ANALYZING BIOLOGICAL CELL MATERIAL BASED ON DIFFERENT INTERACTIONS BETWEEN ILLUMINATION LIGHT AND CELL COMPONENTS

• US 20100105022A1
• Filed: 03/10/2008
• Published: 04/29/2010
• Est. Priority Date: 03/13/2007
• Status: Abandoned Application

• Current Assignee: Koninklijke Philips Electronics N.V. (Koninklijke Philips N.V.)
• Original Assignee: Koninklijke Philips Electronics N.V. (Koninklijke Philips N.V.)
• Inventors: Kuiper, Stein, Hendriks, Bernardus Hendrikus Wilhelmus, Hooft, Gert, De Boer, Ruth Wilhelmine Ireen
• Application Number:
  US12/530,787
• Publication Number:
  US 20100105022A1
• Time in Patent Office: Days
• US Class Current: 435/4
• CPC Class Codes: G01N 21/31 Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry G01N21/72 takes precedence
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/645 Specially adapted constructive features of fluorimeters

Abstract

It is described a device (100) for analyzing biological cell material (115). The device (100) comprises a light source arrangement (120), which is adapted for directing a first (131) and a second illumination light (132) towards the cell material (115), wherein the first (131) and the second (132) illumination light comprises a first and a second spectral radiation component, respectively. The device (100) further comprises a detector arrangement (170), which is adapted for receiving a first measurement light (151) based on a first interaction of the first illumination light (131) with the cell material (115) and a second measurement light (152) based on a second interaction of the second illumination light (152) with the cell material (115). Further, the device (100) comprises an evaluation unit (180), which is coupled the detector arrangement (170) and which is adapted to evaluate a first signal (171a) and a second signal (171b) being indicative for the first (151) and the second measurement light (151), respectively. The device (100) may be used for accomplishing ultraviolet DNA image cytometryin combination with autofluorescence measurements of NAD(P)H.

Claims

1. A device for analyzing biological cell material (115, 215, 315, 415), the device comprising:

a light source arrangement (120, 220, 320, 420), which is adapted for directing a first illumination light (131, 231, 331, 431) and a second illumination light (132, 232, 332, 432) towards the biological cell material (115, 215, 315, 415), wherein the first illumination light (131, 231, 331, 431) comprises a first spectral radiation component and the second illumination light (132, 232, 332, 432) comprises a second spectral radiation component,

a detector arrangement (170, 270, 370, 470), which is adapted for receiving

a first measurement light (151, 251, 351, 451), which is based on a first interaction of the first illumination light (131, 231, 331, 431) with the cell material (115, 215, 315, 415), and

a second measurement light (132, 232, 332, 432), which is based on a second interaction of the second illumination light (132, 232, 332, 432) with the cell material (115, 215, 315, 415), and,

an evaluation unit (180, 280, 380, 480), which is coupled the detector arrangement (170, 270, 370, 470) and which is adapted to evaluate

a first signal (171a, 271a, 371a, 471a) being indicative for the first measurement light (151, 251, 351, 451) and

a second signal (172a, 272a, 372a, 472a) being indicative for the second measurement light (132, 232, 332, 432).

2. The device according to claim 1, further comprising:

a carrier element (110, 210, 310, 410) for supporting the cell material (115, 215, 315, 415).

3. The device according to claim 1, wherein the first interaction is absorption and/or the second interaction is fluorescence.

4. The device according to claim 3, wherein

the first illumination light (131, 231, 331, 431) is adapted to interact with a first cell component of the biological cell material (115, 215, 315, 415) by means of the first interaction and/or

the second illumination light (132, 232, 332, 432) is adapted to interact with a second cell component of the biological cell material (115, 215, 315, 415) by means of the second interaction.

5. The device according to claim 4, wherein

the first cell component is DNA and/or

the second cell component is an enzyme being used for cell metabolism, in particular NAD(P)H.

