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Consepsis

Manufactured by Ultradent
Sourced in United States

Consepsis is a laboratory equipment product designed for cleaning and disinfecting dental instruments. It serves as a solution for the sterilization and preparation of dental tools prior to clinical use.

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8 protocols using consepsis

1

Irrigant Effects on Diabetic Tissues

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All the specimens from both the diabetic and non-diabetic groups were randomly assigned to four subgroups (n=6) in terms of the irrigant used. The lumen of each section was occluded with adhesive wax at the lower surface of the disk and filled with the following irrigants, being refreshed once per minute for a total of 5 minutes:

Subgroup 1: 2.6% NaOCl

Subgroup 2: 17% EDTA (Pulpdent Corp, Watertown, MA)

Subgroup 3: 2% CHX (Consepsis, Ultradent, UT)

Subgroup 4: NSS (control group).

To prevent prolonged effects of the irrigants, the specimens received a final flush of 10 mL of distilled water immediately after the treatment.
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2

Silanized Nanotubes for Disinfection

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One gram of HNs (Sigma–Aldrich, St. Louis, MO, USA) that had been previously dried in a HERAtherm drying oven (Thermo Fisher Scientific, Waltham, MA, USA) was weighed using an analytical balance (Shimadzu Scientific Instruments, Kyoto, Japan). A solution of 3-(trimethoxysilyl) propyl-methacrylate-98% (Sigma–Aldrich, St. Louis, MO, USA) diluted to 5% and 95% acetone (Sigma–Aldrich, St. Louis, MO, USA) was used for the immersion of the nanotubes for 24 h at 110 °C in a drying oven.
Subsequently, 1 g of silanized nanotubes was mixed with 10 mL of 2% CX (Consepsis, Ultradent Products, South Jordan, UT, USA), commonly used for disinfection in dentistry [21 (link)], and 10 mL of 95% pure ethanol and sonicated for 1 h. The CX-loaded nanotubes were then placed in a drying oven for 10 days at 30 °C to eliminate residual solvent [17 (link)].
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3

Root Canal Disinfection Protocols

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One-hundred and forty-four single-rooted human teeth with no cavities and resorption were selected for this study. The teeth were soaked in 5.25% NaOCl for 30 minutes. Calcified root canals with more than one canal were excluded. Access cavity was prepared and working length was determined. Root canals were instrumented to the apical size #35 using Mtwo rotary files (VDW, Munich, Germany) according to the manufacturer’s instructions. All canals were irrigated after using each file by 2 mL of 2.5% NaOCl. To prevent bacterial leakage, apical foramina were sealed with wax. Nail varnish was applied on the surface of roots in two layers. Three mL of 17% EDTA (Meta Biomed Co. Ltd., Mandaluyong, Korea) was used for one minute to remove the smear layer. Then, the canals were irrigated with saline and dried. Finally, 108 teeth (for test groups and positive control) were rinsed with 5 mL of 2% CHX (Consepsis®, Ultradent, South Jordan, UT, USA) for 10 minutes. Thirty-six remaining samples that were not irrigated with CHX were used as negative controls.
The teeth were randomly divided into the following groups:
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4

Dentin Pretreatments with Nanoparticles and CHX

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The specimens were assigned into nine experimental groups (n=10) based on the dentin pretreatments with a 2% CHX solution (Consepsis, Ultradent Inc., South Jordan, UT, USA) or three different NPs (SNPs, TNPs, and ZNPs; purchased from ASEPE Company, Tabriz, Iran). The SNPs, TNPs, and ZNPs had the particle sizes of 20 nm, <50 nm, and 20 nm, respectively.
In group A (control group), a cavity conditioner (Cavity Conditioner, GC Co, Japan) was applied on the prepared dentin surfaces according to the manufacturer’s instructions. 1 mL of a 2% CHX solution was applied on the prepared dentin surfaces using a foam pellet saturated with the solution for 1 minute. Then, the dentin surfaces were blot-dried to remove the excess CHX before applying the conditioner in group B and after applying the conditioner in group F. In groups C, D, and E, the prepared dentin surfaces were pretreated with 1 cc 0.1% SNP, 0.1% TNP, and 0.1% ZNP solutions, respectively, for 1 minute, before applying the conditioner. Then, the dentin surfaces were rinsed thoroughly for 1 minute. SNPs, TNPs, and ZNPs were applied for 1 minute after applying the conditioner in groups G, H, and I, respectively. Then, the dentin surfaces were rinsed thoroughly for 1 minute.
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5

Antimicrobial Efficacy of Dental Irrigants

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The materials tested in this study were: 3% NaOCl (ChlorCid; Ultradent, USA); 2% chlorhexidine gluconate solution (Consepsis; Ultradent, USA); and BioPure MTAD (DENTSPLY Tulsa Dental, USA).
Irrigants were diluted to 0.1 and 100 μl/mL with Dulbecco’s Modified Eagle’s medium (DMEM), following a previously reported protocol [7 (link)].
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6

Dentin Pretreatment with Antioxidants

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The teeth were randomly divided into four groups (n = 24) based on the pretreatments used: (1) Group A (control): no pretreatments; (2) Group B: 2% CHX solution (Consepsis; Ultradent, South Jordan, UT, USA) (Coelho et al., 2020 (link)); (3) Group C: a 10% α‐tocopherol solution was prepared by dissolving 10 g of α‐tocopherol gel (Sigma‐Aldrich, St. Louis, MO, USA) in 100 ml of ethyl alcohol in a standard flask (Kavitha et al., 2016 (link)); and (4) Group D: a 1% quercetin solution (Sigma‐Aldrich) was prepared by dissolving 1 g of quercetin powder directly into pure ethanol under water‐bath heating at 37°C (Li et al., 2017 (link)). The pretreatment solutions were actively applied to the dentin surface by tapping with a microbrush. After 60 s, the teeth were rinsed with water for 10 s and gently dried with a cotton roll.
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7

Dentin Conditioning and CHX Application

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The process of dentin conditioning was performed as described for previous groups. Next, 2% CHX solution (Consepsis; Ultradent Products Inc., South Jordan, UT, USA) was applied
to the prepared surfaces with its applicator for 60 seconds and gently air-dried for 10 seconds according to the manufacturer’s instructions. Afterwards, the RMGIC application
and storage of samples were performed in a similar fashion as in the group Ia. Finally, the samples were thermocycled for 500 cycles.
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8

Antimicrobial Silver Nitrate Protocol

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Silver nitrate (AgNO3, CTR Scientific, Monterrey, Nuevo León, Mexico), gallic acid (C7H6O5, Sigma Aldrich, Saint Louis, MO, USA), sodium hydroxide (NaOH, Jalmek Scientific, San Nicolás de los Garza, Mexico), ammonia hydroxide (NH4OH, Jalmek Scientific), Müller-Hinton broth (MH, BD™ Difco™, Rockville, MD, USA), 2.0% chlorhexidine gluconate (Consepsis, Ultradent Products Inc, South Jordan, UT, USA), were used and stored according to manufacturer’s recommendations.
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