Skip Navigation
Skip to contents

Restor Dent Endod : Restorative Dentistry & Endodontics

OPEN ACCESS

Articles

Page Path
HOME > Restor Dent Endod > Volume 40(3); 2015 > Article
Research Article Chelating and antibacterial properties of chitosan nanoparticles on dentin
Aldo del Carpio-Perochena1, Clovis Monteiro Bramante1, Marco Antonio Hungaro Duarte1, Marcia Regina de Moura2,3, Fauze Ahmad Aouada2, Anil Kishen4
2015;40(3):-201.
DOI: https://doi.org/10.5395/rde.2015.40.3.195
Published online: March 30, 2015

1Department of Dentistry, Endodontics and Dental Materials, Bauru Dental School, University of São Paulo, Bauru-São Paulo, Brazil.

2Department of Physics and Chemistry, FEIS, São Paulo State University, Ilha Solteira-São Paulo, Brazil.

3National Nanotechnology Laboratory for Agriculture, Embrapa, São Carlos-São Paulo, Brazil.

4Discipline of Endodontics, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.

Correspondence to Aldo del Carpio Perochena, DDS, PhD. Research associate, Department of Dentistry, Endodontics and Dental Materials, Bauru Dental School, University of São Paulo, Faculdade de Odontologia de Bauru-USP. Al. Octávio Pinheiro Brisolla, 9-75, Bauru-São Paulo, Brazil 17012-901. TEL, +55-14-3235-8344; FAX, +55-14-3223-4679; aldodelcp@usp.br
• Received: August 28, 2014   • Accepted: February 7, 2015

©Copyrights 2015. The Korean Academy of Conservative Dentistry.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