6. The device according to claim 1, wherein

the first illumination light (131, 231, 331, 431) and the second illumination light (132, 232, 332, 432) is ultraviolet light comprising a wavelength in between 150 nm and 350 nm, preferably in between 200 nm and 300 nm and more preferably in between 230 nm and 270 nm.

7. The device according to claim 1, wherein

the second illumination light (132, 232, 332, 432) is ultraviolet light comprising a wavelength in between 280 nm and 400 nm, preferably in between 320 nm and 360 nm and more preferably in between 330 nm and 350 nm, and

the second measurement light (152, 252, 352, 452) is visible light comprising a wavelength in between 345 nm and 545 nm, preferably in between 400 nm and 490 nm and more preferably in between 430 nm and 460 nm.

8. The device according to claim 1, wherein

the light source arrangement (120, 220, 320, 420) comprises a broad-spectrum ultraviolet light source (121, 221).

9. The device according to claim 1, wherein

the light source arrangement (120, 220, 320, 420) comprises

a first light source (321, 421) generating the first illumination light (131, 231, 331, 431) and

a second light source (322, 422) generating the second illumination light (132, 232, 332, 432).

10. The device according to claim 1, further comprising

an optic arrangement (140, 240, 340, 440) for focusing the first illumination light (131, 231, 331, 431) and/or the second illumination light (132, 232, 332, 432) onto the biological cell material (115, 215, 315, 415).

11. The device according to claim 1, wherein

the detector arrangement (170, 270, 370, 470) comprises

a first detector (171, 471) for receiving the first measurement light (151, 251, 351, 451) and

a second detector (172, 472) for receiving the second measurement light (132, 232, 332, 432).

12. The device according to claim 1, wherein

the detector arrangement (170, 270, 370, 470) comprises

a common detector (270, 370) for receiving both the first measurement light (151, 251, 351, 451) and the second measurement light (132, 232, 332, 432), and wherein

the device further comprises

a chopper device (245, 265, 345, 365) for letting pass the first measurement light (151, 251, 351, 451) and the second measurement light (132, 232, 332, 432) in an alternating manner.

13. The device according to claim 1, wherein

the first illumination light (131, 231, 331, 431) and the second illumination light (132, 232, 332, 432) impinge onto the biological cell material (115, 215, 315, 415) along a common incidence beam path (135, 235, 335, 435) and

the first measurement light (151, 251, 351, 451) and the second measurement light (132, 232, 332, 432) leave the biological cell material (115, 215, 315, 415) along a common exit beam path (155, 255, 355, 455), wherein

the common incidence beam path (135, 235, 335, 435) and the common exit beam path (155, 255, 355, 455) are collinear with respect to each other.

14. The device according to claim 3, wherein

the detector arrangement (470) is adapted to measure a time dependence of the second signal (472a) being indicative for the second measurement light (432) and

the evaluation unit (480) is adapted to evaluate the time dependence of the second signal (472a).

15. The device according to claim 14, further comprising

a light modulation device (490), which is adapted to modulate to intensity of the second illumination light (432) as a function of time.

16. A method for analyzing biological cell material (115, 215, 315, 415), the method comprising

directing a first illumination light (131, 231, 331, 431) comprising a first spectral radiation component from a light source arrangement (120, 220, 320, 420) towards the cell material (115, 215, 315, 415),

directing a second illumination light (132, 232, 332, 432) comprising a second spectral radiation component from the light source arrangement (120, 220, 320, 420) towards the cell material (115, 215, 315, 415),

receiving a first measurement light (151, 251, 351, 451), which is based on a first interaction of the first illumination light (131, 231, 331, 431) with the cell material (115, 215, 315, 415), by means of a detector arrangement (170, 270, 370, 470),

receiving a second measurement light (132, 232, 332, 432), which is based on a second interaction of the second illumination light (132, 232, 332, 432) with the cell material (115, 215, 315, 415), by means of the detector arrangement (170, 270, 370, 470),

evaluating a first signal being indicative for the first measurement light (151, 251, 351, 451), and

evaluating a second signal being indicative for the second measurement light (132, 232, 332, 432).