CN107088661A - A kind of synthetic method of Nano Silver - Google Patents

A kind of synthetic method of Nano Silver Download PDF

Info

Publication number
CN107088661A
CN107088661A CN201710327955.1A CN201710327955A CN107088661A CN 107088661 A CN107088661 A CN 107088661A CN 201710327955 A CN201710327955 A CN 201710327955A CN 107088661 A CN107088661 A CN 107088661A
Authority
CN
China
Prior art keywords
nano silver
synthetic method
silver
nano
quercetin
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
CN201710327955.1A
Other languages
Chinese (zh)
Inventor
袁玉国
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.)
Yangzhou University
Original Assignee
Yangzhou University
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 Yangzhou University filed Critical Yangzhou University
Priority to CN201710327955.1A priority Critical patent/CN107088661A/en
Publication of CN107088661A publication Critical patent/CN107088661A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/16Making metallic powder or suspensions thereof using chemical processes
    • B22F9/18Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
    • B22F9/24Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/24Heavy metals; Compounds thereof
    • A61K33/38Silver; Compounds thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/05Metallic powder characterised by the size or surface area of the particles
    • B22F1/054Nanosized particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nanotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Inorganic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Composite Materials (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Materials Engineering (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A kind of synthetic method of Nano Silver, is related to the technical fields such as environment disinfected and veterinary clinic, and the DMSO solution of quercetin is reacted with silver nitrate aqueous solution mixing, obtains nano silver material.The size nano silver material average diameter of synthesis is 10nm, to drug-resistant pseudomonas aeruginosa and the Mlc of gold-coloured staphylococci(MIC)And bacteriocidal concentration(MBC)Respectively 1 μ g/mL and 2 μ g/mL, 2 μ g/mL and 4 μ g/mL, and Nano Silver effect 24h can completely inhibit resistance bacteria growing.Therefore, the nano silver material synthetic method is simple, can be mass-produced, there is obvious action effect to drug-fast bacteria.

