Polyvinyl siloxane impression materials are addition-reaction silicone elastomers introduced in the 1970s that have gained popularity due to their favorable properties. They are composed of a polymethyl hydrogen siloxane base polymer and a vinyl-terminated polydimethyl siloxane accelerator polymer. On mixing, an addition reaction occurs between the silane and vinyl groups, resulting in minimal dimensional change and no by-products. Modern polyvinyl siloxanes have adequate working and setting times of two and six minutes, respectively.
Polyvinyl siloxane impression materials are addition-reaction silicone elastomers introduced in the 1970s that have gained popularity due to their favorable properties. They are composed of a polymethyl hydrogen siloxane base polymer and a vinyl-terminated polydimethyl siloxane accelerator polymer. On mixing, an addition reaction occurs between the silane and vinyl groups, resulting in minimal dimensional change and no by-products. Modern polyvinyl siloxanes have adequate working and setting times of two and six minutes, respectively.
Polyvinyl siloxane impression materials are addition-reaction silicone elastomers introduced in the 1970s that have gained popularity due to their favorable properties. They are composed of a polymethyl hydrogen siloxane base polymer and a vinyl-terminated polydimethyl siloxane accelerator polymer. On mixing, an addition reaction occurs between the silane and vinyl groups, resulting in minimal dimensional change and no by-products. Modern polyvinyl siloxanes have adequate working and setting times of two and six minutes, respectively.
Polyvinyl siloxane impression materials are addition-reaction silicone elastomers introduced in the 1970s that have gained popularity due to their favorable properties. They are composed of a polymethyl hydrogen siloxane base polymer and a vinyl-terminated polydimethyl siloxane accelerator polymer. On mixing, an addition reaction occurs between the silane and vinyl groups, resulting in minimal dimensional change and no by-products. Modern polyvinyl siloxanes have adequate working and setting times of two and six minutes, respectively.
Polyvinyl siloxane impression materials: An update
on clinical use Michael N. Mandikos, BDSc, MS*
Abstract their different curing reactions.3 As the dimensional
Polyvinyl siloxane impression materials have stability of the polyvinyls is so much improved and applications in a variety of indirect procedures in the setting reaction is sufficiently different from the prosthodontics and restorative dentistry. Favourable condensation curing silicones, the polyvinyl siloxanes handling properties, good patient acceptance and warrant classification as a separate category of excellent physical properties have resulted in their popularity in today’s practice. In this review, the material.4 chemistry and important physical properties of The base material contains a polymethyl hydrogen polyvinyl siloxanes are summarized, and recent siloxane copolymer, which is a moderately low clinical questions of improved hydrophilics, tray molecular mass polymer with silane terminal adhesives, disinfection, and glove-induced polymerization inhibition are addressed. groups.3,5 The accelerator material contains the vinyl-terminated polydimethyl siloxane. This is also Key words: Polyvinyl siloxane, elastomer, impression a moderately low molecular mass polymer but has materials, hydrophilic, polymerization inhibition. vinyl terminal groups.3,5 The accelerator material (Received for publication November 1997. Revised March 1998. Accepted April 1998.) also contains chloroplatinic acid as a homogeneous metal complex catalyst.6-8 On mixing, an addition reaction occurs between the silane and vinyl groups Introduction (Fig. 1). There is minimal dimensional change during The polyvinyl siloxane impression materials are this polymerization and there are no by-products. addition reaction silicone elastomers which were Several authors have reported hydrogen gas first introduced in the 1970s. Since that time and bubble formation on the surface of gypsum dies especially in the past decade, these materials have poured immediately from polyvinyl siloxane gained in their acceptance and account for a large impressions.1,2,6 A side reaction of the hydrides on share of the impression material market. Polyvinyl the base polymer can produce hydrogen gas if siloxanes have applications in fixed prosthodontics, moisture or residual silanol groups are present. operative dentistry, removable prosthodontics and Manufacturers have now eliminated the possibility implant dentistry.1,2 The materials are presented in of this side reaction by proper purification and the form of two pastes (a base and an accelerator) accurate proportioning of the materials, and by the which can be hand spatulated or autodispensed from addition of palladium to the pastes as a hydrogen a dual cartridge, and mixed in equal quantities for absorber.7,8 It is no longer necessary to wait for one use. They have achieved a high level of dentist and hour before pouring these impressions. patient acceptance as they are clean, odourless and tasteless. The base and accelerator pastes also contain fillers. Amorphous silica or fluorocarbons are used Chemistr y as fillers to add bulk and improve the properties of the paste. The filler is also normally silanated to Polyvinyl siloxane materials are a modification of increase the bond strength between filler and the original condensation silicones. Both are based polymer, which better allows it to function as a on the polydimethyl siloxane polymer, however the cross-linker. 6 Colouring agents are added to presence of differing terminal groups accounts for distinguish the base and catalyst pastes and to aid evaluation of mixing. More recently, intrinsic *Advanced Education Program in Prosthodontics, State University surfactants have also been added in an attempt to of New York at Buffalo, New York, USA. negate the hydrophobicity of these materials.9 428 Australian Dental Journal 1998;43:6. Fig. 1. – The accelerator polymer is terminated with vinyl groups which cross-link to the silane terminal groups on the base polymer when activated by a platinum salt catalyst. Note that this is an addition reaction and there are no by-products.
