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Determination method of nucleoside content in Poria cocos

A detection method and nucleoside technology, which can be used in measurement devices, instruments, scientific instruments, etc., can solve the problems of low content, and achieve the effects of high detection efficiency, reduced errors, and strong practicability.

Active Publication Date: 2021-11-26
SHANGHAI INST OF PHARMA IND CO LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Zhou Jun etc. reported (Tianjin Pharmacy, 2015, 27 (6), 12-17) HPLC method to measure the content of pachymic acid in Poria formula granules, but the content of these detection items is extremely low, and the content of single components is mostly insufficient One, this may also be the main reason why the "Chinese Pharmacopoeia" as of the 2015 edition has not listed it as the content determination item of Poria cocos medicinal materials and decoction pieces
[0005] At present, in the prior art, the quality control item for Poria cocos has not yet reached the content standard that can be used as the quality control item of medicine in the Pharmacopoeia. Therefore, a kind of suitable quality control item is urgently needed to carry out effective quality control for Poria cocos

Method used

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  • Determination method of nucleoside content in Poria cocos
  • Determination method of nucleoside content in Poria cocos
  • Determination method of nucleoside content in Poria cocos

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0076] 1. The conditions of the HPLC detection adopted in the present embodiment are as follows: Zorbax SB-Aq chromatographic column (5 μm, 4.6 × 250mm, Agilent), detection wavelength: 260nm, column temperature 30°C, flow rate: 0.8mL / min, Injection volume: 10 μL, the mobile phase is acetonitrile and water, and the gradient elution conditions are shown in Table 2 below:

[0077] Table 2 gradient elution conditions

[0078] time / min water / % Acetonitrile / % 0~12 100 0 12~20 100→98 0→2 20~45 98→80 2→20 45~46 80→100 20→0 46~60 100 0

[0079] The meaning of percent sign in the table is volume percent.

[0080] 2. Preparation of internal standard solution

[0081] Accurately weigh geniposide, place it in a 10mL volumetric flask, add methanol to dissolve to a constant volume, and prepare a 0.6mg / mL internal standard solution.

[0082] 3. Preparation of mixed reference solution containing internal standard

[0083] Accurately measure th...

Embodiment 2

[0125] The conditions for the determination of liquid chromatography adopted in this comparative example are as follows: Zorbax SB-Aq chromatographic column (5 μm, 4.6 × 250mm, Agilent), detection wavelength 260nm, column temperature 30 ℃, flow rate 0.5mL / min, injection volume: 10 μL, the mobile phase is acetonitrile and water, the gradient elution conditions of this comparative example are shown in the following table 9:

[0126] Table 9 gradient elution conditions

[0127] time / min Acetonitrile / % water / % 0~5 0→5 100→95 5~10 5 95 10~20 5→20 95→80 20~25 20 80 25~26 20→0 80→100 26~40 0 100

[0128] The meaning of percent sign in the table is volume percent.

[0129] Prepare the Poria cocos need testing solution that does not contain internal standard according to the method of embodiment 1, detect by the gradient elution condition of table 9, gained chromatogram is as follows Figure 4 shown. It can be seen from the figure...

Embodiment 3

[0131] The conditions for the determination of the liquid chromatography method used in this comparative example are as follows: Zorbax SB-Aq chromatographic column (5 μ m, 4.6 × 250 mm, Agilent), detection wavelength: 260 nm, column temperature 30 ° C, flow rate: 0.5 mL / min, sample injection Volume: 10 μL, mobile phase: acetonitrile and 0.05% formic acid / water solution (V / V), the gradient elution conditions of this comparative example are shown in Table 9 below:

[0132] Table 10 gradient elution conditions

[0133] time / min Acetonitrile / % 0.05% formic acid / water 0~12 0 100 12~17 0→2 100→98 17~27 2 98 27~45 2→20 98→80

[0134] The meaning of percent sign in the table is volume percent.

[0135] Prepare the Poria cocos need testing solution that does not contain internal standard according to the method of embodiment 1, detect by the gradient elution condition of table 10, gained chromatogram is as follows image 3 shown. It can be s...

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Abstract

The invention discloses a method for detecting nucleoside content in poria cocos, which comprises the following steps: using geniposide as an internal standard to detect the content of nucleoside in the poria cocos test solution by high-performance liquid chromatography. The content of each nucleoside measured by the detection method of uridine, guanosine and adenosine in Poria cocos is relatively high, which can effectively control the quality of Poria cocos standard decoction and Poria cocos formula granules, and adopts the internal standard method The content of each nucleoside in the Poria cocos test solution is detected by high performance liquid chromatography, and the external standard point method is used to calculate the content of each nucleoside in the Poria cocos test solution. The error of measurement is small and the operation is simple , stability, good reproducibility, high detection efficiency, and strong practicability.

Description

technical field [0001] The invention relates to a method for detecting nucleoside content in poria cocos. Background technique [0002] Poria cocos (Schw.) Wolf is a commonly used traditional Chinese medicine with a long history of clinical application. It is the dry sclerotium of Poria cocos, a fungus of Polyporaceae. It is sweet, light, and flat in nature. [0003] Traditional Chinese medicine formula granules are made by extracting, concentrating, drying, and granulating single-flavored Chinese medicine decoction pieces. Since the formula granules have lost the external morphological characteristics of traditional Chinese medicine decoction pieces, their quality control and standard formulation are particularly important and critical. The corresponding quality standards established are to effectively and objectively reflect the internal quality and characteristics of different medicinal materials to ensure clinical drug use. Reliable and dose-effective. [0004] At pre...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N30/02G01N30/06
CPCG01N30/02G01N30/06G01N2030/045G01N2030/047
Inventor 华茉莉徐云辉刘洁张倩倩朱敏航周靖
Owner SHANGHAI INST OF PHARMA IND CO LTD