U.S. patent application number 13/881719 was filed with the patent office on 2013-10-10 for cell collecting device.
This patent application is currently assigned to CYTOGEN CO., LTD.. The applicant listed for this patent is Byung Hee Jeon, Jong Kil Lee. Invention is credited to Byung Hee Jeon, Jong Kil Lee.
Application Number | 20130264272 13/881719 |
Document ID | / |
Family ID | 45994539 |
Filed Date | 2013-10-10 |
United States Patent
Application |
20130264272 |
Kind Code |
A1 |
Jeon; Byung Hee ; et
al. |
October 10, 2013 |
CELL COLLECTING DEVICE
Abstract
A cell collecting device is configured to collect target cells
from a fluid sample such as blood or physiological fluid. The cell
collecting device includes a conduit through which a fluid sample
containing target cells passes. The cell collecting device further
includes a screen filter installed inside the conduit and
configured to guide the target cells toward a specified region. The
screen filter includes a plurality of filtering holes for filtering
the target cells.
Inventors: |
Jeon; Byung Hee;
(Seongnam-si, KR) ; Lee; Jong Kil; (Yeonsu-gu,
KR) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Jeon; Byung Hee
Lee; Jong Kil |
Seongnam-si
Yeonsu-gu |
|
KR
KR |
|
|
Assignee: |
CYTOGEN CO., LTD.
Seongnam-si, Gyeonggi-do
KR
|
Family ID: |
45994539 |
Appl. No.: |
13/881719 |
Filed: |
October 25, 2011 |
PCT Filed: |
October 25, 2011 |
PCT NO: |
PCT/KR2011/007976 |
371 Date: |
June 27, 2013 |
Current U.S.
Class: |
210/435 |
Current CPC
Class: |
B01D 39/10 20130101;
C12M 47/04 20130101; A61M 1/34 20130101; A61M 1/341 20140204; G01N
1/4005 20130101; A61M 2205/3334 20130101; G01N 2001/4016
20130101 |
Class at
Publication: |
210/435 |
International
Class: |
A61M 1/34 20060101
A61M001/34 |
Foreign Application Data
Date |
Code |
Application Number |
Oct 25, 2010 |
KR |
10-2010-0104249 |
Oct 25, 2010 |
KR |
10-2010-0104250 |
Claims
1. A cell collecting device, comprising: a conduit through which a
fluid sample containing target cells passes; and a screen filter
installed inside the conduit and configured to guide the target
cells toward a specified region, the screen filter including a
plurality of filtering holes for filtering the target cells.
2. The cell collecting device of claim 1, wherein the conduit
includes a tubular wall defining a passage for passing the fluid
sample therethrough, the screen filter configured to guide the
target cells toward a boundary region where the screen filter meets
with the tubular wall.
3. The cell collecting device of claim 2, wherein the screen filter
is obliquely installed in the passage along a flow direction of the
fluid sample.
4. The cell collecting device of claim 3, wherein the screen filter
includes a trap formed at a downstream end of the screen filter so
as to gather the target cells.
5. The cell collecting device of claim 2, wherein the screen filter
is formed into a curvilinear shape.
6. The cell collecting device of claim 2, wherein the conduit
includes an outlet formed near the boundary region and kept in
communication with the boundary region so that the target cells can
be discharged through the outlet.
7. The cell collecting device of claim 2, wherein the screen filter
includes a convex portion formed to guide the target cells toward
the boundary region.
8. The cell collecting device of claim 1, wherein the screen filter
includes a concave portion formed to guide and gather the target
cells.
9. The cell collecting device of claim 8, wherein the concave
portion is formed at a center of the screen filter so as to gather
the target cells.
10. The cell collecting device of claim 9, wherein the screen
filter further includes a trap formed at a center of the concave
portion so as to receive the target cells.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to a cell collecting device
and, more particularly, to a cell collecting device capable of
filtering and collecting target cells from a fluid sample such as
blood or physiological fluid.
BACKGROUND OF THE INVENTION
[0002] In recent years, regulations are increasingly strengthened
on a biological test and a clinical test conducted for the sake of
treatment of human diseases. As an alternative for the biological
test and the clinical test, research and development have been
extensively made on the collection of live cells from the human
blood. The collection of cells is conducted by different kinds of
cell collecting devices such as a micro-fluidic device, a CTC
(Circulating Tumor Cell) chip, a filter, and so forth.
