US3549328A - Test paper for detector of niacin - Google Patents
Test paper for detector of niacin Download PDFInfo
- Publication number
- US3549328A US3549328A US686494A US3549328DA US3549328A US 3549328 A US3549328 A US 3549328A US 686494 A US686494 A US 686494A US 3549328D A US3549328D A US 3549328DA US 3549328 A US3549328 A US 3549328A
- Authority
- US
- United States
- Prior art keywords
- niacin
- test paper
- reagents
- detector
- test
- 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.)
- Expired - Lifetime
Links
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 title description 17
- 229960003512 nicotinic acid Drugs 0.000 title description 16
- 235000001968 nicotinic acid Nutrition 0.000 title description 16
- 239000011664 nicotinic acid Substances 0.000 title description 16
- 239000003153 chemical reaction reagent Substances 0.000 description 15
- 238000001514 detection method Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 5
- 229960004909 aminosalicylic acid Drugs 0.000 description 5
- VDQQXEISLMTGAB-UHFFFAOYSA-N chloramine T Chemical compound [Na+].CC1=CC=C(S(=O)(=O)[N-]Cl)C=C1 VDQQXEISLMTGAB-UHFFFAOYSA-N 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 4
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 3
- 150000004982 aromatic amines Chemical group 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- -1 cyanogen halide Chemical class 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229940116357 potassium thiocyanate Drugs 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 241000187479 Mycobacterium tuberculosis Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 239000006286 aqueous extract Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 description 1
- QPJDMGCKMHUXFD-UHFFFAOYSA-N cyanogen chloride Chemical compound ClC#N QPJDMGCKMHUXFD-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- JMANVNJQNLATNU-UHFFFAOYSA-N glycolonitrile Natural products N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
- G01N21/78—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/52—Use of compounds or compositions for colorimetric, spectrophotometric or fluorometric investigation, e.g. use of reagent paper and including single- and multilayer analytical elements
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
- Y10T436/145555—Hetero-N
Definitions
- niacin is an important biochemical tool in the identification of Mycobacterium tuberculosis.
- Several methods of the detection of niacin have been proposed, but they suffer from one or more disadvantages.
- the disadvantages is the requirement for using liquid reagents which are unstable upon exposure to light and air. Accordingly, the reagents must be freshly distilled to avoid colors which mask the color test for niacin.
- the art has, therefore, long sought a test procedure which could be used for the detection of niacin which avoids the use of liquid reagents.
- Another object is to provide a niacin test paper which yields reliable and reproducible results.
- a further object is to provide a method for the detection of niacin which is simple and reliable and avoids the use of liquid reagents.
- the test paper of the invention comprises an inert absorbent substrate, such as filter paper and the like which has been impregnated in separate discrete zones with three reagents.
- the reagents are solids at ambient temperatures. Solutions of the reagents are employed to impregnate the substrate and the substrate thereafter dried to yield areas of the three reagents on the substrate.
- the first reagent is a source of cyanide ion which will react with a halogen to form a cyanogen halide.
- Suitable solid sources include potassium thiocyanate and potassium cyanide. Aqueous solutions of such reagents may be used to impregnate the substrate.
- the second reagent is a source of active free halogen.
- Suitable solids include chloramine T and alkali metal hypochlorites, which may be used in aqueous solution to impregnate the substrate.
- the third reagent is an aromatic amine.
- Suitable solid amines include p-aminosalicylic acid, benzidine and pmethylaminophenol sulfate.
- the amine component is preferably dissolved in a non-aqueous solvent for impregnation, since it tends to oxidize in the presence of Water to form colored products.
- the accompanying drawing illustrates a test strip prepared in accordance with the invention.
- the drawing illustrates a strip of filter paper (on an enlarged scale) impregnated with the three reagents at A, B and C.
- the paper has been impregnated with the halogen "ice source.
- the impregnant is the cyanide ion source.
- Zone C contains the aromatic amine.
- aqueous extract of a culture being tested was added to a 13 x 100 mm. screw capped tube.
- the test paper strip was dropped into the extract, the p-aminosalicylic acid end first. Diffusion of the ex tract caused mixing of the reagents.
- the acidified KCNS mixed with the chloramine T, releasing cyanogen chloride which reacts with niacin and p-aminosalicylic acid to form a yellow color in the liquid. Twelve to fifteen minutes, with occasional shaking, are preferably allowed for best development of the color test.
- the yellow color is a derivative of glutaconic aldehyde.
- test strips may bear suita'ble indicia (not shown) to identify one or more reagents on the strip.
