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. 2022 Jan 18;17(1):e0262582. doi: 10.1371/journal.pone.0262582

The effects of provisional resin cements on the color and retentive strength of all-ceramic restorations cemented on customized zirconia abutments

Seyede Mina Salehi Dehno 1, Rashin Giti 1,*, Mohammad Hassan Kalantari 1, Farhad Mohammadi 2
Editor: Antonio Riveiro Rodríguez3
PMCID: PMC8765607  PMID: 35041706

Abstract

This study aimed to evaluate the effects of two types of provisional resin cements on the color and retentive strength of two different all-ceramic restorations cemented onto customized zirconia abutments. Forty-two crowns were made of monolithic zirconia and lithium disilicate ceramics (n = 21 per group) and cemented on customized zirconia abutments by using two provisional resin cements of TempBond Clear and Implantlink Semi, and TempBond serving as the control (n = 7 per cement subgroup). The specimens’ color was measured before and after cementation and after thermocycling. The color difference was calculated by using CIEDE2000 formula (ΔE00). The tensile force was applied to assess the retentive strength. Kruskal-Wallis, Dunn’s post-hoc, and Mann-Whitney non-parametric tests were used to compare ΔE00(1) and ΔE00(2) and two-way ANOVA followed by one-way ANOVA and Tukey’s HSD post hoc test and T-test were used to compare retentive strength between subgroups. In the lithium disilicate group, ΔE00 of the control subgroup (TempBond) was significantly higher than that of Implantlink Semi cements subgroup (P = 0.001). But, in the monolithic zirconia group, ΔE00 of the control subgroup (TempBond) was significantly higher than that of Implantlink Semi (P = 0.020) and TempBond Clear cements (P = 0.007). In the monolithic zirconia group, the control subgroup (TempBond) was significantly more retentive than TempBond Clear (P = 0.003) and Implantlink Semi cement (P = 0.001). However, in the lithium disilicate group, Implantlink Semi cement was significantly more retentive than TempBond Clear (P = 0.019) and TempBond (control) (P = 0.001). The final color of both restorations was significantly affected by the provisional resin cement type. The retentive strength was influenced by both the type of cement and ceramic.

Introduction

An implant is a durable and successful option for esthetic reconstruction and function of the missing teeth [1]. They are attached to the abutments with either screws or cements. The clinical success of cement-retained restorations mainly depends on the retention [2], which is affected by many factors like the geometry of abutment preparation, taper, abutment height, surface area and roughness, luting agent [3], as well as the abutment and coping material. While zirconia copings are said to have higher mean retention than metal copings [4], evidence has shown that the abutment material does not affect the copings dislodgement resistance, regardless of the type of cement [5].

The cement type considerably affects the retention of restorations. Specially-formulated cements have been introduced for the cementation of implant-supported prostheses. New provisional resin cements are reported to be more retentive than the zinc oxide-eugenol and non-eugenol cements while precluding the drawbacks [6, 7]. Another study documented that non-eugenol temporary resin cement had significantly higher tensile strength than the non-eugenol zinc oxide cement and resin-based acrylic urethane cement [8].

New ceramic materials like yttrium-stabilized zirconium oxide polycrystal are popular for their premium mechanical properties and tooth-like color [9]. The final color of restorations is affected by numerous factors such as the material and color of the substrate, cement, thickness and shade of zirconia coping and veneering ceramic, and laboratory process [10]. Capa et al. asserted polycarboxylate cement to be better than resin cement for cementation of zirconia restorations on titanium abutments [11]. Another study reported that the resin cement caused the most unacceptable changes in color and translucency of monolithic zirconia [12].

Although new provisional resin cements are claimed to have better properties than their conventional counterparts [7], limited information is available about their effect on the final color and retentive strength of implant-supported ceramic restorations. Given the lack of studies on the effects of specific types of provisional resin cements on the retentive strength and final color of aged implant-supported all-ceramic restorations, the present study aimed to assess the effect of TempBond Clear and Implantlink Semi provisional resin cements used to attach the crowns onto customized zirconia abutments on the retentive strength and final color of implant-supported all-ceramic restorations before and after aging.

The null hypothesis was that the type of provisional resin cement and type of ceramic restoration would not affect the final color and retentive strength of implant-supported all-ceramic restorations.

Materials and methods

Fabrication of customized zirconia abutments

This experimental in-vitro study involved 6 maxillary right central incisor customized zirconia abutments (ZrGEN; AnyOne; model: AAOIPR4525; Megagen, South Korea). Six implant laboratory analogs (Lab Analog; Blue color; Megagen, South Korea) were embedded in autopolymerizing acrylic resin blocks (Acropars Re; Marlic; Iran) by using a dental surveyor (Marathon-103; Saeyang; Korea).

A single ceramic superstructure was computer-aided designed ([CAD], CAD design software; 3shape, Denmark) and milled out of high translucency zirconia blanks in A2 shade by using a laboratory milling machine (Cori Tec 340i; Imes-Icore GmbH, Germany) with 6-mm axial wall height, 11-degree axial taper, 1-mm deep shoulder finishing line, and 2-plane reduction of labial surface (Fig 1).

Fig 1. Milled customized zirconia abutment superstructure.

Fig 1

A: buccal surface, B: proximal surface, C: lingual surface. The bonding surface of the titanium implant insert (ZrGEN; AnyOne; model: AAOIPR4525; Megagen, South Korea) was abraded with 50-μm aluminum oxide particles at a 10-mm distance for 10 seconds (0.4 MPa). The inner surface of zirconia abutment superstructures was also subjected to airborne particle abrasion with 30-μm silica-coated aluminum oxide (Rocatec Soft; 3M ESPE, USA).

Titanium inserts were screwed to the implant analogs and tightened to 35 Ncm torque by a manual torque wrench (Megagen, South Korea). The superstructures were bonded to titanium inserts by using dual-cure self-adhesive resin cement (RelyXTM U200; 3M ESPE, USA) according to the manufacturer’s instructions. The six abutments were used for 60 crowns and cleaned between each run. Removal of the temporary cement consisted of gross removal with explorer, ultrasonic bath with 70% ethanol for 15 minutes, and application of 37% phosphoric acid for 30 seconds for complete removal of the cement remnants. The specimens were then rinsed and dried.

