Arrangement and process for optical analysis and specific isolation of biological samples
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
G01N-033/50
G01N-001/28
B01D-063/08
B01L-003/00
G01N-015/10
G01N-001/04
G01N-001/40
출원번호
US-0118723
(2012-04-16)
등록번호
US-9958435
(2018-05-01)
우선권정보
DE-10 2011 076 238 (2011-05-20)
국제출원번호
PCT/EP2012/056872
(2012-04-16)
§371/§102 date
20131202
(20131202)
국제공개번호
WO2012/159822
(2012-11-29)
발명자
/ 주소
Bangert, Joachim
Friedrich, Katja
Gumbrecht, Walter
Hiltawsky, Karsten
Paulicka, Peter
Stanzel, Manfred
출원인 / 주소
Siemens Healthcare Diagnostics Inc.
대리인 / 주소
Stein, Kevin
인용정보
피인용 횟수 :
0인용 특허 :
8
초록▼
A process is disclosed for detecting cells in a liquid sample, which includes: i) filtration of the liquid sample through a porous membrane which is suitable for retaining detectable cells, where at least one subregion of a support is configured as transparent supporting body and the membrane is arr
A process is disclosed for detecting cells in a liquid sample, which includes: i) filtration of the liquid sample through a porous membrane which is suitable for retaining detectable cells, where at least one subregion of a support is configured as transparent supporting body and the membrane is arranged over its area on the transparent supporting body in such a way that detectable cells are retained on at least part of the surface of the membrane and that at least part of the sample liquid passes through the membrane, ii) application of a liquid optical medium which has essentially the same refractive index as the supporting body, and iii) optical measurement of at least a subarea of the membrane in order to detect detectable cells.
대표청구항▼
1. A process for detecting cells to be detected in a liquid sample, comprising: i) filtrating the liquid sample through a porous membrane arrayed in a flat configuration on a transparent supporting body, wherein the porous membrane is suitable for retaining the cells to be detected, such that the ce
1. A process for detecting cells to be detected in a liquid sample, comprising: i) filtrating the liquid sample through a porous membrane arrayed in a flat configuration on a transparent supporting body, wherein the porous membrane is suitable for retaining the cells to be detected, such that the cells to be detected are retained on at least part of a surface of the membrane and such that at least part of the liquid sample passes through the membrane, wherein the supporting body is a slide for microscopy, made of glass or plastic;ii) applying a liquid optical medium to the membrane on the transparent supporting body, wherein, the liquid optical medium has essentially the same refractive index as the transparent supporting body; andiii) optically measuring at least a subarea of the membrane on the transparent supporting body in order to detect the cells to be detected, wherein the porous membrane remains in a flat configuration on the transparent support during the entire course of steps i)-iii). 2. The process of claim 1, wherein the cells to be detected are labeled before or after filtration with a first element for labeling the cells to he detected, which contains a first marker. 3. The process of claim 1, wherein the supporting body is at least one of textured, porous, and made of plastic. 4. The process of claim 1, wherein the support and the supporting body are made integrally from a single body and the membrane completely covers the supporting body. 5. The process of claim 1, wherein the supporting body includes channels formed on a side facing the filter membrane, said channels being configured in fluid contact with the membrane. 6. The process of claim, 1, wherein the membrane and the supporting body include a plurality of mutual contact points lying in a plane-parallel, flat plane of the contact surface, and wherein especially the membrane includes a maximum distance from the planar contact surface of less than 100 μm. 7. The process of claim 1, wherein the membrane is a Track Etched filter membrane that is composed of a polycarbonate film or and includes pores with a diameter of 2 μm-100 μm. 8. The process of claim 1, wherein at least one cell to be detected is isolated on the surface of the membrane after the filtrating the liquid sample through the porous membrane. 9. The process of claim 8, wherein the cell to be detected is isolated by laser microdissection. 10. The process of claim 1, wherein the cell to be detected is a tumor cell. 11. The process of claim 3, wherein the support is a slide for microscopy, made of COC. 12. The process of claim 3, wherein the supporting body is made of a same plastic as the support. 13. The process of claim 4, wherein the membrane lies flat on the supporting body. 14. The process of claim 2, wherein at least one of the support is a slide for microscopy, made of glass or plastic; andthe supporting body is at least one of textured, porous, and made of plastic. 15. The process of claim 2, wherein the support and the supporting body are made integrally from a single body and the membrane completely covers the supporting body. 16. The process of claim 11, wherein the supporting body is made of a same plastic as the support. 17. The process of claim 12, wherein the membrane lies flat on the supporting body. 18. The process of claim 2, wherein the element for labeling comprises at least one marker that can stain cells specifically or nonspecifically. 19. The process of claim 18, wherein the nonspecific marker includes at least one of a dye that stain proteins, nucleic acids, or other cell constituents. 20. The process of claim 18, wherein the specific marker includes at least ore of an antibody, oligonucleotide probe, peptide or other molecule that binds specifically to proteins, nucleic acid sequences or other cell-specific structures.
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이 특허에 인용된 특허 (8)
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Baer, Thomas M.; Reamey, Robert H.; Moravick, Keith E.; Head, David F.; Richardson, Bruce J.; Richardson, Derrick A., Laser capture microdissection (LCM) extraction device and device carrier, and method for post-LCM fluid processing.
Bisconte, Jean-Claude, Microscope stage for rapid and indexed analysis of filters and other media carrying multiple samples, and a method of analyzing such samples using said stage.
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