WO1994023061A1 - Method of determining sodium ion - Google Patents
Method of determining sodium ion Download PDFInfo
- Publication number
- WO1994023061A1 WO1994023061A1 PCT/JP1994/000572 JP9400572W WO9423061A1 WO 1994023061 A1 WO1994023061 A1 WO 1994023061A1 JP 9400572 W JP9400572 W JP 9400572W WO 9423061 A1 WO9423061 A1 WO 9423061A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ions
- sodium
- galactosidase
- ion
- sodium ion
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/54—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving glucose or galactose
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/34—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase
-
- 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
- G01N33/84—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving inorganic compounds or pH
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
- G01N2333/914—Hydrolases (3)
- G01N2333/924—Hydrolases (3) acting on glycosyl compounds (3.2)
Definitions
- the present invention relates to a method for quantifying sodium ions using / 3-galactosidase in the presence of a cation that competes with sodium ions.
- the method using a Nitrile-type crown ether such as Crypt Fix 22 1 has a low dissociation rate of the critate, takes a long time to perform a preliminary reaction until measurement, and lacks the simplicity of the measurement operation.
- Kryptofix 222 and) 3-galactosidase the stability of 0-galactosidase is impaired by Cryptofix 221 and the quantification of low concentrations of sodium ion is lacking.
- there are problems such as that the pH of the reaction is limited to the alkaline side, and better methods are being developed. Disclosure of the invention
- the present invention provides a method for quantifying sodium ions in a sample using 13-galactosidase in an aqueous medium, characterized in that a) 3-galactosidase reaction is performed in the presence of a cation that competes with sodium ions. Is what you do.
- the aqueous medium refers to a liquid containing water, such as a buffer or a physiological saline, and the buffer is a tris (hydroxymethyl) aminoaminomonohydrochloride buffer.
- tris-hydrochloric acid buffer phosphate buffer, acetate buffer, succinate buffer, oxalate buffer, phthalate buffer, borate buffer, glycine buffer, valpital buffer Or a good (GOOD) buffer solution.
- Any sample containing sodium ions may be used as long as it is a sample that is miscible with an aqueous medium.
- Whole blood, cells, etc., samples in living organisms that are difficult to measure by atomic absorption spectrometry, flame photometry, etc. Can also be measured.
- Examples of cations that compete with sodium ions include lithium ions, potassium ions, rubidium ions, and cesium ions, and the like. These ions may be used alone or in combination of two or more. Suitable concentrations of cations competing for sodium ions for this reaction are 13 OmM to 0.5 M for lithium ions, 20 to 20 OmM for potassium ions, and 120 to 5 OmM for potassium ions. 0 O mM, 20 to 50 O mM for rubidium ions, and 50 to 50 O mM for ammonium ions.
- Sources of lithium ions or lithium ions include chlorides, nitrates, sulfates, and borohydrides of these ions. Other sources of rubidium ions or cesium ions include chloride salts of these ions. Sources of ammonium ions include ammonium sulfate, ammonium chloride, and the like.
- the 3-galactosidase in the present invention may be any enzyme belonging to the enzyme number [EC. 3.2.1.23], and may be J3-galactosidase collected from animals, microorganisms or plants, or modified by genetic engineering. Includes manufactured enzymes.
- the substrate for 13-galactosidase may be either a synthetic product or a natural product, for example, / 3-D-galactoside, aryl 13-D-galactoside, alkyl / 3-D-galactoside, 3,6-dihi (Droxyfluoran) 3-D-galactoside, nitrophenyl / 3-D- villanoglycoside, nitrophenyl / 3-D-galactoside, lactinol, lactose, 4-methylumbelliferyl) 3-D-gala And Kuttoside.
- magnesium sulfate, magnesium chloride, magnesium nitrate or the like is used as an activator of 3-galactosidase.
- the change in the base mass of J3-galactosidase which decreases in the reaction solution can be determined by measuring the decrease in the aforementioned substrate such as nitrophenyl / 3-D-galactoside by absorbance or the like.
- the amount of the ⁇ -galactosidase reaction product produced in the reaction solution is determined by, for example, colorimetrically determining the amount of galactose, aglycone, 3,6-dihydroxyfluoran, nitrophenol, etc. produced by the -galactosidase reaction from the aforementioned substrate. It can be determined by a method such as a spectrophotometric method, a spectrophotometric method, a fluorometric method, a redox measuring method, a high-performance liquid chromatography method and the like. Further, the enzyme reaction may be conjugated to galactose dehydrogenase or the like to determine the amount of reduced coenzyme produced.