  • 401 Views
  • 8 Download
  • 87 Crossref
prev next
  • Objectives
    The use of chitosan nanoparticles (CNPs) in endodontics is of interest due to their antibiofilm properties. This study was to investigate the ability of bioactive CNPs to remove the smear layer and inhibit bacterial recolonization on dentin.
  • Materials and Methods
    One hundred bovine dentin sections were divided into five groups (n = 20 per group) according to the treatment. The irrigating solutions used were 2.5% sodium hypochlorite (NaOCl) for 20 min, 17% ethylenediaminetetraacetic acid (EDTA) for 3 min and 1.29 mg/mL CNPs for 3 min. The samples were irrigated with either distilled water (control), NaOCl, NaOCl-EDTA, NaOCl-EDTA-CNPs or NaOCl-CNPs. After the treatment, half of the samples (n = 50) were used to assess the chelating effect of the solutions using portable scanning electronic microscopy, while the other half (n = 50) were infected intra-orally to examine the post-treatment bacterial biofilm forming capacity. The biovolume and cellular viability of the biofilms were analysed under confocal laser scanning microscopy. The Kappa test was performed for examiner calibration, and the non-parametric Kruskal-Wallis and Dunn tests (p < 0.05) were used for comparisons among the groups.
  • Results
    The smear layer was significantly reduced in all of the groups except the control and NaOCl groups (p < 0.05). The CNPs-treated samples were able to resist biofilm formation significantly better than other treatment groups (p < 0.05).
  • Conclusions
    CNPs could be used as a final irrigant during root canal treatment with the dual benefit of removing the smear layer and inhibiting bacterial recolonization on root dentin.
Bacterial biofilms are structured communities of cells adhered to an organic surface and stabilized in an extracellular matrix.1 The high density of bacterial cells in biofilm communities and the inherent resistance of biofilm bacteria to antimicrobials/host defence systems are the main factors responsible for most persistent and chronic bacterial infections.1 The combined use of mechanical instrumentation and chemical irrigation has been recommended to obtain effective elimination of biofilms from the root canal system.2 Among the commonly used endodontic irrigants, sodium hypochlorite (NaOCl) is the most recommended irrigant due to its substantial tissue dissolution capacity and antibacterial effect.3,4 However, NaOCl causes dentin collagen denaturation and dissolution. Consequently, the use of a high concentration of this solution for long periods of time may cause ultrastructural damage into the dentin.5 In addition, NaOCl is not capable of completely debriding the root canals or eliminating the biofilm bacteria.4 The chelating agents well remove smear layers from root dentin, thus are used for the final irrigation of the root canals.6 The smear layer is composed of very small particles that may be solubilized in acids.7 The most common chelating solutions contain ethylenediaminetetraacetic acid (EDTA), which reacts with the calcium ions in dentin and forms soluble calcium chelates.8 However, the chelating agents may alter the structural characteristic of the dentin resulting in a compromised mechanical integrity and an increased potential for bacterial adherence on the collagen.9,10
Chitosan is a non-toxic cationic biopolymer usually obtained by alkaline deacetylation from chitin, which is the principal component of crustacean exoskeletons.11 The covalent immobilization of chitosan on dentinal collagen has been proposed to induce the remineralization of the exposed and demineralized dentin structure because its functional phosphate groups might bind to calcium ions to form a favorable surface for crystal nucleation, resulting in the formation of a calcium phosphate layer.12 Chitosan treatment improves the resistance of the dentinal surface to degradation by collagenase.13 Furthermore, chitosan presents with biocompatibility, chelating capacity and also antimicrobial effects against a broad range of gram-positive and gram-negative bacteria as well as fungi.14,15,16,17
Previous in vitro studies have demonstrated the significant antibiofilm efficacy of chitosan nanoparticles (CNPs).14,15 However, testing the efficacy of these nanoparticles on biofilms formed in situ would provide a stronger correlation with the findings from the in vivo studies since coronal leakage of saliva is one of the main factors that allows for bacterial recolonization in root-filled teeth.18 In addition, there is limited information about the use of CNPs as a chelating agent.16,19 The current study aims to investigate the ability of CNPs to act as a final irrigant to remove the smear layer from a root-dentin surface and simultaneously inhibit bacterial recolonization/early biofilm formation when exposed to saliva.
Sample preparation
The present study was performed according to the guidelines of the Institutional Research Human Ethics Committee (Protocol 166/2011). Eighty rectangular dentin blocks (5 mm × 5 mm × 3 mm) were obtained from bovine radicular dentin. Dentin debris were created on the sample surface by sectioning every side of the block. The sectioning procedures were performed using an Isomet saw (Buehler Ltd., Evanston, IL, USA). The dentin blocks were autoclaved for 30 minutes at 121℃ (Sercon-Modelo HS, Mogi das Cruzes, SP, Brazil). The samples were not treated with any chemicals before being autoclaved to maintain the dentin surface debris generated during the sectioning of these samples.
Synthesis of chitosan nanoparticles
The CNPs were synthesized based on a previously published protocol using an ionic gelation method.20 Briefly, the chitosan powder (Polymar Ciência e Nutrição S/A, Fortaleza, Brazil) was dissolved in 1% acetic acid under magnetic stirring at room temperature. Next, 1 mg/mL sodium tripoly-phosphate solution (Sigma-Aldrich Chemical Co., St. Louis, MO, USA) was added into the chitosan solution. The preparations were mixed with a Polytron homogenizer (PT-3000, Brinkman Instruments, Rexdale, ON, Canada) at 5,000 rpm with drop-wise addition of the tripoly-phosphate solution, thus achieving a final CNPs concentration of 1.29 mg/mL. The zone of opalescent suspension was visible with the formation of the nanoparticles, and the solution was further examined for nanoparticle characterization. The concentration of tripolyphosphate solution in the final solution was 0.3 - 0.6 mg/mL. The range of the nanoparticles' size was 85 - 221 nm.
Treatment procedures
The irrigating solutions used included 2.5% NaOCl for 20 minutes, 17% EDTA for 3 minutes and 1.29 mg/mL CNPs for 3 minutes. The NaOCl was replenished every 5 minutes to simulate clinical conditions. One hundred bovine dentin blocks were equally divided in five groups (n = 20 per group) and treated with either distilled water (control, group 1), NaOCl (group 2), NaOCl-EDTA (group 3), NaOCl-EDTA-CNPs (group 4), and NaOCl-CNPs (group 5). The volume was standardized to 3 mL for all of the solutions. The experiments were performed in 24 well tissue culture plates by immersing the dentin samples in the irrigant solutions. After the irrigation procedure was performed, half of the samples (n = 50) were used to analyse the chelating effect of the solutions using a portable scanning electronic microscope (PSEM, Aspex Corporation, Delmont, PA, USA), while the other half (n = 50) was infected intra-orally to assess bacterial biofilm forming capacity using a confocal laser scanning microscope (CLSM, Leica TCS-SPE, Mannheim, Germany). Therefore, the experiment was conducted in two assays, which were formed by five groups each containing 10 samples.
Chelating effect of chitosan nanoparticles
After the irrigation procedures, the samples were dried at room temperature for 24 hours and fixed on stubs. Three micrographs per block were analysed using a PSEM with a magnification of 500 times at 10 kV creating a total of 150 images. The area of each image represented 1,024 µm × 1,024 µm. For quantification purposes, the PSEM pictures were divided into 100 areas using a digital grid, and then examined by three endodontic specialists who assessed the amount of area in each grid that was covered by a smear layer. Each examiner evaluated the pictures twice, with an interval of one week between each observation. The values obtained by one examiner that showed concordance with that from the other examiners and had the lowest amount of discrepancy between these observations were chosen for the statistical analysis. A scores of one to four were ascribed to each sample according to a previously published methodology that was slightly modified.21 Having less than 10% of the area containing open dentinal tubules was scored as one, having 10 - 50% of the area containing open dentinal tubules was scored as two, having 50 - 70% of the area containing open dentinal tubules was scored as three and having more than 70% of the area containing open dentinal tubules was scored as four.
Antibacterial ability of chitosan nanoparticles
An in situ model was modified to simulate the presence of intra-oral dentinal biofilms.4 Twenty treated dentin blocks were fixed in the cavities of a Hawley orthodontic device using sticky wax (Kota Ind. e Com. Ltda., São Paulo, SP, Brazil). The procedure was repeated to complete the infection of all of the samples. To standardize the biofilm thickness as much as possible, one healthy volunteer used the orthodontic device for 48 hours. After this period, the samples were transferred to test tubes containing 5 mL of brain-heart infusion broth, and then incubated at 37℃ for 24 hours. The subject maintained a controlled routine of food and drink consumption while using the intra-oral device during the infection period except during regular oral-hygiene practices. The same diet was supplied during each infection period.
After the dentinal infection period, the samples were rinsed with sterile distilled water to remove the non-adherent cells and culture medium. The biofilms were stained with the Live/Dead BacLight Bacterial Viability kit (Invitrogen, Eugene, OR, USA) and analysed with a CLSM. Four stacks were analysed from random areas of each sample, totalling 200 images. Each block was scanned using a 40 times oil lens, 1.5 µm step-size and a format of 512 pixels × 512 pixels. The area of each image represented 275 µm × 275 µm. The parameters evaluated were the total biovolume expressed in µm3/µm2 in accordance with Heydorn et al. and the percentage of viable cells.22 The software Bioimage_L (http://bioimagel.com) was used to calculate these parameters.23 Representative images obtained from the PSEM (post-irrigation) and CLSM (post-infection) are shown in Figure 1. A previous pilot study has demonstrated that the residual effect of NaOCl did not interfere with the activities of the experimental solutions on the dentinal surface and bacterial biofilm.
rde-40-195-g001.jpg Figure 1 

Representative images from the portable scanning electron microscope (×500) and confocal laser scanning microscope (×40). The irrigated pre-infection samples can be seen in images (a) - (e), and the infected samples after experimental irrigation protocols can be seen in images (f) - (j). A substantial amount of smear layer was observed when the samples were irrigated with sterile distilled water (a) and NaOCl (b). Visible dentinal tubules were seen in the samples treated with NaOCl-EDTA (c), NaOCl-EDTA-CNPs (d) and NaOCl-CNPs (e). A positive cellular viability and evident biomass were observed in the control (f), NaOCl (g) and NaOCl-EDTA (h) groups. The NaOCl-EDTA-CNPs and NaOCl-CNPs groups had decreased biomass (i) and interfered with bacterial growth (j). All bars represent 20 µm.

