[go: up one dir, main page]

WO2016145925A1 - Assemblage de nanoparticules métalliques fortement résistant aux sels et son procédé de fabrication - Google Patents

Assemblage de nanoparticules métalliques fortement résistant aux sels et son procédé de fabrication Download PDF

Info

Publication number
WO2016145925A1
WO2016145925A1 PCT/CN2015/100036 CN2015100036W WO2016145925A1 WO 2016145925 A1 WO2016145925 A1 WO 2016145925A1 CN 2015100036 W CN2015100036 W CN 2015100036W WO 2016145925 A1 WO2016145925 A1 WO 2016145925A1
Authority
WO
WIPO (PCT)
Prior art keywords
product
metal nanoparticle
salt
high salt
mixture
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.)
Ceased
Application number
PCT/CN2015/100036
Other languages
English (en)
Chinese (zh)
Inventor
胡建强
余贵萍
李敏
陈宇宇
邓修龙
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.)
South China University of Technology SCUT
Original Assignee
South China University of Technology SCUT
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 South China University of Technology SCUT filed Critical South China University of Technology SCUT
Publication of WO2016145925A1 publication Critical patent/WO2016145925A1/fr
Anticipated expiration legal-status Critical
Ceased 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
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • 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
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology

Definitions

  • the invention belongs to the technical field of nano materials, and particularly relates to a high salt tolerance metal nanoparticle assembly and a preparation method thereof.
  • Metal nanoparticle assemblies have found wide applications in nanodevices, nanosensors, and nanomedicine.
  • Metal nano-assemblies not only have excellent optical, electrical, catalytic and other properties of isolated nanoparticles, but also have some new properties, such as surface-enhanced Raman properties, due to assembly, which greatly broadens the field of nano-particles in nanotechnology.
  • the scope of application within. With the increasing application of metal nanoparticle assemblies, especially in biomedicine, the salt tolerance is very high.
  • Metal nanoparticles, including metal nanoparticle assemblies are colloids that are particularly sensitive to electrolyte solutions such as salt solutions.
  • the primary object of the present invention is to provide a method for preparing a metal nanoparticle assembly having high salt tolerance, which is simple and efficient, has uniform product morphology, and good dispersibility.
  • Another object of the present invention is to provide a metal nanoparticle assembly obtained by the above production method, and to carry out an experiment for salt tolerance of the assembly.
  • a method for preparing a high salt tolerance metal nanoparticle assembly comprising the following steps:
  • the metal nanoparticle a according to the step (1) is Au, Ag or Cu.
  • the coating agent in the step (1) is sodium dodecyl sulfate (SDS); the coating agent and the metal nanoparticles are added
  • SDS sodium dodecyl sulfate
  • the mass ratio of a to ssDNA mixture a is 0.01% ⁇ 1%
  • PBS phosphate buffered saline
  • the buffer solution has a concentration of 10 to 100 mmol/L in a mixture a of metal nanoparticles a and ssDNA; the salt is added with metal nanoparticles a and
  • the concentration in the mixture of ssDNA a gradually increased from 6 to 24 h to the final 50 to 500 mmol/L.
  • the mixing culture time described in the step (1) is 6 to 24 h.
  • the separation and purification method is centrifugal separation or dialysis.
  • the metal nanoparticles b described in the step (2) and the metal nanoparticles in the step (1) are one or two of Au, Ag or Cu; the metal nanoparticles b have a size of 1 to 100 nm; the metal nanoparticles b
  • the molar ratio to sscDNA is 1:0.2 ⁇ 20.
  • the encapsulating agent in the step (2) is SDS, and the wrapping agent is added with metal nanoparticles b and
  • the mass ratio of the mixture b of sscDNA is 0.01% ⁇ 1%
  • the concentration of the mixture of sscDNA b is 10 ⁇ 100 mmol/L
  • the concentration of the salt in the mixture b of metal nanoparticles b and sscDNA is 50-500. Mmmol/L ;
  • the mixing culture time described in the step (2) is 6 to 24 h.
  • the separation and purification method is centrifugal separation or dialysis.
