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ASSOCIATION REPORTS Revised ANSI/ADA specification no. 5* for dental casting alloys Council on Dental Materials, Instruments, and Equipment R evised American Dental Association specification no. 5 for dental casting alloys has been approved by the Council on Dental Materials, Instruments, and Equipment of the American Dental Association. This and other specifications for dental materials, instruments, and equip- ment are being formulated by subcommittees of the Accredited Standards Committee MD156 for Dental Materials, Instruments, and Equip- ment. The council acts as administrative sponsor of that committee, which has represen- tation from all interests in the United States in the standardization of materials, instru- ments, and equipment in dentistry. The council has adopted the specifications, show- ing professional recognition of their usefulness in dentistry, and has forwarded them to the American National Standards Institute with a recommendation that the specifications be approved as American National Standards. Approval of revised ADA specification no. 5 as an American National Standard was granted by the American National Standards Institute on Dec 14, 1988. This standard becomes effective Dec 14, 1989. The council thanks the subcommittee members and organizations with which they were affiliated at the time the specification was developed: Clyde Ingersoll (chairman), Williams Dental, Buffalo; Ken Anusavice, University of Florida, Gainesville; Arun Prasad, Jeneric Industries, Wallingford, CT; Marcy Kramer, JF Jelenko 8c Co, Armonk, NY; Ronald Dudek, Austenal Dental, Chicago; Lawrence Getlleman, Metairie, LA; Robert Hinman, Naval Dental Clinic, San Diego; T. K. Vaidyanathan, New York University Dental Center, New York; Edward Kaufman, Brookdale Dental Center, New York University, New York; Leon Laub, Loyola University, Maywood, IL; Robert Lorey, University of Michigan, Ann Arbor; and Herbert Mueller, ADA, Chicago. Revised ANSI/ADA specification no. 5 for dental casting alloys is written to assure both the efficacy and safety of clinical restorations in the mouth. Requirements for composition of alloy, mechanical properties, physical properties, casting characteristics, toxicity, tarnish and corrosion resistance, and pack- aging inserts are included to meet these goals. The clinical significance of these requirements follows. In addition to major elements and noble metal constituents, quantitative determination of any hazardous elements must be stated. It is important for the clinician to have this information when selecting an alloy for a patient with known metal hypersensitivity and in the general assessment of health risk to the patient. Depending on its use as an inlay, onlay, crown or bridge, a dental casting alloy should have a combination of mechanical properties that would preserve the anatomy designed into the restoration and permit the clinician to adjust or finish the appliance. A clinician may then designate a brand of alloy based on its mechanical properties. For example, if the margin on an inlay is short, the clinician may need to burnish the region. To achieve this result, the alloy should have a relatively low-yield strength and hardness, and a high elongation. When an alloy for a bridge is selected, a material having a high modulus of elasticity and high-yield strength would be desirable. Yield strength is a measure of how much stress is needed to deform a restoration. Elongation is a measure of the relative ductility or brittleness of an alloy. Modulus of elasticity is a measure of stiffness of an alloy. Hardness is a measure of the difficulty in finishing or polishing a restoration, as well as an indicator of potential wear of opposing natural tooth structure. Melting conditions will affect properties (for example, grain size and homogeneity of the alloy), and ultimately the clinical performance of a cast restoration. To achieve the properties described by a manufacturer, the conditions necessary for melting and casting, according to that manufacturer, must be followed. Clinically, a casting should not contain marginal discrepancies and should fit the prepared tooth. Because there is no compo- sition requirement in the specification (that is, the alloy can be predominantly noble or base metal), castability and fit need to be clinically acceptable. Biological safety of the alloy will be indicated through three toxicity evaluations: in vitro test of cytotoxicity, Ames’ test for potential mutagenic activity, and mucous membrane irritation testing. Neither composition requirements nor designated limits on mechanical property values assure tarnish or corrosion resistance of a casting alloy in the mouth. A tarnish test and evaluation of the effect of corrosion on mechanical properties are included. Packaging requirements include the pro- cessing information needed to achieve the combination of physical and mechanical properties reported by the manufacturer. Alloys are chosen for clinical use based on their properties and if clinical failure occurs, the packing information will help determine whether the cause was a materials problem. In this revision of ANSI/ADA specification no. 5 ,1981, the Accredited Standards Committee MD156 subcommittee has made extensive changes to the specification in response to recent developments in the casting alloy field. No longer are gold alloys dominant in the crown and bridge application of casting alloys. The first revision is the subcommittee’s recommendation for a change in the name of the specification. The word “gold” has been removed to reflect the fact that it is no longer restricted to gold alloys. There are no compositional requirements in the proposed revision of the specification. This reflects the clinical use and general acceptance of alloys containing less than 75% weight of gold and platinum group elements. The reason for the previous restriction to noble metals was the widespread belief that alloys with less than 75% (or 78%) noble metal content would tarnish or corrode in the mouth. This correlation has been disproved. Lower cost alternatives have been demanded by dentistry and have been furnished through advances in metallurgy, and greater knowledge of raw materials and oral tarnish/corrosion effects. Since the original specification no. 5, a considerable proliferation of alloys and alloy systems have proved to be viable substitutes for the high-gold alloys. *ANSI/ADA specification no. 5, 1988. Approved Dec 14, 1988. ---------------- jfiO A ----------------- Copies of this and other ANSI/ADA specifications are available from the American National Standards Institute, 1430 Broadway, New York 10018. JADA, Vol. 118, March 1989 ■ 379

