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Houkangsan quality control method

A quality control method and technology of Hokang powder, applied in the field of quality control of Chinese patent medicines, can solve the problems of difficulty in controlling the sample size, limited detection components, poor separation effect, etc., so as to improve specificity and quality stability, and ensure safety. and effectiveness

Active Publication Date: 2008-11-19
GUANGZHOU BAIYUNSHAN QIXING PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Wherein experiment (3) specificity is not strong, implementation (4) thin-layer chromatography exists the shortcoming that point sample volume is difficult to grasp and reach better separation effect; Wherein, when point sample volume is large, the separation effect of menthol, borneol is poor , when the sample amount is small, the spots of indigo and indirubin are too weak, and the color development is not strong
In addition, thin-layer chromatography only detects Qingdai, borneol, and menthol, and the detection components are limited, which is not enough to effectively identify this product, and there is no method for determining the content of active ingredients, which cannot effectively control product quality

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0030] The present invention will be further described below in conjunction with embodiment.

[0031] Get the Houkang San with batch number 5018 produced by the applicant.

[0032][Identification] (1) Take this product and observe under a microscope: the diameter of calcium oxalate cluster crystals is 20-68 μm, with sharp edges and corners (ginseng). Starch granules are spherical, semicircular or helmet-shaped, with a diameter of 27-48 μm, navel point-like, short-slit-like or herringbone-like, and layer patterns are faintly visible (trichosporin). The parenchyma cells around the fiber bundles contain square crystals of calcium oxalate, forming crystal fibers (licorice).

[0033] (2) Take 0.5g of this product, add 5ml of water, extract by shaking, filter, take 2ml of the filtrate, add barium chloride test solution, and a white precipitate will form, which will not dissolve in hydrochloric acid or nitric acid.

[0034] (3) Take 1g of this product, add 10ml of ethyl acetate, ul...

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PUM

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Abstract

The invention provides a method for controlling the quality of a Chinese traditional throat medicine. The method comprises the steps: (1) discriminating ginseng, radix trichosanthis and liquorice contained in the Chinese traditional throat medicine by the microscope discrimination method; (2) detecting vitriol in natrii sulfas exsiccatus by the barium chloride reagent precipitation method; (3) detecting natural indigo in the Chinese traditional throat medicine by the thin-layer chromatography, and comparing the natural indigo with indigotin and indirubin; (4) detecting borneol and menthol by the thin-layer chromatography; (5) detecting ginseng contained in the Chinese traditional throat medicine by the thin-layer chromatography, and comparing the Chinese traditional throat medicine with ginseng, ginseng saponin Rb1, ginsenoside Re and ginsenoside Rg1; (6) detecting liquorice contained in the Chinese traditional throat medicine by the thin-layer chromatography; and (7) detecting the content of andrographolide and dehydrolyzed andrographolide contained in the Chinese traditional throat medicine. The method used for controlling the quality of the Chinese traditional medicine overcomes the defects of the prior discrimination method that the specificity is not enough; the thin-layer chromatography is used for detecting natural indigo, borneol and menthol simultaneously, the sampling amount is difficult to grasp, and excellent separating effect is difficult to reach, the thin-layer chromatography can just detect limited ingredients, i.e. natural indigo, borneol and menthol, thus failing to effectively discriminate the Chinese traditional throat medicine; the prior discrimination method fails to measure the content of effective ingredients, and can not effectively control the defects of product quality. The method improves the specialty and the quality stability, and ensures security and effective use of the medicine by users.

Description

technical field [0001] The invention relates to a quality control method of Chinese patent medicines, in particular to a quality control method of Houkang Powder. Background technique [0002] Houkang San is a Chinese patent medicine for clearing heat, detoxifying, reducing inflammation and relieving pain. It has been used in my country for many years and is clinically used for various throat diseases, such as acute and chronic pharyngitis, laryngitis, tonsillitis, oral ulcers, etc. Houkang powder is prepared from borneol, nacre powder, ginseng, borax (calcined), xuanming powder, menthol, trichosanthes powder, Qingdai, Andrographis paniculata leaves, and licorice according to the conventional process of Chinese patent medicine powder. This standard is recorded in the Ministry of Health of the People's Republic of China Drug Standards Chinese Medicine Prescriptions Volume 5, Standard No. WS 3 -B-1040-91. The identification methods in this standard include: (1) microscopic i...

Claims

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Application Information

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IPC IPC(8): A61K36/534A61K9/14G01N30/90G01N30/02A61P11/04A61P1/02A61K31/045A61K35/56A61K33/22A61K33/04A61K35/618
Inventor 黄夏敏冯倩玲梁祈辛碧霞伍建芬蒋文庆
Owner GUANGZHOU BAIYUNSHAN QIXING PHARMA
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