[0003] A filter for filtering cells from blood is disclosed in many
patent documents, e.g., U.S. Patent Publication Nos. 2007/0025883A1
and 2009/0188864A1. The filter is formed of a membrane having a
plurality of pores for filtering cells. In the technologies of the
aforementioned patent documents, cancer cells are dispersed over
the entire surface of the filer mounted inside a chamber or a
central square hole. For that reason, there is a problem in that it
becomes difficult to identify the filtered state of the cancer
cells. Moreover, it is difficult to recover and collect the cancer
cells dispersed on the surface of the filter.
SUMMARY OF THE INVENTION
Technical Problems
[0004] In view of the problems noted above, it is an object of the
present invention to provide a cell collecting device capable of
filtering target cells from a fluid sample such as blood or
physiological fluid and collecting the target cells in a region
near a tubular wall.
[0005] Another object of the present invention is to provide a cell
collecting device capable of gathering target cells at a specified
place and collecting the target cells with ease.
Means for Solving the Problems
[0006] In order to achieve these objects, the present invention
provides a cell collecting device, including: a conduit through
which a fluid sample containing target cells passes; and a screen
filter installed inside the conduit and configured to guide the
target cells toward a specified region, the screen filter including
a plurality of filtering holes for filtering the target cells.
[0007] The conduit may include a tubular wall defining a passage
for passing the fluid sample therethrough, the screen filter
configured to guide the target cells toward a boundary region where
the screen filter meets with the tubular wall. The screen filter
may be obliquely installed in the passage along a flow direction of
the fluid sample. The screen filter may include a trap formed at a
downstream end of the screen filter so as to gather the target
cells. The screen filter may be formed into a curvilinear shape.
The conduit may include an outlet formed near the boundary region
and kept in communication with the boundary region so that the
target cells can be discharged through the outlet. The screen
filter may include a convex portion formed to guide the target
cells toward the boundary region. The screen filter may include a
concave portion formed to guide and gather the target cells. The
concave portion may be formed at a center of the screen filter so
as to gather the target cells. The screen filter may further
include a trap formed at a center of the concave portion so as to
receive the target cells.
Advantageous Effects of the Invention
[0008] The present cell collecting device is capable of separating
target cells from a fluid sample, gathering the target cells at a
specified place and collecting the target cells with ease. This
significantly increases the collecting percentage of the target
cells. Accordingly, the present cell collecting device is useful in
collecting target cells from the human blood for the purpose of
analysis, inspection, drug trials and clinical tests.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] FIG. 1 is a perspective view showing the configuration of a
cell collecting device according to one embodiment of the present
invention.
[0010] FIG. 2 is a partially cutaway perspective view of the cell
collecting device shown in FIG. 1.
[0011] FIG. 3 is a section view of the cell collecting device shown
in FIG. 1.
[0012] FIG. 4 is a partially cutaway perspective view showing one
modified example of a screen filter employed in the present cell
collecting device.
[0013] FIG. 5 is a section view of the screen filter shown in FIG.
4.
[0014] FIG. 6 is a partially cutaway perspective view showing
another modified example of a screen filter employed in the present
cell collecting device.
[0015] FIG. 7 is a section view of the screen filter shown in FIG.
6.
[0016] FIG. 8 is a partially cutaway perspective view showing a
further modified example of a screen filter employed in the present
cell collecting device.
[0017] FIG. 9 is a section view of the screen filter shown in FIG.
8.
[0018] FIG. 10 is a partially cutaway perspective view showing a
still further modified example of a screen filter employed in the
present cell collecting device.
[0019] FIG. 11 is a section view of the screen filter shown in FIG.
10.
[0020] FIG. 12 is an exploded perspective view showing a cell
collecting device according to another embodiment of the present
invention.
[0021] FIG. 13 is a partially cutaway perspective view of the cell
collecting device shown in FIG. 12.
[0022] FIG. 14 is a section view of the cell collecting device
shown in FIG. 12.
[0023] FIG. 15 is a partially cutaway perspective view showing a
cell collecting device according to a further embodiment of the
present invention.
[0024] FIG. 16 is a section view of the cell collecting device
shown in FIG. 15.
DETAILED DESCRIPTION OF EMBODIMENTS
[0025] Other objects, specific advantages and novel features of the
present invention will become apparent from the following
description of embodiments made in conjunction with the
accompanying drawings.
