intracellular substance are separated from the cells using the electroporation method, the separation is easy.

In addition, since the central part of the first input channel to which the pulse voltage is applied is formed to be smaller than the width of both ends, the pulse pressure is concentrated at the central part of the first input channel, do. As a result, the extracellular endoplasmic reticulum can be more rapidly separated from the cells.

In addition, the perforations formed in the cells are nano-sized and very fine, so that the cells are able to recover quickly and reuse the cells.

Further, since the extracellular endoplasmic reticulum, the intracellular substance, and the perforated cell are discharged to different channels through the separation method using the pinched flow, the purification rate is improved and separate transport means are required The economical efficiency is improved.

In addition, since the extracellular endoplasmic reticulum and the intracellular substance are separated from the cells without using any separate transport means, the separation operation can be performed quickly and simply.

1 is a schematic diagram of an intracellular material separation and extraction apparatus according to an embodiment of the present invention;
Fig. 2 is a view showing the flow of extracellular endoplasmic reticulum and intracellular material in Fig. 1; Fig.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, an intracellular material separation and extraction apparatus according to a preferred embodiment of the present invention will be described in detail with reference to the accompanying drawings. Here, the same reference numerals are used for the same components, and repeated descriptions and known functions and configurations that may obscure the gist of the present invention will not be described in detail. Embodiments of the invention are provided to more fully describe the present invention to those skilled in the art. Accordingly, the shapes and sizes of the elements in the drawings and the like can be exaggerated for clarity.

1 is a schematic diagram of an intracellular material separation and extraction apparatus according to an embodiment of the present invention. 2 is a view showing the flow of extracellular endoplasmic reticulum and intracellular material in Fig.

1 and 2, the intracellular material separation and extraction apparatus 100 includes a first input channel 110, a pulse voltage generator (not shown), a second input channel 130, A connection channel 140, and a plurality of output channels 150 and 160.

The first input channel 110 receives a first buffer and cells containing a plurality of intracellular substances larger in size than the extracellular endoplasmic reticulum and the extracellular endoplasmic reticulum to be separated.

Here, the first buffer is for smooth flow and focusing of cells, and may be introduced into the first input channel 110 through a pump. The first buffer may be made of phosphate buffered saline (PBS) or a biocompatible fluid such as water.

Specifically, the first input channel 110 may be formed such that the discharge portion from the inlet portion is inclined downward. In addition, the cell and the first buffer may be both introduced into the first input channel 110, and the third input channel 170 may further be connected to the inlet end of the first input channel 110, Respectively.

A pulse voltage generator (not shown) applies a pulse voltage to cells flowing along the first input channel 110 to form perforations, and separates the extracellular endoplasmic reticulum and intracellular material from the perforations. That is, they are separated from the cells into extracellular endoplasmic reticulum and intracellular material through electroporation. Since the pulse voltage generator generates an electric field in the first input channel 110, the pulse voltage generator can be referred to as an electric field generator.

For example, when a pulse voltage is applied to the first input channel 110 through the pulse voltage generator, an electric field is formed in the first input channel 110, and nano-sized holes are formed in the cell membrane due to the intensity of the electric field .

Here, the electric field generated by the pulse voltage generator can be formed in a direction in which the first buffer of the first input channel 110 flows, and the pulse voltage applied to the first input channel 110 is formed to be 75V to 100V . The electrodes of the pulse voltage generating unit may be connected to the first input channel 110 and the second input channel 130, respectively.

As the perforation is formed in the cells through the pulse voltage generator, the extracellular endoplasmic reticulum and intracellular material can be extracted to the outside of the cell through the perforation. At this time, the perforations formed in the cells are nano-sized and very fine, so that the resilience of the cells progresses rapidly.

Meanwhile, in order to concentrate the pulse voltage on the first input channel 110, the width of the center portion of the first input channel 110 may be smaller than the width of both ends. That is, the flow path may be formed so as to be small from both ends of the first input channel 110 to the center. Accordingly, when the pulse voltage is applied to the first input channel 110, the pulse voltage is concentrated at the central portion of the first input channel 110 to increase the strength of the electric field, .

The second input channel 130 is connected to the first input channel 110, and the second buffer is input. Specifically, the discharge end of the second input channel 130 may be radially connected to the discharge end of the first input channel 110. The second input channel 130 may be formed such that the discharge portion from the inlet portion is inclined upward.

The flow rate of the second buffer flowing into the second input channel 130 may be greater than the flow rate of the first buffer. When the second buffer is introduced into the second input channel 130 as the flow rate of the second buffer is larger than the flow rate of the first buffer, So that it can be brought into close contact with one surface of the channel 140.

In order to concentrate the extracellular endoplasmic reticulum, intracellular material, and perforated cells on one surface of the connection channel 140, the particle size of the first buffer is preferably smaller than the size of the extracellular endoplasmic reticulum.