Ada specification n 5 casting alloys

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A S S O C I A T I O N R E P O R T S

Revised ANSI/ADA specification no. 5 * for dental casting alloys

Council on Dental Materials, Instruments, and Equipment

R evised Am erican Dental Association specification no. 5 for dental casting a llo y s has been ap p ro v ed by the

C ouncil on D ental M aterials, In s tru m en ts , an d E q u ip m e n t of th e A m erican D en ta l A ssocia tion . T h is a n d o th e r sp ec ifica tio n s for dental m aterials, instrum ents, and equ ip ­m ent are being form ulated by subcom mittees of the Accredited Standards Com m ittee MD156 for Dental Materials, Instrum ents, and E q u ip ­m ent. T h e council acts as ad m in istra tiv e sponsor of that comm ittee, w hich has represen­tation from all interests in the U nited States in the stan d ard iza tio n of m ateria ls , in s tru ­m en ts , a n d e q u ip m e n t in d e n tis try . T h e council has adopted the specifications, show ­ing professional recognition of their usefulness in dentistry, and has forwarded them to the Am erican N ational Standards Institu te w ith a recom m endation that the specifications be approved as A m erican N a tio n a l S tandards. A pproval of revised ADA sp ec ifica tio n no. 5 as an A m erican N a tio n a l S ta n d a rd was granted by the American N ational Standards In s t i tu te on Dec 14, 1988. T h is s ta n d a rd becomes effective Dec 14, 1989.

T h e c o u n c il th a n k s th e su b c o m m itte e members and organizations w ith w hich they were a ffiliated a t the tim e the specification was developed: Clyde Ingerso ll (chairm an), W illiam s D en tal, B uffalo ; Ken A nusav ice, U n iv e rs ity o f F lo rid a , G a in esv ille ; A ru n Prasad, Jeneric Industries, W allingford, CT; Marcy Kram er, JF Je len k o 8c Co, A rm onk, NY; R onald Dudek, Austenal Dental, Chicago; L aw rence G etllem an, M etairie, LA; R obert H in m an , N aval D ental C lin ic , San Diego; T . K. V aidyanathan , New Y ork U niversity Dental Center, New York; Edward Kaufm an, Brookdale Dental Center, New York University, New York; Leon Laub, Loyola University, Maywood, IL; Robert Lorey, University of M ichigan, Ann Arbor; and H erbert Mueller, ADA, Chicago.

Revised ANSI/ADA specification no. 5 for dental casting alloys is w ritten to assure both the efficacy and safety of clinical restorations in the m outh. Requirem ents for com position of a llo y , m ec h an ic a l p ro p e rtie s , p h y sica l p ro p erties , casting characteris tics , toxicity , ta rn ish an d corrosion resistance, and pack­ag ing inserts are included to meet these goals. T h e clinical significance of these requirem ents follows.

In addition to m ajor elem ents and noble m etal constituents, quantitative determ ination of any hazardous elem ents m ust be stated. It is im portan t for the clin ician to have this in fo rm a tio n w hen se lec ting an a lloy for a p a tie n t w ith know n m eta l hypersensitiv ity and in the general assessment of health risk to the patient.