[0026] Certain embodiments of a cell collecting device according to
the present invention will now be described in detail with
reference to the accompanying drawings.
[0027] Referring first to FIGS. 1 through 3, a cell collecting
device according to the present invention is configured to filter
target cells 4 from non-target cells 6 contained in a fluid sample
2, thereby collecting the target cells 4. The fluid sample 2
includes physiological fluid such as saliva, sweat or urine of a
human or an animal, blood and serum. In addition, the fluid
containing target cells 4 such as cells or tissues of a human, an
animal or a plant and the fluid containing viruses or bacteria may
be selected as the fluid sample 2. If the blood is selected as the
fluid sample 2, the cells of different sizes contained in the blood
may become the target cells 4. Examples of the cells contained in
the blood include red blood cells, white blood cells and cancer
cells. In the embodiments of the present invention, the cancer
cells may be selected as the target cells 4. The red blood cells
and the white blood cells may be selected as the non-target cells
6.
[0028] The present cell collecting device includes a conduit 10
through which the fluid sample 2 can flow. The conduit 10 includes
a tubular wall 14 defining a passage 12 through which a large
amount of fluid sample 2 containing target cells 4 can flow
smoothly. The passage 12 can be formed to have many different
cross-sectional shapes such as a circular cross-sectional shape and
a rectangular cross-sectional shape. The conduit 10 is divided into
an upper conduit part 16a and a lower conduit part 16b. The upper
conduit part 16a and the lower conduit part 16b are combined
together by bonding, press-fit or thread coupling so as to define
the passage 12.
[0029] The present cell collecting device further includes a screen
filter 20 installed in the passage 12 of the conduit 10. The screen
filter 20 includes a front surface 22, a rear surface 24, a
peripheral edge 26 and a plurality of filtering holes 28 formed so
as to filter the target cells 4. The filtering holes 28 are formed
to have a dimension smaller than the diameter of the target cells
4. The screen filter 20 is preferably made of metal, e.g.,
stainless steel, nickel, aluminum or copper. The filtering holes 28
having a micrometer size can be formed by etching or electroforming
through the use of a MEMS (Micro-Electro-Mechanical System)
technology. The screen filter 20 is rigid enough not to be deformed
by the pressure of the fluid sample 2 flowing through the passage
12.
[0030] The peripheral edge 26 of the screen filter 20 is interposed
between the lower end of the upper conduit part 16a and the upper
end of the lower conduit part 16b. The front surface 22 meets with
the tubular wall 14. The screen filter 20 is shaped to guide the
target cells 4 toward a boundary region 30 where the tubular wall
14 adjoins the front surface 22. While the peripheral edge 26 of
the screen filter 20 is interposed between the upper conduit part
16a and the lower conduit part 16b in the present embodiment, the
screen filter 20 may be arranged in the passage 12 such that the
peripheral edge 26 thereof makes contact with the tubular wall
14.
[0031] The screen filter 20 is obliquely installed in the passage
12 along the flow direction of the fluid sample 2 so as to gather
the target cells 4 in the boundary region 30 where the downstream
end of the screen filter 20 meets with the tubular wall 14. In
other words, the target cells 4 are gathered in the boundary region
30 existing between the downstream end portion of the screen filter
20 and the tubular wall 14. In the present embodiment, the slope of
the screen filter 20 is set to ensure that the target cells can
flow down toward the boundary region 30 along the front surface 22
of the screen filter 20.
[0032] As shown in FIG. 3, the conduit 10 has an outlet 18 formed
near the boundary region 30 and kept in communication with the
boundary region 30. The target cells 4 gathered in the boundary
region 30 can be collected by discharging the target cells 4 out of
the conduit 10 through the outlet 18. The outlet 18 may be opened
and closed by a well-known valve.
[0033] In the present cell collecting device configured as above,
the fluid sample 2 is supplied to the upstream end of the conduit
10 by a fluid sample supply means (not shown). Examples of the
fluid sample supply means include a syringe, a blood collection
tube, a bag, a pack or other containers capable of storing a
specified amount of fluid sample and supplying the fluid sample to
the upstream end of the conduit 10. The fluid sample supply means
may be formed of a syringe pump or a plunger pump.