Fabrication of all-ceramic crowns

A full contour right maxillary central incisor crown with a projection on its incisal edge was designed by using CAD software. A 2-mm (diameter) hole was considered in the middle of this projection to attach the crowns to the universal testing machine (Fig 2). The crowns were designed in standard dimensions, 40-μm cement space, and an average 1-mm thickness in the mid-third of the labial surface, where color measurement was done.

Fig 2. A full contour right maxillary central incisor crown with a projection on its incisal edge.

Fig 2

A: buccal surface, B: proximal surface, C: lingual surface. Forty-two ceramic crowns (n = 21 per group) were fabricated with either ultrahigh-translucent monolithic zirconia in A2 shade (ZIRAE; SHT Preshaded Zirconia Block, Nanjing Zirae Advanced Material Co, China) by using a laboratory milling machine (Cori Tec 340i; Imes-Icore GmbH, Germany) or high-translucent lithium disilicate ceramic in A2 shade (IPS e.max Press; Ivoclar Vivadent, Germany). For making lithium disilicate crowns, wax patterns were prepared by a 3D printer (Solidscape D76+; Solidscape, USA) based on the previously CAD-designed shape and dimensions. The wax patterns were sprued, invested, burned out; and lithium disilicate was pressed into the burned-out molds.

The crowns were all sandblasted with 50-μm aluminum oxide particles from a 10-mm distance for 10 seconds, steam-cleaned, and dried with oil-free water. The abutments received no surface treatment and were only steam-cleaned and dried with oil-free air before cementation.

Color measurement and cementation

Having seated the crowns on the abutments, the shade was measured at the mid-third of the crowns by using a spectrophotometer (VITA Easyshade; VITA Zahnfabrik, Germany) on a 3-mm area. The device was calibrated according to the manufacturer’s instruction before each use. To replicate the conditions of spectrophotometry for all specimens and preclude any external light, a silicone putty material (Speedex; Coltène, Switzerland) was molded to the spectrophotometer [13]. Shade parameters (L, a, b) were measured 3 times and the mean value was recorded. The spectrophotometer output was accorded to a 2-degree standard observer and D65 illuminant.

The crowns made with each ceramic system were randomly divided into 3 subgroups (n = 7) to be cemented with provisional dual-cure resin cements of Implantlink Semi (Semipermanent Implant Cement; DETAX, Germany) and Temp-Bond Clear (Temporary crown and bridge cement; Kerr corporation, Italy); while TempBond (TempBond; Kerr, Italy) served as the control (Table 1). The screw access hole of the customized zirconia superstructure was filled with cotton and composite resin and cemented according to the manufacturer’s instructions. To cement with Temp-Bond Clear and Implantlink Semi, the automix tip was placed onto the syringe, the abutment surface and the internal surface of restoration was completely dried, and a thin layer of the mixed cement was applied to the internal surface of the restoration. The crowns were seated on the abutments with firm finger pressure for 10 seconds and subjected to a controlled axial load of 20-N for 10 minutes. It was different from ADA specification #96 (5-kg load) since ceramic fracture along the margin of the implant abutments was reported in pilot studies when loaded with weight greater than 2 kg [14]. The excess cement was removed by a scaler after the initial setting. For the cementation with TempBond (control), after drying the abutment and the internal surface of the restorations, equal lengths of base and accelerator were extruded onto the mixing pad. The paste was thoroughly mixed for approximately 30 seconds and a thin layer of the mixed cement was applied to the internal surfaces of the restoration. The restoration was firmly seated on the abutment. After the material set, the excess material was removed with a scaler and the color was re-measured after final setting of the luting agent. The color measurements were all performed by a single skilled operator blinded to the subgroups. After assessing color and measuring dislodgment force for each crown, the abutment was cleaned and the next crown was cemented.

Table 1. Type, manufacturer, composition (%) and LOT number of the cements.

Cement Cement type Manufacturer Compositions LOT number
TempBond Zinc oxide eugenol Kerr TEMP-BOND NE BASE: zinc oxide (60–100%), White mineral oil (petroleum) (5–10%), 6987471
Temp-Bond Accelerator: Eugenol (30–60%)
Temp-Bond Clear Dual curable temporary resin cement Kerr Dibutyl phthalate (5–10%), 7326030
Hydroxyethyl methacrylate (5–10%), Fumed silica (1–5%),
N-(2-Pyridyl) thiourea (1–5%),
Ethyldimethylaminobenzoate
(0.5–1.5%), Triclosan (0.5–1.5%).
Implantlink Semi Resin-based temporary luting cement DETAX aliphatic urethane acrylate(10 - < 15%), 1-benzyl-5-phenyl-hexahydropyrimidine-2,4,-6-trione(5 - < 10%), 1,6-hexanediol dimethacrylate(5 - < 10%), 2-hydroxyethyl methacrylate(< 1%), triclosan; 2,4,4’-trichloro-2’-hydroxy-diphenyl-ether; 5-chloro-2-(2,4-dichlorophenoxy)phenol(< 1%), 2-Ethylhexyl 4-(dimethylamino)benzoate(< 1%). 220804

Aging process

The specimens were stored at 37°C in 100% humidity for 24 hours and then subjected to 5000 thermal cycles [2] between 5° and 55° with a dwell time of 10 seconds (TC-300; Vafaei Industrial, Tehran, Iran). The color was, then, re-measured to check the effect of aging on the cement color.

The color difference was calculated by using the CIEDE2000 formula [15]:

ΔE00*=(ΔLkLSL)2+(ΔCkCSC)2+(ΔHkHSH)2+RTΔCkCSCΔHkHSH

The pre- and post-cementation color difference was called ΔE00(1) and the post-cementation and post-aging color difference was defined as ΔE00(2).

The perceptibility threshold was set at ΔE00≤1.30 and the clinical acceptability threshold was set at ΔE00>2.25 [15].