  • the concentration of the buffer solution in the mixed solution in which the product a and the product b are mixed is 10 to 100 mmol/L; the concentration of the salt in the mixed solution in which the product a and the product b are mixed is 50 ⁇ 500 mmol/L;
  • the mixed culture time is 6 ⁇ 24 h; the centrifugal speed is 5000 ⁇ 20,000 rpm; the centrifugation time is 5 ⁇ 30 min, centrifugation 1 ⁇ 3 times.
  • Salt tolerance test of the above metal nanoparticle assembly including stability in physiological saline and sodium chloride at different concentrations ( NaCl Stability in solution.
  • the method is easy to operate, has strong controllability and high assembly efficiency, and the obtained product has uniform structure and good dispersibility, and the product has strong salt tolerance and can withstand a salt concentration up to three times the concentration of physiological saline. Therefore, the metal nanoassemblies obtained by the preparation method have potential advantages in biological applications.
  • Figure 1 is a transmission electron micrograph (TEM) of the gold nanoparticle assembly obtained in Example 2;
  • Figure 2 is a transmission electron micrograph of the gold nanoparticle assembly obtained in Example 2 after incubation for 12 h in physiological saline ( TEM );
  • Figure 3 is a gold nanoparticle assembly obtained in Example 2 at different concentrations of NaCl
  • the salt tolerance test result in the solution, that is, the ultraviolet absorption spectrum.
  • the metal nanoparticles used in the method of the present invention are commercially available or can be prepared by themselves using the prior art.
  • the ssDNA and sscDNA used in the following examples were purchased from Shanghai Shenggong Bioengineering Co., Ltd.
  • ssDNA 5' -HS-(CH 2 ) 6 ATC CTG ACA TCG GCA CGA GTA TTT CTA CCA TGT ATC-3'
  • sscDNA 5'-HS-(CH 2 ) 6 GAT ACA TGG TAG AAA TAC TCGTGC CGA TGT CAG GAT-3'.
  • steps (1) and (2) are mixed at a molar ratio of 1:40 and added to a final concentration of 0.2.
  • the obtained gold nanoparticle assembly was subjected to TEM characterization, and the results are shown in Fig. 1.
  • the gold nanoparticles were successfully connected to the surface of 18 nm gold nanoparticles to form a 'nuclear-satellite' assembly.
  • the average number of satellites was nine, and the assembly was well dispersed and uniform in size.
  • steps (1) and (2) are mixed at a molar ratio of 1:80 and added to a final concentration of 0.2.
  • Example 2 The gold nanoparticle assembly of Example 2 was cultured in physiological saline for 12 hours, and then subjected to transmission electron microscopy (TEM). ) characterization. Its TEM image is shown in Figure 2.
  • TEM transmission electron microscopy
  • the gold nanoparticle assembly prepared by the method of the present invention is cultured in physiological saline for up to 12 h. It still retains its intact morphology, indicating its good stability at 0.9% salt concentration.
  • Example 2 The gold nanoparticle assembly of Example 2 was taken at 0.9%, 1.8%, 3.0%, 3.3, respectively. Salt tolerance tests were performed in % and 4.5% (mass fraction) NaCl solutions, and the initial color change of the solution was observed and UV characterized (results shown in Figure 3).
  • the stability of the gold nanoparticle assembly is easily affected by the salt concentration.
  • a normally uniformly dispersed aqueous solution of the assembly is generally ruby red, and agglomeration may occur when it is in a high concentration of salt solution. This is reflected in the appearance of the color change of the solution (usually purple), which is reflected in the ultraviolet spectrum as the red shift of the maximum absorption peak. Therefore, the stability of the solution can be verified by the color of the solution and the ultraviolet absorption spectrum.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Nanotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Physics & Mathematics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Zoology (AREA)
  • Biomedical Technology (AREA)
  • Wood Science & Technology (AREA)
  • General Physics & Mathematics (AREA)
  • General Engineering & Computer Science (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Plant Pathology (AREA)
  • Composite Materials (AREA)
  • Molecular Biology (AREA)
  • Microbiology (AREA)
  • Biophysics (AREA)
  • Manufacturing & Machinery (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • Powder Metallurgy (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)