Description

A kind of synthetic method of Nano Silver
Technical field
The present invention relates to the technical fields such as environment disinfected and veterinary clinic, and in particular to a kind of method of synthesizing nano-silver, It is directed to environment and plant's environment disinfected, sterilization and the Prevention Technique field for treating ox, goat mastitis veterinary clinic disease etc..
Background technology
Mastadenitis of cow is that a kind of inflammatory produced by mammary gland is stimulated by physics, chemistry, microorganism changes, and is milk cow Common disease and frequently-occurring disease.At present, the whole world there are about 2.2 hundred million more bovine cows, wherein about 1/3 suffers from various types of mammary gland Inflammation, the economic loss caused is annual up to 35,000,000,000 dollars.Surpassed the world average level in the incidence of disease of China's mastadenitis of cow, It is annual up to 1.35 hundred million yuan to the economic loss that China brings.Mastitis is mainly caused by a variety of unspecific pathogenic microorganisms, There are bacterium, fungi, virus and mycoplasma etc..Research shows that staphylococcus aureus, streptococcus and Escherichia coli account for whole milk More than the 90% of bovine mastitis case.Since being come out from the 40's of 20th century antibiotic, the treatment of mastitis is depended on Antibiotic, but antibiotherapy the drawbacks of expose it gradually.It is the appearance of antibody-resistant bacterium and changing for pathogenic bacteria first Become, decline antibiotic curative effect.Current research finds that staphylococcus aureus can hide in the hiding in macrophage and breast epithelium for a long time It is intracellular, and traditional antibiotic generally can not penetrate into cell or enter cell concentration it is too low and do not reach and control curative effect Really.Another drawback of antibiotherapy is the antibiotic residue problem in milk, and the antibiotic of Residues in Milk can induce people Hypersensitivity occurs for body, and great threat is caused to human health.And pure Chinese medicinal preparation, although noresidue, toxic side effect are small, but Its antibacterial efficacy can not show a candle to antibiotic.So, it is the task of top priority to find or invent more preferably medicine newly or reagent.
A large amount of with chemicalses such as antibiotic, disinfectant and bactericide use, and the microorganism as caused by drug resistance becomes Xenogenesis group is more and more, and the global microbial plague event thus triggered occurs again and again.In order to prevent microbial plague event Generation, research and development and application novel antibacterial material be a kind of effective method.It is anti-that traditional antiseptic can be divided into inorganic system Microbial inoculum, organic series antibacterial agent and all kinds of antiseptics of natural biological series antibacterial agent have respective advantage and disadvantage.Organic series antibacterial agent it is anti- Bacterium effect is good, with low cost, but its poor heat resistance, or even strong toxicity, can only typically be used for carrying out disposable sterilization or sterilizing.My god Right biomaterial is as antiseptic, and toxicity and environmental pollution are small, but are restricted by security and processing conditions, at present also not Mass market can be realized, is difficult to make nano-class antibacterial agent.With the continuous improvement of people's living standards, wishing to connect with people Tactile various life appliances energy automatic disinfection after by courses of infection is degerming, it is desirable to which the material of life appliance in itself can be chronically Discharge antiseptic or play a part of antiseptic.Numerous studies show that inorganic series antibacterial agent antibacterial spectrum width, toxicity is low, heat-resisting Property it is strong, be suitable for the antibiotic and sterilizing under the various living conditions of the mankind, and be especially suitable for and make nano-class antibacterial agent, inorganic antibacterial material Material has safe, and heat resistance and persistence are good, and the advantages of be not likely to produce the resistance to the action of a drug, from the 80's of 20th century with To obtain exploitation and application successively.Wherein, silver-colored inorganic antibacterial material is carried because its toxicity is low, antibacterial activity is high, has a broad antifungal spectrum, Current most widely used inorganic antibacterial material is turned into.
Invention or content
It is resistance to improve gold-coloured staphylococci and Pseudomonas aeruginosa etc. it is an object of the present invention to provide a kind of method of simple synthesizing nano-silver The killing effect of medicine bacterium.
The technical scheme is that:The DMSO solution of quercetin is reacted with silver nitrate aqueous solution mixing, acquirement is received Rice ag material.
Tests prove that the size nano silver material average diameter of synthesis is 10nm, to drug-resistant pseudomonas aeruginosa and golden grape The Mlc of coccus(MIC)And bacteriocidal concentration(MBC)Respectively 1 μ g/mL and 2 μ g/mL, 2 μ g/mL and 4 μ g/mL, and nanometer Silver effect 24h can completely inhibit resistance bacteria growing.Therefore, the nano silver material synthetic method is simple, can be mass-produced, right Drug-fast bacteria has obvious action effect.
Further, quercetin content is 0.5mg/mL in the DMSO solution of the quercetin.Quercetin has in DMSO Preferable dissolubility, beneficial to the progress of reaction.
Quercetin contains many phenolic hydroxyl group groups that can be combined with free radical, with antioxidation.And quercetin can be very Easily and quickly silver oxide ion, and effectively can prevent Nano Silver from assembling as sealer.Therefore, using the rubber of debita spissitudo Flavine can effectively synthesizing nano-silver material and with good stability as reducing agent.
Silver nitrate concentration is 1mM in the silver nitrate aqueous solution.Reacted, can had with 1mM silver nitrate aqueous solutions and quercetin The synthesizing nano-silver of effect, and can preferably control nano-Ag particles size.
The reaction is carried out under the conditions of 25~50 DEG C.At this temperature, the reduction reaction of Nano Silver can effectively be controlled Speed etc., controls nano-Ag particles size.Reaction is easier control reaction speed etc. under the conditions of 40 DEG C, obtains optimal size chi Very little nano-Ag particles.
Brief description of the drawings
Fig. 1 is the distribution map of the Nano Silver diameter synthesized.
Fig. 2 is the graph of a relation of nanometer silver concentration and bacterial action.
Fig. 3 is the graph of a relation that Nano Silver suppresses time and bacterial action.
Embodiment
1st, Nano Silver is prepared:
Weigh quercetin and be dissolved in the solution that 0.5mg/mL is made into DMSO.
Weigh silver nitrate powder and be dissolved in water and be configured to 1mM solution.
Quercetin solution is mixed in equal volume with silver nitrate solution, at 25~50 DEG C(It is preferred that 40 DEG C)At a temperature of stirring reaction 1h, in the process it can be seen that solution becomes dark brown by yellow, you can complete the synthesis of Nano Silver.
The dark brown mixed liquor that reaction is obtained moves into the 24h that dialysed in the bag filter of 12kDa sizes, then moves into solution In 50mL test tubes, freeze-drying produces nano silver material.
2nd, Nano Silver diameter is detected:
Appropriate amount of deionized water is added in the Nano Silver of acquirement and is made into 0.5mg/mL Nano Silver water mixed liquids, by transmission electron microscope and Particle diameter distribution instrument detects synthesizing nano-silver size.
As seen from Figure 1:Nano Silver diameter is distributed between 1 ~ 21nm, and Nano Silver average diameter is 10nm.
3rd, application of the Nano Silver on drug-fast bacteria:
Separated with Conventional bacteria separation method from the milk for suffering from mammitis sheep and obtain Pseudomonas aeruginosa and gold-coloured staphylococci, entered respectively Row experiment.
Bacterium is cultivated into 12h in 37 DEG C of nutrient broth nutrient solution, fresh medium culture 24h is added, bacterium solution from Supernatant is removed after the heart, precipitation is blown and beaten with deionized water disperses, and bacterium solution is diluted into 106Individual/mL, adds nanometer into bacterium solution respectively Silver, is made under the conditions of 0,0.2,0.4,0.6,0.8,1,2 μ g/mL Nano silver solution, 37 DEG C and is further cultured for after 24h, different Time point(0、4、8、12、16、20、24h)100 μ L bacterium solutions are taken to calculate CFU respectively, to detect that the antibacterial of Nano Silver and sterilization are imitated Really.
Pseudomonas aeruginosa is respectively adopted and gold-coloured staphylococci carries out result of the test as shown in Figure 2,3.
As seen from Figure 2:Nano Silver is respectively 1 μ g/ to the minimum inhibitory concentration of drug-resistant pseudomonas aeruginosa and gold-coloured staphylococci ML and 2 μ g/mL, bacteriocidal concentration is respectively 2 μ g/mL and 4 μ g/mL.
As seen from Figure 3:Resistance bacteria growing can be completely inhibited after Nano Silver effect 24h.