Pull-out test

The specimens were attached to the universal testing machine (Zwick/Roell Z020, Ulm, Germany) and subjected to a tensile force at a crosshead speed of 5 mm/min [16]. The retentive force causing the detachment of specimens was recorded in Newton. The pull-out tests were done by the same blinded operator. The specimens were examined by using a light microscope and their failure mode was classified as an adhesive (complete separation of the cement from the abutment or the crown), cohesive (failure within the cement), and mixed (a combination of adhesive and cohesive). Fracture of the crowns or abutments was also assessed.

Statistical analysis

The data were analyzed by using SPSS software (IBM SPSS Statistics for Windows, v22.0; IBM Corp., IL, USA). Normal distribution was tested with the Kolmogorov-Smirnov test (P<0.05 indicates lack of normality). Kruskal-Wallis, Dunn’s post-hoc, and Mann-Whitney non-parametric tests were used to compare ΔE00(1) and ΔE00(2) among the study groups and subgroups, because the data for these two variables (ΔE00(1) and ΔE00(2)) were not normal. After the normality test showed that the data for retentive strength was normal, the mean retentive strength was analyzed with two-way ANOVA followed by one-way ANOVA and Tukey’s HSD post hoc test to determine statistically significant differences among the three employed cements. T-test was used to compare the retention of ceramic crowns as a function of the type of cement. To consider the effect of inflated type 1 error through Bonferroni correction, the P value obtained by Mann-Whitney U or T test was multiplied by 3 (number of comparisons). P<0.05 was considered to be statistically significant in all tests.

Results

Color change (ΔE00)

Kruskal-Wallis test revealed that unlike ΔE00(2), ΔE00(1) was significantly different among the types of cement with both monolithic zirconia (P = 0.004) and lithium disilicate ceramic crowns (P = 0.002) (Table 2, Fig 3). Pairwise comparison of the cements through Dunn’s post-hoc test revealed that in monolithic zirconia crowns, the mean ΔE00(1) in TempBond was significantly higher than that in Temp-Bond Clear (P = 0.007) and Implantlink Semi cement (P = 0.020). Similarly, in lithium disilicate ceramic crowns, TempBond had a significantly higher mean ΔE00(1) than Implantlink Semi cement (P<0.001) (Table 2).

Table 2. Mean±SD and median [minimum, maximum] of ΔE00(1) and ΔE00(2) and the results of Kruskal-Wallis H test and Dunn’s post-hoc test comparisons of the cements.

Type of restoration ΔE00 Type of cement P value
TempBond Temp-Bond Clear Implantlink Semi
Monolithic Zirconia ΔE00(1) 3.57±0.19 2.12±0.35 2.41±0.15 0.004
3.50 [3.10,4.60] 2.10[0.8,3.60] 2.20[1.90,2.90]
P Value 0.007ac© 0.999ab© 0.020bc©
ΔE00(2) 0.83±0.18 0.93±0.35 1.13±0.21 0.509
0.80[0.20,1.40] 0.50[0.2,2.5] 1.10[0.30,2.0]
P value --- ---- ---
Lithium disilicate ΔE00(1) 4.91±0.66 2.08±0.54 0.78±0.18 0.002
4.3[2.90,7.40] 2.30[0.30,4.10] 0.70[0.20,1.70]
P value 0.067ac© 0.635ab© 0.001bc©
ΔE00(2) 1.11±0.35 1.46±0.46 1.40±0.31 0.735
0.70[0.2,2.50] 1.0[0.30,3.30] 1.5[0.30,2.40]
P value ----- ------ ------

ab: Temp-Bond Clear vs. Implantlink Semi

ac: Temp-Bond Clear vs. TempBond

bc: Implantlink Semi vs. TempBond

¶: Results Of Kruskal-Wallis H test

©: Results of Dunn’s post-hoc test comparisons of the cements

Fig 3. Mean and standard deviation of ΔE00(1) and ΔE00(2).

Fig 3

Mann-Whitney test compared the mean ΔE00(1) and ΔE00(2) among the cement groups as a function of the type of ceramic crown. Accordingly, only in presence of Implantlink Semi cement, ΔE00(1) of monolithic zirconia was significantly higher than that of the lithium disilicate ceramic (P = 0.003). Yet, ΔE00(2) was not significantly different between the two ceramics with any of the employed cements (Table 3).

Table 3. Results of Mann-Whitney test for ΔE00 differences between ceramic restorations in each temporary cement.

Cement ΔE00 Ceramic P value
TempBond ΔE00(1) Monolithic zirconia 0.777
Lithium disilicate
ΔE00(2) Monolithic zirconia >0.999
Lithium disilicate
Temp-Bond Clear ΔE00(1) Monolithic zirconia >0.999
Lithium disilicate
ΔE00(2) Monolithic zirconia 0.627
Lithium disilicate
Implantlink Semi ΔE00(1) Monolithic zirconia 0.003
Lithium disilicate
ΔE00(2) Monolithic zirconia >0.999
Lithium disilicate

Retentive strength

Two-way ANOVA showed that the retentive strength was significantly influenced by both the type of ceramic crown (P = 0.018) and cement (P = 0.016). Interaction between the ceramic crown and cement type was also significant (P<0.001) (Table 4). Meanwhile, one-way ANOVA showed significant differences among the three cements in both monolithic zirconia (P = 0.001) and lithium disilicate (P = 0.002) ceramic restorations (Table 5).

Table 4. Two-way ANOVA results for retentive strength (N).

Type III Sum of Squares Df Mean square F Sig.
Type of ceramic 866.050 1 866.050 6.128 .018
Type of cements 1311.627 2 655.813 4.641 .016
Ceramic×cements 5888.943 2 2944.471 20.836 < .001

Table 5. Mean and standard deviation and pairwise comparison of retentive strength (N).

