Won-Jun Shon

Lifespan of One Nickel-Titanium Rotary File with Reciprocating Motion in Curved Root Canals

INTRODUCTION The purpose of this study was to examine the lifespan of one nickel-titanium (NiTi) rotary file when used in reciprocating motion and to compare the time required for its preparation of a curved root canal using both reciprocating and continuous motion. METHODS One hundred twenty curved canals from 60 extracted maxillary and mandibular molars were selected for measuring the mean number of uses. Each canal was prepared with reciprocating motion until the ProTaper F2 single file (Dentsply Maillefer, Ballaigues, Switzerland) reached the working length. One file was used until it was fractured. Another 60 canals were divided into two groups. 30 canals in the continuous rotation motion (CM) group were prepared using continuous rotation following the sequence of ProTaper files, whereas the canals in the reciprocating motion (RM) group (n = 30) were prepared with reciprocating motion with the sole use of the ProTaper F2. The total root canal preparation time was measured until the F2 file finally reached the working length in both groups. RESULTS A total of 11 files were used in the preparation of 120 curved root canals. The average lifespan of one F2 file was 10.60 ± 4.35 canals with the longest lifespan of 21 canals. The total time for canal preparation was 46.42 ± 18.12 seconds and 21.15 ± 6.70 seconds in the CM and RM groups, respectively. There was a statistically significant difference between the groups (p < 0.01). CONCLUSION Within the limitation of this study, one F2 file can be safely used to the working length of curved canals at least six times under reciprocating motion. Reciprocating preparation with only one F2 file was much faster than root canal instrumentation with continuous rotation.

Effect of final irrigation regimen on sealer penetration in curved root canals.

INTRODUCTION The purpose of this study was to evaluate the effect of different final irrigation regimens on the sealer penetration into dentinal tubules of curved root canals. METHODS The mesiobuccal canals from 45 extracted maxillary and mandibular molars were instrumented with sodium hypochlorite (NaOCl) irrigation. The samples were divided into 3 groups according to the final irrigation used: group N (control), 3.5% NaOCl; group E, 17% ethylenediaminetetraacetic acid (EDTA); and group EN, 17% EDTA followed by 3.5% NaOCl. All teeth were obturated with gutta-percha and AH Plus sealer labeled with fluorescent dye. Transverse sections at 2 mm (apical) and 5 mm (coronal) from root apex were examined by using confocal laser scanning microscopy. Then, total percentage and maximum depth of sealer penetration were measured. RESULTS The apical sections in each group showed significantly lower percentage and maximum depth of sealer penetration than the coronal sections (P < .05). In apical levels, group E and EN resulted in a higher percentage of sealer penetration than the control group (P < .05), but there was no significant difference of maximum depth between group E and the control group (P > .05). CONCLUSIONS In curved canal, final rinse with NaOCl after the use of EDTA had no additional effect on sealer penetration. Complete debridement with a 1-minute application of EDTA remains a challenge in the apical area of curved canals.

Heat shock protein-mediated cell penetration and cytosolic delivery of macromolecules by a telomerase-derived peptide vaccine

A reverse-transcriptase-subunit of telomerase (hTERT) derived peptide, GV1001, has been developed as a vaccine against various cancers. Here, we report an unexpected function of GV1001 as a cell-penetrating peptide (CPP). GV1001 was delivered into a variety of cells including various cancer cell lines and primary blood cells. Moreover, the delivered GV1001 was predominantly located in the cytoplasm of the cells, while a significantly higher proportion of TAT peptide was localized in the nucleus. Macromolecules such as proteins, DNA and siRNA, which were linked to GV1001 by direct covalent conjugation or non-covalent complexation through poly-lysine, were successfully delivered into cells, indicating that GV1001 can be used as a carrier for macromolecules. Expression of the delivered DNA, and lowered expression of the target gene by the delivered siRNA, suggest the potential therapeutic use of GV1001. Pull-down analysis identified Heat Shock Protein 90 (HSP90) and 70 (HSP70) as GV1001 interacting proteins. Treatment of Anti-HSP90 and HSP70 antibodies lowered the internalization of GV1001, indicating that the interaction is critical for the efficient internalization of GV1001. Collectively, the results of this study suggest the pharmaceutical potential of GV1001, already proven safe in clinical trials, as a carrier for the delivery of macromolecular therapeutics into cells, in addition to its own anti-cancer activity.