Abstract

L'invention concerne un procédé de fabrication d'un assemblage de nanoparticules métalliques fortement résistant aux sels, ledit procédé consistant à : obtenir une nanoparticule métallique (a) et l'ADNss, ajouter ces derniers à un mélange (a) d'un agent de revêtement, d'une solution tampon et d'un sel, et séparer et purifier ces derniers après mélange et mise en culture, ce qui permet d'obtenir un produit (a) ; obtenir une nanoparticule métallique (b) et l'ADNssc, ajouter ces derniers à un mélange (b) de l'agent de revêtement, de la solution tampon et du sel, et séparer et purifier ces derniers après mélange et mise en culture, ce qui permet d'obtenir un produit (b) ; et mélanger le produit (a) et le produit (b), dissoudre ces derniers dans une solution mixte constituée de l'agent de revêtement, de la solution tampon et du sel, et centrifuger et laver ces derniers après agitation et mise en culture de ces derniers, ce qui permet d'obtenir l'assemblage de nanoparticules métalliques fortement résistant aux sels. L'invention concerne un assemblage de nanoparticules métalliques fortement résistant aux sels qui est fabriqué par le procédé ci-dessus. Le procédé est simple, très efficace et présente une contrôlabilité élevée. Le produit résultant présente un aspect uniforme, une bonne dispersibilité et une résistance élevée aux sels.
PCT/CN2015/100036 2015-03-18 2015-12-31 Assemblage de nanoparticules métalliques fortement résistant aux sels et son procédé de fabrication Ceased WO2016145925A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201510118750.3 2015-03-18
CN201510118750.3A CN104923777A (zh) 2015-03-18 2015-03-18 一种高耐盐性金属纳米粒子组装体及其制备方法

Publications (1)

Publication Number Publication Date
WO2016145925A1 true WO2016145925A1 (fr) 2016-09-22

Family

ID=54111378

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2015/100036 Ceased WO2016145925A1 (fr) 2015-03-18 2015-12-31 Assemblage de nanoparticules métalliques fortement résistant aux sels et son procédé de fabrication

Country Status (2)

Country Link
CN (1) CN104923777A (fr)
WO (1) WO2016145925A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117123794A (zh) * 2023-08-23 2023-11-28 哈尔滨工业大学(深圳)(哈尔滨工业大学深圳科技创新研究院) 一种表面具有纳米级棒状结构的微米银颗粒及其制备方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104923777A (zh) * 2015-03-18 2015-09-23 华南理工大学 一种高耐盐性金属纳米粒子组装体及其制备方法

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050136439A1 (en) * 2003-09-12 2005-06-23 North Carolina State University Novel methods of inorganic compound discovery and synthesis
WO2006024023A2 (fr) * 2004-08-24 2006-03-02 Nanomix, Inc. Dispositifs de detection a nanotubes, destines a la detection de sequences d'adn
CN101541961A (zh) * 2006-10-04 2009-09-23 布鲁克哈文科学协会 Dna指导的纳米颗粒组装体
CN101987364A (zh) * 2010-09-14 2011-03-23 江南大学 一种高稳定性和功能化的金纳米粒子的制备方法
CN102080131A (zh) * 2010-12-10 2011-06-01 郑州大学 发夹式dna修饰的金胶纳米粒子及其合成方法
CN102203246A (zh) * 2008-06-02 2011-09-28 布鲁克哈文科学协会有限公司 通过蛋白质和dna剂可控组装和解组装的纳米颗粒体系
CN102556959A (zh) * 2011-12-30 2012-07-11 中国科学院苏州纳米技术与纳米仿生研究所 一种金属纳米颗粒二聚体的制备方法
CN103539065A (zh) * 2012-07-10 2014-01-29 中国科学院苏州纳米技术与纳米仿生研究所 构建纳米颗粒和纳米棒组合结构的方法及构建的组合结构
CN104923777A (zh) * 2015-03-18 2015-09-23 华南理工大学 一种高耐盐性金属纳米粒子组装体及其制备方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6974669B2 (en) * 2000-03-28 2005-12-13 Nanosphere, Inc. Bio-barcodes based on oligonucleotide-modified nanoparticles
US20090258355A1 (en) * 2008-04-11 2009-10-15 Brookhaven Science Associates, Llc Nanoscale Clusters and Methods of Making Same
EP2511231B1 (fr) * 2009-12-11 2015-03-11 Korea Research Institute Of Chemical Technology Nanoparticle coeur-écorce hétérodimère dans laquelle des molécules actives à effet raman sont situées au niveau d'une partie de liaison d'une nanoparticule hétérodimère, utilisation de celle-ci, et procédé de préparation correspondant
CN102127542B (zh) * 2010-12-27 2012-05-23 江南大学 一种具有表面增强拉曼活性的自组装材料的制备方法
CN102442638A (zh) * 2011-09-15 2012-05-09 王利兵 一种具有手性信号的不对称金纳米粒子二聚体的制备方法
CN102382816B (zh) * 2011-09-15 2013-03-13 王利兵 一种具有手性的自组装材料的制备方法
CN102367589B (zh) * 2011-09-15 2013-02-27 王利兵 一种二元金纳米粒子Janus组装体的制备方法