- a dry test strip for the detection of niacin comprising an inert absorbent substrate impregnated in discrete separate zones with (1) a solid stable source of free active halogen ion (2) a solid stable source of cyanide ion, and
- a method for the detection of niacin in an aqueous medium comprising adding the test strip of claim 2 to the medium whereby a yellow color develops in said medium if niacin is present.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Immunology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Physics & Mathematics (AREA)
- Pathology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Cell Biology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plasma & Fusion (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Description
TEST PAPER FOR DETECTOR OF NIACIN Filed Nov. 29, 1967 INVENTOR JAMES 0. KILBURN ATTORNEY! United States Patent 3,549,328 TEST PAPER FOR DETECTOR OF NIACIN James O. Kilburn, Chamblee, Ga., assignor t0 the United States of America as represented by the Secretary of Health, Education, and Welfare Filed Nov. 29, 1967, Ser. No. 686,494 Int. Cl. G01n 31 00, 33/00; C09k 3/00 US. Cl. 23253 3 Claims ABSTRACT OF THE DISCLOSURE This invention relates to a test paper for the detection of niacin.
As is known, the detection of niacin is an important biochemical tool in the identification of Mycobacterium tuberculosis. Several methods of the detection of niacin have been proposed, but they suffer from one or more disadvantages. Among the disadvantages is the requirement for using liquid reagents which are unstable upon exposure to light and air. Accordingly, the reagents must be freshly distilled to avoid colors which mask the color test for niacin. The art has, therefore, long sought a test procedure which could be used for the detection of niacin which avoids the use of liquid reagents.
It is an object of this invention to provide a dry, stable test paper which greatly facilitates the detection of niacin.
Another object is to provide a niacin test paper which yields reliable and reproducible results.
A further object is to provide a method for the detection of niacin which is simple and reliable and avoids the use of liquid reagents.
Other objects and advantages will be apparent to those skilled in the art from the description herein.
The test paper of the invention comprises an inert absorbent substrate, such as filter paper and the like which has been impregnated in separate discrete zones with three reagents. The reagents are solids at ambient temperatures. Solutions of the reagents are employed to impregnate the substrate and the substrate thereafter dried to yield areas of the three reagents on the substrate.
The first reagent is a source of cyanide ion which will react with a halogen to form a cyanogen halide. Suitable solid sources include potassium thiocyanate and potassium cyanide. Aqueous solutions of such reagents may be used to impregnate the substrate.
The second reagent is a source of active free halogen. Suitable solids include chloramine T and alkali metal hypochlorites, which may be used in aqueous solution to impregnate the substrate.
The third reagent is an aromatic amine. Suitable solid amines include p-aminosalicylic acid, benzidine and pmethylaminophenol sulfate. The amine component is preferably dissolved in a non-aqueous solvent for impregnation, since it tends to oxidize in the presence of Water to form colored products.
The accompanying drawing illustrates a test strip prepared in accordance with the invention. The drawing illustrates a strip of filter paper (on an enlarged scale) impregnated with the three reagents at A, B and C. At zone A the paper has been impregnated with the halogen "ice source. At zone B the impregnant is the cyanide ion source. Zone C contains the aromatic amine.
EXAMPLE Filter paper strips, 6 cm. x 8 mm., are impregnated in three zones as shown in the drawing. At zone A,
one drop of 50% aqueous chloramine T was applied. At zone B, a drop of 60% potassium thiocyanate dissolved in 8% aqueous citric acid was applied. At zone C, one drop of a 10% solution of p-aminosalicylic acid in ethanol was applied. The strips were air-dried at room temperature in the dark for 24 hours and thereafter stored at 4 C. in 13 x mm. screw capped tubes. The strips remained stable and useable for more than three months.
In use, 0.6 ml. of an aqueous extract of a culture being tested was added to a 13 x 100 mm. screw capped tube. The test paper strip was dropped into the extract, the p-aminosalicylic acid end first. Diffusion of the ex tract caused mixing of the reagents.
The acidified KCNS mixed with the chloramine T, releasing cyanogen chloride which reacts with niacin and p-aminosalicylic acid to form a yellow color in the liquid. Twelve to fifteen minutes, with occasional shaking, are preferably allowed for best development of the color test.
While it is not intended to be bound by any theory of operation, it is believed that the yellow color is a derivative of glutaconic aldehyde.
In practice, the test strips may bear suita'ble indicia (not shown) to identify one or more reagents on the strip.
While the invention has been described in terms of certain embodiments, they are to be considered illustrative rather than limiting, and it is intended to cover all modifications which fall within the spirit and scope of the appended claims.