Properties b. Working and setting times
a. Viscosity Modern polyvinyl siloxanes have a working time Polyvinyl siloxanes are available in viscosities ranging of two minutes and a setting time of six minutes from very low (for pouring, syringing or wash use), (with slight variation). 1,2 These times are considered to medium, high and very high. The viscosity of the to be adequate if not ideal. Occasionally, situations material increases with the proportion of filler present. will present which require extended working times and some methods of altering working and setting Viscosity is also affected by the shear force placed on times have been reported in the literature. Alteration the material. The mixed base and catalyst pastes of the proportion of catalyst is to be avoided as this exhibit a decrease in their relative viscosities in leads to variable results and has been suggested to response to high shear stresses. This is termed shear facilitate the side reaction which produces hydrogen thinning. Thus a medium body impression material gas. can possess sufficient viscosity to avoid excess flow if Some manufacturers supply a retarder that can be loaded into an impression tray, yet it can also exhibit incorporated into the mix to provide additional an apparent lowered viscosity suitable for intrasulcular working time without compromising other properties.2 impressions, when it is expressed through an The retarder is a small, reactive, tetracyclic vinyl impression syringe tip.5,10 The higher the viscosity of molecule that polymerizes preferentially to the the material, the more pronounced is the effect of siloxane copolymers. This small molecule is cyclic shear thinning. This phenomenon is suggested to be and does not form a chain. It is thus a chain stopper, due to the extremely small filler particle size.10 and temporarily prevents polymerization of the Thixotropy is the property of certain gels to linear siloxane molecules. The retarder continues to liquefy when subjected to vibrating forces (for polymerize until it is completely consumed and then example, ultrasonic waves) and then to solidify when the linear siloxane molecules polymerize causing the left to stand again. Polyvinyl siloxanes behave impression material to set. The retarder was used by similarly to this but have not been sufficiently two dental schools in the USA to provide students investigated to be classified as thixotropic materials. with extended working times in a teaching Australian Dental Journal 1998;43:6. 429 environment. It has become less commonly used Long term dimensional stability of polyvinyl since the polyvinyl siloxanes became available in siloxanes is reported in the literature. This is because automix dual cartridges. they are not susceptible to changes in humidity, and The most convenient and widely advocated they do not undergo any further chemical reactions method for extending working time is to refrigerate or release any by-products.1-3,5,16-18 Polyvinyl siloxane the materials before mixing. Gains of up to 90 impressions may be repoured to produce stone dies seconds have been reported when the materials are which are as accurate as the original, as many as chilled to 2°C. 2,11 seven days later.1,16,19 The linear coefficient of thermal contraction is c. Reproduction of detail relatively high for all elastomers. When an impression Polyvinyl siloxanes are currently considered to is removed from the mouth, there is an element of reproduce the greatest detail of all the impression shrinkage due to the decrease in temperature that materials. The international standard for dental occurs as the material moves from the mouth to the bench. Lower viscosity materials show the greatest elastomeric impression materials1 states that a type change (0.02-0.05 per cent shrinkage) due to their III (light body) impression material must reproduce lower filler content.16,17 Reheating an impression to a line 0.020 mm in width. With the exception of the 37°C before pouring has been demonstrated to very high viscosity putty materials, all polyvinyl improve the accuracy of the resultant die; however it siloxanes (light, medium and heavy body) achieve is doubtful that this is clinically significant.11,17 this. Very low viscosity materials can reproduce lines 1-2 µm wide. 5,12,13 e. Tear energy, elastic recovery and It should be noted that the literature does not tend deformation to support the use of putty and wash impression Impression materials must have sufficient strength techniques for greatest accuracy in impressions. to