Biosens

Gold nanoparticles

bSens Materials

Research use

A colloidal solution of citrate-stabilized gold nanoparticles (AuNPs), with a surface ready for functionalization. Stable in ethanol and isopropanol.

  • What it provides: a colloidal solution of gold nanoparticles, with the specifications of datasheet no. 98.

For research use only. Not for use in diagnostic procedures.

Specifications

Synthesis route
Chemical reduction
Medium
Ultrapure water
Appearance
Ruby red liquid
pH
6.0 to 7.0
Maximum absorbance band
521 nm
Optical density
1.462 (at 521 nm)
Mean size
12 to 16 nm

Values from Biosens datasheet no. 98, version 260107.

Characterization

4004505005506006507007508000.00.20.40.60.81.01.21.41.6Wavelength (nm)Absorbance521 nm
Ultraviolet-visible spectroscopy. Absorbance peak at 521 nm. Curve redrawn from the datasheet.
Gold nanoparticles under a transmission electron microscope: dark, rounded dots, alone and in clusters.
Transmission electron microscopy. Scale bar: 100 nm.

Use and storage

  • Store refrigerated, between 2 and 8 °C.
  • If particles settle, vortex the solution for 30 minutes.

Scientific context

What the studies say.

Data from scientific papers and books. They describe the condition, the field and the technology, not bSens products.

  • 1951

    Reducing a gold salt with citrate in water is one of the most widely used ways to make gold nanoparticles. In the Turkevich method, from 1951, citrate acts as both the reducing and the stabilizing agent. In 1973, Frens showed that particle size can be controlled by varying the ratio of gold to citrate. 1,2,3

  • 500 to 550 nm

    In water, spherical gold nanoparticles show colors such as brown, orange, red and purple as the core grows from 1 to 100 nm. They have an absorption band, the surface plasmon band, caused by the collective oscillation of conduction electrons excited by light, which generally lies between 500 and 550 nm depending on size. Particles smaller than 2 nm lack this band. When the particles aggregate, the band shifts from about 520 nm to about 650 nm and the solution turns from red to blue, an effect used in colorimetric sensors. 1,2,4

  • 5 to 100 nm

    A 2007 study calculated how the optical properties of spherical gold nanoparticles vary with size and compared the calculation with particles of 5 to 100 nm, synthesized and characterized by transmission electron microscopy and UV-Vis spectroscopy. Theory and experiment agreed. The authors derived equations to determine particle size and concentration directly from the UV-Vis spectrum and discussed the precision of various methods. 5

  • Proper surface functionalization is a prerequisite for any application of colloidal inorganic nanoparticles, because it determines how they interact with their environment. On gold it is usually based on the gold-sulfur bond: thiols can displace citrate from the surface, and the particles can carry oligonucleotides, antibodies and proteins. During this exchange, citrate-stabilized particles can aggregate irreversibly, and strategies exist to prevent it. 2,6,7,8

  • In lateral flow tests, whose best-known application is the pregnancy test, colloidal gold is the most used label material, according to a 2009 literature survey; colored latex particles come next. A 2016 review describes it as the most widely used label in commercial lateral flow immunoassays: it has an intense color and needs no development step to be seen. 9,10

  • Two reviews, from 2012 and 2015, point to three properties that make gold nanoparticles useful for electrochemical detection: conductivity, a large surface area and catalytic properties. The gold surface allows biomolecules to be bound, and electrodes with gold nanoparticles can act as electron wires that facilitate electron transfer between redox proteins and the electrode without redox mediators. 1,7

References

  1. 1.Saha K, Agasti SS, Kim C, Li X, Rotello VM. Gold nanoparticles in chemical and biological sensing. Chem Rev. 2012;112:2739-2779. doi:10.1021/cr2001178
  2. 2.Yeh YC, Creran B, Rotello VM. Gold nanoparticles: preparation, properties, and applications in bionanotechnology. Nanoscale. 2012;4:1871-1880. doi:10.1039/c1nr11188d
  3. 3.Dreaden EC, Alkilany AM, Huang X, Murphy CJ, El-Sayed MA. The golden age: gold nanoparticles for biomedicine. Chem Soc Rev. 2012;41:2740-2779. doi:10.1039/c1cs15237h
  4. 4.Elghanian R, Storhoff JJ, Mucic RC, Letsinger RL, Mirkin CA. Selective colorimetric detection of polynucleotides based on the distance-dependent optical properties of gold nanoparticles. Science. 1997;277:1078-1081. doi:10.1126/science.277.5329.1078
  5. 5.Haiss W, Thanh NTK, Aveyard J, Fernig DG. Determination of size and concentration of gold nanoparticles from UV-Vis spectra. Anal Chem. 2007;79:4215-4221. doi:10.1021/ac0702084
  6. 6.Sperling RA, Parak WJ. Surface modification, functionalization and bioconjugation of colloidal inorganic nanoparticles. Philos Trans A Math Phys Eng Sci. 2010;368:1333-1383. doi:10.1098/rsta.2009.0273
  7. 7.Zhou W, Gao X, Liu D, Chen X. Gold nanoparticles for in vitro diagnostics. Chem Rev. 2015;115:10575-10636. doi:10.1021/acs.chemrev.5b00100
  8. 8.Mirkin CA, Letsinger RL, Mucic RC, Storhoff JJ. A DNA-based method for rationally assembling nanoparticles into macroscopic materials. Nature. 1996;382:607-609. doi:10.1038/382607a0
  9. 9.Posthuma-Trumpie GA, Korf J, van Amerongen A. Lateral flow (immuno)assay: its strengths, weaknesses, opportunities and threats. A literature survey. Anal Bioanal Chem. 2009;393:569-582. doi:10.1007/s00216-008-2287-2
  10. 10.Koczula KM, Gallotta A. Lateral flow assays. Essays Biochem. 2016;60:111-120. doi:10.1042/EBC20150012

Contact

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