CN105232540A - Drug combination for treating infection after burn - Google Patents

Drug combination for treating infection after burn Download PDF

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Publication number
CN105232540A
CN105232540A CN201510629893.0A CN201510629893A CN105232540A CN 105232540 A CN105232540 A CN 105232540A CN 201510629893 A CN201510629893 A CN 201510629893A CN 105232540 A CN105232540 A CN 105232540A
Authority
CN
China
Prior art keywords
compound
burn
infections
pharmaceutical composition
treatment
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201510629893.0A
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Chinese (zh)
Inventor
王洪燕
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201710122496.3A priority Critical patent/CN106806367A/en
Priority to CN201510629893.0A priority patent/CN105232540A/en
Publication of CN105232540A publication Critical patent/CN105232540A/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Preparation (AREA)

Abstract

The invention relates to a drug combination for treating infection after burn. The drug combination comprises a compound in effective quantity and a pharmaceutically-acceptable carrier, and structure of the compound is shown as follows. The compound has remarkable effect on pathogenic bacteria causing infection after burn, and can be developed into a novel drug combination which is clinically effective.

Description

A kind of pharmaceutical composition for the treatment of infections after burn
Technical field
The present invention relates to field of medicaments, specifically, the present invention relates to a kind of pharmaceutical composition for the treatment of infections after burn.
Background technology
Infections after burn is common clinical frequently-occurring disease, and the cause of disease is many caused by cause pathogeny imcrobe infection, causes the pathogenic microorganism of infection to mainly contain antibacterial, virus and mycoplasma, chlamydia.Find after deliberation, in the secretions at patient infection position, various pathogens detected, find that in the recent period Venice acinetobacter calcoaceticus ATCC31012 is also one of pathogenic bacterium wherein.
Summary of the invention
The object of the present invention is to provide a kind of pharmaceutical composition for the treatment of infections after burn.
In order to realize object of the present invention, the invention provides a kind of compound for the treatment of infections after burn, this compound has having structure:
The present invention also provides a kind of pharmaceutical composition for the treatment of infections after burn, and described pharmaceutical composition includes the compound of effective amount and pharmaceutically acceptable carrier, and described compound has having structure:
Preferably, described pharmaceutically acceptable carrier is diluent, disintegrating agent, binding agent, lubricant, stabilizing agent or corrigent.
Preferably, described diluent is sugar derivatives, starch derivatives or cellulose derivative.
Preferably, described diluent is lactose.
Preferably, described pharmaceutical composition is powder, microgranule, granule, capsule or tablet.
The present invention also provides the purposes of compound in the medicine of preparation treatment infections after burn, and this compound has having structure:
Preferably, described infections after burn is caused by Venice acinetobacter calcoaceticus ATCC31012.
The present invention also provides the purposes of compound in the medicine of preparation vitro inhibition Venice acinetobacter calcoaceticus ATCC31012, and this compound has having structure:
Term used herein " pharmaceutically acceptable " refers to not eliminate the biologic activity of compound as herein described or the material of character, as carrier or diluent.This kind of material is applied to and individual does not cause undesirable biological action or not with harmful way and any component interaction comprised in its compositions.
" pharmaceutically acceptable carrier " comprises any and all solvents as the term is employed herein, disperse medium, coating material, surfactant, antioxidant, antiseptic (such as antibacterial, antifungal), isotonic agent, absorption delay agent, salt, antiseptic, drug stabilizing agent, binding agent, excipient, disintegrating agent, lubricant, sweeting agent, correctives, dyestuff etc. and its combination, this is well-known to those skilled in the art (for example, see Remington'sPharmaceuticalSciences, 18thEd.MackPrintingCompany, 1990, pp.1289-1329).Except with except the inconsistent carrier of active component, consider to use any conventional carrier in treatment or pharmaceutical composition.
Compound of the present invention, for the pathogen Be very effective causing infections after burn, can be developed to pharmaceutical composition effectively new clinically.
Detailed description of the invention
Below by way of the description of detailed description of the invention, the invention will be further described, but this is not limitation of the present invention, those skilled in the art are according to basic thought of the present invention, various amendment or improvement can be made, but only otherwise depart from basic thought of the present invention, all within the scope of the present invention.
The research of the purposes of experimental example the compounds of this invention in the medicine of preparation vitro inhibition Venice acinetobacter calcoaceticus ATCC31012
Bacteriostatic test
Use following compounds, adopt filter paper enzyme classical in this area to carry out bacteriostatic test, wherein:
The structural formula of compound is:
For examination strain Venice acinetobacter calcoaceticus ATCC31012 purchased from Fu Xiang bio tech ltd, Shanghai.
Culture fluid
Nutrient agar and nutrient broth, purchased from Chen Yu experimental facilities company limited of BeiJing ZhongKe.
Test method
Venice acinetobacter calcoaceticus ATCC31012 is inoculated in agar plate nutritional solution plane, evenly gathers during inoculation.
Take target compound 0.12 gram, add 5000 ml sterile waters, ultrasonic 30 minutes, then the filtering with microporous membrane of 0.22 μm, obtained solution.The aseptic circular filter paper sheet of tweezer, sprays above-mentioned solution to complete wetting, is attached in the agar plate nutritional solution plane of inoculated bacteria.Agar plate is placed in the incubator of 37 DEG C, incubation 4 hours.Measure the diameter of bacterial restrain.Measure and average for 3 times.
1.4 result
The average diameter of the bacterial restrain of Venice acinetobacter calcoaceticus ATCC31012 is 13.86mm, and this shows that target compound has the effect of extremely strong suppression Venice acinetobacter calcoaceticus ATCC31012.