Ceramic Cement Mean SD P* Tukey’s HSD post hoc test P
Monolithic zirconia TempBond 28.20 6.75 0.001 TempBond vs. Temp-Bond Clear 0.003
Temp-Bond Clear 17.40 3.66 Temp-Bond Clear vs. Implantlink Semi 0.659
Implantlink Semi 11.69 8.00 Implantlink Semi vs. TempBond 0.001
Lithium disilicate TempBond 8.03 4.67 0.002 TempBond vs. Temp-Bond Clear 0.151
Temp-Bond Clear 24.30 12.77 Temp-Bond Clear vs. Implantlink Semi 0.019
Implantlink Semi 49.51 23.24 Implantlink Semi vs. TempBond 0.001

P*: results of one-way ANOVA

P: results of Tukey’s HSD post hoc test

Tukey’s HSD post hoc test showed that in the monolithic zirconia group, TempBond created significantly more retention than TempBond Clear (P = 0.003) and Implantlink Semi cement (P = 0.001). However, in the lithium disilicate ceramic group, the specimens cemented with Implantlink Semi cement were significantly more retentive than those cemented with TempBond Clear (P = 0.019) and TempBond (P = 0.001) (Table 5, Fig 4).

Fig 4. The mean and standard deviation of retentive strength of cements as a function of the type of restorations.

Fig 4

Concerning the effect of ceramic restoration, the mean retention was significantly different between the two ceramic types only when cemented with TempBond (P<0.001) and Implantlink Semi cement (P = 0.004); that is, the mean retentive strength of TempBond was significantly higher in monolithic zirconia restorations; while in lithium disilicate, Implantlink Semi was more retentive (Table 6).

Table 6. Comparing the mean retentive strength of ceramic crowns as a function of the type of cement.

Type of cement Type of restoration Mean SD P value
TempBond Monolithic zirconia 28.20 6.76 < .001
Lithium disilicate 8.03 4.67
Temp-Bond Clear Monolithic zirconia 14.70 3.67 0.098
Lithium disilicate 24.30 12.77
Implantlink Semi Monolithic zirconia 11.69 8.01 0.004
Lithium disilicate 49.51 23.24

Table 7 displays the pattern of cement distribution after the removal of cemented crowns. None of the crowns broke during applying dislodgment force; nor was any of the zirconia superstructures of the customized zirconia abutments separated from the titanium inserts.

Table 7. Frequency of mode of failure in different groups (%).

Type of cement/crown Adhesive (cement-abutment interface) Adhesive (cement-crown interface) Cohesive (within the cement) Mixed
TempBond / monolithic zirconia 0 0 0 100
Temp-Bond Clear / monolithic zirconia 0 100 0 0
Implantlink Semi / monolithic zirconia 20 80 0 0
TempBond / lithium disilicate 100 0 0 0
Temp-Bond Clear / lithium disilicate 50 30 0 20
Implantlink Semi / lithium disilicate 70 0 0 30

Discussion

The present findings rejected the null hypothesis since the type of provisional resin cement and ceramic restoration affected the final color of ceramic crowns and retentive strength of implant-supported all-ceramic restorations.

Luting cement and color (ΔE00(1))

This study showed that the provisional resin cement significantly improved the color match of monolithic zirconia and lithium disilicate ceramic restorations over the zirconia abutment by reducing the ΔE00(1) values compared with the control group. Considering the previously established clinical perceptibility and acceptability thresholds [15], the color change for the control group was clinically unacceptable (ΔE00>2.25) for both ceramic restorations, and also unacceptable for Implantlink Semi cement in the monolithic zirconia group (ΔE00>2.25).

The color of ceramic restorations is reported to be affected by the luting cement [12, 17, 18]; as Carrabba et al. [17] documented imperceptible color change only with the clear shade of resin cements in combination with the thickest CAD/CAM feldspathic ceramic (2 mm). Tabatabaian et al. [18] detected that zinc phosphate and TempBond cements caused unacceptable color changes on a zirconia framework; while, a glass ionomer and resin cement led to acceptable results. However, Malkondu et al. [12] found the lowest and highest ΔE in monolithic zirconia crowns cemented with resin-modified glass ionomer and zirconia crowns cemented with resin cement, respectively.

Although the provisional resin cement used in this study significantly improved the color match of both types of ceramic restorations, it was still clinically unacceptable for Implantlink Semi cement in monolithic zirconia group (ΔE00>2.25); but, using this cement with lithium disilicate resulted in a great color match (ΔE00<1.3). However, it should be noted that the final color of all-ceramic restorations might be unpredictable after the use of temporary cements, as reported by Liu et al. [19]. They also suggested that for a 1-mm-thick high or ultrahigh-translucent all-ceramic restoration, non-opaque or natural opaque shade cements can improve the color match before and after cementation more than the opaque cements did; however, it might be insufficient to make the final color clinically acceptable. The role of cement is even more imperative in more translucent ceramics restorations, where opaque cements create a lighter shade and transparent cements create a darker shade due to changes in L* values [20].

The effect of luting cement on the color of an all-ceramic restoration is in association with the thickness of the ceramic and cement, as well as the cement shade [13, 21]. Tabatabaian et al. [13] defined the minimum thickness of 1 mm for acceptable masking ability and a minimum thickness of 1.6 mm for the ideal masking ability of a zirconia ceramic on a black and white substrate. In addition, Vichi et al. [21] showed that differences in cement thickness (0.1 or 0.2 mm) slightly affected the final color of an all-ceramic crown. Since the current study used ceramic and cement in a single thickness (1.0 and 0.04 mm, respectively), no conclusion can be drawn regarding the ceramic and cement thicknesses.

The wide variety of color measurement methods restricts the comparison between studies. Tsiliagkou et al. [22] assessed the repeatability and accuracy of Easyshade (Vita), SpectroShade (MHT Optic Research), and ShadeVision (XRite) dental spectrophotometers and reported SpectroShade as the most accurate and reliable of the three color-matching devices. It was corroborated by Mehl et al.’s [23] and Khurana et al.’s [24] studies. However, Dozic et al. reported Easyshade (the one used in the present study) as the most reliable instrument of shade matching both in vitro and in vivo [25]. The difference among the studies can also be due to the employed color difference formulae. Although some researchers might still use the CIE 76 formula, CIEDE2000 is suggested as a more applicable and reliable formula in dentistry [26].

