Amalgam (dentistry)

For other uses, see Amalgam.
Amalgam filling on first molar

Dental amalgam is a liquid mercury and metal alloy mixture used to fill cavities caused by tooth decay.[1] Low-copper amalgam commonly consists of mercury (50%), silver (~22–32% ), tin (~14%), copper (~8%) and other trace metals.[2][3] Dental amalgams were first documented in a Tang Dynasty medical text written by Su Kung in 659, and appeared in Germany in 1528.[4][5] In the 1800s, amalgam became the dental restorative material of choice due to its low cost, ease of application, strength, and durability.[6]

Recently however, concern for appearance, environmental pollution, health, and the availability of improved, reliable, composite materials diminished its popularity.[7] In particular, concerns about the toxicity of mercury have made its use increasingly controversial.

History of use

There are, according to Geir Bjørklund, indications that dental amalgam was used in the first part of the Tang Dynasty in China (AD 618–907), and in Germany by Strockerus in about 1528.[4] Evidence of a dental amalgam first appears in the Tang Dynasty medical text Hsin Hsiu Pen Tsao written by Su Kung in 659, manufactured from tin and silver.[5] Historical records hint that the use of amalgams may date even earlier in the Tang Dynasty.[5] It was during the Ming Dynasty that the composition of an early dental amalgam was first published, and a text written by Liu Wen Taiin 1505 states that it consists of "100 shares of mercury, 45 shares of silver and 900 shares of tin."[5] Ever since its introduction in the Western World in the 1830s, amalgam has been the subject of recurrent controversies because of its mercury content. Early amalgam was made by mixing mercury with the filings of silver coins.[4]

In 1833 two natives of England, Edward Crawcour and his nephew Moses Crawcour (incorrectly referred to as "the Crawcour brothers"), brought amalgam to the United States, and in 1844 it was reported that fifty percent of all dental restorations placed in upstate New York consisted of amalgam.[8] However, at that point the use of dental amalgam was declared to be malpractice, and the American Society of Dental Surgeons (ASDS), the only US dental association at the time, forced all of its members to sign a pledge to abstain from using the mercury fillings.[9] This was the beginning of what is known as the first dental amalgam war.[10]

The dispute ended in 1856 with the disbanding of the old association. The American Dental Association (ADA) was founded in its place in 1859, which has since then strongly defended dental amalgam from allegations of being too risky from the health standpoint.[11]

The ratio of the mercury to the remaining metallic mixture in dental amalgam has not always been 50:50. It was as high as 66:33 in 1930. Relative ratios between the other metals used in dental amalgams has also been highly variable. Conventional (or gamma2)-amalgams have 32% silver and 14% tin, and they are most susceptible to corrosion due to their low copper content. Non-gamma2 dental amalgams have been developed that were, however, found to release higher levels of mercury vapor compared with traditional amalgams. Amalgam is the dental material that has the strongest tendency to create galvanic currents and high electric potentials as it ages. The rate of mercury release with the corrosion is accelerated when the amalgam filling is in contact with old restorations or coupled with gold artifacts present in the mouth.

In 2008, Sweden, Norway and Denmark deliberated a ban of mercury dental amalgam in favor of alternative fillings.[12] Since 1 April 2008, dentists in Denmark are forbidden to use mercury in fillings, except for molar masticating surface fillings in permanent (adult) teeth. The Swedish amalgam ban is for both environmental and health issues, according to the Swedish authorities.[12][13]

Amalgam's setting reaction

Amalgam alloy has two main product types, designated low- and high-copper. The phases involved in the dental silver amalgam system are:

γ  : Ag3Sn (mechanically the strongest)
γ1 : Ag4Hg5 (main reaction product in set amalgam)
γ2 : Sn7.6Hg (weakest phase, corrodes easily)
β  : Ag5Sn 
η' : Cu6Sn5
ε  : Cu3Sn

The properties of set amalgam depends upon the proportions of the phases. If more unconsumed Ag3Sn is present, the stronger the amalgam.

Low copper alloy

Ag3Sn, Ag5Sn + Hg → Ag4Hg5 + Sn7.6

i.e. (γ + β) + Hg → γ1 + γ2

High copper alloy

In high copper alloy, high copper is added to improve mechanical properties, resistance to corrosion and marginal integrity. It has 2 types:

  1. Admixed alloy [2 Powders with different contents are mixed with mercury]
  2. Uni/single-composition alloy [1 powder is made available instead of 2 (that's why uni) to mix with mercury]

Admixed alloy setting reaction

Made by mixing 1/3 high-copper particles and 2/3 silver–tin alloy (low-copper, lathe-cut) particles. Here copper avoids Sn to react with Hg for avoiding gamma2 phase (weakest phase) formation, leading to new phase formation called Cu6Sn5 (eta phase).