- a surfactant such as Triton X-100 can be added as necessary to prevent the occurrence of turbidity in the reaction solution.
- a surfactant such as Triton X-100
- the effect of albumin in the sample can be reduced and the serum albumin
- BSA human serum albumin
- HSA human serum albumin
- proteins such as human immunoglobulin and ovalbumin, dimethyl sulfonate, etc.
- a solubilizing agent such as foxide and an antioxidant such as dithiothreitol can be added.
- the method of the present invention includes ethylene bis (oxyethylene nitrite) tetraacetic acid (EGTA), ethylene diamine tetraethylene, etc. in order to eliminate interference of divalent to trivalent metals and enhance the effect of cations that compete with sodium ions.
- EGTA ethylene bis (oxyethylene nitrite) tetraacetic acid
- EDTA acetic acid
- binders of sodium ions such as monocyclic crown ethers can be added to improve the accuracy of the measurement and enhance the effect of cations competing with sodium ions.
- Monocyclic crown ethers include 18-crown-16, N- [2- (methoxy) ethyl] monoaza-15-crown-15 or N- [2- (2-methoxyethoxy) Monoethyl] Monother 1 5—Crown 5 etc.
- the concentration of the monocyclic crown ether is usually 5 to 100 mM, preferably 10 to 50 mM. By adding these chelating ligands and binders, it is possible to reduce the suitable concentration of the ion that competes with sodium ions.
- the cation that competes with the sodium ion used in the present invention reduces the activity of the sodium ion as necessary and sufficiently. Therefore, in the quantification method of the present invention, the preliminary reaction until the measurement does not take a long time, and the reaction with / 3-galactosidase is not performed. No need for incubation. Therefore, the enzyme can be measured in a stable state without impairing the stability of / 3-galactosidase. Further, in the present invention, the pH application range of the reaction solution is wider than the reaction using Krybtofix. Therefore, according to the present invention, a novel quantitative method of sodium ion in a living body with good quantification, which is quick and simple is provided. BRIEF DESCRIPTION OF THE FIGURES
- FIG. 1 is a diagram showing a calibration curve of sodium ions by lithium ions of 22 O mM or more.
- the (1-1) and (I) markers represent calibration curves of sodium ions when the concentrations of lithium ions are 22 OmM and 26 OmM, respectively.
- FIG. 2 is a diagram showing a calibration curve of sodium ions using lithium ions of 13 O mM or less.
- the (- ⁇ -) and (-San-ichi) marks are The calibration curve of sodium ion is shown when the concentration of sodium ion is 9 OmM and 13 OmM.
- FIG. 3 is a diagram showing a calibration curve of sodium ions by potassium ions.
- the (-1-1) mark and the (I-San-ichi) mark indicate o-nitrofuunil (sodium ion when the concentration of 31-D-viranoglycoside is 1.5 mM and 3 mM, respectively). Represents a calibration curve.
- FIG. 4 is a diagram showing a calibration curve of sodium ions by ammonium ions.
- (1-1) and (1) are the calibration curves of sodium ion when the concentration of ammonium ion is 5 OmM and 10 OmM, respectively.
- FIG. 5 is a diagram showing a calibration curve of sodium ions by cesium ions.
- the (- ⁇ -1) and (1-1) marks represent the calibration curves of sodium ions when the cesium ion concentration is 14 OmM and 27 OmM, respectively.
- Dilute sodium salt (manufactured by Wako Pure Chemical Industries) was diluted with distilled water to prepare a standard solution for a sodium ion calibration curve of 10 to 18 OmM in the reaction solution.
- the sodium ions were quantified in the same manner as in Example 1 except that the concentration of lithium chloride (Wako Pure Chemical) was changed to 90 or 13 OmM.
- the obtained calibration curve is shown in FIG. Lithium chloride showed linearity at a concentration of 13 OmM.
- a sodium ion was prepared in the same manner as in Example 1 except that 5 OmM lithium chloride was used instead of lithium chloride, and that the concentration of o-diethyl phenyl 3-D-viranoglycoside was 1.5 or 3 mM. Was quantified. The obtained calibration curve is shown in FIG.