Download Figure Download Figure
Statistical analysis
All statistical analyses were performed with the Prism 5.0 software (GraphPad Software Inc., La Jolla, CA, USA). The Kappa test was utilized to determinate the concordance among the examiners (Kappa ≥ 0.75). The non-parametric Kruskal-Wallis and Dunn tests (p < 0.05) were used to perform multiple comparisons among the groups as the data did not show a normal distribution.
The results of the Kappa tests showed good interexaminer agreement with values of 0.8 or above for all of the different categories.
Chelating effect of chitosan nanoparticles
The smear layer was significantly reduced in the groups treated with NaOCl-EDTA, NaOCl-EDTA-CNPs and NaOCl-CNPs in comparison with that of the control and NaOCl groups (p < 0.05). The percentage of areas with or without observable dentinal tubules per score and the statistical differences among the groups are shown in the Figure 2.
rde-40-195-g002.jpg Figure 2 

The percentage of areas with open dentinal tubules for each score (1 to 4). Having less than 10% of the area containing open dentinal tubules was scored as one, having 10 - 50% of the area containing open dentinal tubules was scored as two, having 50 - 70% of the area containing open dentinal tubules was scored as three and having more than 70% of the area containing open dentinal tubules was scored as four.

*Different letters within a column depict a significant difference (p < 0.05).
NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochloriteethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.
Download Figure Download Figure
Antibacterial ability of chitosan nanoparticles
The biovolume and bacterial viability were significantly lower in the samples receiving final irrigation with CNPs than those in the control were (p < 0.05). The NaOCl-EDTA-CNPs and NaOCl-CNPs groups were not statistically different (p > 0.05). The bacterial colonization and cell viability in the NaOCl and NaOCl-EDTA groups were not statically different than those in the control group (p > 0.05). The comparison of the medians and 25 - 75% percentiles of the total biovolume and the percentage of live cells among all of the groups are shown in Table 1.
Table 1

Medians (25 - 75 percentiles) of the total biovolume and the percentage of live cells of the comparisons among the groups

Total Biovolume (µm3/µm2) Percentage of live cells
Control 5.0 (4.0 - 5.4)a 92 (90 - 96)a
NaOCl 3.9 (3.1 - 5.1)ab 90 (85 - 92)a
NaOCl-EDTA 3.6 (2.8 - 5.1)ab 91 (87 - 94)a
NaOCl-EDTA-CNPs 2.6 (0.85 - 4.4)c 73 (51 - 86)b
NaOCl-CNPs 2.7 (1.8 - 4.2)bc 77 (60 - 83)b

*Different superscript letters in each column represent significant differences (p < 0.05).

NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochlorite-ethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.

Download Table Download Table
The bovine dentin was chosen as a substrate in the present study because it is a suitable substitute for human dentin when testing for erosion/abrasion, which is closely related with smear layer removal.24 In addition, the topography of the substrate is an important factor when discussing the survival of biofilms since rough surfaces will increase bacterial adhesion and retention providing anchor points for microorganisms and their nutrients.25 Thus, it should be logical to assume that the bovine dentin facilitate bacterial invasion due to the significantly greater tubular diameter when compared with that of human dentinal tubules.26 However, these factors do not substantially affect studies focused on evaluating the bacterial volume and cell viability of mature biofilms localized from the dentinal surface to the highest part of the biofilm.4,27,28
The chelating capacity of chitosan on root canal dentin has been assessed by only two previous studies, which showed that the irrigation of the root canals with a CNPs-based solution for 3 minutes effectively removed the smear layer from the root canals.16,19 These results were in accordance with those obtained in the present study, where the final irrigation with CNPs for 3 minutes effectively removed the inorganic contents from the dentin. Even though all the EDTA- and CNPs-treated experimental groups showed similar efficacy in removing the smear layer, the use of CNPs after irrigation with NaOCl is recommended because of the ability of the CNPs on dentin to resist bacterial adherence and early biofilm formation.15 This resistance is an important advantage of using CNPs over EDTA, which presented a similar chelating effect.
The chelating effect of CNPs and EDTA could cause dentin demineralization.16 However, a previous study has shown that dentin surfaces coated with chitosan have the potential to remineralize the demineralized dentin.12 The results of the present study suggest that the chelating effect of CNPs irrigation following 17% EDTA is similar to the effect caused by each of these solutions when they are used independently. This observation could be explained by the finding that the chelating ability of the polymeric chitosan matrices was maintained when it was modified with the chemical immobilization of EDTA.29
The chelating mechanism of chitosan on dentin has previously not been well documented. However, this bioactive biopolymer is widely used as a chelating agent to absorb heavy metals from wastewater.30 Two theories have been used to explain the chelating mechanism of chitosan. First, the bridge model states that two or more amino groups of chitosan bind to the same metal ion.31 Second, the pendant model suggests that one amino group is utilized in the binding, and the metal ion is linked to the amino group like a pendant.32 Either of the two mechanisms could be responsible for the chelation of calcium ions in dentin resulting in the depletion of inorganic matter from the smear layer.33
In the present study, the bacterial infection was created in situ because biofilm development in a natural environment has been demonstrated to be profoundly different from the biofilm formed in vitro.34 Many factors have been associated with failures in endodontic treatment. Yet, bacterial re-entry and re-contamination of the root canal by coronal microleakage subsequent to root-filling, is suggested to be one of most important causes for endodontic treatment failure.35 In addition to salivary microleakage, the filled root canals may be exposed to the oral environment in certain situations such as during the loss or fracture of dental structures/restorations as well as during intraradicular preparations for prosthetic purposes, thereby allowing the more than 175 bacterial species present in human saliva to invade the root canal spaces.36,37 It is important to note that intracanal salivary penetration via coronal leakage in endodontically treated teeth can occur in only 2 - 3 days.38,39
In this study, the bacterial volume and cell viability were found to be highest when the samples were irrigated with NaOCl and NaOCl-EDTA. EDTA has been reported as a weak antibacterial agent, and its effect against gram-positive bacteria has been found to be almost nil.40 EDTA has shown selectivity for gram-negative bacteria and is known to destabilize the bacterial cell membrane and cause release of lipopolysaccharides. In contrast, the biofilm formed after treatment with NaOCl-EDTA-CNPs and NaOCl-CNPs were significantly lower than that in the control and NaOCl-EDTA groups. These results corroborate the theory that chitosan has the ability to interfere with bacterial adhesion thereby hindering the biofilm formation, and that EDTA has the power to alter the physicochemical properties of dentin that contribute to the bacterial adhesion.10,15
The antibacterial mechanism of chitosan has been attributed to its polycationic nature that interacts with the negatively charged surface of bacteria, altering cell permeability and resulting in the leakage of intracellular components.41,42 In addition, CNPs are able to inhibit bacterial enzymatic degradation reducing the possibility of bacterial penetration and dentinal micro-fractures.43 This biopolymer is also capable of improving the mechanical properties of the root dentin.13 Grande et al. showed that the reaction between NaOCl and EDTA led a very slow degradation of the acid.44 Although degradation of EDTA was progressive, its properties were not affected in periods of time clinically realistic. In addition, the structure and molecular weight of chitosan have been found to be affected by oxidation caused by NaOCl.45 However, more detailed evidence on the interaction of NaOCl with chitosan applicable to root canal disinfection is required.
CNPs have the potential to be used as a final irrigant and a useful alternative to EDTA in root canal treatment due to its ability to act as an antibiofilm agent and a chelating agent on root dentin.
This study was supported by the São Paulo Research Foundation (FAPESP 2011/08184-8 and 2012/06738-9) and the National Counsel of Technological and Scientific Development (CNPq).