The second buffer may be introduced into the second input channel 130 through a pump as well as the first buffer, and may be formed of the same material as the first buffer. That is, the second buffer may be composed of PBS (Phosphate Buffered Saline) or a biocompatible fluid such as water.

The connection channel 140 is connected to the first input channel 110 and the second input channel 130 at one end. Here, the extracellular endoplasmic reticulum, intracellular material, and perforated cells may be closely attached to the inner surface of the connection channel 140 by the second buffer.

The width of the connection channel 140 is smaller than the widths of the first input channel 110 and the second input channel 130 and the first output channel 150 and the second output channel 160 . This is to separate the extracellular endoplasmic reticulum, intracellular material, and perforated cells depending on the size of the particle by causing a pinched flow.

Here, a "pinched flow" is a method using a fluid flowing along a wire. That is, since the width of the connection channel 140 is formed to be smaller than the widths of the first output channel 150 and the second output channel 160, the discharge portion of the connection channel 140 and the first output channel 150, The point where the inlet portion of the second output channel 160 meets is suddenly depressurized and thus the laminar flow is formed at the discharge portion of the connection channel 140. [ By the laminar flow, the extracellular endoplasmic reticulum, the intracellular material, and the cells having the perforated cells are classified according to sizes and discharged to the first output channel 150 and the second output channel 160, which will be described later. The detailed principle of this pinched flow is already known, and will be omitted.

The output channels 150 and 160 include a first output channel 150 and a second output channel 160.

The first output channel 150 is connected to the other end of the connection channel 140. Specifically, the inlet end of the first output channel 150 may be radially connected to the outlet end of the connection channel 140. The first output channel 150 may be arranged in the vertical direction such that the discharge portion from the inlet is located at the top.

As the first output channel 150 is arranged perpendicular to the connection, the extracellular endoplasmic reticulum, the intracellular material, and the extracellular endoplasmic reticulum having the smallest size among the perforated cells are connected to the first output channel 150 . This is due to the effect of the above-described pinched flow, and a detailed description thereof will be omitted.

The plurality of second output channels 160 are connected to the connection channel 140 and the first output channel 150. At this time, one output channel 110 and one of the second output channels 160 may be arranged at intervals of 180 degrees in order to improve a pinched flow effect. The first output channel 150 and the second output channel 160 are radially connected to the other end of the connection channel 140 and may be disposed at equal intervals.

Specifically, the second output channel 160 may include a first output member 161, a second output member 162, a third output member 163, and a fourth output member 164 .

The first output member 161 can be radially connected to the inflow end of the first output channel 150, with the inflow end being a discharge of intracellular material. Specifically, the first output member 161 may be formed such that the discharge portion from the inlet portion is inclined upward. Since the intracellular material is larger than the extracellular endoplasmic reticulum and smaller than the perforated cell size, the intracellular material is discharged to the first output member 161 by the principle of the pinched flow. do.

The second output member 162 is such that the perforated cells are discharged, and the inlet end can be radially connected to the inlet end of the first output member 161. Specifically, the first output member 161 may be formed in parallel with the connection channel 140 by arranging the discharge portion from the inlet portion in the horizontal direction. Here, since the perforated cells are larger than the extracellular endoplasmic reticulum and the intracellular substance, the perforated cells are discharged to the second output member 162 by the principle of the pinched flow.

The third output member 163 can be radially connected to the inlet end of the second output member 162 with the second buffer being drained. Specifically, the third output member 163 may be formed such that the discharge from the inlet portion is inclined downward. At this time, since the intracellular substance is disposed on the upper side wall of the connecting member by the second buffer, the intracellular substance is first discharged through the first output member 161 formed upwardly inclined. Therefore, the second buffer is discharged to the third output member 163.

The fourth output member 164 can be radially connected between the outlet end of the connecting channel 140 and the inlet end of the third output member 163, with the inlet end being the outlet of the second buffer. Specifically, the fourth output member 164 may be arranged in a vertical direction such that the outlet from the inlet is located below. At this time, since the intracellular substance is disposed on the upper side wall of the connecting member by the second buffer, the extracellular endoplasmic reticulum is firstly discharged through the first output channel 150. Therefore, the second buffer is discharged to the fourth output member 164.

At least one of the third output member 163 and the fourth output member 164 may be connected to the first input channel 110 or the second input channel 130. As the third output member 163 and the output member 164 from which the buffer is discharged are connected to the first input channel 110 or the second input channel 130 to which the buffer is inputted, the third output member 163 And the fourth output member 164 can be recovered and reused.

As described above, the intracellular material separation and extraction apparatus separates the extracellular endoplasmic reticulum and the intracellular material from the cells using the electroporation method, so that it is easy to separate.

In addition, since the central part of the first input channel to which the pulse voltage is applied is formed to be smaller than the width of both ends, the pulse pressure is concentrated at the central part of the first input channel, do. As a result, the extracellular endoplasmic reticulum can be more rapidly separated from the cells.

In addition, the perforations formed in the cells are nano-sized and very fine, so that the cells are able to recover quickly and reuse the cells.