Effect of Laser-activated Irrigation of 1320-Nanometer Nd:YAG Laser on Sealer Penetration in Curved Root Canals

INTRODUCTION The purpose of this study was to investigate the efficacy of laser-activated irrigation (LAI) of 1320-nm neodymium-doped:yttrium-aluminum-garnet (Nd:YAG) laser on sealer penetration into dentinal tubules in the presence of 5.25% sodium hypochlorite (NaOCl) or 17% ethylenediaminetetraacetic acid (EDTA). METHODS The curved root canals (>20°) from 63 extracted human molars (negative control, n = 3) were prepared to size #30.06 with NaOCl irrigation. Teeth were divided into 4 groups (n = 15) as follows: group N, NaOCl irrigation without LAI; group E, EDTA irrigation without LAI; group NL, LAI with NaOCl; group EL, LAI with EDTA. In all groups, the laser fiber was inserted and withdrawn 4 times for 5 seconds each. Teeth were obturated with gutta-percha and fluorescent-labeled sealer. Transverse sections at 2 and 5 mm from root apex were examined with confocal laser scanning microscopy, and the percentage of sealer penetration into dentinal tubules was measured. RESULTS Groups E, NL, and EL showed higher percentage of sealer penetration than group N (P < .05). With NaOCl as irrigant, LAI (group NL) resulted in significantly higher amount of sealer penetration than nonactivated group (group N) in both levels (P < .05). However, with EDTA, no significant differences in sealer penetration were observed between the laser-activated group (group EL) and its nonactivated counterpart (group E) in both levels (P > .05). CONCLUSIONS The 1320-nm Nd:YAG laser activation with either NaOCl or EDTA was much better than NaOCl irrigation alone and as effective as EDTA final flush for sealer penetration into dentinal tubules. Additional use of laser with EDTA did not improve the quality of obturation in the curved canals.

Peri‐implant bone formation of non‐thermal atmospheric pressure plasma–treated zirconia implants with different surface roughness in rabbit tibiae

OBJECTIVES The aim of this study was to evaluate and compare the osseointegration of powder-injection molded (PIM) zirconia implants in rabbit tibiae with or without He plasma treatment. MATERIAL AND METHODS Twenty-five rabbits received 4 types of external hex implants with identical geometry in the tibiae: PIM zirconia implants, roughened PIM zirconia implants, plasma-treated PIM zirconia implants, and plasma-treated roughened PIM zirconia implants. The contact angles of the four types of implants were evaluated. Removal torque tests and histomorphometric analyses were performed. RESULTS The plasma treatment markedly enhanced the hydrophilicity, but did not seem to change the surface topography of the PIM zirconia implants. There were statistically significant differences in the bone-to-implant contact (BIC) ratios, bone volume (BV/TV), and removal torque values (RTQ) among the tested implant types (P < 0.001). The plasma-treated implants exhibited significantly higher BIC and BV/TV values than the untreated implants. However, the removal torque values favored the rough surface. CONCLUSIONS The He plasma treatments on PIM zirconia implants made the surface more hydrophilic and enhanced the osseointegration of the implants without changing the micro-topography.

Clinical efficiency and reusability of the reciprocating nickel–titanium instruments according to the root canal anatomy

The application of the single-file technique using the reciprocating motion is gaining concern in root canal preparation. The purpose of this research is to compare the efficiency of the reciprocating motion-employing files (RECIPROC and WaveOne) by measuring the working time for complete canal shaping, and to evaluate their reusability under scanning examinations. One hundred curved root canals of the extracted molars were used. The working length was determined and the glide path was confirmed using a #15 K-file. Canals shaping was completed to the length either with RECIPROC R25 file (n = 50), or with WaveOne Primary file (n = 50). The time taken for the file to reach the working length was also measured. Each file was repeatedly used in a maximum of 10 canals for comparing the change of the efficiency (shaping time) according to the working length, canal curvature, and number of file re-use. The deformations or surface defects of the files after the in vitro use were observed using a scanning electron microscope (SEM). There was no difference under the SEM between the 2 file groups with no initiation of micro-cracks until they were re-used up to 5 canals. WaveOne Primary file showed significantly shorter working time than RECIPROC R25 (p < 0.05). There was a statistically significant correlation between the working time and three variables. As the working length and the curvature of the canal increased, the shaping time was increased in both file systems. Reusability of these reciprocating instruments might be maximum 5 canals with minimal surface deformations.

Tumor-suppressive effect of a telomerase-derived peptide by inhibiting hypoxia-induced HIF-1α-VEGF signaling axis.

A reverse-transcriptase-subunit of telomerase (hTERT) derived peptide, GV1001, has been developed as a vaccine against various cancers. Previously, we have shown that GV1001 interacts with heat shock proteins (HSPs) and penetrates cell membranes to be localized in the cytoplasm. In this study, we have found that GV1001 lowered the level of intracellular and surface HSPs of various cancer cells. In hypoxic conditions, GV1001 treatment of cancer cells resulted in decreases of HSP90, HSP70, and HIF-1α. Subsequently, proliferation of cancer cells and synthesis of VEGF were significantly reduced by treatment using GV1001 in hypoxic conditions. In an experiment using a nude mouse xenograft model, GV1001 exerted a similar tumor suppressive effect, further confirming its anti-tumor efficacy. Higher apoptotic cell death, reduced proliferation of cells, and fewer blood vessels were observed in GV1001-treated tumors compared to control. In addition, significant reduction of Tie2+ CD11b+ monocytes, which were recruited by VEGF from tumor cells and play a critical role in angiogenesis, was observed in GV1001-treated tumors. Collectively, the results suggest that GV1001 possesses potential therapeutic efficacy in addition to its ability to induce anti-cancer immune responses by suppressing both HSP70 and HSP90.

