ABSTRACT
Astracts Objective: Studies have focused on use of non-expired composites. Unfortunately some clinicians still use expired composite resins without considering their effects. The objective of this in vitro preliminary research was to investigate cytotoxicity of expired(6-months) and non-expired composite resins. Materials and methods: Expired (E) and non-expired (NE) samples of one bulk-fill (Tetric N-Ceram Bulk-fill (TNB), Ivoclar Vivadent), two nano-hybrid (Tetric N-Ceram (TN), Ivoclar Vivadent; Clearfil Majesty ES-2 (CM), Kuraray) composite resins were tested on L929 fibroblast cells. Medium covering cells was removed then plastic rings (2-mm height) were filled with non-polymerized composite resins, placed in direct contact with cells and polymerized with LED light curing unit (LCU). Three samples were prepared for each group. After polymerization, removed medium was added to the cells. Cells that were left without medium (WOM) and cells that were exposed to LCU were used as positive control groups. Cells without any treatment were used as negative control group (C). Cells were incubated with tested materials for 7-days to evaluate cytotoxicity. Cell viability was calculated by sulforhodamine B test as a percentage (%). One-way ANOVA and post-hoc Tukey tests were used for statistical analyses (p0.05), except between TN NE and TN E (p0.05). All experimental groups compared with C group showed statistically significant cytotoxicity (p<0.05). A statistically significant difference existed between LCU and C groups (p<0.05). Conclusions: In clinical practice, expired composite resins should never be used. Although a correlation was found between expiration dates of nano-hybrid composite resins and cell viability, opposite data were obtained for bulk- fill composite resin. Researches are still required to evaluate biocompatibility of bulk- fill composite resins at various thicknesses with current LCUs.
Resumen Objetivo: Los estudios se han concentrado en el uso de resinas compuestas no vencidos. Desafortunadamente, algunos clínicos aún usan resinas caducadas sin considerar sus efectos. El objetivo de este estudio preliminar in vitro fue investigar la citotoxicidad de resinas compuestas caducadas (6 meses) y no caducadas. Materiales y métodos: muestras caducadas (E) y no caducadas (NE) de una resina bulk-fill (Tetric N-Ceram Bulk-fill (TNB), Ivoclar Vivadent) y dos resinas nanohíbridas (Tetric N-Ceram (TN) Ivoclar Vivadent) (Clearfil Majesty ES-2 (CM), Kuraray), se probaron en células de fibroblastos L929. Se retiraron las células que cubrían el medio, luego se llenaron anillos de plástico (2 mm de altura) con resinas no polimerizadas, se colocaron en contacto directo con las células y se polimerizaron con una unidad de fotocurado LED (LCU). Se prepararon tres muestras para cada grupo. Después de la polimerización, se añadió el medio eliminado a las células. Las células que quedaron sin medio (WOM) y las células que se expusieron a LCU se usaron como grupos de control positivo. Las células sin ningún tratamiento se utilizaron como grupo de control negativo (C). Las células se incubaron con las resinas durante 7 días para evaluar la citotoxicidad. La viabilidad celular se calculó mediante la prueba de sulforodamina B como un porcentaje (%). ANOVA unidireccional y pruebas post-hoc de Tukey se utilizaron para los análisis estadísticos (p 0.05), excepto entre TN NE y TN E (p 0.05). Todos los grupos experimentales en comparación con el grupo C mostraron citotoxicidad estadísticamente significativa (p <0,05). Existió una diferencia estadísticamente significativa entre LCU y grupos C (p <0.05). Conclusiones: En la práctica clínica, las resinas compuestas caducadas nunca deben usarse. Aunque se encontró una correlación entre las fechas de vencimiento de las resinas compuestas nano-híbridas y la viabilidad celular, se obtuvieron datos opuestos para la resina bulk-fill. Se requieren nuevas investigaciones para evaluar la biocompatibilidad de las resinas bulk-fill en distintos espesores con las LCU actuales.