[0034] If the fluid sample 2 is supplied to the upstream end of the
conduit 10 as shown in FIG. 3, the target cells 4 contained in the
fluid sample 2 flowing along the passage 12 cannot pass through the
filtering holes 28 but obliquely move down along the front surface
22 toward the downstream end portion of the screen filter 20. Thus,
the target cells are gathered in the boundary region 30 where the
downstream end of the front surface 22 meets with the tubular wall
14.
[0035] The flow velocity profile P of the fluid sample 2 shows such
a pattern that the flow velocity becomes highest in the central
region of the passage 12 and grows lower toward the tubular wall 14
due to the pile friction loss. The pressure is high and the flow
velocity is low at the upstream end of the front surface 22 and the
downstream end of the rear surface 24 adjacent to the tubular wall
14.
[0036] The target cells 4 filtered by the filtering holes 28 in the
central region of the screen filter 20 where the flow velocity is
highest rapidly flow down toward the downstream end of the screen
filter 20 along the front surface 22. The non-target cells 6, e.g.,
red blood cells, rapidly pass through the filtering holes 28 in the
central region of the screen filter 20. Accordingly, it is possible
to prevent the filtering holes 28 from being clogged by the target
cells 4 and the non-target cells 6. This makes it possible to
maintain smooth flow of the fluid sample 2, thereby efficiently
filtering the target cells 4 from the fluid sample 2.
[0037] The screen filter 20 of the present cell collecting device
is formed into a linear shape as shown in FIG. 1. Alternatively,
the screen filter 20 may be formed into a curvilinear shape with an
apex point existing at the center, a monotonously increasing
curvilinear shape or a monotonously decreasing curvilinear shape.
In case of the screen filter having a curvilinear shape with an
apex point existing at the center, the slope of the tangential line
becomes gentlest in the central region of the screen filter and
grows gradually larger toward the peripheral edge of the screen
filter. For that reason, even if the flow velocity of the fluid
sample 2 is not high in the central region of the passage 12, it is
possible to efficiently gather the target cells 4 in a region near
the tubular wall 14.
[0038] The target cells 4 gathered in the boundary region 30 can be
collected by discharging the target cells 4 out of the conduit 10
through the outlet 18. In this collecting process, the target cells
4 discharged out of the conduit 10 may be received in a test tube
or a culture dish.
[0039] FIGS. 4 and 5 show one modified example of the screen filter
employed in the present cell collecting device. Referring to FIGS.
4 and 5, the screen filter 120 according to one modified example
includes a front surface 122, a rear surface 124, a peripheral edge
126 and a plurality of filtering holes 128 formed so as to filter
the target cells 4. The screen filter 120 is obliquely installed in
the passage 12 along the flow direction of the fluid sample 2 so as
to gather the target cells 4 in a boundary region 130 where the
downstream end of the screen filter 120 meets with the tubular wall
14.
[0040] The screen filter 120 is formed into a double-curve shape to
have a concave portion 132 positioned more upward than the center
of the screen filter 120 and a convex portion 134 positioned more
downward than the center of the screen filter 120. The concave
portion 132 and the convex portion 134 are connected to each other
in a smooth wave form. In the concave portion 132, the non-target
cells 6 can smoothly pass through the filtering holes 28. The
target cells 4 are rapidly moved toward the boundary region 30
across the convex portion 134 and are gathered in the boundary
region 30. It is therefore possible to separate the target cells 4
from the non-target cells 6 and to gather the target cells 4 in a
region near the tubular wall 14.
[0041] In the screen filter 120 of a double-curve shape including
the concave portion 132 and the convex portion 134, the slope of
the tangential line is changed depending on the curvature of the
screen filter 120. The slope of the tangential line affects the
efficiency of guiding the target cells 4 toward the tubular wall
14. The collection efficiency of the target cells 4 can be
increased by appropriately changing the curvature of the screen
filter 120 depending on the flow velocity profile of the fluid
sample 2.
[0042] FIGS. 6 and 7 show another modified example of the screen
filter employed in the present cell collecting device. Referring to
FIGS. 6 and 7, the screen filter 220 according to another modified
example includes a front surface 222, rear surface 224, a
peripheral edge 226 and a plurality of filtering holes 228 formed
so as to filter the target cells 4. The screen filter 220 is
obliquely installed in the passage 12 along the flow direction of
the fluid sample 2 so as to gather the target cells 4 in a boundary
region 230 where the downstream end of the screen filter 220 meets
with the tubular wall 14.
