CN103134919A - Detection reagent for quantitative detection of 6-methyl-2-thiopyridine-N-acetyl-beta-D-glucosaminide - Google Patents
Detection reagent for quantitative detection of 6-methyl-2-thiopyridine-N-acetyl-beta-D-glucosaminide Download PDFInfo
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- CN103134919A CN103134919A CN 201110381308 CN201110381308A CN103134919A CN 103134919 A CN103134919 A CN 103134919A CN 201110381308 CN201110381308 CN 201110381308 CN 201110381308 A CN201110381308 A CN 201110381308A CN 103134919 A CN103134919 A CN 103134919A
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Abstract
The invention discloses a detection reagent for quantitative detection of 6-methyl-2-thiopyridine-N-acetyl-beta-D-glucosaminide (MPT-NAG). The reagent is characterized by comprising the following components: a citric acid-sodium citrate buffer solution with a pH value of 4.0-5.0 and a citric acid-sodium citrate concentration of 30-500 mmol/L, MgCl2 with a concentration of 2-20 mmol/L, EDTA.2Na with a concentration of 0.5-10 mmol/L, N-acetyl-beta-D-glucosaminidase with a concentration of 5-20 KU/L, polyethylene glycol 6000 with a concentration of 2-10 g/L, ethylene glycol with a concentration of 20-100 ml/L, and sucrose with a concentration of 5-50 g/L, wherein a concentration of a sample requiring detection is 0.005-16.5 g/L. The method has the following characteristics that: the used chemicals are non-toxic and easy to obtain so as to meet requirements of green detection method development, detection sensitivity is high, linearity and precision are good, the result is accurate, operation is convenient and rapid, the method can be applicable for various types of analyzers, and requirements of large scale sample measurements can be met.
Description
Technical field
The invention belongs to the biological chemical reagent detection field, be specifically related to the detection reagent of a kind of quantitative detection 6-methyl-2-sulfo-pyridine-N-acetyl-β-D-glucosaminide (MPT-NAG).
Background technology
6-methyl-2-sulfo-pyridine-N-acetyl-β-D-glucosaminide (MPT-NAG) is the new substrate of the mensuration N-acetyl-β-D-glucosaminidase (NAG) that synthesizes in recent years.Take MPT-NAG as main raw material(s) the liquid-type NAG of exploitation measure reagent has stable, antijamming capability good, can realize the characteristics such as automated analysis, is able to widespread use clinical.The height appreciable impact NAG of MPT-NAG content measures the sensitivity of reagent, is to control NAG to measure one of very important empirical factor of reagent difference between batch.
At present all adopt high performance liquid chromatography (HPLC) method during experimental determination MPT-NAG content, this method needs special-purpose large-scale instrument, needs standard items to do contrast, during check fee and cost high, also need to use toxic solvent methyl alcohol during detection, easily cause environmental pollution.
Therefore, seek a kind of easy and simple to handle, highly sensitive, result method accurately, MPT-NAG is carried out quantitative detection just seem particularly important.
Summary of the invention
The objective of the invention is in order to solve the deficiency of above-mentioned technology, utilize N-acetyl-β-D-glucosaminidase to the catalytic decomposition of MPT-NAG, by assaying reaction absorbance of solution under specific wavelength after a period of time, calculate MPT-NAG concentration in sample to be determined., environmental protection green according to the mensuration reagent that this method builds realize that single stage method directly measures, and measure reagent and are placed in 2-8 ℃ of environment and can stablize and preserved 12 months, just can realize detection with common ultraviolet spectrophotometer.
Measuring principle of the present invention is: the N-acetyl-β-D-glucosaminidase of measuring in reagent produces 6-methyl-2 mercaptopyridine (MPT) and N-acetyl-β-D-Glucosamine with the MPT-NAG catalytic decomposition.There is absorption maximum at MPT 205nm, the 270nm that generates in reaction, 340nm place, by measuring after 37 ℃ of reaction a period of times the absorbance of solution under specific wavelength, calculates the content of MPT-NAG in sample.