allow removal from a gingival sulcus without Wassell and Ibbetson14 reported that heavy body and tearing. Tear energy is that energy required to wash impressions were more accurate than putty and sustain a tear through a material, and is of obvious wash impressions. Frederick and Caputo15 further importance in thin intrasulcular or interproximal showed that the putty and wash technique was areas. significantly less accurate than polyether (heavy and light body) or reversible hydrocolloid impressions. Elasticity is inherent to all the elastomeric impression materials as they are polymers with highly flexible kinked segments that allow freedom d. Dimensional stability of movement. Under a load, the flexible kinked The accuracy of an impression material is segments of these polymers will uncoil allowing dependent on the dimensional stability. There are a movement. Upon removal of the load, an ideal number of possible causes for dimensional changes elastomer will exhibit complete elastic recovery and in elastomeric impression materials. All rubber return to its prestressed configuration. The degree polymers must contract slightly during polymerization to which this occurs is a measure of the elastic as a result of reduction in spatial volume as they recovery of the material. Permanent deformation cross-link. If the setting reaction produces a by- occurs when a polymer is elongated beyond the product or if accelerator components are liberated, point where elastic recovery is possible. Permanent then the set volume is further decreased. Some deformation is related to the degree of cross-linking impression materials like the polyethers are less of the polymer strands, temperature, and the rate of hydrophobic and can absorb and then even lose applied stress.20 water if they are placed in wet or varying humidity The ideal impression material should exhibit environments. Changes in temperature can also lead maximum energy absorption with minimal distortion. to varying changes in the final dimensions. However, it is also desirable that the material tears Polyvinyl siloxanes show the smallest dimensional rather than deforms past a critical point such as a changes on setting of all the elastomeric impression margin. Polyvinyl siloxanes deform at much slower materials. The majority of this shrinkage is due to rates and tear at points of less permanent deformation continued polymerization occurring within the first than do the other elastomeric materials.20 Polyvinyl three minutes of removal of the impression from the siloxanes are frequently reported to be the most mouth.2 Reductions in volume due to polymerization ideally elastic impression materials because they have been reported to be as low as 0.1 to 0.05 per exhibit better elastic recovery and less permanent cent.5,7 This linear contraction is well matched to the deformation than the other elastomers. They can setting expansion of modern type III and type IV die absorb over three times more energy up to the point stones and results in a slightly larger replication of of permanent deformation than other elastomers, the preparation.5,13,16 and if elongated to over 100 per cent (strain at tear), 430 Australian Dental Journal 1998;43:6. they rebound to only 0.6 per cent permanent in this area has involved observations of the wetting deformation.16,20 of set surfaces of polyvinyl siloxanes. The conclusion then is that the ‘hydrophilic’ statements refer to the f. Creep compliance newer materials being more readily poured up with All elastomers are viscoelastic materials, implying a gypsum-based die stone than the previous that deformation and elastic recovery are time generation materials. There is no scientific evidence dependent as well. Therefore, the longer the material to indicate that polyvinyl siloxanes advertised as is deformed (as occurs when impressions are ‘hydrophilic’ can be syringed into a wet sulcus for an removed slowly from the mouth or separated slowly accurate impression.2,9,12,23 from a poured model), then the longer time it takes This has been confirmed by Takahashi and for elastic recovery and the possibility of permanent Finger,24 who demonstrated that under a simulated deformation becomes higher.5 Polyvinyl siloxanes clinically dry field, both the hydrophilic and original have the least viscoelastic qualities thus requiring the formulations of polyvinyl siloxane wet tooth structure least time for recovery from viscoelastic deformation. with equal results. It has also been shown that the Blomberg et al.21 reported that polyvinyl siloxanes