Aging and the final color (ΔE00(2))

The present study also assessed the effect of aging and thermocycling on the final color of all-ceramic restorations. Concerning the aging, although the post-aging ΔE00(2) did not increase as much as ΔE00(1), it was above the clinically perceptible threshold in lithium disilicate crowns cemented with Implantlink Semi and Temp-Bond Clear cements; indicating the mild influence of cement type on pre- and post-aging ΔE00, to be considered by the clinicians. Gürdal et al. [27] reported that the aging process increased the b* value. Gradual changes of camphorquinone towards yellow have also been reported [28, 29], as it is possible in the newly developed photoinitiator in the tested resin cements, which is yellow in color [27]. In the current study, increasing the number of cycles (5000 times between 5° and 55° with a dwell time of 10 seconds was applied) might have had resulted in more intense color changes. Mesbah et al. [30] noted an increase in ΔE in all cements by increasing the number of thermal cycles.

Retentive strength (N)

The present study also found that the type of cement and ceramic significantly influenced the retention. The mean retention strength decreased in the monolithic zirconia crowns as the cement changed from TempBond to Temp-Bond Clear and then to Implantlink Semi cement; whereas, quite the opposite trend occurred in the lithium disilicate ceramic crowns.

Sarfaraz et al. [8] cemented the metal copings on metal abutments by using three cements and observed that the retentive strength was the highest in non-eugenol temporary resin cement, followed by non-eugenol zinc oxide cement, and resin-based acrylic urethane cement, respectively. They concluded that non-eugenol temporary resin cement might be better for cementation of implant prosthesis due to its superior mechanical properties.

Manufacturers of some new provisional resin cements claim to have higher retentive strength [6]. It has been corroborated by some previous [7, 8] and the present study in the lithium disilicate ceramic group; although, some other research documented the opposite, even compared with other temporary cements [31]. However, resin-based provisional cement has certain advantages such as ease of retrievability with adequate strength and excess cement removal, and excellent marginal adaptability [32, 33].

As the manufacturers recommended avoiding the surface preparation on the abutments or intaglio surface of the crowns, the two currently-employed resin-based provisional cements used mechanical retention to adhere the crown to the abutment. Although the inner surface of both crown groups was sandblasted, they were not prepared on the abutments. Recent reports have shown that the bond strength of zirconium oxide ceramics could be improved only by airborne particle abrasion on the ceramic surface and the use of a composite resin cement containing an adhesive phosphate monomer [34, 35]. Nejatidanesh et al. [16] reported that silicoating improved the retentive strength of zirconia copings more than aluminum oxide airborne particle abrasion. The alloy primers cannot improve the bond of temporary resin cements since these cements lack 10-methacryloyloxydecyl dihydrogen phosphate, which exists in many resin cements like Panavia F [36].

Among the limitations of this study was the 0.04-mm cement space, which might have compromised the retentive properties of the resin‑based luting cements, as a higher film thickness would have compromised their physical properties. Moreover, using a constant removing force might have affected the results, since intraoral occlusal forces have a dynamic nature and not a monotonic static load; therefore, cement behavior might be different under fatigue loading rather than a static force load. Nor did the current study measure the retentive strength before aging. Further studies are recommended to assess the effect of aging and methods of surface treatment on the retentive strength of currently-studied resin-based temporary cements.

Conclusions

Within the limitations of this in-vitro study, it can be concluded that:

  1. In the monolithic zirconia crowns, the mean ΔE00(1) of TempBond (control) was higher than TempBond Clear and Implantlink Semi. Similarly, in the lithium disilicate ceramic group, ΔE00(1) of TempBond was higher than Implantlink Semi.

  2. The mean retentive strength in the monolithic zirconia group was the highest for TempBond (control), followed by TempBond Clear, and Implantlink Semi cement. However, for the lithium disilicate ceramic crowns, the mean retentive strength was the highest for Implantlink Semi cement, followed by TempBond Clear, and TempBond.

Supporting information

S1 Table. Raw data of ΔE00(1) and ΔE00(2).

(XLSX)

S2 Table. Raw data of retentive strength.

(XLSX)

Acknowledgments

This article was based on the postgraduate thesis by Dr. Seyede Mina Salehi Dehno. The authors would like to thank Dr. Vossoughi from the Dental Research Development Center of School of Dentistry for the statistical analyses and Miss Farzaneh Rasooli for proofreading, copyediting, and improving the use of English in this manuscript. Appreciations are also expressed to ArmanSalamat Dental laboratory and Mr. Abdi for the preparation of the laboratory specimens.

Data Availability

All relevant data are within the manuscript and its Supporting Information files.

Funding Statement

The Vice-Chancellry of Shiraz University of Medical Sciences for supporting this research (grant #21860). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Decision Letter 0

Antonio Riveiro Rodríguez

2 Nov 2021

PONE-D-21-30628The effects of provisional resin cements on the color and retentive strength of all-ceramic restorations cemented on customized zirconia abutmentsPLOS ONE

Dear Dr. Giti,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. Please, address all the comments made by the reviewers.

Please submit your revised manuscript by Dec 17 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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We look forward to receiving your revised manuscript.

Kind regards,

Antonio Riveiro Rodríguez, PhD

Academic Editor

PLOS ONE

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Reviewers' comments:

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Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

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2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: I Don't Know

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3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: No

Reviewer #2: Yes

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Reviewer #1: Yes

Reviewer #2: Yes

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5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This in vitro research assesses the effect of two different provisional resin cements (ie, TempBond Clear and Implantlink Semi) on the color and retentive strength of implant crowns manufactured from two different ceramics (ie, monolithic zirconia and lithium disilicate). Crowns cemented with conventional zinc oxide-eugenol cement (ie, TempBond) served as control.

The study is of interest to the scientific community. However, statistical analysis and reporting should comply with standards regarding the publication of results derived from material laboratory research. Therefore, the following issues should be corrected:

- TempBond is a conventional zinc oxide-eugenol cement and NOT a provisional resin cement. Only two different provisional resin cements (ie, TempBond Clear and Implantlink Semi) were used while TempBond served as control. Please make this clear throughout the whole manuscript.

- Which delivery option of TempBond was used (ie, automix syringe, tube delivery, or unidose)?

- What was your rationale for the low number of thermocycles (ie, 500)? The applied number of cycles corresponds to about 2.6 weeks clinical service (Gale and Darvell 1999).