The present invention is achieved through the following technical solutions:
The detection method of a kind of quantitative detection 6-methyl-2-sulfo-pyridine-N-acetyl-β-D-glucosaminide (MPT-NAG) is characterized in that comprising the steps:
1) preparation contains MgCl
2, EDTA2Na, N-acetyl-β-D-glucosaminidase, Macrogol 6000, ethylene glycol, sucrose pH4.0-5.0 citric acid-trisodium citrate damping fluid;
2) add the testing sample that contains MPT-NAG, reaction a period of time, the N-acetyl-β-D-glucosaminidase in reagent produces 6-methyl-2 mercaptopyridine (MPT) and N-acetyl-β-D-Glucosamine with the MPT-NAG catalytic decomposition;
3) by measuring the absorbance of solution under specific wavelength, calculate the content of MPT-NAG in testing sample.
Described in step (1), the concentration of pH4.0-5.0 citric acid-trisodium citrate damping fluid is 30-500mmol/L, MgCl
2Concentration is that 2-20mmol/L, EDTA2Na concentration are that 0.5-10mmol/L, N-acetyl-β-D-glucosaminidase concentration are that 5-20KU/L, Macrogol 6000 concentration are that 2-10g/L, glycol concentration are that 20-100ml/L, sucrose concentration are 5-50g/L.
Reaction conditions in step (2) is for to react 5-10min in 37 ℃ of environment.
6-methyl-2 mercaptopyridine (MPT) that reaction generates in step (2) has absorption maximum at 205nm, 270nm, 340nm place respectively, especially 340nm.
In sample, the computing formula of MPT-NAG is: sample liquid MPT-NAG content (mmol/L)=(A
u-A
0) * V
1* 10
3/ (ε * V
2), A wherein
uBe sample hose reaction absorbance, A
0For the deionized water with volume replaces the measured absorbance of sample, V
1Be total reaction volume, V
2Be sample volume, ε is the molar absorptivity value of MPT-NAG under specific wavelength.
The detection reagent that the purpose of this invention is to provide a kind of quantitative detection 6-methyl-2-sulfo-pyridine-N-acetyl-β-D-glucosaminide (MPT-NAG), it is characterized in that: containing citric acid in pH4.0-5.0 citric acid-trisodium citrate damping fluid-trisodium citrate concentration is 30-500mmol/L, MgCl
2Concentration is that 2-20mmol/L, EDTA2Na concentration are that 0.5-10mmol/L, N-acetyl-β-D-glucosaminidase concentration are that 5-20KU/L, Macrogol 6000 concentration are that 2-10g/L, glycol concentration are that 20-100ml/L, sucrose concentration are 5-50g/L, and the concentration of testing sample is 0.005-16.5g/L.
Utilize the enzymatic detection method of quantitative detection 6-methyl of the present invention-2-sulfo-pyridine-N-acetyl-β-D-glucosaminide (MPT-NAG), the scope that can accurately detect the 6-methyl that contains in testing sample-2-sulfo-pyridine-N-acetyl-β-D-glucosaminide (MPT-NAG) is 0.015-50 mmol/L.
Chemicals involved in the present invention all nontoxic, be easy to get, meet the requirement of development green test method.This detection method is compared with high efficiency liquid phase (HPLC) method and be the results are shown in Table 1.
Table 1
| Detection method | HPLC | This law |
| Detection time | 60min | 5~10min |
| Testing cost | 200 | Very low |
| Standard items | Need | Do not need |
| Detecting step | Multistep | One step direct method |
| Manual method/automatic method | Manual method | Manual method or automatic method all can |
| The noxious material that contains | Methyl alcohol | Do not contain noxious material |
The method of the invention is highly sensitive, and is linear, precision is good, and result is accurate, and easy and simple to handlely and can be used for various types of analysers fast, reaches the requirement of extensive mensuration sample.
Embodiment
Below in conjunction with embodiment, further set forth principle of the present invention and its application, but the present invention is not limited to this.
Sample liquid: accurately take 0.1 gram left and right sample, be settled to deionized water the sample liquid that the sample final concentration is 0.005-16.5g/L.
The computing formula of MPT-NAG in sample liquid: sample liquid MPT content (mmol/L)=(A
u-A
0) * V
1* 10
3/ (ε * V
2), A wherein
uBe sample hose reaction absorbance, A
0For the deionized water with volume replaces the measured absorbance of sample, V
1Be total reaction volume, V
2Be sample volume, ε is the molar absorptivity value of MPT-NAG under specific wavelength.