newer hydrophilic materials perform no better than have sufficient elastic recovery to allow an impression the original formulations of polyvinyl siloxane in to be poured only six minutes after removal from the wettability for pouring dies, if a compatible, extrinsic, mouth. spray-on surfactant is applied before pouring.9,23 The application of an extrinsic surfactant to the g. Radiopacity surface against which an impression is to be made Radiopacity of impression materials is important has also been suggested. Millar and co-workers25 for radiographic identification of excess material reported a significant reduction in the number of which may be accidentally swallowed, aspirated or voids and an overall increased quality of polyvinyl left in gingival tissues. Presently, only the poly- siloxane impression when a modified polydimethyl sulphide materials exhibit significant radiopacity due siloxane wetting agent was applied to the prepared to their lead dioxide content. tooth surfaces before impressions were made. Shillingburg et al.22 tested an experimental polyvinyl siloxane material containing 20 per cent Impression trays and adhesives barium sulphate to improve radiopacity. Although Tray spacing and tray design have often been cited they were able to demonstrate qualities of radiopacity as potential sources of error in impressions for fixed equal to that of the polysulphides, there were prosthodontic procedures. When only polysulphide associated physical property drawbacks including materials were available, even tray spacing was hydrogen bubble formation in dies poured from the critical to minimize distortion due to uneven poly- impressions, and evidence of long term breakdown merization shrinkage in areas of greater impression limiting the shelf life. material bulk. The improved physical properties of modern elastomers and particularly polyvinyl h. The hydrophilic question siloxanes have diminished this concern and now the According to O’Brien,8 wetting describes the use of stock trays for impressions has become common relative affinity of a liquid for a solid. It is the degree practice for reasons of cost and convenience.26 to which a drop will spread on a solid surface, and Common stock trays made of polystyrene or can be quantified by observing the contact angle. chromium plated brass are reported to be suitably High angles (greater than ninety degrees) indicate stiff to prevent flexure or distortion, although there poor wetting, whilst a zero angle would indicate remains some possibility of tray wall flexure with perfect wetting of the surface. When discussing the polystyrene trays.27 Wassell and Ibbetson14 and Payne wetting characteristics of impression materials, it is and Pereira 28 identified poor fitting stock trays and important to distinguish between the ability of the consequent tray wall flexure as the greatest concern material to flow around the soft and hard tissues of for inaccuracy. the mouth, and the ability of the material to be wet Whether custom or stock trays are used for by a gypsum slur ry. impressions, another potential source of error may Polyvinyl siloxanes are inherently hydrophobic.3,7 arise if the material is not adequately retained in the However in recent times, new ‘hydrophilic’ polyvinyl impression tray when it is removed from the mouth. siloxanes have been introduced with manufacturer The use of adhesives in trays has been shown to claims that they better wet moist dental surfaces. achieve higher material bond strengths for polyvinyl These new formulations have intrinsic surfactants siloxanes than has mechanical retention.28,29 The added. Typically these are non-ionic surfactants of adhesives used are usually polydimethyl siloxane and nonylphenoxypolyethanol homologues.7,23 Research ethylsilicate. The adhesive reacts with the surface of Australian Dental Journal 1998;43:6. 431 the tray material and forms a chemical bond to the Herrera and Merchant33 tested the dimensional tray and to the impression material. It is generally stability of different impression materials following recommended to wait ten to fifteen minutes after immersion disinfection for thirty minutes. They application of the adhesive before making the observed that polyvinyl siloxane and polysulphide impression.29 This allows time for the solvent to were unaffected after immersion in sodium react with the tray material. hypochlorite, 2 per cent glutaraldehyde, 0.5 per cent The polyether systems have the greatest bond povidone-iodine and 0.16 per cent halogenated strengths while the