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050136439A1 (en) * 2003-09-12 2005-06-23 North Carolina State University Novel methods of inorganic compound discovery and synthesis
WO2006024023A2 (fr) * 2004-08-24 2006-03-02 Nanomix, Inc. Dispositifs de detection a nanotubes, destines a la detection de sequences d'adn
CN101541961A (zh) * 2006-10-04 2009-09-23 布鲁克哈文科学协会 Dna指导的纳米颗粒组装体
CN102203246A (zh) * 2008-06-02 2011-09-28 布鲁克哈文科学协会有限公司 通过蛋白质和dna剂可控组装和解组装的纳米颗粒体系
CN101987364A (zh) * 2010-09-14 2011-03-23 江南大学 一种高稳定性和功能化的金纳米粒子的制备方法
CN102080131A (zh) * 2010-12-10 2011-06-01 郑州大学 发夹式dna修饰的金胶纳米粒子及其合成方法
CN102556959A (zh) * 2011-12-30 2012-07-11 中国科学院苏州纳米技术与纳米仿生研究所 一种金属纳米颗粒二聚体的制备方法
CN103539065A (zh) * 2012-07-10 2014-01-29 中国科学院苏州纳米技术与纳米仿生研究所 构建纳米颗粒和纳米棒组合结构的方法及构建的组合结构
CN104923777A (zh) * 2015-03-18 2015-09-23 华南理工大学 一种高耐盐性金属纳米粒子组装体及其制备方法

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117123794A (zh) * 2023-08-23 2023-11-28 哈尔滨工业大学(深圳)(哈尔滨工业大学深圳科技创新研究院) 一种表面具有纳米级棒状结构的微米银颗粒及其制备方法

Also Published As

Publication number Publication date
CN104923777A (zh) 2015-09-23

Similar Documents

Publication Publication Date Title
Sarkar et al. Green synthesis of silver nanoparticles and its optical properties
CN106715009A (zh) 金属质铜粒子及其制备方法
FR2633940A1 (fr) Scleroglucane traite au glyoxal et son procede d'obtention
BRPI0719483A2 (pt) processo para produção de nanoparticula sestáveis e monodispersas de prata metálica e pasta de nanoparticulas de prata metálica
FR2689515A1 (fr) Procédé pour la préparation des pigments composites.
FR2714368A1 (fr) Procédé de production de silice amorphe granulaire.
WO2016145925A1 (fr) Assemblage de nanoparticules métalliques fortement résistant aux sels et son procédé de fabrication
CN103923643B (zh) 一种银复合的手性量子点纳米材料及其制备方法
JPS5869863A (ja) 小さい過酸化ベンゾイル結晶を製造する方法
JPS5913547B2 (ja) ビ−ズ形状の顔料組成物の製造法
TW201144222A (en) A method for the silicon recycling
JP2001512169A (ja) 水性セラック溶液または分散液
CN108165094B (zh) 一种纳米纤维素基笔芯水性墨及其制备方法
JPS63185999A (ja) ツエインの製造法
EP0188979B1 (fr) Procédé de préparation d'anthraquinone
JP6695682B2 (ja) 精製水溶性種子系多糖類の製造方法
TW201241103A (en) Process of preparing product based on copper phthalocyanine (CuPc) particles
JP2015143368A (ja) イプシロン結晶形態を示す銅フタロシアニン(CuPc)粒子の製造方法
CN105111758B (zh) 沥青混合料高模量剂及其制备方法以及沥青组合物
JP7359813B2 (ja) 樹脂ビーズ、樹脂ビーズの製造方法、及び樹脂ビーズを用いた製品
US1880968A (en) Process of purifying bodies insoluble in water
JPH0635488B2 (ja) 塩素化ポリオレフィンの製造方法
JP6511611B2 (ja) マスターバッチの製造方法及びエラストマー組成物の製造方法
US1906357A (en) Parting compound for treating sand molds
CN104150490B (zh) 纳米二氧化硅的制备方法

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 15885293

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 15885293

Country of ref document: EP

Kind code of ref document: A1

32PN Ep: public notification in the ep bulletin as address of the adressee cannot be established

Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 112(1) EPC (EPO FORM 1205A DATED 18/01/2018)

122 Ep: pct application non-entry in european phase

Ref document number: 15885293

Country of ref document: EP

Kind code of ref document: A1