Colloidal gold



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Colloidal gold, also known as "nanogold", is a suspension (or gold in a fluid — usually water. The liquid is usually either an intense red colour (for particles less than 100 nm), or a dirty yellowish colour (for larger particles)[1][2]. The nanoparticles themselves can come in a variety of shapes. Spheres, rods, cubes, and caps are some of the more frequently observed ones.

Known since ancient times, the synthesis of colloidal gold was originally used as a method of staining glass. Modern scientific evaluation of colloidal gold did not begin until nanotechnology[5][6], and the synthesis of novel materials with unique properties.

Synthesis

Generally, gold nanoparticles are produced in a liquid ("liquid chemical methods") by precipitate in the form of sub-nanometer particles. The rest of the gold atoms that form stick to the existing particles, and, if the solution is stirred vigorously enough, the particles will be fairly uniform in size.

To prevent the particles from aggregating, some sort of stabilizing agent that sticks to the nanoparticle surface is usually added. They can be functionalized with various organic ligands to create organic-inorganic hybrids with advanced functionality. [3]

Turkevich et al. method

Pioneered by J. Turkevich et al. in 1951 and refined by G. Frens in 1970s, this recipe is the simplest one available. Generally, it is used to produce modestly monodisperse spherical gold nanoparticles suspended in water of around 10–20 nm in diameter. Larger particles can be produced, but this comes at the cost of monodispersity and shape.

  • Take 5.0×10−6 deionized water (the result should be a faintly yellowish solution) .
  • Heat it until it boils.
  • Continue the heating and, while stirring vigorously, add 1 ml of 0.5% sodium citrate solution; keep stirring for the next 30 minutes.
  • The colour of the solution will gradually change from faint yellowish to clear to grey to purple to deep purple, until settling on wine-red.
  • Add water to the solution as necessary to bring the volume back up to 20 ml (to account for evaporation).

The sodium citrate first acts as a adsorbed onto the gold nanoparticles, introducing the surface charge that repels the particles and prevents them from aggregating.

To produce larger particles, less sodium citrate should be added (possibly down to 0.05%, after which there simply would not be enough to reduce all the gold). The reduction in the amount of sodium citrate will reduce the amount of the citrate ions available for stabilizing the particles, and this will cause the small particles to aggregate into bigger ones (until the total surface area of all particles becomes small enough to be covered by the existing citrate ions).

Brust et al. method

This method was discovered by Brust and Schiffrin in early 1990s, and can be used to produce gold nanoparticles in toluene).

  • Dissolve 9.0×10−4 mol of HAuCl4 (about 0.3 g) in 30 ml of water.
  • Dissolve 4.0×10−3 mol of tetraoctylammonium bromide (TOAB) (about 2.187 g) in 80 ml of toluene.
  • Add the HAuCl4 solution to the TOAB and stir vigorously for about 10– minutes. The colour of the aqueous phase should become clear, and the colour of the organic phase (the toluene) should become orange.
  • While stirring vigorously, add (preferably dropwise, but really doesn't matter) BH4); the colour should change from orange to white to purple to eventually reddish, although the latter colours will be poorly discernible, since the solution will be quite concentrated and thus will look very dark.
  • Keep stirring the solution for up to 24 hours to ensure monodispersity (especially if NaBH4 was not added dropwise; otherwise just an hour or two is enough).
  • Separate the organic phase, wash it once with dilute distilled water.

Here, the gold nanoparticles will be around 5–6 nm. NaBH4 is the reducing agent, and TOAB is both the phase transfer catalyst and the stabilizing agent.

It is important to note that TOAB does not bind to the gold nanoparticles particularly strongly, so the solution will aggregate gradually over the course of two weeks or so, which can be very annoying. To prevent this, one can add a stronger binding agent, like a soxhlet extraction.