- How did you define the required number of specimens? Was any sample size calculation performed?

- Were fabricated crowns randomly assigned to each treatment group?

- How many operators performed the experiments?

- Was the operator of the testing machine blinded regarding the treatment group?

- Please supply LOT numbers of all materials used and provide a table depicting each cements' composition (%).

- Please use uniform spelling/capitalization of all materials throughout the manuscript's main text and figures.

- Please provide the Weibull distribution parameters (Weibull modulus and characteristic strength) of the retentive strength.

- Were all data distributed normally? You only state that normal distribution was tested with Kolmogorov-Smirnov test. However, subsequently both non-parametric tests and parametric tests were used.

- Results from Mann–Whitney U test were not corrected for multiple testing.

Reviewer #2: This research is under the scope of this journal; the topic is relevant for readers, and this research deals with potentially significant knowledge to the field.

However, there are some concerns in the about the present manuscript:

Introduction

(Statement of Relevance) What is the importance of this study for the clinical? You do not think this study is included in the others already done? Which results are comparable? What this study has new?

Materials and Methods

This section would better communicate to readers if restructured. A flowchart or diagram of the experimental processing would be valuable.

How was the sample calculated? Did the authors perform a power analysis to evaluate if this sample size was appropriate?

When mentioning materials or devices: for some of them you don't mention the manufacturer at all, for some you mention only the manufacturer, for some the manufacturer and city, for some you mention the manufacturer and city/ country. Standarized these presentation.

Line 129 - What was the manufacturer's instruction at the time?

Please confirme the tensile force at a crosshead speed of 5 mm/min or 0.5 mm/min. Please read this article(https://doi.org/10.1007/s00784-020-03640-7) or https://doi.org/10.1590/S1678-77572009000600012.

Results

- Improve the resolution quality of all figures and graphs (and a presentation). The font/ language in the figure/caption is different from the text. Please, standardized the size and the font in the figures and charts with the font of the manuscript. 

Conclusions

The conclusion section should more thoroughly summarize the results, this section is too long and sometime too ambiguous.

**********

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Reviewer #1: No

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

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PLoS One. 2022 Jan 18;17(1):e0262582. doi: 10.1371/journal.pone.0262582.r002

Author response to Decision Letter 0


12 Nov 2021

Reviewer #1

1) TempBond is a conventional zinc oxide-eugenol cement and NOT a provisional resin cement. Only two different provisional resin cements (ie, TempBond Clear and Implantlink Semi) were used while TempBond served as control. Please make this clear throughout the whole manuscript.

Response: According to the reviewer's precise comment, the control group was clearly defined throughout the manuscript.

2) Which delivery option of TempBond was used (ie, automix syringe, tube delivery, or unidose)?

Response: The tube delivery of TempBond was used and completely described in the revised manuscript.

3) - What was your rationale for the low number of thermocycles (ie, 500)? The applied number of cycles corresponds to about 2.6 weeks clinical service (Gale and Darvell 1999).

Response: The number of thermal cycles was mistyped as 500 instead of 5000 cycles. It was corrected in the revised manuscript and respective citation was added.

4) - How did you define the required number of specimens? Was any sample size calculation performed?

Response: Although the sample size had not been statistically calculated, the tests resulted in significant p-values where the effect sizes were moderate to large, indicating that the sample size in each category was sufficient to interpret the results.

5) - Were fabricated crowns randomly assigned to each treatment group?

Response: yes, the fabricated crowns were randomly assigned to each cement group.

6) - How many operators performed the experiments?

Response: As mentioned in the revised manuscript, all color measurements and pull-out tests were performed by a single skilled operator.

7) - Was the operator of the testing machine blinded regarding the treatment group?

Response: Yes, the operator of the testing machine was blinded to the treatment groups.

8) - Please supply LOT numbers of all materials used and provide a table depicting each cements' composition (%).

Response: According to the reviewer's precise comment, a new table was added to mention the LOT number, type and manufacturer of all cements. However, since the composition of provisional resin cements (%) was not clearly reported by the manufacturers, such data could not be included in the table.

9) - Please use uniform spelling/capitalization of all materials throughout the manuscript's main text and figures.

Response: The spelling/capitalization was uniformly revised all over the text and figures.

10) - Please provide the Weibull distribution parameters (Weibull modulus and characteristic strength) of the retentive strength.

Response: The Weibull distribution parameters were not reported in the present study as in the preceding research.

11) - Were all data distributed normally? You only state that normal distribution was tested with Kolmogorov-Smirnov test. However, subsequently both non-parametric tests and parametric tests were used.

Response: In the statistical analysis section, it was stated that Kolmogorov-Smirnov test was used to test normality assumption. The two variables of ΔE00(1) and ΔE00(2) were not normally distributed; hence, non-parametric tests were used for the comparisons. Distribution of retentive strength was normal; thus, parametric tests were employed for the statistical comparisons. The revised manuscript clearly explains the tests used for each variable in.

- Results from Mann–Whitney U test were not corrected for multiple testing.

Response: The results of post-hoc tests (Dunn’s test for nonparametric and Tukey’s test for One-way ANOVA) were displayed in Tables 2 and 5 for each type of restoration. Moreover, the results of Mann-Whitney and t test (p-values) were adjusted based on the number of comparisons. Because the two ceramic restorations were separately compared in each cement (3 cements), the p-values were multiplied by 3 and reported in the revised tables.

Reviewer #2

Introduction

1)(Statement of Relevance) What is the importance of this study for the clinical? You do not think this study is included in the others already done? Which results are comparable? What this study has new?

Response: As mentioned in the Introduction section of the revised manuscript, limited information is available about the effect of provisional resin cements on the final color and retentive strength of implant-supported ceramic restorations. Nor has any study evaluated the effect of TempBond Clear and Implantlink Semi provisional resin cements on the retentive strength and final color of implant-supported all-ceramic restorations before and after thermocycling.

Materials and Methods

2)This section would better communicate to readers if restructured. A flowchart or diagram of the experimental processing would be valuable.

Response: The structure of Materials and Methods section was revised and divided into subsections with definite subheadings.