Conflict of Interest: No potential conflict of interest relevant to this article was reported.

Figure 1

Representative images from the portable scanning electron microscope (×500) and confocal laser scanning microscope (×40). The irrigated pre-infection samples can be seen in images (a) - (e), and the infected samples after experimental irrigation protocols can be seen in images (f) - (j). A substantial amount of smear layer was observed when the samples were irrigated with sterile distilled water (a) and NaOCl (b). Visible dentinal tubules were seen in the samples treated with NaOCl-EDTA (c), NaOCl-EDTA-CNPs (d) and NaOCl-CNPs (e). A positive cellular viability and evident biomass were observed in the control (f), NaOCl (g) and NaOCl-EDTA (h) groups. The NaOCl-EDTA-CNPs and NaOCl-CNPs groups had decreased biomass (i) and interfered with bacterial growth (j). All bars represent 20 µm.

rde-40-195-g001.jpg
Figure 2

The percentage of areas with open dentinal tubules for each score (1 to 4). Having less than 10% of the area containing open dentinal tubules was scored as one, having 10 - 50% of the area containing open dentinal tubules was scored as two, having 50 - 70% of the area containing open dentinal tubules was scored as three and having more than 70% of the area containing open dentinal tubules was scored as four.

*Different letters within a column depict a significant difference (p < 0.05).
NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochloriteethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.
rde-40-195-g002.jpg
Table 1

Medians (25 - 75 percentiles) of the total biovolume and the percentage of live cells of the comparisons among the groups

Total Biovolume (µm3/µm2) Percentage of live cells
Control 5.0 (4.0 - 5.4)a 92 (90 - 96)a
NaOCl 3.9 (3.1 - 5.1)ab 90 (85 - 92)a
NaOCl-EDTA 3.6 (2.8 - 5.1)ab 91 (87 - 94)a
NaOCl-EDTA-CNPs 2.6 (0.85 - 4.4)c 73 (51 - 86)b
NaOCl-CNPs 2.7 (1.8 - 4.2)bc 77 (60 - 83)b

*Different superscript letters in each column represent significant differences (p < 0.05).

NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochlorite-ethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.