Sonolysis

Another method for the experimental generation of gold particles is by sonolysis. In one such process based on ultrasound, the reaction of an aqueous solution of HAuCl4 with cyclodextrin (a glucose oligomer) only spherical gold particles are obtained suggesting that glucose is essential in directing the morphology towards a ribbon.

History

A so-called Elixir of Life, a potion made from gold, was discussed, if not actually manufactured, in ancient times. Colloidal gold has been used since Ancient Roman times to colour glass intense shades of yellow, red, or mauve, depending on the concentration of gold. In the 16th century, the gold chloride. Faraday was the first to recognise that the colour was due to the minute size of the gold particles.

Current research

Research in 2005 demonstrated that nanogold-coated bacteria can be used for electronic wiring [7]. Bacillus cereus was deposited on a Fowler-Nordheim equation is obeyed when the interbacterial distance is very small.

The circular dichroism.

Health/Medical Applications

Colloidal gold has been successfully used as a therapy for rheumatoid arthritis [10][11]. In a related study[12], the implantation of gold beads near arthritic hip joints in dogs has been found to relieve pain.

When used in conjunction with weak microwaves, colloidal gold has successfully destroyed the beta-amyloid fibrils and plaque which may contribute to the mental degradation associated with Alzheimer's disease [13]. The possibilities for numerous similar radiative applications are also currently under exploration[14].

Gold nanoparticles are being investigated as carriers for drugs such as Paclitaxel [15]. The administration of hydrophobic drugs require encapsulation and it is found that nanosized particles are particularly efficient in evading the reticuloendothelial system.

See also

References

  1. ^ Bernhard Wessling, Conductive Polymer / Solvent Systems: Solutions or Dispersions?, 1996 (on-line here)
  2. ^ University of Edinburgh School of Physics: Colloids (mentions Elixir of Life)
  3. ^ a b V. R. Reddy, "Gold Nanoparticles: Synthesis and Applications" 2006, 1791, and references therein
  4. ^ Michael Faraday, Philosophical Transactions of the Royal Society, London, 1857
  5. ^ Paul Mulvaney, University of Melbourne, The beauty and elegance of Nanocrystals, Use since Roman times
  6. ^ C. N. Ramachandra Rao, Giridhar U. Kulkarni, P. John Thomasa, Peter P. Edwards, Metal nanoparticles and their assemblies, Chem. Soc. Rev., 2000, 29, 27-35. (on-line here; mentions Cassius and Kunchel)
  7. ^ Sonochemical Formation of Single-Crystalline Gold Nanobelts Jianling Zhang, Jimin Du, Buxing Han, Zhimin Liu, Tao Jiang, Zhaofu Zhang Angewandte Chemie International Edition Volume 45, Issue 7 , Pages 1116 - 1119 2006 Abstract
  8. ^ Self-Assembly of Nanoparticles on Live Bacterium: An Avenue to Fabricate Electronic Devices Vikas Berry, Ravi F. Saraf Angewandte Chemie International Edition Volume 44, Issue 41 , Pages 6668 - 6673 2005 Abstract
  9. ^ Large Optical Activity of Gold Nanocluster Enantiomers Induced by a Pair of Optically Active Penicillamines Hiroshi Yao, Kanae Miki, Naoki Nishida, Akito Sasaki, and Keisaku Kimura J. Am. Chem. Soc.; 2005
  10. ^ Amelioration of collagen-induced arthritis in rats by nanogold.
  11. ^ Repeated Colloidal Gold Tests in Rheumatoid Arthritis
  12. ^ Two years follow-up study of the pain-relieving effect of gold bead implantation in dogs with hip-joint arthritis.
  13. ^ Gold is newest weapon in battle against Alzheimer's
  14. ^ Therapeutic possibilities of plasmonically heated gold nanoparticles.
  15. ^ Paclitaxel-Functionalized Gold Nanoparticles Jacob D. Gibson, Bishnu P. Khanal, and Eugene R. Zubarev J. Am. Chem. Soc. 2007, 129, 11653-11661 doi:10.1021/ja075181k
 
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