I claim:
1. A dry test strip for the detection of niacin comprising an inert absorbent substrate impregnated in discrete separate zones with (1) a solid stable source of free active halogen ion (2) a solid stable source of cyanide ion, and
(3) a solid stable aromatic amine.
2. The test strip set forth in claim 1 wherein (1) is chloramine T (2) is potassium thiocyanate (3) is p-aminosalicylic acid.
3. A method for the detection of niacin in an aqueous medium comprising adding the test strip of claim 2 to the medium whereby a yellow color develops in said medium if niacin is present.
References Cited FOREIGN PATENTS 3,409,405 11/1968 Mohan 23253 3,411,887 11/1968 Chiu-Choon Kn 23253 3,434,801 3/1969 Scherr 23253' 3,453,180 7/1969 Fraser 23-253 OTHER REFERENCES Goldthorpe et al., Estimation of Nicotinic Acid In Tissues by the Cyanogen Bromide Reaction, Analytical Chemistry, vol. 23, No. 3, March 1951, pages 484- 487.
MORRIS O. W-OLK, Primary Examiner R. E. SERWIN, Assistant Examiner US. Cl. X.R. 23- 230; 252-408
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68649467A | 1967-11-29 | 1967-11-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3549328A true US3549328A (en) | 1970-12-22 |
Family
ID=24756522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US686494A Expired - Lifetime US3549328A (en) | 1967-11-29 | 1967-11-29 | Test paper for detector of niacin |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3549328A (en) |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3770383A (en) * | 1971-04-05 | 1973-11-06 | Akzona Inc | Diagnostic test slide |
| US3941876A (en) * | 1973-04-25 | 1976-03-02 | Gte New Ventures Corporation | In vitro method for determining allergic hypersensitivity |
| US4031197A (en) * | 1973-04-25 | 1977-06-21 | Gte New Ventures Corporation | In vitro method for determining allergic hypersensitivity |
| US4178153A (en) * | 1977-11-21 | 1979-12-11 | Damon Corporation | Method and apparatus for chemical spot test analysis |
| US4208399A (en) * | 1978-08-16 | 1980-06-17 | The University Of Pittsburgh | Tolyl isocyanate test antigens, methods for their preparation and use in detecting diisocyanates and antibodies to diisocyanates |
| US4216245A (en) * | 1978-07-25 | 1980-08-05 | Miles Laboratories, Inc. | Method of making printed reagent test devices |
| US4298345A (en) * | 1977-11-21 | 1981-11-03 | Damon Corporation | Method and apparatus for chemical spot test analysis |
| US4383984A (en) * | 1978-08-16 | 1983-05-17 | University Of Pittsburgh | Tolyl isocyanate and toluene diisocyanate test antigens, methods for their preparation and use in detecting diisocyanates and antibodies to diisocyanates |
| USD293374S (en) | 1984-11-19 | 1987-12-22 | Orgenics, Ltd. | Assay cards |
| US4877745A (en) * | 1986-11-17 | 1989-10-31 | Abbott Laboratories | Apparatus and process for reagent fluid dispensing and printing |
| US5126276A (en) * | 1984-11-27 | 1992-06-30 | Falk Fish | Method for the determination and measurements of more than one unknown material in a single surface of a multianalytic assay |
| US5927547A (en) * | 1996-05-31 | 1999-07-27 | Packard Instrument Company | System for dispensing microvolume quantities of liquids |
| US6203759B1 (en) | 1996-05-31 | 2001-03-20 | Packard Instrument Company | Microvolume liquid handling system |
| US6521187B1 (en) | 1996-05-31 | 2003-02-18 | Packard Instrument Company | Dispensing liquid drops onto porous brittle substrates |
| US6537817B1 (en) | 1993-05-31 | 2003-03-25 | Packard Instrument Company | Piezoelectric-drop-on-demand technology |
| USD800001S1 (en) * | 2016-05-09 | 2017-10-17 | Hach Company | Water test strip |
| CN109655436A (en) * | 2018-12-07 | 2019-04-19 | 武汉工程大学 | Cryanide ion fluorescence detection test of a kind of column aromatic hydrocarbons modification and preparation method thereof, detection method |
| USD1008661S1 (en) * | 2022-01-28 | 2023-12-26 | No Sacrifice Bags, Inc. | Purse base shaper |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3409405A (en) * | 1965-02-17 | 1968-11-05 | Raam R. Mohan | Diagnostic preparation for the detection of formaldehyde |
| US3411887A (en) * | 1964-06-15 | 1968-11-19 | Miles Lab | Diagnostic composition |
