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ISSN (Print) 1013-9052
EISSN 1658-3558

The Saudi Dental Journal,
P.O. Box 52500,
Riyadh 11563,
Kingdom of Saudi Arabia
Tel.
966-1-467-7328
Fax.
933-1-467-7308 /
966-1-467-7534
Email
saudidj@ksu.edu.sa

Comparative study of composite, compomer and ormocer

bi-axial flexural strength

 

Nadia M. Taher, BDS, MSc
Department of Restorative Dental Sciences, College of Dentistry, King Saud University, Riyadh, Saudi Arabia

Abstract 

 

The aim of this study was to measure and compare the bi-axial flexural strength of newly developed restorative ormocers with other composite and compomer restorative materials. Eight restorative materials were selected: two ormocers (Admira and Definite), three composite resins (Z-100, Z-250, and Pyramid), and three compomers (Compoglass F, Dyract AP and Composan Glass).  Five 14 mm diameter x 2 mm thick disc-shaped specimens were prepared of each material using a silicone lubricated teflon mold.  The specimens were stored in distilled water at 37oC for 24 hours before the biaxial flexural strengths were measured using an Instron universal testing machine. Definite had the lowest flexural strength mean (160.63 MPa) while Compoglass F had the highest (291.93 MPa).  Admira had a statistically insignificant difference (201.53 MPa) when compared to Definite.  The strength of Compoglass F and Composan Glass were statistically equal to but different statistically from Dyract AP.  The figures for Z-100 and Z-250 were not statistically different, but the strength of Z-250 was statistically different from Pyramid.

 

Introduction

 

New dental restorative materials have made great strides in recent years.1 The use of amalgam as a standard filling material has become more and more controversial.  Since Bowen's early studies (1962), the demands made on resin-based restorative materials have been considerable and fundamental changes have occurred in the matrix chemistry.1 In the last few years, hybrid resin-modified glass ionomer cement (RMGIC) restorative materials have been introduced.  The RMGICs have higher resistance than regular glass ionomer cement restorative materials to early moisture contact and desiccation and also have   improved mechanical properties.3  Another class of restorative materials, the polyacid modified resin composites, or compomers, were marketed in the early 1990s.3 Their mechanical properties were higher than those of glass-ionomer cement restorative materials but less than those of composites (Z-100).4

New filling materials, called ormocers, were developed in 1998.1 Ormocer is an abbreviation for organically modified ceramic.  Ormocers combine glass-like components with polymer components nearly as hard as glass and with similar characteristics as synthetic material.3 Ormocers are equipped with an inorganic SiO2 backbone to which polymerizable organic units are added.  This results in three dimensionally cured co-polymers with filler particles incorporated into the cross-linked inorganic  organic network.  No studies have been done regarding its physical and mechanical properties.  Flexural and tensile strengths are considered the most important mechanical properties of resin-based material.  The flexural strength test is considered to be sensitive to surface imperfections such as cracks, voids and related flaws which can influence the fracture strength of brittle materials.2 High flexural strength values reflect a limited tendency to crazing and high resistance to surface defects and erosion.5

Therefore, the aim of this study was to investigate the bi-axial flexural strength of these new materials (Admira and Definite) and compare it to composite resins and compomers.

 

Materials and Methods

  

The materials used in this study are listed in Table 1. These materials included two ormocers (Definite and Admira), three compomers (Composan Glass, Compoglass F, and Dyract AP) and three composites (Pyramid, Z-100, and Z-250).

Specimen preparation

Five disc shaped specimens (14 mm diameter x 2 mm thickness) were prepared for each material utilizing a silicone lubricated teflon mold.  The mold was placed on a transparent matrix strip supported by a glass microscope slide.  The mold was overfilled with material.  The mold and material were covered with another matrix strip and a glass microscope slide.  Light pressure was applied until the upper matrix strip and slide came into contact with the mold to expel excess material and avoid air entrapment.  The material was light cured in four quadrants from each opposing surface to ensure adequate polymerization of the material.  All eight curing times were for the duration recommended by the manufacturers.  The specimens were removed from the molds without any flexing and stored in distilled water at 37oC for 24 hours.  Particular care was taken to ensure that the discs were flat to avoid uneven loading during subsequent testing.