  • 1. Costerton JW, Stewart PS, Greenberg EP. Bacterial biofilms: a common cause of persistent infections. Science 1999;284:1318-1322.ArticlePubMed
  • 2. Siqueira JF Jr, Paiva SS, Rôças IN. Reduction in the cultivable bacterial populations in infected root canals by a chlorhexidine-based antimicrobial protocol. J Endod 2007;33:541-547.ArticlePubMed
  • 3. Pascon FM, Kantovitz KR, Sacramento PA, Nobredos-Santos M, Puppin-Rontani RM. Effect of sodium hypochlorite on dentin mechanical properties. A review. J Dent 2009;37:903-908.PubMed
  • 4. Del Carpio-Perochena AE, Bramante CM, Duarte MA, Cavenago BC, Villas-Boas MH, Graeff MS, Bernardineli N, de Andrade FB, Ordinola-Zapata R. Biofilm dissolution and cleaning ability of different irrigant solutions on intraorally infected dentin. J Endod 2011;37:1134-1138.ArticlePubMed
  • 5. Zhang K, Kim YK, Cadenaro M, Bryan TE, Sidow SJ, Loushine RJ, Ling JQ, Pashley DH, Tay FR. Effects of different exposure times and concentrations of sodium hypochlorite/ethylenediaminetetraacetic acid on the structural integrity of mineralized dentin. J Endod 2010;36:105-109.ArticlePubMed
  • 6. Calt S, Serper A. Time-dependent effects of EDTA on dentin structures. J Endod 2002;28:17-19.ArticlePubMed
  • 7. Torabinejad M, Handysides R, Khademi AA, Bakland LK. Clinical implications of the smear layer in endodontics: a review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2002;94:658-666.ArticlePubMed
  • 8. Violich DR, Chandler NP. The smear layer in endodontics - a review. Int Endod J 2010;43:2-15.ArticlePubMed
  • 9. Garberoglio R, Becce C. Smear layer removal by root canal irrigants. A comparative scanning electron microscopic study. Oral Surg Oral Med Oral Pathol 1994;78:359-367.PubMed
  • 10. Kishen A, Sum CP, Mathew S, Lim CT. Influence of irrigation regimens on the adherence of Enterococcus faecalis to root canal dentin. J Endod 2008;34:850-854.ArticlePubMed
  • 11. Sinha VR, Singla AK, Wadhawan S, Kaushik R, Kumria R, Bansal K, Dhawan S. Chitosan microspheres as a potential carrier for drugs. Int J Pharm 2004;274:1-33.PubMed
  • 12. Xu Z, Neoh KG, Lin CC, Kishen A. Biomimetic deposition of calcium phosphate minerals on the surface of partially demineralized dentin modified with phosphorylated chitosan. J Biomed Mater Res B Appl Biomater 2011;98:150-159.PubMed
  • 13. Shrestha A, Friedman S, Kishen A. Photodynamically crosslinked and chitosan-incorporated dentin collagen. J Dent Res 2011;90:1346-1351.ArticlePubMedPDF
  • 14. No HK, Park NY, Lee SH, Meyers SP. Antibacterial activity of chitosans and chitosan oligomers with different molecular weights. Int J Food Microbiol 2002;74:65-72.ArticlePubMed
  • 15. Kishen A, Shi Z, Shrestha A, Neoh KG. An investigation on the antibacterial and antibiofilm efficacy of cationic nanoparticulates for root canal disinfection. J Endod 2008;34:1515-1520.ArticlePubMed
  • 16. Silva PV, Guedes DF, Nakadi FV, Pécora JD, Cruz-Filho AM. Chitosan: a new solution for removal of smear layer after root canal instrumentation. Int Endod J 2013;46:332-338.ArticlePubMed
  • 17. Calamari SE, Bojanich MA, Barembaum SR, Berdicevski N, Azcurra AI. Antifungal and post-antifungal effects of chlorhexidine, fluconazole, chitosan and its combinations on Candida albicans. Med Oral Patol Oral Cir Bucal 2011;16:e23-e28.ArticlePubMed
  • 18. Magura ME, Kafrawy AH, Brown CE Jr, Newton CW. Human saliva coronal microleakage in obturated root canals: an in vitro study. J Endod 1991;17:324-331.ArticlePubMed
  • 19. Silva PV, Guedes DF, Pécora JD, da Cruz-Filho AM. Time-dependent effects of chitosan on dentin structures. Braz Dent J 2012;23:357-361.ArticlePubMed
  • 20. De Moura MR, Aouada FA, Avena-Bustillos RJ, McHugh TH, Krochta JM, Mattoso LHC. Improved barrier and mechanical properties of novel hydroxypropyl methylcellulose edible films with chitosan/tripolyphosphate nanoparticles. J Food Eng 2009;92:448-453.Article
  • 21. Zandim DL, Corrêa FO, Rossa Júnior C, Sampaio JE. In vitro evaluation of the effect of natural orange juices on dentin morphology. Braz Oral Res 2008;22:176-183.ArticlePubMed
  • 22. Heydorn A, Nielsen AT, Hentzer M, Sternberg C, Givskov M, Ersbøll BK, Molin S. Quantification of biofilm structures by the novel computer program COMSTAT. Microbiology 2000;146:2395-2407.ArticlePubMed
  • 23. Chávez de Paz LE. Image analysis software based on color segmentation for characterization of viability and physiological activity of biofilms. Appl Environ Microbiol 2009;75:1734-1739.ArticlePubMedPMCPDF
  • 24. Wegehaupt F, Gries D, Wiegand A, Attin T. Is bovine dentin an appropriate substitute for human dentin in erosion/abrasion tests? J Oral Rehabil 2008;35:390-394.PubMed
  • 25. Whitehead KA, Rogers D, Colligon J, Wright C, Verran J. Use of the atomic force microscope to determine the effect of substratum surface topography on the ease of bacterial removal. Colloids Surf B Biointerfaces 2006;51:44-53.ArticlePubMed
  • 26. Lopes MB, Sinhoreti MA, Gonini Júnior A, Consani S, McCabe JF. Comparative study of tubular diameter and quantity for human and bovine dentin at different depths. Braz Dent J 2009;20:279-283.ArticlePubMed
  • 27. Del Carpio-Perochena A, Bramante CM, Hungaro Duarte MA, de Andrade FB, Cavenago BC, Villas-Bôas MH, Ordinola-Zapata R, Amoroso-Silva P. Application of laser scanning microscopy for the analysis of oral biofilm dissolution by different endodontic irrigants. Dent Res J (Isfahan) 2014;11:442-447.PubMedPMC
  • 28. Ordinola-Zapata R, Bramante CM, Cavenago B, Graeff MS, Gomes de Moraes I, Marciano M, Duarte MA. Antimicrobial effect of endodontic solutions used as final irrigants on a dentin biofilm model. Int Endod J 2012;45:162-168.PubMed
  • 29. Inoue K, Yoshizuka K, Ohto K. Adsorptive separation of some metal ions by complexing agent types of chemically modified chitosan. Anal Chim Acta 1999;388:209-218.Article
  • 30. Bassi R, Prasher SO, Simpson BK. Effects of organic acids on the adsorption of heavy metal ions by chitosan flakes. J Environ Sci Health 1999;34:289-294.Article
  • 31. Blair HS, Ho TC. Studies in the adsorption and diffusion of ions in chitosan. J Chem Technol Biotechnol 1981;31:6-10.Article
  • 32. Vold IMN, Vårum KM, Guibal E, Smidsrød O. Binding of ions to chitosan-selectivity studies. Carbohydr Polym 2003;54:471-477.Article
  • 33. Pimenta JA, Zaparolli D, Pécora JD, Cruz-Filho AM. Chitosan: effect of a new chelating agent on the microhardness of root dentin. Braz Dent J 2012;23:212-217.ArticlePubMed
  • 34. Costerton JW, Cheng KJ, Geesey GG, Ladd TI, Nickel JC, Dasgupta M, Marrie TJ. Bacterial biofilms in nature and disease. Annu Rev Microbiol 1987;41:435-464.ArticlePubMed
  • 35. Wang QQ, Zhang CF, Chu CH, Zhu XF. Prevalence of Enterococcus faecalis in saliva and filled root canals of teeth associated with apical periodontitis. Int J Oral Sci 2012;4:19-23.ArticlePubMedPMCPDF
  • 36. Saunders WP, Saunders EM. Coronal leakage as a cause of failure in root-canal therapy: a review. Endod Dent Traumatol 1994;10:105-108.ArticlePubMed
  • 37. Hasan NA, Young BA, Minard-Smith AT, Saeed K, Li H, Heizer EM, McMillan NJ, Isom R, Abdullah AS, Bornman DM, Faith SA, Choi SY, Dickens ML, Cebula TA, Colwell RR. Microbial community profiling of human saliva using shotgun metagenomic sequencing. PLoS One 2014;9:e97699.ArticlePubMedPMC
  • 38. Madison S, Swanson K, Chiles SA. An evaluation of coronal microleakage in endodontically treated teeth. Part II. Sealer types. J Endod 1987;13:109-112.ArticlePubMed
  • 39. Madison S, Wilcox LR. An evaluation of coronal microleakage in endodontically treated teeth. Part III. In vivo study. J Endod 1988;14:455-458.ArticlePubMed
  • 40. Gray GW, Wilkinson SG. The effect of ethylenediaminetetra-acetic acid on cell walls of some gram-negative bacteria. J Gen Microbiol 1965;39:385-399.PubMed
  • 41. Rabea EI, Badawy ME, Stevens CV, Smagghe G, Steurbaut W. Chitosan as antimicrobial agent: applications and mode of action. Biomacromolecules 2003;4:1457-1465.ArticlePubMed
  • 42. Young DH, Köhle H, Kauss H. Effect of chitosan on membrane-permeability of suspension-cultured glycine-max and phaseolus-vulgaris cells. Plant Physiol 1982;70:1449-1454.ArticlePubMedPMC
  • 43. Persadmehr A, Torneck CD, Cvitkovitch DG, Pinto V, Talior I, Kazembe M, Shrestha S, McCulloch CA, Kishen A. Bioactive chitosan nanoparticles and photodynamic therapy inhibit collagen degradation in vitro. J Endod 2014;40:703-709.ArticlePubMed
  • 44. Grande NM, Plotino G, Falanga A, Pomponi M, Somma F. Interaction between EDTA and sodium hypochlorite: a nuclear magnetic resonance analysis. J Endod 2006;32:460-464.ArticlePubMed
  • 45. Yoo SH, Lee JS, Park SY, Kim YS, Chang PS, Lee HG. Effects of selective oxidation of chitosan on physical and biological properties. Int J Biol Macromol 2005;35:27-31.ArticlePubMed