[0043] The screen filter 220 includes a concave portion 232 gently
curved from the upstream end toward the downstream end and a convex
portion 234 extending further downward from the concave portion
232. The screen filter 220 further includes a concave trap 236
formed at the most downstream end of the screen filter 220 so as to
accommodate the target cells 4. The trap 236 is formed into a
pocket shape so as to gather the target cells 4 in between the
tubular wall 14 and the trap 236. The concave portion 232 and the
convex portion 234 serve to guide the target cells 4 toward the
trap 236. The target cells 4 move downward along the front surface
222 and come into the trap 236. Accordingly, it is possible to
separate the target cells 4 from the non-target cells 6 and to
efficiently gather the target cells 4 in the trap 236. The target
cells 4 gathered in the trap 236 can be discharged out of the
conduit 10 through the outlet 18.
[0044] FIGS. 8 and 9 show a further modified example of the screen
filter employed in the present cell collecting device. Referring to
FIGS. 8 and 9, the screen filter 320 according to a further
modified example includes a front surface 322, a rear surface 324,
a peripheral edge 326 and a plurality of filtering holes 328 formed
so as to filter the target cells 4. The screen filter 320 is
obliquely installed in the passage 12 along the flow direction of
the fluid sample 2 such that the target cells 4 moving down along
the front surface 322 are gathered in a trap 336. The screen filter
320 includes a convex portion 334 formed between the trap 336 and
the upstream end of the screen filter 320 so as to bulge obliquely
upward. The convex portion 334 serves to guide the target cells 4
toward the trap 336. It is therefore possible to separate the
target cells 4 from the non-target cells 6 and to gather the target
cells 4 in the trap 336.
[0045] FIGS. 10 and 11 show a still further modified example of the
screen filter employed in the present cell collecting device.
Referring to FIGS. 10 and 11, the screen filter 420 according to a
still further modified example includes a front surface 422, a rear
surface 424, a peripheral edge 426 and a plurality of filtering
holes 428 formed so as to filter the target cells 4. The peripheral
edge 426 is interposed between the upper conduit part 16a and the
lower conduit part 16b and is arranged on a plane orthogonal to the
tubular wall 14.
[0046] The screen filter 420 includes a convex portion 438 formed
so as to guide the target cells 4 toward a boundary region 430
where the downstream end of the screen filter 420 meets with the
tubular wall 14. The convex portion 438 is formed into a
substantially dome-like shape such that the target cells 4 are
guided from the central peak of the convex portion 438 toward the
boundary region 430. The target cells 4 that cannot pass through
the filtering holes 428 are moved down along the convex portion 438
toward the boundary region 430. The target cells 4 are gathered in
the boundary region 430, i.e., at the edge of the convex portion
438. This prevents the filtering holes 428 from being clogged by
the target cells 4. While the convex portion 438 is formed into a
substantially dome-like shape in the present modified example, the
present invention is not limited thereto. Alternatively, the convex
portion 438 may be formed into a conical shape, a triangular
pyramidal shape, a rectangular pyramidal shape or other shapes
suitable for guiding the target cells 4 from the center of the
passage 12 toward the tubular wall 14.
[0047] FIGS. 12 through 14 show a cell collecting device according
to another embodiment of the present invention. Referring to FIGS.
12 through 14, the cell collecting device according to another
embodiment includes a conduit 50 through which a fluid sample 2 can
flow. The conduit 50 has a passage 52 through which the fluid
sample 2 can pass. The conduit 50 is divided into an upper conduit
part 54a and a lower conduit part 54b. The upper conduit part 54a
and the lower conduit part 54b are combined together by bonding,
press-fit or thread coupling so as to define the passage 52. The
passage 52 can be formed into many different cross-sectional shapes
such as a circular cross-sectional shape and a rectangular
cross-sectional shape so as to smoothly pass the fluid sample 2
therethrough.
[0048] The present cell collecting device further includes a screen
filter 520 installed in the passage 52 of the conduit 50 so as to
filter the target cells 4. The screen filter 520 includes a front
surface 522, a rear surface 524, a peripheral edge 526 and a
plurality of filtering holes 528 formed so as to filter the target
cells 4. The peripheral edge 526 of the screen filter 520 is
interposed between the lower end of the upper conduit part 54a and
the upper end of the lower conduit part 54b. Alternatively, the
screen filter 520 may be press-fitted to the passage 52 so that the
peripheral edge 526 can make contact with the inner circumferential
surface of the conduit 50. While the screen filter 520 shown in
FIG. 12 has a circular shape, the present invention is not limited
thereto. The shape of the screen filter 520 may be appropriately
changed to, e.g., a rectangular shape or an elliptical shape,
depending on the shape of the passage 52.