Evaluation of the safety and efficiency of novel metallic ultrasonic scaler tip on titanium surfaces

AIM To evaluate the safety and efficiency of novel ultrasonic scaler tips, conventional stainless-steel tips, and plastic tips on titanium surfaces. MATERIAL AND METHODS Mechanical instrumentation was carried out using conventional ultrasonic scalers (EMS, Nyon, Switzerland) with novel metallic implant tip (BS), a plastic-headed tip (ES), a plastic tip (PS) and a conventional stainless-steel tip (CS) on 10 polished commercially pure titanium disks (Grade II) per group. Arithmetic mean roughness (R(a) ) and maximum height roughness (R(y) ) of titanium samples were measured and dissipated power of the scaler tip in the tip-surface junction was estimated to investigate the scaling efficiency. The instrumented surface morphology of samples was viewed with a scanning electron microscope (SEM) and surface profile of the each sample was investigated using contact mode with a commercial atomic force microscope (AFM). RESULTS There were no significant differences in surface roughness (R(a) and R(y) ) among BS, ES, and PS group. However, CS group showed significant higher surface roughness (R(a) and R(y) ). The efficiency of CS tip is twice as much higher than that of BS tip, the efficiency of BS tip is 20 times higher than that of PS tip, and the efficiency of BS tip is 90 times higher than that of ES tip. CONCLUSION Novel metallic copper alloy ultrasonic scaler tips may minimally influence the titanium surface, similar to plastic tip. Therefore, they can be a suitable instrument for implant maintenance therapy.

Effect of Conditioned Medium from Preameloblasts on Regenerative Cellular Differentiation of the Immature Teeth with Necrotic Pulp and Apical Periodontitis

INTRODUCTION The purpose of this study was to investigate the effect of conditioned medium (CM) from murine preameloblasts on the cellular differentiation of mesenchymal stem cells (MSCs) in immature teeth with necrotic pulp and apical periodontitis. METHODS Pulp necrosis and apical periodontitis were induced in 30 immature permanent double-rooted premolars of 3 beagles and were randomly assigned to the following treatment groups: group CM (n = 10), revascularization treatment was performed using CM from preameloblasts of C57BL/6 mice apical bud cells; group CR (n = 10), conventional revascularization treatment was performed; positive control group (n = 5), left infected; and negative control group (n = 5), untreated. The dogs were followed up for 12 weeks and assessed for treatment outcomes with radiographic and histologic analyses. The effect of the CM on sequential Runx2 and osterix messenger RNA gene expression during the differentiation of MG63 osteoblastlike cells was analyzed with real-time polymerase chain reaction. RESULTS The overall treatment outcomes were not significantly different between the 2 treatment groups. However, the teeth in the CM group showed significantly more mature apices and a higher degree of hard tissue formation with projections intercalating into the pre-existing root dentin (P < .05). In CM-treated teeth, regenerated pulplike tissue was more frequently observed (P < .05). During differentiation, the CM induced early peak expression of Runx2 followed by sustained osterix overexpression. CONCLUSIONS CM from preameloblasts rendered a favorable effect in providing a physiologic microenvironment for the differentiation of MSCs after revascularization treatment.

Antifungal effects of synthetic human β-defensin 3-C15 peptide

Objectives The purpose of this ex vivo study was to compare the antifungal activity of a synthetic peptide consisting of 15 amino acids at the C-terminus of human β-defensin 3 (HBD3-C15) with calcium hydroxide (CH) and Nystatin (Nys) against Candida albicans (C. albicans) biofilm. Materials and Methods C. albicans were grown on cover glass bottom dishes or human dentin disks for 48 hr, and then treated with HBD3-C15 (0, 12.5, 25, 50, 100, 150, 200, and 300 µg/mL), CH (100 µg/mL), and Nys (20 µg/mL) for 7 days at 37℃. On cover glass, live and dead cells in the biomass were measured by the FilmTracer Biofilm viability assay, and observed by confocal laser scanning microscopy (CLSM). On dentin, normal, diminished and ruptured cells were observed by field-emission scanning electron microscopy (FE-SEM). The results were subjected to a two-tailed t-test, a one way analysis variance and a post hoc test at a significance level of p = 0.05. Results C. albicans survival on dentin was inhibited by HBD3-C15 in a dose-dependent manner. There were fewer aggregations of C. albicans in the groups of Nys and HBD3-C15 (≥ 100 µg/mL). CLSM showed C. albicans survival was reduced by HBD3-C15 in a dose dependent manner. Nys and HBD3-C15 (≥ 100 µg/mL) showed significant fungicidal activity compared to CH group (p < 0.05). Conclusions Synthetic HBD3-C15 peptide (≥ 100 µg/mL) and Nys exhibited significantly higher antifungal activity than CH against C. albicans by inhibiting cell survival and biofilm.