JP2014171389A5 - - Google Patents
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- JP2014171389A5 JP2014171389A5 JP2013043424A JP2013043424A JP2014171389A5 JP 2014171389 A5 JP2014171389 A5 JP 2014171389A5 JP 2013043424 A JP2013043424 A JP 2013043424A JP 2013043424 A JP2013043424 A JP 2013043424A JP 2014171389 A5 JP2014171389 A5 JP 2014171389A5
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- hole
- holding member
- disposed
- cell culture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000758 substrate Substances 0.000 claims description 19
- 238000004113 cell culture Methods 0.000 claims description 3
- 229910001172 neodymium magnet Inorganic materials 0.000 description 2
- 210000002381 Plasma Anatomy 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N Simethicone Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating Effects 0.000 description 1
- 210000004027 cells Anatomy 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 238000004987 plasma desorption mass spectroscopy Methods 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
Description
本実施例の第1基板11と第3基板51は、PDMSから成る20mm角の基板である。
第1基板11は、厚み1.3mmであり、中央には直径2.5mmの貫通孔12が形成されている。ここで、第1基板11において、貫通孔12の中心軸側を基板の中心側、その反対を外側とし、培養時に細胞培養ディッシュ21と接する側の面を底面、その反対の面を上面とする。第1基板11の上面には、2本の流路(幅0.5mm深さ0.2mm)17a及び17bが形成されており、各流路17a、17bの一端は貫通孔12へ連通している。第1基板11の底面には、貫通孔12を取り囲むように環状凹部14が形成されている。貫通孔12は、培養室の壁面に起因する影によって培養室71内の細胞が観察できないことがないように、観察に用いる顕微鏡のレンズの性能に合わせて、すり鉢状とすることが望ましい。
The first substrate 11 and the third substrate 51 of the present embodiment are 20 mm square substrates made of PDMS.
The first substrate 11 has a thickness of 1.3 mm, and a through hole 12 having a diameter of 2.5 mm is formed at the center. Here, in the first substrate 11, the central axis side of the through hole 12 is the center side of the substrate, the opposite is the outer side, the surface in contact with the cell culture dish 21 during culture is the bottom surface, and the opposite surface is the upper surface. . Two channels (width 0.5 mm, depth 0.2 mm) 17 a and 17 b are formed on the upper surface of the first substrate 11, and one ends of the channels 17 a and 17 b communicate with the through hole 12. An annular recess 14 is formed on the bottom surface of the first substrate 11 so as to surround the through hole 12. It is desirable that the through-hole 12 has a mortar shape according to the performance of the lens of the microscope used for observation so that the cells in the culture chamber 71 cannot be observed due to shadows caused by the wall surface of the culture chamber.
第3基板51は、厚み3mmであり、内部に内径6mm外径10mm厚さ2mmのネオジム磁石31(第1保持部材に該当する)が封入されている。第3基板51には、ネオジム磁石31より外側の部分に2つの孔(直径1.5mm)52a及び52bが形成されており、本細胞培養デバイス70を組み立てると、この孔52a、52bは、それぞれ、流路17a、17bの他端に連通する。
第1基板11と第3基板51は、例えば真空プラズマなどで表面を活性化させて接合されている。
The third substrate 51 has a thickness of 3 mm and encloses a neodymium magnet 31 (corresponding to the first holding member) having an inner diameter of 6 mm, an outer diameter of 10 mm, and a thickness of 2 mm. Two holes (diameter 1.5 mm) 52a and 52b are formed in the third substrate 51 on the outer side of the neodymium magnet 31, and when the cell culture device 70 is assembled, the holes 52a and 52b are respectively It communicates with the other ends of the flow paths 17a and 17b.
The first substrate 11 and the third substrate 51 are bonded by activating their surfaces with, for example, vacuum plasma.
Claims (1)
前記貫通孔の一端を塞ぐように前記第1基板の一面側に配置された第2基板と、
前記第1基板と前記第2基板とを磁気吸引力によって接合させる磁力対である第1保持部材及び第2保持部材と
を含み、前記第1保持部材は前記貫通孔を取り囲むように環状に前記第1基板側に配置され、及び前記第2保持部材は前記第2基板側に配置されていることを特徴とする細胞培養デバイス。 A first substrate having a through hole;
A second substrate disposed on one side of the first substrate so as to close one end of the through hole;
A first holding member and a second holding member, which are magnetic pairs for joining the first substrate and the second substrate by a magnetic attractive force, and the first holding member is annularly formed so as to surround the through hole. cell culture device disposed on the first substrate side, and the second holding member is characterized by being disposed on the second substrate side.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013043424A JP6120314B2 (en) | 2013-03-05 | 2013-03-05 | Cell culture devices |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013043424A JP6120314B2 (en) | 2013-03-05 | 2013-03-05 | Cell culture devices |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2014171389A JP2014171389A (en) | 2014-09-22 |
JP2014171389A5 true JP2014171389A5 (en) | 2016-02-12 |
JP6120314B2 JP6120314B2 (en) | 2017-04-26 |
Family
ID=51693369
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013043424A Active JP6120314B2 (en) | 2013-03-05 | 2013-03-05 | Cell culture devices |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6120314B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6183289B2 (en) * | 2014-05-14 | 2017-08-23 | 株式会社島津製作所 | Cell culture devices |
JP2021069344A (en) * | 2019-10-31 | 2021-05-06 | 株式会社リコー | Sample container, sample container with lid, and cell-containing container |
CN114107194B (en) * | 2021-11-22 | 2024-01-30 | 颐华国韵(河南)生物科技有限公司 | Immune cell expansion culture method and device |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0853659B1 (en) * | 1995-10-06 | 2000-05-10 | Microcloning CCCD AB | Compact cell culture slide |
JP3878709B2 (en) * | 1997-03-31 | 2007-02-07 | ミクロクローニング シーシーシーデー エイビー | Sequence for culturing a biological sample, its production method and measurement method thereby |
JP2004000163A (en) * | 2002-03-29 | 2004-01-08 | Shimadzu Corp | Cell used for treating cell |
JP4078425B2 (en) * | 2003-11-25 | 2008-04-23 | 独立行政法人産業技術総合研究所 | Sample substrate holder and method of using the same |
JP4475525B2 (en) * | 2005-02-10 | 2010-06-09 | 国立大学法人京都工芸繊維大学 | Biopolymer screening method by depolarization |
JP2009022247A (en) * | 2007-07-23 | 2009-02-05 | Toshiba Corp | Culturing container and method for recovering cultured tissue |
-
2013
- 2013-03-05 JP JP2013043424A patent/JP6120314B2/en active Active
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