CN103830226A - New medicinal application of silymarin - Google Patents

New medicinal application of silymarin Download PDF

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Publication number
CN103830226A
CN103830226A CN201210490269.3A CN201210490269A CN103830226A CN 103830226 A CN103830226 A CN 103830226A CN 201210490269 A CN201210490269 A CN 201210490269A CN 103830226 A CN103830226 A CN 103830226A
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China
Prior art keywords
silymarin
endotoxin
injection
group
application
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Pending
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CN201210490269.3A
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Chinese (zh)
Inventor
毕玉轩
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Qingdao Baicaohui Institute of Chinese Herbal Medicine
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Qingdao Baicaohui Institute of Chinese Herbal Medicine
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Priority to CN201210490269.3A priority Critical patent/CN103830226A/en
Publication of CN103830226A publication Critical patent/CN103830226A/en
Pending legal-status Critical Current

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Abstract

The invention relates to an application of silymarin in treating injury caused by bacterial infection, and particularly relates to an application in treating the endotoxemia and endotoxin shock resulting from the injury caused by bacterial infection.

Description

The new medical use of silymarin
Summary
The present invention relates to the application of silymarin in damage due to preparation treatment antibacterial infects, the application in endotoxemia and endotoxin shock that due to treatment antibacterial infects, damage causes particularly.
Technical field
The present invention relates to silymarin and infect the application in endotoxemia and the endotoxin shock causing on treatment antibacterial.
Background technology
The clinical case fatality rate that antibacterial infects the endotoxemia that causes and shock thereof is very high, is a great problem in anti-infective therapy.Endotoxin (Endotoxin) is a kind of constituent of bacteria cell wall, its chemical nature is lipopolysaccharide (Lipopolysaccharide, LPS), when antibacterial infects, antibacterial or lipopolysaccharide (Lipopolysaccharide, LPS) are that endotoxin (Endotoxin) enters blood circulation, activate inflammation cell and discharge inflammatory mediator, the reaction that causes inflammation, can cause multiple organ dysfunction syndrome when serious.Therefore study effective anti-endotoxin medicine highly significant.
Silymarin is from Herba Silybi mariani, to extract the active component separating, and it has free radical resisting, stabilizing cell membrane and anti-liver injury effect bibliographical information.We study and find that silymarin can obviously reduce the dead mouse being caused by endotoxin; find that silymarin has obvious rising effect to the Blood pressure drop of the Shock in Rats being caused by endotoxin, the damage that endotoxemia causes has significant protective effect simultaneously.Based on this, the inventor provides silymarin to infect the application in the medicine of the endotoxemia that causes and shock on preparation treatment antibacterial.
Summary of the invention
The invention provides the application of silymarin in endotoxemia and endotoxin shock that due to treatment antibacterial infects, damage causes.
The invention provides taking silymarin as active component be used for the treatment of antibacterial infect due to the endotoxemia that causes of damage and the pharmaceutical composition of shock.This pharmaceutical composition can pass through oral, injection administration.Can there is with the form of tablet, pill, granule, capsule, suspension, solution, syrup, injection the preferred freeze-dried powder of injection preparation, injection vein emulsion.Various pharmaceutical dosage form provided by the present invention all can be prepared from pharmacy conventional method.
Silymarin of the present invention is when for above-mentioned arbitrary purposes, and its using dosage scope is 100-3000mg.
The inventor has confirmed the application of silymarin in the medicine of endotoxemia that due to treatment antibacterial infects, damage causes and shock by following test, but effect is not limited to this.
detailed description of the invention:
Preparation example 1: preparation injection silymarin freeze-dried powder
Take 100g silymarin, add water for injection 1000ml, adjusting pH is 8.5, adds 85 DEG C of insulations of 0.1% needle-use activated carbon 30 minutes, G 3sintered glass funnel filters, the filtering with microporous membrane of 0.22um; Filtrate is sub-packed in 10ml cillin bottle, and every loading amount 2ml, makes freeze-dried powder through freeze dryer lyophilizing.
Preparation example 2: preparation injection silymarin freeze-dried powder
Take 100g silymarin, add water for injection 1000ml, adjusting pH is 8.5, adds 85 DEG C of insulations of 0.1% needle-use activated carbon 30 minutes, G 3sintered glass funnel filters, the filtering with microporous membrane of 0.22um; Filtrate is sub-packed in 10ml cillin bottle, and every loading amount 2ml, makes freeze-dried powder through freeze dryer lyophilizing.
Preparation example 3: preparation injection silymarin Emulsion
Silymarin 100mg
Refined soybean oil 10g
Refining soybean phospholipid 2.0g
Poloxamer 1.0g
Glycerol 2.5g
Cholesterol 0.5g
Water for injection Add to 100ml
Silymarin, fabaceous lecithin, cholesterol, with joining after dissolve with ethanol in refined soybean oil, are mixed to clear and brightly, and by rotary evaporation or pass into vaporized nitrogen and remove alcohol, obtain the soybean oil solution containing silibinin 10mg/ml and 50mg/ml cholesterol.
Poloxamer, glycerol are dispersed in water for injection, and under high-speed stirred condition, the phospholipid that slowly dropping contains silymarin, the oil solution of cholesterol, in dispersion, are made thick Emulsion.By obtained thick Emulsion under the condition of pressure 100Mpa, by the further emulsifying of dispersing emulsification machine, after emulsifying finishes in 115 DEG C, 30min sterilizing, subpackage and get final product.
Preparation example 6: prepare silymarin tablet
100g silymarin is crossed to 100 orders (lower same) sieve, add starch 100g to mix, sieve, obtain mixed powder, 75% ethanol water 120ml makes binding agent, make suitable soft material, 18 mesh sieves are granulated, 60 DEG C of oven dryings 2 hours, 16 order nylon mesh granulate, add magnesium stearate 8g, mix, oval special-shaped stamping is made 1000, the heavily about 200mg/ sheet of sheet.
the impact test that experimental example 1 silymarin is lethal on mice endotoxin
1 experiment material
Endotoxin: microorganism teaching and research room of Shanghai The 2nd Army Medical College;
Secondary Kunming kind white mice, body weight 19-21g.
Dexamethasone sodium phosphate injection (Pharmaceutical Lianshui, Tianjin company limited, specification: 5mg)
2 experimental techniques and result
Mice is divided into 8 groups at random: NS group, Dexamethasone group, intravenous injection silymarin 400mg/kg group, 100mg/kg group, 50mg/kg group, 20mg/kg group, 10mg/kg group, gastric infusion silymarin (600mg/kg) group, every group 20, male and female half and half, every mouse mainline endotoxin 20mg/kg, respectively organize immediately administration, NS group gives the NS of same volume, and mice occurs dead after 8 hours, stop to 48 hours dead mouses, respectively organize and between mortality rate group, carry out X 2inspection, carries out statistical procedures.
Table 1 result of the test show intravenous injection silymarin 20mg/kg, gastric infusion silymarin 600mg/kg can obviously reduce by endotoxin induced mice mortality rate (with NS group relatively, p<0.05), intravenous injection silymarin 50mg/kg, 100mg/kg, 400mg/kg, can significantly reduce by endotoxin induced mice mortality rate (with NS group relatively, p<0.01).
The impact (n=20) that table 1 silymarin is lethal on mice endotoxin
Figure 780773DEST_PATH_IMAGE002
Compare with NS group, : p<0.05; △ △: p<0.01.