Measurement procedure

Each specimen was placed on a circular 10 mm knife-edge support and loaded centrally at a rate of 0.2 mm/min with a 1mm diameter steel piston in an Instron Universal testing machine. The specimens were tested to failure and the maximum load was recorded by the Instron software.  The bi-axial flexural strength of each disc was calculated according to the equation:6,7

                                    P                                                                a

smax =    ----------   (1+v)[0.485 ln (------) +0.52]+0.48                     

                                    h2                                                h

            smax  = The maximum flexural strength

            P          = The measured load at fracture

            a          = The radius of the knife-edge support

            h          = The specimen thickness

            v          = The poisson's ratio for all the materials                       (0.25)8

 

Results

 

The mean bi-axial flexural strength values and standard deviation of the tested materials are listed in Table 2 in order of increasing stress and depicted graphically in Fig. 1.  Definite was the weakest and had the lowest mean strength (160.63 + 28.73 MPa).  The material that had the highest mean strength value was Compoglass F (291.93 + 19.98 MPa).  As seen in Table 2, One-way Analysis of variance (ANOVA) and a Student  Newman  Keuls multiple comparison test revealed that there was no significant difference between Definite (160.63 MPa) and Admira (201.53 MPa).  Z-100 (234.10 MPa) and Z-250 (259.00 MPa) were statistically equal but differed from Pyramid (198.87 MPa).  There was no difference between Composan Glass (275.33 MPa) and Compoglass F (291.93 MPA) although they were significantly different from Dyract AP (175.63 MPa).  Definite, Dyract AP, Pyramid, and Admira were statistically equal.  Z-100, Z-250, Composan Glass, and Compoglass F were also statistically equal.

The mean bi-axial flexural strength values and standard deviation of the tested materials are listed in Table 2 in order of increasing stress and depicted graphically in Fig. 1.  Definite was the weakest and had the lowest mean strength (160.63 + 28.73 MPa).  The material that had the highest mean strength value was Compoglass F (291.93 + 19.98 MPa).  As seen in Table 2, One-way Analysis of variance (ANOVA) and a Student  Newman  Keuls multiple comparison test revealed that there was no significant difference between Definite (160.63 MPa) and Admira (201.53 MPa).  Z-100 (234.10 MPa) and Z-250 (259.00 MPa) were statistically equal but differed from Pyramid (198.87 MPa).  There was no difference between Composan Glass (275.33 MPa) and Compoglass F (291.93 MPA) although they were significantly different from Dyract AP (175.63 MPa).  Definite, Dyract AP, Pyramid, and Admira were statistically equal.  Z-100, Z-250, Composan Glass, and Compoglass F were also statistically equal.

 

Discussion

 

Bi-axial flexural strength is considered one of the significant parameters to characterize the bulk of a material.9 It usually involves supporting a disc shaped specimen on either a ring with a knife-edge or on three or more points near the periphery and equidistant from the center of the disc.  The central portion is then loaded such that maximum stress occurs at the center of the lower face of the disc.  The results obtained are independent of the condition of the edge of the specimen disc.3

The bi-axial flexural test has been used frequently in many studies where different formulas7-10 have been used to determine the flexural stress.  Timoshenko's formula,6 the basis for many studies2,7,10 was used here. From the results of this study, the materials tested can be ranked as follows: The compomer group (Compoglass F and Composan Glass) had the highest flexural strength values and it was close to the composite group (Z-100, Z-250) but different from Dyract AP.  This may be related to filler content as noted in Table 1.  This result was in agreement with El-Kalla and Godoy4 who reported that the flexural strength of Dyract was less than for Z-100.  Pyramid and Dyract AP were statistically equal (amount of filler was 75% by weight for both) suggesting that composites and compomers would behave similarly. 

Z-100 and Z-250 are representative of hybrid composites known to be the most universal composites and having superior strength characteristics.11 While Z-100 has been used in many studies as a control or reference composite material,4,11 Z-250 has little, if any, published studies regarding its properties.  The results of this study showed that the flexural strength of Z-250 was not significantly higher than Z-100.  Z-250 had a significantly higher flexural strength than Pyramid.  This difference may be related to the filler type or the resin (Bis-GMA, TEGDMA)12 since filler weight % was close to Z-100.  The manufacturer has claimed that changes were made to the resin matrix for Z-250.  Pyramid is a highly filled packable composite with a unique resin.  According to this study, its strength was the lowest among the composite group.