[0049] The filtering holes 528 are formed to have a dimension
smaller than the diameter of the target cells 4. The screen filter
520 is preferably made of metal, e.g., stainless steel, nickel,
aluminum or copper. The filtering holes 528 having a micrometer
size can be formed by etching or electroforming through the use of
a MEMS (Micro-Electro-Mechanical System) technology. The screen
filter 520 is rigid enough not to be deformed by the pressure of
the fluid sample 2 flowing through the passage 52.
[0050] The screen filter 520 is shaped to guide the target cells 4
toward a specified region along the front surface 522. The screen
filter 520 includes a concave portion 530 formed to gather the
target cells 4 in the central region thereof. The concave portion
530 is formed into a substantially hemi-spherical shape.
Alternatively, the concave portion 530 may be formed into a conical
tube shape, a triangular pyramidal tube shape, a rectangular
pyramidal tube shape or other shapes having a cross section
gradually decreasing toward the downstream end of the conduit 50.
Moreover, the concave portion 530 may be formed into many other
shapes so that the target cells 4 can be gathered in the central
region of the screen filter 520.
[0051] In the present cell collecting device configured as above,
the fluid sample 2 is supplied to the upstream end of the conduit
50 by a fluid sample supply means (not shown). Examples of the
fluid sample supply means include a syringe, a blood collection
tube, a bag, a pack or other containers capable of storing a
specified amount of fluid sample and supplying the fluid sample to
the upstream end of the conduit 50. The fluid sample supply means
may be formed of a syringe pump or a plunger pump.
[0052] If the fluid sample 2 is supplied to the upstream end of the
conduit 50 as shown in FIG. 14, the target cells 4 contained in the
fluid sample 2 flowing along the passage 52 cannot pass through the
filtering holes 528 but obliquely move down along the front surface
522 toward the central region of the concave portion 530. Thus, the
target cells 4 are gathered in the central region of the concave
portion 530. Non-target cells 6, e.g., red blood cells, can rapidly
pass through the filtering holes 528. Since the target cells 4 are
gathered in the central region of the concave portion 530, it is
possible to collect the target cells 4 with ease. In particular,
cancer cells contained in the blood can be gathered in a specified
place and collected in an efficient manner.
[0053] FIGS. 15 and 16 show a cell collecting device according to a
further embodiment of the present invention. Referring to FIGS. 15
and 16, the cell collecting device according to a further
embodiment includes a conduit 50 having a passage 52 defined
therein and a screen filter 620 installed in the passage 52 of the
conduit 10. The screen filter 620 includes a front surface 622, a
rear surface 624, a peripheral edge 626 and a plurality of
filtering holes 628 formed so as to filter the target cells 4.
[0054] The screen filter 620 includes a concave portion 630 formed
to guide the target cells 4 downward along the front surface 622
and a trap 632 formed at the center of the concave portion 630 so
as to gather the target cells 4. The trap 632 is formed into a
pocket shape so as to hold the target cells 4 therein. The target
cells 4 contained in the fluid sample 2 are moved downward along
the concave portion 630 and are gathered in the trap 632. It is
therefore possible to separate the target cells 4 from the
non-target cells 6 and to gather the target cells 4 in the trap
632.
[0055] The target cells 4 filtered and gathered in the trap 632 can
be discharged out of the trap 632 through the passage 52 by
supplying a solution, e.g., water, into the passage 52 in a
backward or forward direction. The target cells 4 discharged
through the passage 52 may be received in a container such as a
test tube or a culture dish. Since the target cells 4 are filtered
from the fluid sample 2 by the screen filter 620 and then detached
from the screen filter 620 by supplying the solution, it is
possible to efficiently collect live cancer cells from the human
blood.
[0056] While certain embodiments of the invention have been
described above, the scope of the present invention is not limited
to these embodiments. It will be apparent to those skilled in the
art that various changes, modifications and substitutions may be
made without departing from the scope of the invention defined in
the claims. Such changes, modifications and substitutions shall be
construed to fall within the scope of the present invention.
* * * * *