2/3 silver tin alloy + 1/3 Eutectic alloy+Hg → Alloy-Hg + halo of Cu6Sn5+Unreacted particles of silver tin powder + unreacted particles of eutectic alloy.

i.e. 2/3 (Ag3Sn+AgSn) + 1/3 (AgCu)+Hg → Ag2Hg3 + Cu6Sn5+unreacted (Ag3Sn+AgSn)+unreacted (AgCu).

i.e. 2/3 (γ+β) + 1/3 eutectic alloy+Hg → γ1 + η + unreacted (γ+β)+unreacted eutectic alloy.

The main role of adding eutectic alloy of copper is to stop Sn from reacting with Hg, and to react with Cu itself,to avoid formation of Sn7–8Hg or gamma2 phase, which is responsible for tarnish and corrosion, thus reducing the same property just to increase mechanical properties. Instead, there is new phase formed because of binding of Cu to Sn called η (eta) phase, which will eventually benefit by reacting with unreacted particles of AgCu to form gamma1 phase, thus creating a cascade.

Uni/single composition alloy

Here, only 1 powder is added with mercury having all the contents of admixed alloy powders, which uses 2 powders, thus the name is derived. In addition indium/palladium in smaller amounts is added.

Ag-Sn-Cu + Hg → Cu6Sn5 + Ag2Hg3+ unreacted powder.

i.e. (γ β ε) + Hg → η + γ1 + (γ β ε)

The difference in eta phase of admixed alloy and unicomposition alloy is that in unicomposition alloy Cu6Sn5 crystals are much larger and rod-shaped than those in admixed alloy. Copper is added in unicomposition also, which causes removal of gamma2 phase. Gamma2 phase causes tarnish and corrosion. Gamma2 phase also causes amalgam to go in permanent deformation and if you send this amalgam in higher loading like occlusion then this phenomenon of deformation is called "creep". So, in short, Cu reduces the amount of creep by avoiding formation of gamma2 phase. Gamma2 phase starts corroding from its surface of restoration and not from center of restoration so it is like going on penetrating the center of amalgam from the surface, which is why it is called "penetration" type of corrosion. Now by linking above sentences we can say that (amount of) copper is responsible for tarnish and corrosion "indirectly". Low-copper amalgam has been thought to undergo more penetration type of corrosion indirectly due to its low copper content and directly due to its high tin content, which makes it more porous, thus reducing its mechanical strength compared with high-copper amalgam.[14][15] However, in fact there is little difference.[16]

Amalgam vs. polymer resins

Amalgam is tolerant to a wide range of clinical placement conditions and moderately tolerant to the presence of moisture during placement.[17] In contrast, the techniques for composite resin placement are more sensitive to many factors.[18][19]

Mercury has properties of a bacteriostatic agent whereas certain methacrylate polymers (for example TEGMA, triethylene glycol methacrylate) composing the matrix of resin composites "encourages the growth of microorganisms". In the Casa Pia study in Portugal (1986–1989), 1,748 posterior restorations were placed and 177 (10.1%) of them failed during the course of the study. Recurrent marginal decay was the main reason for failure in both amalgam and composite restorations, accounting for 66% (32/48) and 88% (113/129), respectively.[20] Polymerization shrinkage, the shrinkage that occurs during the composite curing process, has been implicated as the primary reason for postoperative marginal leakage.[21][22]

These are some of the reasons why amalgam has remained a superior restorative material over resin-base composites. The New England Children's Amalgam Trial (NECAT), a randomized controlled trial, yielded results "consistent with previous reports suggesting that the longevity of amalgam is higher than that of resin-based compomer in primary teeth[17][23] and composites in permanent teeth.[17][24] Compomers were seven times as likely to require replacement and composites were seven times as likely to require repair.[17]

There are circumstances in which composite serves better than amalgam. For example, when a more conservative preparation would be beneficial, composite is the recommended restorative material. These situations would include small occlusal restorations, in which amalgam would require the removal of more sound tooth structure,[25] as well as in "enamel sites beyond the height of contour".[26] For cosmetic purposes, composite is preferred when a restoration is required on an immediately visible portion of a tooth.