3)How was the sample calculated? Did the authors perform a power analysis to evaluate if this sample size was appropriate?

Response: Although the sample size had not been statistically calculated, the tests resulted in significant p-values where the effect sizes were moderate to large, indicating that the sample size in each category was sufficient to interpret the results.

4)When mentioning materials or devices: for some of them you don't mention the manufacturer at all, for some you mention only the manufacturer, for some the manufacturer and city, for some you mention the manufacturer and city/ country. Standardized this presentation.

Response: With respect to the reviewer's meticulous suggestion, the manufacturer's detail for each material was standardized as trade name, manufacturer, country.

5)Line 129 - What was the manufacturer's instruction at the time?

Response: The manufacturer's instruction for all the three cements was described in the revised manuscript

6)Please confirm the tensile force at a crosshead speed of 5 mm/min or 0.5 mm/min. Please read this article(https://doi.org/10.1007/s00784-020-03640-7) or https://doi.org/10.1590/S1678-77572009000600012.

Response: The tensile force was applied at a crosshead speed of 5 mm/min as mentioned in the manuscript and the respective reference was cited.

Results

7) Improve the resolution quality of all figures and graphs (and a presentation). The font/ language in the figure/caption is different from the text. Please, standardized the size and the font in the figures and charts with the font of the manuscript.

Response: The size and the font in the figures, charts, and body of the manuscript was standardized.

8)Conclusions

The conclusion section should more thoroughly summarize the results, this section is too long and sometime too ambiguous.

Response: The Conclusion section was thoroughly summarized in the revised manuscript.

Attachment

Submitted filename: Response to Reviewers.docx

Decision Letter 1

Antonio Riveiro Rodríguez

18 Nov 2021

PONE-D-21-30628R1The effects of provisional resin cements on the color and retentive strength of all-ceramic restorations cemented on customized zirconia abutmentsPLOS ONE

Dear Dr. Giti,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please, address all the comments made by the reviewers. As notice in the review reports, some of the issues given by reviewer 1 remain not satisfactorily answered. 

Please submit your revised manuscript by Jan 02 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Antonio Riveiro Rodríguez, PhD

Academic Editor

PLOS ONE

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Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: All comments have been addressed

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2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Partly

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The authors have revised their manuscript. Some of the issues raised during the previous review round were answered / corrected. However, many issues still remain:

Former 3rd comment:

The number of thermocycles was not changed within the discussion section. The manuscript still reads 500 cycles ("500 times between 5° and 55° with a dwell time of 10 seconds was applied").

Former 4th comment:

Missing sample size calculations increase the risk of bias in laboratory research. Please see the scoring systems for the risk of bias assessment utilized within the following systematic reviews:

- Pires et al.: Is adhesive bond strength similar in primary and permanent teeth? A systematic review and meta-analysis. J Adhes Dent 2018; 20:87–97.

- Isolan et al.: Bonding to sound and caries-affected dentin: a systematic review and meta-analysis. J Adhes Dent 2018; 20:7–18.

- Soares et al.: Bovine tooth is a substitute for human tooth on bond strength studies: a systematic review and meta-analysis of in vitro studies. Dent Mater2016; 32:1385–93.

Former 5th comment:

For the above-mentioned reason, information regarding the random assignment of the fabricated crowns should be mentioned within the manuscript.

Former 7th comment:

For the above-mentioned reason, information regarding the blinded operator should be mentioned within the manuscript.

Former 8th comment:

Please extract composition (chemicals and %) from safety data sheets which are provided by the manufacturers.

Former 10th comment:

The missing Weibull parameters are a shortcoming of the present study. The authors' reply regardring this topic is unsatisfactory. Please see the following citations for further information regarding the importance of Weibull statistics within the context of dental materials research:

- McCabe and Carrick: A statistical approach to the mechanical testing of dental materials. Dent Mater 1986; 2:139-142.

- Quinn and Quinn: A practical and systematic review of Weibull statistics for reporting strengths of dental materials. Dent Mater 2010; 26:135-147.

Former 11th comment:

Information regarding the results of the Kolmogorov-Smirnov test are still missing within the text. Also, mentioned statistical test differ between the abstract and the main text. Also information regarding the meaning of the error bars shown in figures 3 and 4 is missing (eg, stand error, standard deviation).

I noticed the revised p-values derived from the Mann-Whitney U tests. Based on the authors' reply, a Bonferroni correction was utilized. However, this information is missing within the text.

Reviewer #2: This research is under the scope of this journal; the topic is interesting for readers and this research deals with potentially significant knowledge to the field and an open new way for future studies.

The authors improved the quality of the manuscript after the reviewer's indications.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2022 Jan 18;17(1):e0262582. doi: 10.1371/journal.pone.0262582.r004

Author response to Decision Letter 1


26 Nov 2021

Reviewer #1

1)The number of thermocycles was not changed within the discussion section. The manuscript still reads 500 cycles ("500 times between 5° and 55° with a dwell time of 10 seconds was applied").

Response: The number of thermal cycles was corrected in the Discussion section of revised manuscript.

2)Missing sample size calculations increase the risk of bias in laboratory research. Please see the scoring systems for the risk of bias assessment utilized within the following systematic reviews:

Response: Despite missing to calculate the sample size in advance, the statistical tests yienled significant p-values where the effect sizes were moderate to large. It indicated that the sample size in each category was sufficient in this study.

3) For the above-mentioned reason, information regarding the random assignment of the fabricated crowns should be mentioned within the manuscript.

Response: According to the reviewer's wise comment, it was stated in the revised manuscript that the fabricated crowns were randomly assigned to three cement subgroups.

4) For the above-mentioned reason, information regarding the blinded operator should be mentioned within the manuscript.

Response: The operator's blindness to the tested subgroups was clearly mentioned in the revised manuscript.

5) Please extract composition (chemicals and %) from safety data sheets which are provided by the manufacturers.

Response: All of the chemical compositions and % were extracted from safety data sheets and embedded in Table 1.

6)The missing Weibull parameters are a shortcoming of the present study. The authors' reply regarding this topic is unsatisfactory. Please see the following citations for further information regarding the importance of Weibull statistics within the context of dental materials research:

- McCabe and Carrick: A statistical approach to the mechanical testing of dental materials. Dent Mater 1986; 2:139-142.