Claims (5)

1. a kind of synthetic method of Nano Silver, it is characterised in that the DMSO solution of quercetin is mixed into progress with silver nitrate aqueous solution Reaction, obtains Nano Silver.
2. the synthetic method of Nano Silver according to claim 1, it is characterised in that rubber is yellow in the DMSO solution of the quercetin Cellulose content is 0.5mg/mL.
3. the synthetic method of Nano Silver according to claim 1, it is characterised in that silver nitrate is dense in the silver nitrate aqueous solution Spend for 1mM.
4. the synthetic method of Nano Silver according to claim 1 or 2 or 3, it is characterised in that the reaction is in 25~50 DEG C of bars Carried out under part.
5. the synthetic method of Nano Silver according to claim 4, it is characterised in that carried out under the conditions of 40 DEG C.
CN201710327955.1A 2017-05-11 2017-05-11 A kind of synthetic method of Nano Silver Pending CN107088661A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710327955.1A CN107088661A (en) 2017-05-11 2017-05-11 A kind of synthetic method of Nano Silver

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710327955.1A CN107088661A (en) 2017-05-11 2017-05-11 A kind of synthetic method of Nano Silver

Publications (1)

Publication Number Publication Date
CN107088661A true CN107088661A (en) 2017-08-25

Family

ID=59638727

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710327955.1A Pending CN107088661A (en) 2017-05-11 2017-05-11 A kind of synthetic method of Nano Silver

Country Status (1)

Country Link
CN (1) CN107088661A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110272922A (en) * 2019-03-14 2019-09-24 浙江大学 It is a kind of to utilize method of careless pseudomonad cell-free supernatants synthesizing nano-silver and products thereof and application