Dental amalgam toxicity

The greatest toxicity concern with dental amalgam is the potential for mercury poisoning when used as the dental material in a dental filling. Major health and professional organizations say that amalgam is safe.[27][28][29] However, critics argue that it has toxic effects that make it unsafe, both for the patient and perhaps even more so for the dental professional manipulating it during a restoration.[30] A study by the Life Sciences Research Office found that studies on mercury vapor and dental amalgam "provided insufficient information to enable definitive conclusions."[31] They identified several "research gaps", including: "well-controlled studies using standardized measures that evaluate whether low level [mercury vapor exposures] produce neurotoxic and/or neuropsychological effect", studies on "co-exposure to HgO and methylmercury", studies on "in utero exposure to HgO", "occupational studies on [pregnant workers] with well-defined HgO exposure", studies on the absorption of Hg2+ by the "human neonatal gut from breast milk", studies on "whether dental professionals have increased incidences of kidney disease, emotional instability, erethrism, pulmonary dysfunction, or other characteristics of occupational HgO exposure", studies on whether there exist "potential gender differences" or "genetic basis for sensitivity to mercury exposure."[31] The removal of amalgam fillings is not recommended for reasons other than a true hypersensitivity to Mercury.[32] Mercury levels in blood and urine have been shown to rise for a short period of time following the removal of amalgam restorations and no studies have demonstrated any health gain from restoration removal.[32] Removal involves exposure to mercury vapor released during the removal process.[27] Amalgams also contribute to mercury toxicity in the environment.[33] With regards to amalgam placement and removal in pregnancy, research has not shown any adverse effects for the mother or fetus. However, research is inadequate to determine the chance of harm occurring and therefore placement and removal should be avoided during pregnancy if possible.[34]

Metallurgy of amalgam

To fabricate an amalgam filling, the dentist uses a mixing device to blend roughly equal parts (by mass) of shavings of a silver-base alloy with mercury until the shavings are thoroughly wetted. The silver alloy is typically 40–70% Ag, 25-29% Sn, 2–40% Cu and 0–2% Zn (when the alloy is formulated. Zn is a scavenger and is mostly consumed during melting and lost as oxide). The dentist packs the plastic mass, before it sets, into the cavity. The amalgam expands ~0.1% over 6–8 hours on setting.

The final structure is a metal matrix composite, where γ1, η and γ2 phases, are a matrix for unreacted original alloy, minus the fast-reacting β-phase and excess Sn.[35][36]