Tables & Figures

rde-40-195-g001.jpg Figure 1 

Representative images from the portable scanning electron microscope (×500) and confocal laser scanning microscope (×40). The irrigated pre-infection samples can be seen in images (a) - (e), and the infected samples after experimental irrigation protocols can be seen in images (f) - (j). A substantial amount of smear layer was observed when the samples were irrigated with sterile distilled water (a) and NaOCl (b). Visible dentinal tubules were seen in the samples treated with NaOCl-EDTA (c), NaOCl-EDTA-CNPs (d) and NaOCl-CNPs (e). A positive cellular viability and evident biomass were observed in the control (f), NaOCl (g) and NaOCl-EDTA (h) groups. The NaOCl-EDTA-CNPs and NaOCl-CNPs groups had decreased biomass (i) and interfered with bacterial growth (j). All bars represent 20 µm.

Download Figure Download Figure
rde-40-195-g002.jpg Figure 2 

The percentage of areas with open dentinal tubules for each score (1 to 4). Having less than 10% of the area containing open dentinal tubules was scored as one, having 10 - 50% of the area containing open dentinal tubules was scored as two, having 50 - 70% of the area containing open dentinal tubules was scored as three and having more than 70% of the area containing open dentinal tubules was scored as four.

*Different letters within a column depict a significant difference (p < 0.05).
NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochloriteethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.
Download Figure Download Figure
Table 1

Medians (25 - 75 percentiles) of the total biovolume and the percentage of live cells of the comparisons among the groups

Total Biovolume (µm3/µm2) Percentage of live cells
Control 5.0 (4.0 - 5.4)a 92 (90 - 96)a
NaOCl 3.9 (3.1 - 5.1)ab 90 (85 - 92)a
NaOCl-EDTA 3.6 (2.8 - 5.1)ab 91 (87 - 94)a
NaOCl-EDTA-CNPs 2.6 (0.85 - 4.4)c 73 (51 - 86)b
NaOCl-CNPs 2.7 (1.8 - 4.2)bc 77 (60 - 83)b

*Different superscript letters in each column represent significant differences (p < 0.05).

NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochlorite-ethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.

Download Table Download Table
Figure 1

Representative images from the portable scanning electron microscope (×500) and confocal laser scanning microscope (×40). The irrigated pre-infection samples can be seen in images (a) - (e), and the infected samples after experimental irrigation protocols can be seen in images (f) - (j). A substantial amount of smear layer was observed when the samples were irrigated with sterile distilled water (a) and NaOCl (b). Visible dentinal tubules were seen in the samples treated with NaOCl-EDTA (c), NaOCl-EDTA-CNPs (d) and NaOCl-CNPs (e). A positive cellular viability and evident biomass were observed in the control (f), NaOCl (g) and NaOCl-EDTA (h) groups. The NaOCl-EDTA-CNPs and NaOCl-CNPs groups had decreased biomass (i) and interfered with bacterial growth (j). All bars represent 20 µm.

rde-40-195-g001.jpg
Figure 2

The percentage of areas with open dentinal tubules for each score (1 to 4). Having less than 10% of the area containing open dentinal tubules was scored as one, having 10 - 50% of the area containing open dentinal tubules was scored as two, having 50 - 70% of the area containing open dentinal tubules was scored as three and having more than 70% of the area containing open dentinal tubules was scored as four.