Since the extracellular endoplasmic reticulum, the intracellular substance, and the perforated cell are discharged to different channels through the separation method using the pinched flow, the purification rate is improved and separate conveying means are not required Economic efficiency is improved.

In addition, since the extracellular endoplasmic reticulum and the intracellular substance are separated from the cells without using any separate transport means, the separation operation can be performed quickly and simply.

While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is clearly understood that the same is by way of illustration and example only and is not to be taken by way of limitation and that those skilled in the art will recognize that various modifications and equivalent arrangements may be made therein. It will be possible. Accordingly, the true scope of protection of the present invention should be determined only by the appended claims.

110 .. First input channel
130 .. Second input channel
140 .. connection channel
150 .. The first output channel
160 .. Second output channel

Claims (14)

A cell comprising a plurality of intracellular materials of varying sizes; a first input channel through which a buffer is introduced;
An electric field generating unit for applying an electric field to the cells flowing along the first input channel to form perforations, and separating the intracellular substances from the perforations;
A second input channel coupled to the first input channel and having a buffer therein;
A connection channel, one end of which is connected to the first input channel and the second input channel; And
A plurality of output channels extending at different angles at the other end of the connection channel and discharging at least one of the intracellular material and buffer introduced into the first input channel and the intracellular material being classified according to size;
And an intracellular material separation and extraction device. The method according to claim 1,
Wherein the plurality of output channels are connected to the other end of the connection channel and have a first output channel through which the extracellular endoplasmic reticulum separated by the pulse voltage generation unit is discharged; And
And a plurality of second output channels connected to the connection channel and the first output channel, the plurality of second output channels discharging the extracellular endoplasmic reticulum isolated by the electric field generating unit and the cells formed with the intracellular material and the perforated cells, respectively Separation and extraction equipment. 3. The method of claim 2,
Wherein a width of the connection channel is smaller than a width of the first input channel, the second input channel, the first output channel, and the second output channel. The method according to claim 1,
Wherein a width of a center portion of the first input channel is smaller than a width of both end portions, so that a pulse voltage is concentrated. The method according to claim 1,
And an electrode of the electric field generating unit is connected to the first input channel and the second input channel, respectively. The method according to claim 1,
Wherein at least two of the plurality of output channels are arranged at intervals of 180 degrees. The method according to claim 1,
Wherein the plurality of output channels are radially connected to the other end of the connection channel, and are arranged at equal intervals. The method according to claim 1,
Wherein an electric field generated by the electric field generating unit is formed in a direction in which a buffer of the first input channel flows. The method according to claim 1,
Wherein the flow rate of the buffer flowing through the second input channel is greater than the flow rate of the buffer flowing through the first input channel. The method according to claim 1,
Wherein the cells introduced into the first input channel by the electric field generating unit are separated into extracellular endoplasmic reticulum, intracellular material, and perforated cells,
Wherein the extracellular endoplasmic reticulum, the intracellular substance, and the perforated cell are attached to one surface of the connection channel. 3. The method of claim 2,
Wherein the first input channel is formed such that the discharge portion from the inlet portion is inclined downward,
Wherein the second input channel is formed such that the outlet from the inlet is inclined upwardly and the outlet end is radially connected to the outlet end of the first input channel. 12. The method of claim 11,
Wherein the second output channel comprises:
A first output member having an inlet end radially connected to an inlet end of the first output channel and an inlet outlet outlet formed with an upward slope,
A second output member having an inlet end radially connected to the inlet end of the first output member and an outlet from the inlet arranged in a horizontal direction,
A third output member in which the inlet end is radially connected to the inlet end of the second output member and the outlet from the inlet is formed in a downwardly inclined manner,
And a fourth output member arranged in a vertical direction such that the inlet end is radially connected between the outlet end of the connecting channel and the inlet end of the third output member and the outlet from the inlet is located underneath Apparatus for the separation and extraction of intracellular substances. 12. The method of claim 11,
Wherein at least one of the third output member and the fourth output member is connected to the first input channel or the second input channel so that the used buffer is recovered again. An extracellular endoplasmic reticulum and a plurality of intracellular substances larger in size than the extracellular endoplasmic reticulum; a first input channel through which the first buffer is introduced;
A pulse voltage generator for applying a pulse voltage to the cells flowing along the first input channel to form perforations, and separating the extracellular endoplasmic reticulum and the intracellular material from the perforations;
A second input channel coupled to the first input channel, the second input channel receiving a second buffer;
A connection channel, one end of which is connected to the first input channel and the second input channel;
A first output channel connected to the other end of the connection channel and through which the extracellular matrix separated by the pulse voltage generator is discharged; And
And a plurality of second output channels connected to the connection channel and the first output channel and through which the intracellular material separated by the pulse voltage generation unit and the perforated cells are discharged,
Wherein a width of the connection channel is smaller than a width of the first input channel, the second input channel, the first output channel, and the second output channel.

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