- Quinn and Quinn: A practical and systematic review of Weibull statistics for reporting strengths of dental materials. Dent Mater 2010; 26:135-147.

Answer: With all due respect to the reviewer's wise comment, the present study missed performing the Weibull statistics.

7) Information regarding the results of the Kolmogorov-Smirnov test is still missing within the text. Also, mentioned statistical test differ between the abstract and the main text. Also, information regarding the meaning of the error bars shown in figures 3 and 4 is missing (eg, stand error, standard deviation). I noticed the revised p-values derived from the Mann-Whitney U tests. Based on the authors' reply, a Bonferroni correction was utilized. However, this information is missing within the text.

Answer: The information regarding the Kolmogorov-Smirnov test was completely added to the Statistical analysis section of revised manuscript, also the total statistical test was added to the Abstract section of revised manuscript. Besides, the legends of Figures 3 and 4 state that the means and standard deviations of each variable were shown in the figures.

As presented in the Statistical Analysis section, all the statistical teste used in the presented study are as follows: Normal distribution was tested with the Kolmogorov-Smirnov test. Kruskal-Wallis, Dunn’s post-hoc, and Mann-Whitney non-parametric tests were used to compare ΔE00(1) and ΔE00(2) among the study groups and subgroups, because the data for these two variables (ΔE00(1) and ΔE00(2)) were not normal. After the normality test showed that the data for retentive strength was normal, the mean retentive strength was analyzed with two-way ANOVA followed by one-way ANOVA and Tukey's HSD post hoc test to determine statistically significant differences among the three employed cements. T-test was used to compare the retention of ceramic crowns as a function of the type of cement. P<0.05 was considered to be statistically significant in all tests.

Attachment

Submitted filename: Response to Reviewers.docx

Decision Letter 2

Antonio Riveiro Rodríguez

19 Dec 2021

PONE-D-21-30628R2The effects of provisional resin cements on the color and retentive strength of all-ceramic restorations cemented on customized zirconia abutmentsPLOS ONE

Dear Dr. Giti,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Notice that some minor revisions are still required in the manuscript. Please, address the remaining comments pointed out by the reviewer 1.

Please submit your revised manuscript by Feb 02 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

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We look forward to receiving your revised manuscript.

Kind regards,

Antonio Riveiro Rodríguez, PhD

Academic Editor

PLOS ONE

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The presented manuscript significantly improved during the previous review rounds. Despite the missing Weibull analysis, the manuscript might be acceptable after addressing the following remaining issues:

1. Information regarding my previous 7th comment is still missing ("Based on the authors' reply, a Bonferroni correction was utilized. However, this information is missing within the text."). Please add information within the statistical analysis section, if and how p-values derived from Mann-Whitney U and t tests were adjusted for multiple testing (eg, Bonferroni correction, Bonferroni-Holm correction).

2. Table 2: The Lilliefors correction is related to the Kolmogorov-Smirnov test for normality. Therefore, the footnote "* Lilliefors Significance Correction is P<0.05" is misleading.

3. Table 2: "0.999a©b" should be written as "0.999ab©".

4. Tables 5: The footnote "Significance correction is P<0.05" not required.

5. Tables 3 and 6: Again, the footnote "Significance correction is P<0.05" not required if information regarding the level of significance and adjustment for multiple testing is given within the statistical analysis section.

6. Please write p-values as "<.001" instead of ".000".

Reviewer #2: (No Response)

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2022 Jan 18;17(1):e0262582. doi: 10.1371/journal.pone.0262582.r006

Author response to Decision Letter 2


21 Dec 2021

Reviewer #1

1. Information regarding my previous 7th comment is still missing ("Based on the authors' reply, a Bonferroni correction was utilized. However, this information is missing within the text."). Please add information within the statistical analysis section, if and how p-values derived from Mann-Whitney U and t tests were adjusted for multiple testing (eg, Bonferroni correction, Bonferroni-Holm correction).

Response: Details of the employed Bonferroni correction was added to the statistical analysis section of revised manuscript and highlighted.

2. Table 2: The Lilliefors correction is related to the Kolmogorov-Smirnov test for normality. Therefore, the footnote "* Lilliefors Significance Correction is P<0.05" is misleading.

Response: This part was deleted as suggested by the reviewer.

3. Table 2: "0.999a©b" should be written as "0.999ab©".

Response: It was corrected as recommended.

4. Tables 5: The footnote "Significance correction is P<0.05" not required.

Response: It was omitted according to reviewer's comment.

5. Tables 3 and 6: Again, the footnote "Significance correction is P<0.05" not required if information regarding the level of significance and adjustment for multiple testing is given within the statistical analysis section.

Response: It was omitted as suggested.

6. Please write p-values as "<.001" instead of ".000".he footnote "* Lilliefors Significance Correction is P<0.05" is misleading.

Response: The P-values were corrected according to the reviewer's meticulous comment.

Attachment

Submitted filename: Response to Reviewers.docx

Decision Letter 3

Antonio Riveiro Rodríguez

30 Dec 2021

The effects of provisional resin cements on the color and retentive strength of all-ceramic restorations cemented on customized zirconia abutments

PONE-D-21-30628R3

Dear Dr. Giti,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Antonio Riveiro Rodríguez, PhD

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Authors have addressed all the comments made by the reviewer 1.

Acceptance letter

Antonio Riveiro Rodríguez

7 Jan 2022

PONE-D-21-30628R3

The effects of provisional resin cements on the color and retentive strength of all-ceramic restorations cemented on customized zirconia abutments

Dear Dr. Giti:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Antonio Riveiro Rodríguez

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Table. Raw data of ΔE00(1) and ΔE00(2).

    (XLSX)

    S2 Table. Raw data of retentive strength.

    (XLSX)

    Attachment

    Submitted filename: Response to Reviewers.docx

    Attachment

    Submitted filename: Response to Reviewers.docx

    Attachment

    Submitted filename: Response to Reviewers.docx

    Data Availability Statement

    All relevant data are within the manuscript and its Supporting Information files.


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