*Different letters within a column depict a significant difference (p < 0.05).
NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochloriteethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.
rde-40-195-g002.jpg
Table 1

Medians (25 - 75 percentiles) of the total biovolume and the percentage of live cells of the comparisons among the groups

Total Biovolume (µm3/µm2) Percentage of live cells
Control 5.0 (4.0 - 5.4)a 92 (90 - 96)a
NaOCl 3.9 (3.1 - 5.1)ab 90 (85 - 92)a
NaOCl-EDTA 3.6 (2.8 - 5.1)ab 91 (87 - 94)a
NaOCl-EDTA-CNPs 2.6 (0.85 - 4.4)c 73 (51 - 86)b
NaOCl-CNPs 2.7 (1.8 - 4.2)bc 77 (60 - 83)b

*Different superscript letters in each column represent significant differences (p < 0.05).

NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochlorite-ethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.

REFERENCES

  • 1. Costerton JW, Stewart PS, Greenberg EP. Bacterial biofilms: a common cause of persistent infections. Science 1999;284:1318-1322.ArticlePubMed
  • 2. Siqueira JF Jr, Paiva SS, Rôças IN. Reduction in the cultivable bacterial populations in infected root canals by a chlorhexidine-based antimicrobial protocol. J Endod 2007;33:541-547.ArticlePubMed
  • 3. Pascon FM, Kantovitz KR, Sacramento PA, Nobredos-Santos M, Puppin-Rontani RM. Effect of sodium hypochlorite on dentin mechanical properties. A review. J Dent 2009;37:903-908.PubMed
  • 4. Del Carpio-Perochena AE, Bramante CM, Duarte MA, Cavenago BC, Villas-Boas MH, Graeff MS, Bernardineli N, de Andrade FB, Ordinola-Zapata R. Biofilm dissolution and cleaning ability of different irrigant solutions on intraorally infected dentin. J Endod 2011;37:1134-1138.ArticlePubMed
  • 5. Zhang K, Kim YK, Cadenaro M, Bryan TE, Sidow SJ, Loushine RJ, Ling JQ, Pashley DH, Tay FR. Effects of different exposure times and concentrations of sodium hypochlorite/ethylenediaminetetraacetic acid on the structural integrity of mineralized dentin. J Endod 2010;36:105-109.ArticlePubMed
  • 6. Calt S, Serper A. Time-dependent effects of EDTA on dentin structures. J Endod 2002;28:17-19.ArticlePubMed
  • 7. Torabinejad M, Handysides R, Khademi AA, Bakland LK. Clinical implications of the smear layer in endodontics: a review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2002;94:658-666.ArticlePubMed
  • 8. Violich DR, Chandler NP. The smear layer in endodontics - a review. Int Endod J 2010;43:2-15.ArticlePubMed
  • 9. Garberoglio R, Becce C. Smear layer removal by root canal irrigants. A comparative scanning electron microscopic study. Oral Surg Oral Med Oral Pathol 1994;78:359-367.PubMed
  • 10. Kishen A, Sum CP, Mathew S, Lim CT. Influence of irrigation regimens on the adherence of Enterococcus faecalis to root canal dentin. J Endod 2008;34:850-854.ArticlePubMed
  • 11. Sinha VR, Singla AK, Wadhawan S, Kaushik R, Kumria R, Bansal K, Dhawan S. Chitosan microspheres as a potential carrier for drugs. Int J Pharm 2004;274:1-33.PubMed
  • 12. Xu Z, Neoh KG, Lin CC, Kishen A. Biomimetic deposition of calcium phosphate minerals on the surface of partially demineralized dentin modified with phosphorylated chitosan. J Biomed Mater Res B Appl Biomater 2011;98:150-159.PubMed
  • 13. Shrestha A, Friedman S, Kishen A. Photodynamically crosslinked and chitosan-incorporated dentin collagen. J Dent Res 2011;90:1346-1351.ArticlePubMedPDF
  • 14. No HK, Park NY, Lee SH, Meyers SP. Antibacterial activity of chitosans and chitosan oligomers with different molecular weights. Int J Food Microbiol 2002;74:65-72.ArticlePubMed
  • 15. Kishen A, Shi Z, Shrestha A, Neoh KG. An investigation on the antibacterial and antibiofilm efficacy of cationic nanoparticulates for root canal disinfection. J Endod 2008;34:1515-1520.ArticlePubMed
  • 16. Silva PV, Guedes DF, Nakadi FV, Pécora JD, Cruz-Filho AM. Chitosan: a new solution for removal of smear layer after root canal instrumentation. Int Endod J 2013;46:332-338.ArticlePubMed
  • 17. Calamari SE, Bojanich MA, Barembaum SR, Berdicevski N, Azcurra AI. Antifungal and post-antifungal effects of chlorhexidine, fluconazole, chitosan and its combinations on Candida albicans. Med Oral Patol Oral Cir Bucal 2011;16:e23-e28.ArticlePubMed
  • 18. Magura ME, Kafrawy AH, Brown CE Jr, Newton CW. Human saliva coronal microleakage in obturated root canals: an in vitro study. J Endod 1991;17:324-331.ArticlePubMed
  • 19. Silva PV, Guedes DF, Pécora JD, da Cruz-Filho AM. Time-dependent effects of chitosan on dentin structures. Braz Dent J 2012;23:357-361.ArticlePubMed
  • 20. De Moura MR, Aouada FA, Avena-Bustillos RJ, McHugh TH, Krochta JM, Mattoso LHC. Improved barrier and mechanical properties of novel hydroxypropyl methylcellulose edible films with chitosan/tripolyphosphate nanoparticles. J Food Eng 2009;92:448-453.Article
  • 21. Zandim DL, Corrêa FO, Rossa Júnior C, Sampaio JE. In vitro evaluation of the effect of natural orange juices on dentin morphology. Braz Oral Res 2008;22:176-183.ArticlePubMed
  • 22. Heydorn A, Nielsen AT, Hentzer M, Sternberg C, Givskov M, Ersbøll BK, Molin S. Quantification of biofilm structures by the novel computer program COMSTAT. Microbiology 2000;146:2395-2407.ArticlePubMed