Claims (9)

1. treat a compound for infections after burn, it is characterized in that, this compound has having structure:
2. treat a pharmaceutical composition for infections after burn, it is characterized in that, described pharmaceutical composition includes the compound of effective amount and pharmaceutically acceptable carrier, and described compound has having structure:
3. the pharmaceutical composition for the treatment of infections after burn according to claim 2, is characterized in that, described pharmaceutically acceptable carrier is diluent, disintegrating agent, binding agent, lubricant, stabilizing agent or corrigent.
4. the pharmaceutical composition for the treatment of infections after burn according to claim 3, is characterized in that, described diluent is sugar derivatives, starch derivatives or cellulose derivative.
5. the pharmaceutical composition for the treatment of infections after burn according to claim 4, is characterized in that, described diluent is lactose.
6. the pharmaceutical composition for the treatment of infections after burn according to claim 3, is characterized in that, described pharmaceutical composition is powder, microgranule, granule, capsule or tablet.
7. the purposes of compound in the medicine of preparation treatment infections after burn, it is characterized in that, this compound has having structure:
8. purposes according to claim 7, is characterized in that, described infections after burn is caused by Venice acinetobacter calcoaceticus ATCC31012.
9. the purposes of compound in the medicine of preparation vitro inhibition Venice acinetobacter calcoaceticus ATCC31012, it is characterized in that, this compound has having structure:
CN201510629893.0A 2015-09-29 2015-09-29 Drug combination for treating infection after burn Pending CN105232540A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201710122496.3A CN106806367A (en) 2015-09-29 2015-09-29 A kind of pharmaceutical composition for treating infections after burn
CN201510629893.0A CN105232540A (en) 2015-09-29 2015-09-29 Drug combination for treating infection after burn

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510629893.0A CN105232540A (en) 2015-09-29 2015-09-29 Drug combination for treating infection after burn

Related Child Applications (1)

Application Number Title Priority Date Filing Date
CN201710122496.3A Division CN106806367A (en) 2015-09-29 2015-09-29 A kind of pharmaceutical composition for treating infections after burn

Publications (1)

Publication Number Publication Date
CN105232540A true CN105232540A (en) 2016-01-13

Family

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Family Applications (2)

Application Number Title Priority Date Filing Date
CN201710122496.3A Withdrawn CN106806367A (en) 2015-09-29 2015-09-29 A kind of pharmaceutical composition for treating infections after burn
CN201510629893.0A Pending CN105232540A (en) 2015-09-29 2015-09-29 Drug combination for treating infection after burn

Family Applications Before (1)

Application Number Title Priority Date Filing Date
CN201710122496.3A Withdrawn CN106806367A (en) 2015-09-29 2015-09-29 A kind of pharmaceutical composition for treating infections after burn

Country Status (1)

Country Link
CN (2) CN106806367A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105777612A (en) * 2016-03-07 2016-07-20 王保亮 Medicine composition for treating children recurrent respiratory infection

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070238782A1 (en) * 2006-04-07 2007-10-11 Sunten Phytotech Co., Ltd. Naphthalenedione Compounds
CN101553471A (en) * 2006-12-06 2009-10-07 詹森药业有限公司 Antibacterial quinoline derivatives

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070238782A1 (en) * 2006-04-07 2007-10-11 Sunten Phytotech Co., Ltd. Naphthalenedione Compounds
CN101553471A (en) * 2006-12-06 2009-10-07 詹森药业有限公司 Antibacterial quinoline derivatives

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105777612A (en) * 2016-03-07 2016-07-20 王保亮 Medicine composition for treating children recurrent respiratory infection

Also Published As

Publication number Publication date
CN106806367A (en) 2017-06-09

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Application publication date: 20160113