JPS5663260A - Clinical test device - Google Patents
Clinical test deviceInfo
- Publication number
- JPS5663260A JPS5663260A JP14061079A JP14061079A JPS5663260A JP S5663260 A JPS5663260 A JP S5663260A JP 14061079 A JP14061079 A JP 14061079A JP 14061079 A JP14061079 A JP 14061079A JP S5663260 A JPS5663260 A JP S5663260A
- Authority
- JP
- Japan
- Prior art keywords
- electrode
- sample
- detector
- detection side
- flow paths
- 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.)
- Pending
Links
- 238000001514 detection method Methods 0.000 abstract 3
- 239000000243 solution Substances 0.000 abstract 3
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 abstract 2
- 238000000502 dialysis Methods 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108010046334 Urease Proteins 0.000 abstract 1
- 239000007853 buffer solution Substances 0.000 abstract 1
- 239000003792 electrolyte Substances 0.000 abstract 1
- 238000005070 sampling Methods 0.000 abstract 1
Landscapes
- Investigating Or Analysing Biological Materials (AREA)
Abstract
PURPOSE: To realize a quick analysis for multiple components with a small amount of sample, by providing the sample flow path passing the center part plus two detection side flow paths holding the sample between centering on the dialyais film within a dialysis cell and then connecting a detector to the detection side flow paths each.
CONSTITUTION: The sample 8 and the standard sample 29 are sucked up into the sample flow path 24 of the dialysis cell 21 by the liquid supply pump 30 and via the sampling device 9. On the other hand, the buffer solutions 27 and 28 are led to the detection side flow paths 25 and 26 of the cell 21 as well as to the electrolyte detector 40 and the urea nitrogen detector 50 each by the liquid supply pumps 31 and 32. The low molecular weight components of the samples 8 and 29 are sampled into the solutions 27 and 28. For the solution 27, the potential difference to the electrode 44 is measured by the detector 40 and through the sensing parts of the Na+ electrode 41, K+ electrode 42, C- electrode 43 and the comparison electrode 44 each, thus obtaining the concentration. On the other hand, the solution 28 affects via the detector 50 the enzyme reactor 54 formed by solidifying the urease, and then the NH4 + amount before and after the reactor 54 is measured through the NH4 + electrodes 51 and 52 plus the comparison electrode 53 each. Based on this difference, the amount of urea nitrogen is calculated.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14061079A JPS5663260A (en) | 1979-10-30 | 1979-10-30 | Clinical test device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14061079A JPS5663260A (en) | 1979-10-30 | 1979-10-30 | Clinical test device |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5663260A true JPS5663260A (en) | 1981-05-29 |
Family
ID=15272703
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14061079A Pending JPS5663260A (en) | 1979-10-30 | 1979-10-30 | Clinical test device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5663260A (en) |
-
1979
- 1979-10-30 JP JP14061079A patent/JPS5663260A/en active Pending
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