Although the flexural strength of materials in the ormocer group (Admira, Definite) were statistically similar, Admira was lower in flexural strength than Composan Glass and Compoglass F and Definite was lower in flexural strength than the composite materials (Z-100, Z-250) and the compomer materials (Composan Glass, and Compoglass F).  This difference may be related to the filler characteristics or the resin13 since the inorganic filler content is similar (Table 1).  The ormocer group can be ranked between the composite and compomer groups. The newly developed ormocer restorative materials have desirable flexural strength properties, especially Admira.  However, further research is indicated to gain a clearer picture of other properties.  For clinical success, the dentist should know the properties of the materials, choose accordingly, and manipulate them properly.

 

Conclusions

 

1.         The Ormocer materials were not significantly different in flexural strength.

2.         Compoglass F and Composan Glass are the hardest, are statistically equal, and different from Dyract AP in flexural strength.

3.         The figures for Z-100 and Z-250 are statistically equal, and Z-250 differs statistically from           Pyramid.

4.         The Ormocer material can be ranked between the compomer group and the composite       group.

 

Acknowledgement

 

The author wishes to express her sincere appreciation to Dr. Ahmed El-Hejazi and Dr. Nazeer Khan for their advice and assistance with the manuscript.  Special thanks to Prof. Abdullah R. Al-Shammery for his cooperation and usual support.  This research (NF 1774) is registered with the College of Dentistry (CDRC), King Saud University.

 

References

 

  1. Degussa Dental Research. Technical manual,  September 1998.
  2. El Hejazi AA. Bi-axial tensile strength for glass- ionomer cement. Cairo Dental Journal 2000; 4:275-  277.
  3. Van Dijken Jan WV.  Longevity of new hybrid restorative materials in class III cavities.  Eur J OralSci 1999; 107: 215-219.
  4. El-Kalla IH, Godoy FG.  Mechanical properties ofcompomer restorative materials. Operative Dentistry 1999; 24:2-8.
  5. Combe EC, Shaglouf A-MS, Watts DC.  Mechanical properties of direct core build-upmaterials.  Dental Materials1999; 15:158-165.
  6. Timoshenko S, Woinowsky-Krieger S.  Symmetrical bending of circular plates.  Theory of plates and shells; New York:  McGraw-Hill.Second Edition, chap. 3, pp  87-121, 1959.
  7. Fleming GJP, Shaini FJ, Marquis PM.  An  assessment of the influence of mixing induced  variability on the biaxial flexure strength  of dentineporcelain discs and the implication for laboratory  testing of porcelain specimens. Dental Materials  2000; 16:114-119.
  8. Frankel N, Pearson GJ, Labella R. Long-term  strength of aesthetic restoratives.  Journal of Oral Rehabilitation 1999; 25:89-93.
  9. Cattani-Lorente MA, Dupuis V, Payan J, Moya F, Meyer JM.  Effect of water on the physical properties of resin-modified  glass ionomer cements.  DentalMaterials 1999; 15:71-78.
  10. Khouw-Liu VHW, Anstice HM, Pearson GJ.  An in vitro investigation of a poly (vinyl phosphonic acid)based  cement with four conventional glass-ionomer cements. Part I: Flexural strength and fluoride release.  Journal of Dentistry 1999; 27:351-357.
  11. Willems G, Lambrechts P, Braem M, Celes JP,  Vanherle G.  A classification of dental composites according to their  morphological and mechanicalcharacteristics.  Dental Materials 1992; 8:310-319.
  12. Yap W, Teoh SH, Tan KB. Influence of water  exposure on three-body wear of compositerestoratives. J Biomed Mater Res 2000; 53:547-553.
  13. Park C, Robertson RE.  Mechanical properties ofresin composites with filler particles aligned by an  electric filed. Dental Materials  1998; 14:385-393.

 

Tables

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2002-1-09

 
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