polyvinyl siloxanes show great phenol whilst polyethers were significantly unstable. variability between manufacturers with some being Even after extending the immersion times to sixty very poor, and others rivalling the polyether minutes, del Pilar Rios et al.34 agreed with the findings systems.27 Bond strengths will also vary depending of Herrera and Merchant. Johansen and Stackhouse35 on the tray material. In contrast to the polyethers demonstrated that polyvinyl siloxanes were able to and polysulphides, Chai et al.27 reported that be immersed in 2 per cent glutaraldehyde for 16 adhesive strength to acrylic resin (custom trays) was hours without any observed dimensional changes, significantly lower than polystyrene or metal stock whilst polyether materials showed dramatic distortions trays for the polyvinyl siloxanes. under the same conditions. Holtan et al.36 measured the dimensional stability Visible light-cured tray materials based on urethane of polyvinyl siloxanes after sterilization procedures dimethacrylate have found recent acceptance. using a conventional steam autoclave, and an Investigations into their bond strengths with ethylene oxide gas autoclave. They determined that polyvinyl siloxane adhesives indicate that they bond sterilization in ethylene oxide gas resulted in gas better than polymethyl methacrylate mat e ri a l s inclusions into the impression material which then provided that the air inhibited non-polymerized formed bubbles in dies poured immediately from layer is removed with isopropyl alcohol or a carbide them. Waiting to pour dies for 24 hours after gas bur.28,30 Sulong and Setchell31 demonstrated that autoclaving prevented this problem. Impressions roughening the surface of the impression tray will sterilized in the steam autoclave did undergo significantly improve the effectiveness of polyvinyl distortion that would have been significant enough siloxane adhesives. to prevent a casting from seating. It was concluded It is important to note that although other that steam autoclaving was a suitable sterilization elastomers have stronger bonding adhesives, these method if the impressions were not to be used for cannot be substituted for use with polyvinyl fixed prostheses. siloxanes. Also, polyvinyl siloxane putties are reported Most recently, radiofrequency glow discharging to show no chemical adhesion to their adhesive and has been advocated for use as a disinfecting so the use of putties requires mandatory mechanical procedure for polyvinyl siloxane impressions.37 retention in the impression tray.27 Whilst this procedure is claimed to clean and In many clinical situations, the impression tray must improve the wettability of the impression surface, it be tried in the mouth prior to impression making is not clear if glow discharging results in sterilization.† and this leads to saliva contamination. If the tray has already been painted with adhesive, then subsequent Compatibility with die materials application is recommended to maintain bond The hydrophobicity of polyvinyl siloxanes is well strengths. Contaminated adhesives have shown a drop established, however, as mentioned previously, the in bond strength to one-fifth of their original amount.32 introduction of newer materials with intrinsic surfactants or the conjunctive use of extrinsic Disinfection surfactants topically, can greatly improve wettability. Disinfection is the inhibition or destruction of This makes polyvinyl siloxanes compatible with pathogens and can be achieved by immersion of an gypsum, epoxy resin, and polyurethane resin impression into antimicrobial chemical solutions for materials.9,12,38 3 to 90 minutes depending on the agent. Sterilization Gypsum stones cannot reproduce detail much is the total elimination of all micro-organisms and smaller than 20 µm because their crystal size ranges spores and requires immersion periods of 6 to 10 hours. from 15 to 25 µm. Epoxy and polyurethane resins Extended periods of immersion can risk distorting can reproduce detail down to 1 to 2 µm making impressions by liquid uptake and subsequent them highly compatible with the detail capture swelling of the material. Consequently, procedures possible with polyvinyl siloxane impressions.12 currently used to control the transmission of Polyvinyl siloxanes can also be silver electroplated. pathogens from impressions have tended to be This procedure can be facilitated by soaking the disinfecting and not sterilizing due to concern for the accuracy of the impression. † Baier RE. Written communication, September 1996.