Claims (2)

1. the application of silymarin in damage due to preparation treatment antibacterial infects.
2. the application of silymarin in endotoxemia and endotoxin shock that due to treatment antibacterial infects, damage causes.
CN201210490269.3A 2012-11-27 2012-11-27 New medicinal application of silymarin Pending CN103830226A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210490269.3A CN103830226A (en) 2012-11-27 2012-11-27 New medicinal application of silymarin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210490269.3A CN103830226A (en) 2012-11-27 2012-11-27 New medicinal application of silymarin

Publications (1)

Publication Number Publication Date
CN103830226A true CN103830226A (en) 2014-06-04

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210490269.3A Pending CN103830226A (en) 2012-11-27 2012-11-27 New medicinal application of silymarin

Country Status (1)

Country Link
CN (1) CN103830226A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016065609A1 (en) * 2014-10-31 2016-05-06 Kimberly-Clark Worldwide, Inc. Anti-adherent botanical compositions
US9969885B2 (en) 2014-07-31 2018-05-15 Kimberly-Clark Worldwide, Inc. Anti-adherent composition
US10028899B2 (en) 2014-07-31 2018-07-24 Kimberly-Clark Worldwide, Inc. Anti-adherent alcohol-based composition
US10238107B2 (en) 2014-07-31 2019-03-26 Kimberly-Clark Worldwide, Inc. Anti-adherent composition
US11168287B2 (en) 2016-05-26 2021-11-09 Kimberly-Clark Worldwide, Inc. Anti-adherent compositions and methods of inhibiting the adherence of microbes to a surface
US11737458B2 (en) 2015-04-01 2023-08-29 Kimberly-Clark Worldwide, Inc. Fibrous substrate for capture of gram negative bacteria

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9969885B2 (en) 2014-07-31 2018-05-15 Kimberly-Clark Worldwide, Inc. Anti-adherent composition
US10028899B2 (en) 2014-07-31 2018-07-24 Kimberly-Clark Worldwide, Inc. Anti-adherent alcohol-based composition
US10238107B2 (en) 2014-07-31 2019-03-26 Kimberly-Clark Worldwide, Inc. Anti-adherent composition
US10292916B2 (en) 2014-07-31 2019-05-21 Kimberly-Clark Worldwide, Inc. Anti-adherent alcohol-based composition
WO2016065609A1 (en) * 2014-10-31 2016-05-06 Kimberly-Clark Worldwide, Inc. Anti-adherent botanical compositions
GB2547153A (en) * 2014-10-31 2017-08-09 Kimberly Clark Co Anti-adherent botanical compositions
GB2547153B (en) * 2014-10-31 2020-08-05 Kimberly Clark Co Anti-adherent botanical compositions
US11737458B2 (en) 2015-04-01 2023-08-29 Kimberly-Clark Worldwide, Inc. Fibrous substrate for capture of gram negative bacteria
US11168287B2 (en) 2016-05-26 2021-11-09 Kimberly-Clark Worldwide, Inc. Anti-adherent compositions and methods of inhibiting the adherence of microbes to a surface

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Application publication date: 20140604