Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for detecting related substances in tauroursodeoxycholic acid

A technology of tauroursodeoxycholic acid and related substances, which is applied in the field of high-performance liquid chromatography-evaporative light scattering detection method, can solve the problems of low sensitivity, low accuracy, and interference of components to be measured, and achieve a reduction in chromatographic The effect of peak broadening behavior, good specificity and accuracy, and improved quality controllability

Active Publication Date: 2016-07-20
YAOPHARMA CO LTD
View PDF4 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The ultraviolet absorption of bile acids is weak, or only at the end. When using ultraviolet detectors for detection, low wavelengths should be used for detection, but many organic solvents have absorption in the wavelength range of 190nm~220nm (the cut-off wavelength of common organic solvents: Methanol 205nm, acetonitrile 190nm, isopropanol 205nm), there is interference in the components to be measured, there are problems such as baseline fluctuations, large noise, low sensitivity, poor linearity, and low accuracy
Moreover, the existing literature reports only detect 4 kinds of impurities at most, which cannot control the quality of tauroursodeoxycholic acid well.
Among the 8 known impurities of tauroursodeoxycholic acid, there are components with large difference in polarity and components with close polarity. Multiple chromatographic systems are usually used for detection, especially taurine- 7-ketocholic acid and taurochenodeoxycholic acid, cholic acid and ursodeoxycholic acid, 7-ketocholic acid and chenodeoxycholic acid are close in polarity, it is difficult to effectively separate; tauroursodeoxycholic acid Cholic acid has a large polarity difference with cholic acid and gallstone acid. Under the same chromatographic conditions, the retention time of the components differs greatly. The peak shape of the strong retention component will broaden with the extension of the retention time, which reduces the detection sensitivity. Even some components cannot be eluted, and it is difficult to quickly detect 8 known impurities and other unknown impurities of tauroursodeoxycholic acid at the same time using one chromatographic condition

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for detecting related substances in tauroursodeoxycholic acid
  • Method for detecting related substances in tauroursodeoxycholic acid
  • Method for detecting related substances in tauroursodeoxycholic acid

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0046] The determination of embodiment 1 chromatographic column

[0047] Preliminary mobile phase: mobile phase A-mobile phase B;

[0048] Mobile phase A is 50mmol / L ammonia water (adjust the pH to 3.5 with formic acid), and mobile phase B is acetonitrile;

[0049] The column temperature is 40°C;

[0050] The flow rate is 1.0ml / min;

[0051] Evaporative light scattering detector, drift tube temperature is 115°C, carrier gas flow rate is 2.5L / min;

[0052] The test solution: take an appropriate amount of tauroursodeoxycholic acid raw material, and prepare a solution of about 10 mg / ml to obtain the product;

[0053] System Suitability Solution: Take Tauroursodeoxycholic Acid, Tauro-7-ketocholic Acid, Taurochenodeoxycholic Acid, Taurocholic Acid, Cholic Acid, Ursodeoxycholic Acid, 7-Ketocholic Acid Appropriate amounts of cholelithic acid, chenodeoxycholic acid, and cholelithic acid reference substances were prepared into a mixed solution containing about 250 μg / ml of each com...

Embodiment 2

[0058] The selection of embodiment 2 mobile phases

[0059] Accurately measure tauroursodeoxycholic acid reference solution 1 (2.5 μg / ml) or tauroursodeoxycholic acid reference solution 2 (5.0 μg / ml) and system suitability solution respectively, under different mobile phase conditions Next, inject into the high performance liquid chromatograph and record the chromatogram. Investigate the effects of different types and concentrations of buffer salts and different pH regulators on component separation (the number of system suitability solution peaks) and detection sensitivity. The results are shown in Table 2:

[0060] Table 2 buffer salt selection results

[0061]

[0062] Column: The chromatographic column number is the same as in Table 1.

[0063] The above results show that: using 2.5mmol / L to 50mmol / L ammonium salt buffer and adjusting the pH value to the range of 2.5 to 3.5 with formic acid, acetic acid or trifluoroacetic acid can obtain higher sensitivity and ensure ...

Embodiment 3

[0077] Embodiment 3 Determination of Evaporative Light Scattering Detector Conditions

[0078] Chromatographic conditions:

[0079] Chromatographic column: with the chromatographic column 3 in embodiment 1;

[0080] Mobile phase: the same as buffer salt 6 in Example 2;

[0081] Gradient elution conditions:

[0082]

[0083] Flow rate: 1.0ml / min;

[0084] The injection volume is 10 μl;

[0085] Investigate the influence of evaporative light scattering detector conditions, drift tube temperature in the range of 70-115 °C, and carrier gas flow rate in the range of 2.5-4.0 L / min, take 10 μg / ml tauroursodeoxycholic acid reference solution 10 μl respectively Inject into a liquid chromatograph, record the chromatogram, and investigate the sensitivity of tauroursodeoxycholic acid response under different conditions. Other chromatographic conditions are as above, and the results are shown in Table 7.

[0086] Table 7 Effect of evaporative light scattering detector conditions on...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
separationaaaaaaaaaa
recovery rateaaaaaaaaaa
Login to View More

Abstract

The invention relates to a method for detecting related substance in tauroursodeoxycholic acid, and especially relates to a method using a HPLC-ELSD technology to simultaneously detect eight related substances in tauroursodeoxycholic acid. According to the method, an octyl bonded silica gel chromatographic column and an evaporative light-scattering detector are adopted; and a mobile phase (A) and a mobile phase (B) are mixed to carry out isocratic elution or gradient elution, wherein the mobile phase (A) is an ammonium salt buffer solution with a concentration of 2.5 to 50 mmol / L, and the mobile phase (B) is methanol or acetonitrile. The provided method has the advantages of simpleness, rapidness, accuracy, reliability, and good resolution of chromatographic peaks, and is capable of simultaneously detecting eight related substances in tauroursodeoxycholic acid quantitatively or qualitatively.

Description

technical field [0001] The invention relates to a high-performance liquid chromatography-evaporative light scattering detection method (HPLC-ELSD) for detecting related substances in tauroursodeoxycholic acid, belonging to the technical field of chemical drug analysis. Background technique [0002] The chemical name of tauroursodeoxycholic acid (TUDCA) is 2-[[(3α,5β,7β)-3,7-dihydroxy-24-oxocholan-24-yl]amino]ethane Sulfonic acid is a combined bile acid formed by condensation between the carboxyl group of ursodeoxycholic acid and the amino group of taurine. It has one more taurine group than ursodeoxycholic acid, and its polarity is greatly increased. Cholesterol capacity is also greatly improved. Tauroursodeoxycholic acid can increase the concentration of bile acids in bile, inhibit the formation of cholesterol crystals, and promote the dissolution of cholesterol gallstones, which is of great significance in reducing the recurrence rate of gallstone removal and improving th...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): G01N30/02G01N30/06G01N30/74
Inventor 李睿钟家庆曾加智周莎
Owner YAOPHARMA CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products