432 Australian Dental Journal 1998;43:6.
impressions in water for 24 hours before application adequate tear strengths, and exceptional dimensional of the silver powder. It is thought that this alters the stability. They are compatible with all common die concentration of surfactants in the surface layers of materials, can be disinfected or sterilized, and can be the impression.‡ Crispin et al.39 reported that silver repoured after delayed periods. They are dispensed dies recovered from polyvinyl siloxane impressions in convenient automixing dual cartridges or single are the most accurate dies. tubes and are available in several viscosities. If The ability to pour duplicate dies from one handled appropriately, polyvinyl siloxanes can be impression is highly advantageous. Morgano et al.40 applied in almost any indirect procedure. reported that the removal of dies and subsequent repouring of polyvinyl siloxane impressions produced Acknowledgements clinically accurate duplicate models. The author would like to thank Dr J. Malcolm Carter, Associate Professor Biomaterials, Department Gloves and the inhibition of polymerization of Restorative Dentistry, State University of New Occasionally an inhibition or retarding effect is York at Buffalo, for his advice in preparing this seen on polyvinyl siloxanes when they are used in a manuscript. clinical setting. This phenomenon can occur after direct contact between the impression material and References latex gloves, or a region of the mucosa previously 1. I n t e rn ational Standards Organization. Dental elastomeric impression material. ISO 4823-1992. Section 5.11 Detail touched by latex gloves.41-45 It was initially suspected reproduction. Stand alone document. Chicago: A m e ri c a n that the corn starch powder used as a lubricant in Dental Association Department of Standards Administration, the gloves was interacting,41 while other authors 1992. suggested atmospheric oxygen inhibition, or inter- 2. Chee WWL, Donovan TE. Polyvinyl siloxane impression materials: A review of properties and techniques. J Prosthet actions with haemostatic agents were the cause. Dent 1992;68:728-32. Several haemostatic agents were tested before de 3. van Noort R. Introduction to dental materials. Spain: Mosby, Camargo et al.46 concluded that they were not the 1994. inhibitors. Jones et al.47 were able to show that 4. Shillingburg HT, Hobo S, Whitsett LD. Fundamentals of fixed prosthodontics. 2nd edn. Chicago: Quintessence Publishing Co., provisional luting agents did not interfere with the 1981. polymerization. 5. Craig RG. Restorative dental materials. 9th edn. St Louis: A sulphur compound has since been identified as Mosby, 1993. being responsible for the retarding effect on poly- 6. Williams JR, Craig RG. Physical properties of addition silicones as a function of composition. J Oral Rehabil 1988;15:639-50. merization. Zinc diethyl dithiocarbamate is an 7. Craig RG, O’Brien WJ, Powers JM. Dental materials. Properties accelerator used in the manufacture of the latex and manipulation. 6th edn. St Louis: Mosby, 1996. gloves. It reacts with the platinum catalyst in the 8. O’Brien WJ. Dental materials. Properties and selection. polyvinyl siloxane to cause a delay or total inhibition Chicago: Quintessence Books, 1989. of polymerization.44,45,48 Baumann44 reported that 9. Panichuttra R, Jones RM, Goodacre C, Munoz CA, Moore KB. Hydrophilic poly(vinyl siloxane) impression mat e ri a l s : even in concentrations as low as 0.005 per cent, total dimensional accuracy, wettability, and effect on gypsum inhibition of polymerization of polyvinyl siloxane hardness. Int J Prosthodont 1991;4:240-8. can be observed. It is also believed that the 10. Chai J, Pang I. A study of the “thixotropic” property of compound can remain on a previously gloved hand, elastomeric impression materials. Int J Prosthodont 1994;7:155- 8. and so washing gloves or washing hands after glove 11. Chew C, Chee WWL, Donovan TE. The influence of use is not recommended as a means of avoiding temperature on dimensional stability of poly(vinyl siloxane) contamination. impression materials. Int J Prosthodont 1993;6:528-32. 12. Derrien G, Le Menn G. Evaluation of detail reproduction for Interestingly, not all latex gloves will cause an three die materials by using scanning electron microscopy and inhibition of set. It has been observed that synthetic two-dimensional profilometry. J Prosthet Dent 1995;74:1-7. latex gloves do not produce this phenomenon, while 13. Chee WWL, Donovan TE. Fine detail reproduction of very high some natural latex gloves do.42-44 One’s own testing viscosity poly(vinyl siloxane) impression materials. Int J Prosthodont 1989;2:368-70. and subsequent use of a non-retarding glove is 14. Wassell RW, Ibbetson RJ. The accuracy of polyvinyl siloxane recommended. impressions made with standard and reinforced stock trays. J Prosthet Dent 1991;65:748-57. Conclusions 15. Frederick DR, Caputo A. Comparing the accuracy of reversible hydrocolloid and elastomeric impression materials. J Am Dent The results of investigations into polyvinyl siloxane Assoc 1997;128:183-8. impression materials indicate that they produce 16. Phillips RW. Skinner’s science of dental materials. 