Embodiment 1:
Preparation contains MgCl
2The 500mmol/L pH5.0 citric acid of 20mmol/L, EDTA2Na 10mmol/L, N-acetyl-β-D-glucosaminidase 20KU/L, Macrogol 6000 10g/L, ethylene glycol 100ml/L, sucrose 50g/L-trisodium citrate damping fluid is for measuring reagent, in the time of should measuring reagent for working sample liquid, the instrument that adopts is Hitachi's 7080 automatic clinical chemistry analyzers, the assay method type is end-point method, temperature is 37 ℃, V
SampleBe 3 μ l, V
ReagentBe 300 μ l, mensuration master/commplementary wave length is 340/800nm, and reagent reads absorbance in the mensuration thermotonus after 5 minutes after adding sample.In sample liquid, the computing formula of MPT-NAG is: MPT-NAG content (mmol/L)=(A
u-A
0) * V
1* 10
3/ (10063 * V
2), A wherein
uBe sample hose reaction absorbance, A
0For the deionized water with volume replaces the measured absorbance of sample, V
1Be total reaction volume, V
2Be sample volume, 10063 is MPT-NAG molar absorptivity value under 340nm.Measured simultaneously MPT-NAG content in 25 routine sample liquid with this law and HPLC method.
The value table of comparisons that table 2 is measured MPT-NAG content for measured value and the HPLC method of MPT-NAG content in the sample liquid that contains MPT-NAG of the described method mensuration of the present embodiment.
Table 2
| Sample number | HPLC method measured value (mmol/L) | This law measured value (mmol/L) |
| 1 | 0.023 | 0.025 |
| 2 | 0.117 | 0.114 |
| 3 | 0.507 | 0.503 |
| 4 | 0.752 | 0.748 |
| 5 | 1.132 | 1.119 |
| 6 | 2.254 | 2.261 |
| 7 | 4.985 | 4.971 |
| 8 | 7.588 | 7.541 |
| 9 | 10.023 | 9.991 |
| 10 | 12.250 | 12.188 |
| 11 | 15.381 | 15.298 |
| 12 | 17.571 | 17.520 |
| 13 | 20.652 | 20.587 |
| 14 | 22.235 | 22.145 |
| 15 | 25.034 | 25.039 |
| 16 | 27.560 | 27.833 |
| 17 | 30.001 | 29.692 |
| 18 | 32.612 | 32.454 |
| 19 | 35.420 | 35.503 |
| 20 | 37.451 | 37.338 |
| 21 | 40.012 | 40.223 |
| 22 | 42.527 | 42.588 |
| 23 | 45.321 | 45.228 |
| 24 | 47.255 | 47.553 |
| 25 | 49.703 | 49.111 |
As known from Table 2, the correlation coefficient r of the described method of the present embodiment and HPLC method is 0.9999, and both have shown fabulous correlativity.
Embodiment 2:
Preparation contains MgCl
2The 250mmol/L PH4.5 citric acid of 10mmol/L, EDTA2Na 5mmol/L, N-acetyl-β-D-glucosaminidase 12.5KU/L, Macrogol 6000 6g/L, ethylene glycol 60ml/L, sucrose 25g/L-trisodium citrate damping fluid is for measuring reagent, in the time of should measuring reagent for working sample liquid, the instrument that adopts is Shimadzu UV-2550 ultraviolet-visible pectrophotometer, temperature is 37 ℃, V
SampleBe 30 μ l, V
ReagentBe 3000 μ l, the mensuration wavelength is 270nm, and reagent reads absorbance in the mensuration thermotonus after 7.5 minutes after adding sample.In sample liquid, the computing formula of MPT-NAG is: MPT-NAG content (mmol/L)=(A
u-A
0) * V
1* 10
3/ (9919 * V
2), A wherein
uBe sample hose reaction absorbance, A
0For the deionized water with volume replaces the measured absorbance of sample, V
1Be total reaction volume, V
2Be sample volume, 9919 is MPT-NAG molar absorptivity value under 270nm.
