JPS578447A - Method and apparatus for analysis of guanidine derivative - Google Patents
Method and apparatus for analysis of guanidine derivativeInfo
- Publication number
- JPS578447A JPS578447A JP8413680A JP8413680A JPS578447A JP S578447 A JPS578447 A JP S578447A JP 8413680 A JP8413680 A JP 8413680A JP 8413680 A JP8413680 A JP 8413680A JP S578447 A JPS578447 A JP S578447A
- Authority
- JP
- Japan
- Prior art keywords
- fluorescence
- reaction
- solution
- reagent
- sent
- 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.)
- Granted
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/84—Preparation of the fraction to be distributed
Abstract
PURPOSE:To make a determination of guanidine derivates in a short time with a good sensibility, by adding an aqueous solution of ninhydrin after adding the aqueous sodium hydroxide solution at first as a fluorescent reagent. CONSTITUTION:A sample containing a very small amount of guanidine derivatives is injected into a column 4 of high speed liquid chromatography connected with a stepwise gradient apparatus 1 and a feeding pump 2 for high speed liquid chromatography from a sample introducing opening 3. An aqueous sodium hydroxide solution 5 and an aqueous solution of nihydrin 7 are consecutively added to said eluate by using feeding pumps of reagent 6, 8 and the reaction is performed. Said mixed solution is sent to a reaction coil 10 of fluorescence reaction part 9 and the fluorescence reaction is performed. Next, the reacted solution is sent to a fluorescence photometer 11 and an intensity of fluorescence is measured and then, guanidine derivatives are determined. Hereby, conventional amino acid does not emit fluorescence and also, the analysis is not interrupted by any deposited matter because the reagent is soluble in water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8413680A JPS578447A (en) | 1980-06-20 | 1980-06-20 | Method and apparatus for analysis of guanidine derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8413680A JPS578447A (en) | 1980-06-20 | 1980-06-20 | Method and apparatus for analysis of guanidine derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS578447A true JPS578447A (en) | 1982-01-16 |
JPH0210380B2 JPH0210380B2 (en) | 1990-03-07 |
Family
ID=13822073
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8413680A Granted JPS578447A (en) | 1980-06-20 | 1980-06-20 | Method and apparatus for analysis of guanidine derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS578447A (en) |
-
1980
- 1980-06-20 JP JP8413680A patent/JPS578447A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0210380B2 (en) | 1990-03-07 |
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