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102202815A (en) * 2008-05-16 2011-09-28 维鲁泰克技术股份有限公司 Green synthesis of nanometals using plant extracts and use thereof
CN103302306A (en) * 2013-06-19 2013-09-18 东南大学 Method for reducing and preparing functionalized nano-silver based on polyphenol
CN103990793A (en) * 2014-05-09 2014-08-20 北京威士恩科技有限公司 High-length-to-diameter-ratio solid-walled hollow gold/gold-silver nanotube and manufacturing method thereof
CN104858448A (en) * 2015-05-11 2015-08-26 华南理工大学 Green synthesis method for nanogold in lignin solution
CN104889419A (en) * 2015-05-18 2015-09-09 湖州品创孵化器有限公司 Biological synthesis method for spherical silver nanoparticle
CN104999091A (en) * 2015-08-22 2015-10-28 钱景 Nano-silver particles and preparation thereof
CN105664168A (en) * 2016-03-02 2016-06-15 中国科学院武汉植物园 Preparation method and application of drug-loading nano silver particles
CN106270548A (en) * 2016-09-06 2017-01-04 西南大学 Utilize method of sericin green syt nanometer silver in situ and products thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102202815A (en) * 2008-05-16 2011-09-28 维鲁泰克技术股份有限公司 Green synthesis of nanometals using plant extracts and use thereof
CN103302306A (en) * 2013-06-19 2013-09-18 东南大学 Method for reducing and preparing functionalized nano-silver based on polyphenol
CN103990793A (en) * 2014-05-09 2014-08-20 北京威士恩科技有限公司 High-length-to-diameter-ratio solid-walled hollow gold/gold-silver nanotube and manufacturing method thereof
CN104858448A (en) * 2015-05-11 2015-08-26 华南理工大学 Green synthesis method for nanogold in lignin solution
CN104889419A (en) * 2015-05-18 2015-09-09 湖州品创孵化器有限公司 Biological synthesis method for spherical silver nanoparticle
CN104999091A (en) * 2015-08-22 2015-10-28 钱景 Nano-silver particles and preparation thereof
CN105664168A (en) * 2016-03-02 2016-06-15 中国科学院武汉植物园 Preparation method and application of drug-loading nano silver particles
CN106270548A (en) * 2016-09-06 2017-01-04 西南大学 Utilize method of sericin green syt nanometer silver in situ and products thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110272922A (en) * 2019-03-14 2019-09-24 浙江大学 It is a kind of to utilize method of careless pseudomonad cell-free supernatants synthesizing nano-silver and products thereof and application

Similar Documents

Publication Publication Date Title
WO2009133616A1 (en) Versatile disinfectant
CN109364100A (en) A kind of nanometer vulcanization iron mixture of high-efficiency antimicrobial and its preparation method and application
JP5669943B2 (en) Antibacterial agent and production method thereof
CN104336101A (en) Air sterilization method for edible mushroom culture room
CN1918999A (en) Preparation process of nano antibacterial agent
Li et al. Stabilizing the bactericidal activity of hydrogen peroxide: a brandnew function of certain chinese herbs
CN107836466A (en) A kind of tea tree ethereal oil natural disinfectant agent for animals and preparation method thereof
CN111296496A (en) Disinfectant for farm, preparation method and application
CN109260222A (en) Cysteine base antimicrobial nano vulcanizes iron mixture and its preparation method and application
CN102839535A (en) Manufacturing method of durable composite antibacterial textile
CN101199319A (en) Enzyme composite bactericide with broad-spectrum high-efficient bactericidal action and its preparation method
CN101578984A (en) Algaecide combined by cinnamic aldehyde, eugenol and citric acid
CN101803611B (en) Citric acid iodine disinfectant and method for preparing same
CN102405935B (en) Protamine compounded preparation, preparation method and application thereof
CN102349548A (en) Environment biological disinfectant with phages as main components and application thereof
CN108315276A (en) A kind of multifunctional microbial compound deodorizer and its preparation method and application
CN107088661A (en) A kind of synthetic method of Nano Silver
Piskaeva et al. Comparative analysis of the activity of silver nanoparticles against native microflora from poultry processing plants wastes
CN102939966B (en) A kind of compound disinfectant, its preparation method and application
CN101926830B (en) Antibacterial agent
CN102586136A (en) Microbial inoculant for improving disease resistance and promoting growth of plants
CN102388925B (en) Plant-sourced bactericide for controlling bacterial wilt of tobacco
CN104524558A (en) Enzyme compounded preparation and preparation method thereof
CN101239034A (en) High-efficiency sterilization shampoo
CN103951732A (en) Antibacterial peptide

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20170825