| US3434801A (en) * | 1964-02-21 | 1969-03-25 | Colab Lab Inc | Diagnostic test material for determination of ovulatory function and method for production of said test material |
| US3453180A (en) * | 1965-08-02 | 1969-07-01 | Miles Lab | Test article |
-
1967
- 1967-11-29 US US686494A patent/US3549328A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3434801A (en) * | 1964-02-21 | 1969-03-25 | Colab Lab Inc | Diagnostic test material for determination of ovulatory function and method for production of said test material |
| US3411887A (en) * | 1964-06-15 | 1968-11-19 | Miles Lab | Diagnostic composition |
| US3409405A (en) * | 1965-02-17 | 1968-11-05 | Raam R. Mohan | Diagnostic preparation for the detection of formaldehyde |
| US3453180A (en) * | 1965-08-02 | 1969-07-01 | Miles Lab | Test article |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3770383A (en) * | 1971-04-05 | 1973-11-06 | Akzona Inc | Diagnostic test slide |
| US3941876A (en) * | 1973-04-25 | 1976-03-02 | Gte New Ventures Corporation | In vitro method for determining allergic hypersensitivity |
| US4031197A (en) * | 1973-04-25 | 1977-06-21 | Gte New Ventures Corporation | In vitro method for determining allergic hypersensitivity |
| US4178153A (en) * | 1977-11-21 | 1979-12-11 | Damon Corporation | Method and apparatus for chemical spot test analysis |
| US4298345A (en) * | 1977-11-21 | 1981-11-03 | Damon Corporation | Method and apparatus for chemical spot test analysis |
| US4216245A (en) * | 1978-07-25 | 1980-08-05 | Miles Laboratories, Inc. | Method of making printed reagent test devices |
| US4208399A (en) * | 1978-08-16 | 1980-06-17 | The University Of Pittsburgh | Tolyl isocyanate test antigens, methods for their preparation and use in detecting diisocyanates and antibodies to diisocyanates |
| US4383984A (en) * | 1978-08-16 | 1983-05-17 | University Of Pittsburgh | Tolyl isocyanate and toluene diisocyanate test antigens, methods for their preparation and use in detecting diisocyanates and antibodies to diisocyanates |
| USD293374S (en) | 1984-11-19 | 1987-12-22 | Orgenics, Ltd. | Assay cards |
| US5126276A (en) * | 1984-11-27 | 1992-06-30 | Falk Fish | Method for the determination and measurements of more than one unknown material in a single surface of a multianalytic assay |
| US4877745A (en) * | 1986-11-17 | 1989-10-31 | Abbott Laboratories | Apparatus and process for reagent fluid dispensing and printing |
| US6537817B1 (en) | 1993-05-31 | 2003-03-25 | Packard Instrument Company | Piezoelectric-drop-on-demand technology |
| US6079283A (en) * | 1996-05-31 | 2000-06-27 | Packard Instruments Comapny | Method for aspirating sample liquid into a dispenser tip and thereafter ejecting droplets therethrough |
| US6083762A (en) * | 1996-05-31 | 2000-07-04 | Packard Instruments Company | Microvolume liquid handling system |
| US6112605A (en) * | 1996-05-31 | 2000-09-05 | Packard Instrument Company | Method for dispensing and determining a microvolume of sample liquid |
| US6203759B1 (en) | 1996-05-31 | 2001-03-20 | Packard Instrument Company | Microvolume liquid handling system |
| US6422431B2 (en) | 1996-05-31 | 2002-07-23 | Packard Instrument Company, Inc. | Microvolume liquid handling system |
| US6521187B1 (en) | 1996-05-31 | 2003-02-18 | Packard Instrument Company | Dispensing liquid drops onto porous brittle substrates |
| US5927547A (en) * | 1996-05-31 | 1999-07-27 | Packard Instrument Company | System for dispensing microvolume quantities of liquids |
| US6592825B2 (en) | 1996-05-31 | 2003-07-15 | Packard Instrument Company, Inc. | Microvolume liquid handling system |
| USD800001S1 (en) * | 2016-05-09 | 2017-10-17 | Hach Company | Water test strip |
| CN109655436A (en) * | 2018-12-07 | 2019-04-19 | 武汉工程大学 | Cryanide ion fluorescence detection test of a kind of column aromatic hydrocarbons modification and preparation method thereof, detection method |
| CN109655436B (en) * | 2018-12-07 | 2021-03-30 | 武汉工程大学 | Column aromatic modified cyanide ion fluorescence detection test paper, and preparation method and detection method thereof |
| USD1008661S1 (en) * | 2022-01-28 | 2023-12-26 | No Sacrifice Bags, Inc. | Purse base shaper |
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