Subject(s)
Composite Resins/toxicity , Date of Validity of Products , In Vitro TechniquesABSTRACT
Abstract Gap formation of composite resin restorations is a serious shortcoming in clinical practice. Polymerization shrinkage stress exceeds the tooth-restoration bond strength, and it causes bacterial infiltration within gaps between cavity walls and the restorative material. Thus, an intermediate liner application with a low elastic modulus has been advised to minimize polymerization shrinkage as well as gap formation. Objective: The purpose of this in vitro study was to assess gap formation volume in premolars restored with different bulk-fill composites, with and without a resin-modified glass-ionomer cement (RMGIC) liner, using x-ray micro-computed tomography (micro-CT). Methodology: Sixty extracted human maxillary premolars were divided into six groups according to bucco-palatal dimensions (n=10). Standardized Class II mesio-occluso-distal cavities were prepared. G-Premio Bond (GC Corp., Japan) was applied in the selective-etch mode. Teeth were restored with high-viscosity (Filtek Bulk Fill, 3M ESPE, USA)-FB, sonic-activated (SonicFill 2, Kerr, USA)-SF and low viscosity (Estelite Bulk Fill Flow, Tokuyama, Japan)-EB bulk-fill composites, with and without a liner (Ionoseal, Voco GmbH, Germany)-L. The specimens were subjected to 10,000 thermocycles (5-55°C) and 50,000 simulated chewing cycles (100 N). Gap formation based on the volume of black spaces at the tooth-restoration interface was quantified in mm3 using micro-computed tomography (SkyScan, Belgium), and analyses were performed. Data were analyzed using repeated-measures ANOVA and the Bonferroni correction test (p < 0.05). Results: The gap volume of all tested bulk-fill composites demonstrated that Group SF (1.581±0.773) had significantly higher values than Group EB (0.717±0.679). Regarding the use of a liner, a significant reduction in gap formation volume was observed only in Group SFL (0.927±0.630) compared with Group SF (1.581±0.773). Conclusion: It can be concluded that different types of bulk-fill composite resins affected gap formation volume. Low-viscosity bulk-fill composites exhibited better adaptation to cavity walls and less gap formation than did sonic-activated bulk-fill composites. The use of an RMGIC liner produced a significant reduction in gap formation volume for sonic-activated bulk-fill composites.
Subject(s)
Humans , Composite Resins/chemistry , Imaging, Three-Dimensional/methods , Dental Cavity Preparation/methods , Dental Materials/chemistry , Dental Restoration, Permanent/methods , Polymerization , In Vitro Techniques , Materials Testing , Resin Cements , Dental Stress Analysis , X-Ray MicrotomographyABSTRACT
SUMMARY: Paramolar tubercle (PT) is an additional cusp occuring on buccal surface of both upper and lower permanent molars. PT is also known as parastyle when tubercle is present in upper molars, as protostylid when tubercle is present in lower molars. The aim of this study was to evaluate prevalence of PTs in Turkish population with cone beam computed tomography (CBCT). Presence of PT in molar teeth were evaluated retrospectively using CBCT images of 210 patients (102 male, 108 female) between 18-77 years old. A total of 909 teeth were analyzed. Because of various reasons some teeth were excluded and final analyze was done with 653 teeth. Prevalence of PT was found as 2.76 % (18 out of 653). Highest frequency of PT was detected 5 in #27, 4 in #17, 2 in #48 among all molar teeth respectively. In two cases; 2 PTs were on the same tooth, bilateral PT was found only in one case. PT was undetected on upper first molars. Prevalence of PTs on permanent molars is a rare phenomenon in the studied population. Use of CBCT in such anatomic variations will provide valuable and detailed information during treatment modalities. Since this pilot study represents Turkish subpopulation, comprehensive studies with increased number of cases should be undertaken to clarify the prevalence of paramolars in Turkish population. Advanced imaging techniques like CBCT will be more helpful in understanding and detecting exact morphological and anatomical variations of PTs during treatment modalities.
RESUMEN: El tubérculo paramolar (TP) es una cúspide adicional que está en la superficie vestibular de los molares permanentes superiores e inferiores. El objetivo de este estudio fue evaluar la predisposición de TP en la población turca con tomografía computarizada de haz cónico (TCHC). Presencia de TP en dientes molares se evaluaron retrospectivamente utilizando imágenes de tomografia de 210 pacientes (102 hombres, 108 mujeres) entre 18-77 años de edad. Se analizó un total de 909 dientes. Por varias razones, algunos dientes fueron excluídos y el análisis final se realizó con 653 dientes. Prevalencia de PTP se encontró en el 2,76 % (18 dientes de 653). La frecuencia más alta de TP se detectó: 5 en # 27, 4 en # 17, 2 en # 48, entre todos los dientes molares, respectivamente. En dos casos, 2 de los TP fueron observados en el mismo diente; TP bilateral sólo se encontró en un caso. El TP no fue detectado en los primeros molares superiores. La prevalencia de TP en los molares permanentes es un fenómeno poco frecuente en la población estudiada. El uso de la TCHC en tales variaciones anatómicas, proporcionará información valiosa y detallada para definir la aplicación de diferentes modalidades de tratamiento. Dado que este estudio piloto representa a una subpoblación turca, estudios exhaustivos con un mayor número de casos deben llevarse a cabo para determinar la prevalencia en la población turca total. Técnicas avanzadas de imagen como TCHC serán más útiles para detectar variaciones morfológicas y anatómicas exactas de TP durante diversas modalidades de tratamiento.