See also

References

  1. ↑ "About Dental Amalgam Fillings". U.S. Food and Drug Administration. U.S. Food and Drug Administration. Retrieved 2 October 2015.
  2. ↑ Materials in Dentistry: Principles and Applications - Jack L. Ferracane - Google Boeken. Books.google.com. Retrieved 2012-09-19.
  3. ↑ Ferracane, Jack L. (2001). Materials in Dentistry: Principles and Applications. Lippincott Williams & Wilkins. p. 3. ISBN 0-7817-2733-2.
  4. 1 2 3 Bjørklund, G (1989). "The history of dental amalgam (in Norwegian)". Tidsskr Nor Laegeforen 109 (34–36): 3582–3585. PMID 2694433.
  5. 1 2 3 4 Czarnetzki, A.; Ehrhardt S. (1990). "Re-dating the Chinese amalgam-filling of teeth in Europe". International Journal of Anthropology 5 (4): 325–332.
  6. ↑ Bharti R, Wadhwani KK, Tikku AP, Chandra A (2010). "Dental amalgam: An update". J Conserv Dent 13 (4): 204–208. doi:10.4103/0972-0707.73380. PMC 3010024. PMID 21217947.
  7. ↑ Shenoy, A (2008). "Is it the end of the road for dental amalgam? A critical review". J Conserv Dent 11 (3): 99–107. doi:10.4103/0972-0707.45247. PMC 2813106. PMID 20142895.
  8. ↑ Westcott, A. (1844). "Report to the Onondonga Medical Society on metal paste (amalgam)". American Journal of Dental Science IV. 1st Ser: 175–201.
  9. ↑ American Society of Dental Surgeons. (1845). American Journal of Dental Science. Harvard University. p. 170.
  10. ↑ Molin, C (February 1992). "Amalgam—fact and fiction". Scandinavian Journal of Dental Research 100 (1): 66–73. doi:10.1111/j.1600-0722.1992.tb01811.x. PMID 1557606.
  11. ↑ Bremner MDF. (1939). The Story of Dentistry from the Dawn of Civilization to the Present Dental Items of Interest Pub. Co. p 86–87
  12. 1 2 "Dental Mercury Use Banned in Norway, Sweden and Denmark Because Composites Are Adequate...". Reuters. 2008-01-03. Retrieved 2012-09-19.
  13. ↑ "News". Dentistry.co.uk. Retrieved 2012-09-19.
  14. ↑ http://books.google.co.in/books/about/Phillips_Science_of_Dental_Materials.html?id=ZtFwJCAiF3wC
  15. ↑ Phillip's Science of Dental Materials, 12th ed. ISBN 978-1437724189
  16. ↑ Darvell BW. Effect of corrosion on the strength of dental silver amalgam. Dent Mater 28: e160–e167 (2012)
  17. 1 2 3 4 Soncini JA, Maserejian NN, Trachtenberg F, Tavares M, Hayes C (2007). "The longevity of amalgam versus compomer/composite restorations in posterior primary and permanent teeth: findings From the New England Children's Amalgam Trial". J Am Dent Assoc 138 (6): 763–772. PMID 17545265.
  18. ↑ Christensen, GJ (2005). "Longevity of posterior tooth dental restorations". J Am Dent Assoc 136 (3): 201–203. PMID 15782524.
  19. ↑ Bohaty BS, Ye Q, Misra A, Sene F, Spencer P (2013). "Posterior composite restoration update: focus on factors influencing form and function". Clin Cosmet Investig Dent 5: 33–42. doi:10.2147/CCIDE.S42044. PMC 3666491. PMID 23750102.
  20. ↑ Bernardo, M; Martin, MD; Lerouz, BG (2007). "Survival and reasons for failure of amalgam versus resin-based composites posterior restorations placed in a randomized clinical trial". The Journal of the American Dental Association 138: 775–783.
  21. ↑ Burgess, JO; Walker, R; Davidson, JM (2002). "Posterior resin-based composite: review of the literature". Journal of Pediatric Dentistry 24 (5): 465–479.
  22. ↑ Estefan, D.; Agosta, C. (2003). "Eliminating microleakage from the composite resin system". General dentistry 51 (6): 506–509.
  23. ↑ Forss, H; Widstrom, E (2003). "The post-amalgam era: a selection of materials and their longevity in the primary and young permanent dentition. Others express concern regarding the Children's Amalgam Trial's elevated serum and urine mercury content in the children with the amalgams". International Journal of Paediatric Dentistry 13 (3): 158–164.
  24. ↑ Qvist, V; Thylstrup, A (1986). "Restorative treatment patterns and longevity of amalgam restorations in Denmark.". Acta Odontologica Scandinavica 44 (6): 343–349.
  25. ↑ Fuks, AB (2002). "The use of amalgam in pediatric patients". Journal of Pediatric Dentistry 24 (5): 448–455.
  26. ↑ Newman, SM (1991). "Amalgam alternatives: what can compete?". The Journal of the American Dental Association 122 (8): 67–71.
  27. 1 2 "About Dental Amalgam Fillings". Food and Drug Administration. Retrieved 19 April 2015.
  28. ↑ "Final opinion on dental amalgam". European Commission. 2 June 2015. Retrieved 17 January 2016.
  29. ↑ "Dental Amalgam: What Others Say". American Dental Association. May 2015. Retrieved 17 January 2016.
  30. ↑ Mutter, J; Naumann, J; Walach, H; Daschner, F (2005). "Amalgam: Eine Risikobewertung unter Berücksichtigung der neuen Literatur bis 2005" [Amalgam risk assessment with coverage of references up to 2005]. Gesundheitswesen (Bundesverband der Arzte des Offentlichen Gesundheitsdienstes (Germany)) (in German) 67 (3): 204–16. doi:10.1055/s-2005-857962. PMID 15789284.
  31. 1 2 "Review and Analysis of the Literature on the Health Effects of Dental Amalgams" (PDF). Life Sciences Research Office. Retrieved 29 July 2009.
  32. 1 2 "British Dental Association" (PDF). www.bda.org. March 2008. Retrieved 2016-01-27.
  33. ↑ "Mercury in Health Care" (PDF). World Health Organization. 2005.
  34. ↑ "British Dental Association" (PDF). www.bda.org. March 2008. Retrieved 2016-01-27.
  35. ↑ Mitchell RJ, Okabe T (1996). "Setting reactions in dental amalgam. Part 1. Phases and microstructures between one hour and one week". Crit Rev Oral Biol Med 7 (1): 12–22. doi:10.1177/10454411960070010101. PMID 8727104.
  36. ↑ Mitchell RJ, Okabe T (1996). "Setting reactions in dental amalgam. Part 2. The kinetics of amalgamation". Crit Rev Oral Biol Med 7 (1): 23–25. doi:10.1177/10454411960070010201. PMID 8727105.

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