- Sodium ions were quantified in the same manner as in Example 1, except that 50 or 10 OmM ammonium chloride was used instead of lithium chloride.
- the calibration curve obtained is shown in FIG.
- 150 mM sodium ion standard was used in the same manner as in Example 1 except that 150 mM potassium chloride was used instead of lithium chloride, and o-nitrophenyl) 3-D-viranoglycoside was used at a concentration of 2 mM.
- the coefficient of variation (hereinafter referred to as “CV”) of the quantitative value was 1.5 to 2.8%.
- the CV of the sodium ion quantitative value was measured in the same manner as in Example 7, except that the concentration of potassium chloride was 75 mM, and 19 mM 18-crown 6 was added together with potassium salt. It was 88%.
- the concentration of lithium chloride was set to 150 mM, and 5 OmM of N- [2- (methoxy) ethyl] monoaza 15-crown-15 was added together with lithium chloride, and the concentration of o-ditrophenyl / 3-D-viranoglycoside was increased to 2 mM.
- the present invention quantitative and reproducibility is good, is how power s offers can be measured easily and quickly sodium ions.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Wood Science & Technology (AREA)
- Immunology (AREA)
- General Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Biotechnology (AREA)
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Urology & Nephrology (AREA)
- Biomedical Technology (AREA)
- Inorganic Chemistry (AREA)
- Cell Biology (AREA)
- Emergency Medicine (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
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- Pathology (AREA)
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Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP94912059A EP0702088A4 (en) | 1993-04-07 | 1994-04-06 | METHOD FOR DETERMINING SODRIUMIONS |
US08/530,336 US5700652A (en) | 1993-04-07 | 1994-04-06 | Quantitative determination method for sodium ions |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8081793 | 1993-04-07 | ||
JP5/80817 | 1993-04-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1994023061A1 true WO1994023061A1 (en) | 1994-10-13 |
Family
ID=13729009
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1994/000572 WO1994023061A1 (en) | 1993-04-07 | 1994-04-06 | Method of determining sodium ion |
Country Status (3)
Country | Link |
---|---|
US (1) | US5700652A (ja) |
EP (1) | EP0702088A4 (ja) |
WO (1) | WO1994023061A1 (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060121548A1 (en) * | 2004-11-09 | 2006-06-08 | Remote Clinical Solutions, Inc. | Systems and methods for measuring sodium concentration in saliva |
US20070015287A1 (en) * | 2005-07-15 | 2007-01-18 | Remote Clinical Solutions, Inc. | Methods and devices for measuring analyte concentration in a nonblood body fluid sample |
KR102080417B1 (ko) * | 2015-07-06 | 2020-02-21 | 후지필름 가부시키가이샤 | 혈액 검사 키트 및 혈액 분석 방법 |
JP6495768B2 (ja) * | 2015-07-06 | 2019-04-03 | 富士フイルム株式会社 | 血液分析方法及び血液検査キット |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01503596A (ja) * | 1987-04-10 | 1989-12-07 | ザ フリンダーズ ユニヴアーシテイ オブ サウス オーストラリア | 体液中のカリウムイオンを測定する方法及びそのための組成物 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5384247A (en) * | 1987-04-10 | 1995-01-24 | Boehringer Mannheim, Gmbh | Determination of sodium ions in fluids |
US5196306A (en) * | 1989-03-29 | 1993-03-23 | E. I. Du Pont De Nemours And Company | Method for the detection or quantitation of an analyte using an analyte dependent enzyme activation system |
-
1994
- 1994-04-06 WO PCT/JP1994/000572 patent/WO1994023061A1/ja not_active Application Discontinuation
- 1994-04-06 US US08/530,336 patent/US5700652A/en not_active Expired - Fee Related
- 1994-04-06 EP EP94912059A patent/EP0702088A4/en not_active Ceased
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01503596A (ja) * | 1987-04-10 | 1989-12-07 | ザ フリンダーズ ユニヴアーシテイ オブ サウス オーストラリア | 体液中のカリウムイオンを測定する方法及びそのための組成物 |
Non-Patent Citations (1)
Title |
---|
See also references of EP0702088A4 * |
Also Published As
Publication number | Publication date |
---|---|
EP0702088A1 (en) | 1996-03-20 |
US5700652A (en) | 1997-12-23 |
EP0702088A4 (en) | 1998-04-29 |
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