9th edn. highly accurate impressions because they reproduce Philadelphia: Saunders, 1991. fine surface detail, and have excellent elastic recovery, 17. Tjan AHL, Li T. Effects of reheating on the accuracy of addition silicone putty-wash impressions. J Prosthet Dent 1991;65:743-8. 18. Lewinstein I, Craig RG. Accuracy of impression materials measured with a vertical height gauge. J Oral Rehabil ‡Garlapo DG. Written communication, February 1996. 1990;17:303-10. Australian Dental Journal 1998;43:6. 433 19. DeWald JP, Nakajima H, Bell JL. Bond strengths between 35. Johansen RE, Stackhouse JA. Dimensional changes of elastomers elastomeric impression materials and disinfected preliminary during cold sterilization. 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Quintessence Int 1989;20:657-63. reproduction of type IV dental stones with selected polyvinyl siloxane impression materials. Quintessence Int 1991;22:51-5. 23. Chai JY, Yeung T. Wettability of nonaqueous elastomeric impression materials. Int J Prosthodont 1991;4:555-60. 39. Crispin BJ, Watson JF, Frawley KR. Silver plated dies. Part II: marginal accuracy of cast restorations. J Prosthet Dent 24. Takahashi H, Finger WJ. Dentin surface reproduction with 1984;51:768-73. hydrophilic and hydrophobic impression materials. Dent Mater 1991;7:197-201. 40. Morgano SM, Milot P, Ducharme P, Rose L. Ability of various impression materials to produce duplicated dies from successive 25. Millar BJ, Dunne SM, Robinson PB. The effect of a wetting impressions. J Prosthet Dent 1995;73:333-40. agent on void formation in impressions. J Prosthet Dent 1997;77:54-6. 41. Duncan JD. Prevention of catalyst contamination of vinyl poly- siloxane silicone impression material during the impression 26. Tjan AHL, Nemetz H, Nguyen LTP, Contino R. Effect of tray procedure. J Prosthet Dent 1991;66:277. space on the accuracy of monophasic polyvinyl siloxane 42. Chee WWL, Donovan TE, Kahn RL. Indirect inhibition of poly- impressions. J Prosthet Dent 1992;68:19-28. merization of a polyvinyl siloxane impression material: a case 27. Chai JY, Jameson LM, Moser JB, Hesby RA. Adhesive report. Quintessence Int 1991;22:133-5. properties of several impression material systems: Part 1. J 43. Rosen M, Touyz LZG, Becker PJ. The effect of latex gloves on Prosthet Dent 1991;66:201-9. setting time of vinyl polysiloxane putty impression material. Br 28. Payne JA, Pereira BP. Bond strength of three nonaqueous Dent J 1989;166:374-5. elastomeric impression materials to a light-activated resin tray. 44. Baumann MA. The influence of dental gloves on the setting of Int J Prosthodont 1992;5:55-8. impression materials. Br Dent J 1995;179:130-5. 29. Cho GC, Donovan TE, Chee WWL, White SN. Tensile bond 45. Kahn RL, Dono van TE, Chee WWL. Interaction of gloves and strength of polyvinyl siloxane impressions bonded to a custom rubber dam with a poly(vinyl siloxane) impression material: a tray as a function of drying time. Part 1. J Prosthet Dent screening test. Int J Prosthodont 1989;2:342-6. 1995;73:419-23. 46. de Camargo LM, Chee WW, Donovan TE. Inhibition of poly- 30. Dixon DL, Breeding LC, Bosser MJ, Nafso AJ. The effect of merisation of polyvinyl siloxanes by medicaments used on custom tray material type and surface treatment on the tensile gingival retraction cords. J Prosthet Dent 1993;70:44-7. bond strength of an impression material/adhesive system. Int J Prosthodont 1993;6:303-6. 47. Jones RH, Cook GS, Moon MG. Effect of provisional luting agents on polyvinyl siloxane impression material. J Prosthet Dent 31. Sulong MZAM, Setchell DJ. Properties of the tray adhesive of an 1996;75:360-3. addition polymerizing silicone to impression tray materials. J 48. Causton BE, Burke FJT, Wilson NHF. Implications of the Prosthet Dent 1991;66:743-7. presence of dithiocarbamate in latex gloves. Dent Mater 32. Chai JY, Jameson LM, Moser JB, Hesby RA. Adhesive 1993;9:209-13. properties of several impression material systems: Part II. J Prosthet Dent 1991;66:287-92. 33. Herrera SP, Merchant VA. Dimensional stability of dental Address for correspondence/reprints: impressions after immersion disinfection. J Am Dent Assoc Dr Michael N. Mandikos, 1986;113:419-22. 1st Floor, Loyal House, 34. del Pilar Rios M, Morgano SM, Stein RS, Rose L. Effects of chemical disinfectant solutions on the stability and accuracy of 245 Albert Street, the dental impression complex. J Prosthet Dent 1996;76:356-62. Brisbane, Queensland 4000.