Embodiment 3:
Preparation contains MgCl
2The 30mmol/L pH4.0 citric acid of 2mmol/L, EDTA2Na 0.5mmol/L, N-acetyl-β-D-glucosaminidase 5KU/L, Macrogol 6000 2g/L, ethylene glycol 20ml/L, sucrose 5g/L-trisodium citrate damping fluid is for measuring reagent, in the time of should measuring reagent for working sample liquid, the instrument that adopts is Shimadzu UV-2201 ultraviolet-visible pectrophotometer, temperature is 37 ℃, V
SampleBe 25 μ l, V
ReagentBe 2500 μ l, the mensuration wavelength is 205nm, and reagent reads absorbance in the mensuration thermotonus after 10 minutes after adding sample.In sample liquid, the computing formula of MPT-NAG is: MPT-NAG content (mmol/L)=(A
u-A
0) * V
1* 10
3/ (8329 * V
2), A wherein
uBe sample hose reaction absorbance, A
0For the deionized water with volume replaces the measured absorbance of sample, V
1Be total reaction volume, V
2Be sample volume, 8329 is MPT-NAG molar absorptivity value under 205nm.
Those skilled in the art should understand; the present invention is not restricted to the described embodiments; that describes in above-described embodiment and instructions just illustrates principle of the present invention; under the prerequisite that does not break away from connotation of the present invention and scope; various variations, modification and improvement to invention all should fall in the claimed scope of claims.
Claims (4)
1. a detection reagent that quantitatively detects 6-methyl-2-sulfo-pyridine-N-acetyl-β-D-glucosaminide (MPT-NAG), is characterized in that reagent contains following component: pH4.0-5.0 citric acid-trisodium citrate damping fluid, MgCl
2, EDTA2Na, N-acetyl-β-D-glucosaminidase concentration be, Macrogol 6000, ethylene glycol, sucrose.
2. detection reagent as claimed in claim 1, it is characterized in that: in described pH4.0-5.0 citric acid-trisodium citrate damping fluid, citric acid-trisodium citrate concentration is 30-500mmol/L.
3. detection reagent as claimed in claim 2, is characterized in that: described MgCl
2Concentration is that 2-20mmol/L, EDTA2Na concentration are that 0.5-10mmol/L, N-acetyl-β-D-glucosaminidase concentration are that 5-20KU/L, Macrogol 6000 concentration are that 2-10g/L, glycol concentration are that 20-100ml/L, sucrose concentration are 5-50g/L.
4. detection reagent as claimed in claim 3, it is characterized in that: the concentration of testing sample is 0.005-16.5g/L.
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|---|---|---|---|
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|---|---|---|---|
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103755754A (en) * | 2013-12-20 | 2014-04-30 | 宁波大学 | N-acetyl-3,4,6-triacetyl-beta-D-glucosaminidase compound and hydrolyzate thereof and preparation methods of compound and hydrolyzate |
| CN110849870A (en) * | 2019-11-26 | 2020-02-28 | 吉林省富生医疗器械有限公司 | Detection reagent for N-acetyl- β -D-glucosaminidase |
| CN111826417A (en) * | 2020-08-04 | 2020-10-27 | 武汉生之源生物科技股份有限公司 | N-acetyl-beta-D-glucosaminidase detection kit with good stability, preparation method and application |
-
2011
- 2011-11-26 CN CN 201110381308 patent/CN103134919A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103755754A (en) * | 2013-12-20 | 2014-04-30 | 宁波大学 | N-acetyl-3,4,6-triacetyl-beta-D-glucosaminidase compound and hydrolyzate thereof and preparation methods of compound and hydrolyzate |
| CN110849870A (en) * | 2019-11-26 | 2020-02-28 | 吉林省富生医疗器械有限公司 | Detection reagent for N-acetyl- β -D-glucosaminidase |
| CN111826417A (en) * | 2020-08-04 | 2020-10-27 | 武汉生之源生物科技股份有限公司 | N-acetyl-beta-D-glucosaminidase detection kit with good stability, preparation method and application |
| CN111826417B (en) * | 2020-08-04 | 2023-01-17 | 武汉生之源生物科技股份有限公司 | N-acetyl-beta-D-glucosaminidase detection kit with good stability, preparation method and application |
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Application publication date: 20130605 |