D epending on its use as an in lay , onlay, crown or bridge, a dental casting alloy should have a com bination of m echanical properties th a t w ou ld preserve the an a to m y designed into the restoration and perm it the clinician to adjust or finish the appliance. A clinician m ay then designate a b ra n d of a lloy based on its m echanical p roperties. For exam ple, if the m argin on an inlay is short, the clinician may need to burn ish the region. T o achieve this result, the alloy should have a relatively low-yield strength and hardness, and a h igh elongation.

W hen an alloy for a bridge is selected, a m aterial having a h igh m odulus of elasticity and h igh-yield strength w ould be desirable. Y ield s tre n g th is a m easu re of how m uch stress is needed to d efo rm a re s to ra tio n . E longation is a measure of the relative ductility or brittleness of an alloy. M odulus of elasticity is a measure of stiffness of an alloy. Hardness is a m easure of the d iff icu lty in f in ish in g o r p o lis h in g a re s to ra t io n , as w ell as an indicator of po tential wear of opposing natural tooth structure.

M elting co n d itio n s w ill affect p roperties (for ex am p le , g ra in size an d hom o g en e ity of th e a llo y ), a n d u ltim a te ly th e c lin ica l perform ance of a cast restoration. T o achieve the p roperties described by a m anufacturer, th e c o n d it io n s necessary fo r m e ltin g and casting, according to that m anufacturer, must be followed.

C lin ica lly , a cas tin g sh o u ld no t co n ta in m arg in a l d isc rep an cies an d sh o u ld fit the prepared tooth. Because there is no com po­sition requirem ent in the specification (that is, the alloy can be predom inantly noble or base m eta l), c as ta b ility a n d f it need to be clinically acceptable.

B io lo g ica l safety of th e a llo y w ill be indicated th rough three toxicity evaluations: in v itro test of cy to tox icity , A m es’ test for p o te n tia l m u ta g e n ic ac tiv ity , a n d m ucous m em brane irrita tion testing.

N e ith e r c o m p o s itio n re q u ire m e n ts no r

d es ig n a ted lim its o n m ech an ica l p ro p e rty values assure tarn ish or corrosion resistance of a cas tin g a llo y in the m o u th . A ta rn ish test and evaluation of the effect of corrosion on m echanical properties are included.

Packaging requirem ents include the p ro ­cessing in fo rm a tio n needed to ach ieve the c o m b in a tio n of p h y s ic a l a n d m ec h an ic a l properties reported by the m anufacturer. Alloys are ch o sen fo r c lin ic a l use based o n th e ir p roperties and if c lin ical failure occurs, the p a c k in g in fo rm a t io n w ill h e lp d e te rm in e whether the cause was a m aterials problem.

In this revision of ANSI/ADA specification no. 5 ,1981, the Accredited Standards Com m ittee MD156 su bcom m ittee has m ade extensive changes to the specification in response to recent developm ents in the casting alloy field. No longer are gold alloys dom inan t in the crown and bridge app lication of casting alloys.

T h e firs t re v is io n is the su b c o m m itte e ’s reco m m en d a tio n for a change in the nam e of the sp ec ifica tio n . T h e w ord “ g o ld ” has been rem oved to re flec t the fact th a t i t is no lo n g e r re s tr ic te d to g o ld a llo y s. T h ere a re no c o m p o s itio n a l re q u ire m e n ts in the p roposed revision of the specification. T h is reflects the clinical use and general acceptance of a llo y s c o n ta in in g less th a n 75% w eig h t of gold and p la tin u m group elements.

T h e reason for the previous restriction to noble m etals was the widespread belief that alloys w ith less than 75% (or 78%) noble metal content w ould tarn ish or corrode in the m outh. T h is corre lation has been disproved. Lower cost a lte rn a tiv e s have been d em an d ed by d en tistry an d have been fu rn ish ed th ro u g h advances in m etallurgy, and greater knowledge of raw m ateria ls and oral ta rn ish /co rro s io n effects. Since th e o rig in a l spec ifica tion no. 5, a considerable p ro liferation of alloys and a llo y system s have p ro v ed to be v iab le substitutes for the h igh-gold alloys.

* A N S I/A D A sp e c if ic a tio n no . 5, 1988. Approved Dec 14, 1988.

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Copies of this an d o ther ANSI/ADA specifications are available from the Am erican N ational Standards Institu te , 1430 Broadway, New York 10018.

JA D A , Vol. 118, March 1989 ■ 379