  • 23. Chávez de Paz LE. Image analysis software based on color segmentation for characterization of viability and physiological activity of biofilms. Appl Environ Microbiol 2009;75:1734-1739.ArticlePubMedPMCPDF
  • 24. Wegehaupt F, Gries D, Wiegand A, Attin T. Is bovine dentin an appropriate substitute for human dentin in erosion/abrasion tests? J Oral Rehabil 2008;35:390-394.PubMed
  • 25. Whitehead KA, Rogers D, Colligon J, Wright C, Verran J. Use of the atomic force microscope to determine the effect of substratum surface topography on the ease of bacterial removal. Colloids Surf B Biointerfaces 2006;51:44-53.ArticlePubMed
  • 26. Lopes MB, Sinhoreti MA, Gonini Júnior A, Consani S, McCabe JF. Comparative study of tubular diameter and quantity for human and bovine dentin at different depths. Braz Dent J 2009;20:279-283.ArticlePubMed
  • 27. Del Carpio-Perochena A, Bramante CM, Hungaro Duarte MA, de Andrade FB, Cavenago BC, Villas-Bôas MH, Ordinola-Zapata R, Amoroso-Silva P. Application of laser scanning microscopy for the analysis of oral biofilm dissolution by different endodontic irrigants. Dent Res J (Isfahan) 2014;11:442-447.PubMedPMC
  • 28. Ordinola-Zapata R, Bramante CM, Cavenago B, Graeff MS, Gomes de Moraes I, Marciano M, Duarte MA. Antimicrobial effect of endodontic solutions used as final irrigants on a dentin biofilm model. Int Endod J 2012;45:162-168.PubMed
  • 29. Inoue K, Yoshizuka K, Ohto K. Adsorptive separation of some metal ions by complexing agent types of chemically modified chitosan. Anal Chim Acta 1999;388:209-218.Article
  • 30. Bassi R, Prasher SO, Simpson BK. Effects of organic acids on the adsorption of heavy metal ions by chitosan flakes. J Environ Sci Health 1999;34:289-294.Article
  • 31. Blair HS, Ho TC. Studies in the adsorption and diffusion of ions in chitosan. J Chem Technol Biotechnol 1981;31:6-10.Article
  • 32. Vold IMN, Vårum KM, Guibal E, Smidsrød O. Binding of ions to chitosan-selectivity studies. Carbohydr Polym 2003;54:471-477.Article
  • 33. Pimenta JA, Zaparolli D, Pécora JD, Cruz-Filho AM. Chitosan: effect of a new chelating agent on the microhardness of root dentin. Braz Dent J 2012;23:212-217.ArticlePubMed
  • 34. Costerton JW, Cheng KJ, Geesey GG, Ladd TI, Nickel JC, Dasgupta M, Marrie TJ. Bacterial biofilms in nature and disease. Annu Rev Microbiol 1987;41:435-464.ArticlePubMed
  • 35. Wang QQ, Zhang CF, Chu CH, Zhu XF. Prevalence of Enterococcus faecalis in saliva and filled root canals of teeth associated with apical periodontitis. Int J Oral Sci 2012;4:19-23.ArticlePubMedPMCPDF
  • 36. Saunders WP, Saunders EM. Coronal leakage as a cause of failure in root-canal therapy: a review. Endod Dent Traumatol 1994;10:105-108.ArticlePubMed
  • 37. Hasan NA, Young BA, Minard-Smith AT, Saeed K, Li H, Heizer EM, McMillan NJ, Isom R, Abdullah AS, Bornman DM, Faith SA, Choi SY, Dickens ML, Cebula TA, Colwell RR. Microbial community profiling of human saliva using shotgun metagenomic sequencing. PLoS One 2014;9:e97699.ArticlePubMedPMC
  • 38. Madison S, Swanson K, Chiles SA. An evaluation of coronal microleakage in endodontically treated teeth. Part II. Sealer types. J Endod 1987;13:109-112.ArticlePubMed
  • 39. Madison S, Wilcox LR. An evaluation of coronal microleakage in endodontically treated teeth. Part III. In vivo study. J Endod 1988;14:455-458.ArticlePubMed
  • 40. Gray GW, Wilkinson SG. The effect of ethylenediaminetetra-acetic acid on cell walls of some gram-negative bacteria. J Gen Microbiol 1965;39:385-399.PubMed
  • 41. Rabea EI, Badawy ME, Stevens CV, Smagghe G, Steurbaut W. Chitosan as antimicrobial agent: applications and mode of action. Biomacromolecules 2003;4:1457-1465.ArticlePubMed
  • 42. Young DH, Köhle H, Kauss H. Effect of chitosan on membrane-permeability of suspension-cultured glycine-max and phaseolus-vulgaris cells. Plant Physiol 1982;70:1449-1454.ArticlePubMedPMC
  • 43. Persadmehr A, Torneck CD, Cvitkovitch DG, Pinto V, Talior I, Kazembe M, Shrestha S, McCulloch CA, Kishen A. Bioactive chitosan nanoparticles and photodynamic therapy inhibit collagen degradation in vitro. J Endod 2014;40:703-709.ArticlePubMed
  • 44. Grande NM, Plotino G, Falanga A, Pomponi M, Somma F. Interaction between EDTA and sodium hypochlorite: a nuclear magnetic resonance analysis. J Endod 2006;32:460-464.ArticlePubMed
  • 45. Yoo SH, Lee JS, Park SY, Kim YS, Chang PS, Lee HG. Effects of selective oxidation of chitosan on physical and biological properties. Int J Biol Macromol 2005;35:27-31.ArticlePubMed

Citations

Citations to this article as recorded by  
  • Comparison of Various Irrigation Techniques for the Removal of Silicone Oil-Based Calcium Hydroxide Intracanal Medicament from the Apical Third: An SEM Study
    Shalin Ann Saji, Chitharanjan Shetty, Gurmeen Kaur, Sunheri Bajpe, Chandraprabha Chandraprabha, Rashi Shroff, Shazeena Qaiser, Surabhi Gupta
    Journal of Health and Allied Sciences NU.2025; 15(01): 103.     CrossRef
  • Comparative evaluation of smear layer removal and dentin wettability using 1% phytic acid with and without 0.2% chitosan nanoparticles: An in vitro study
    Rahul Halkai, Kiran R. Halkai, Syeda Uzma Mahveen
    Saudi Endodontic Journal.2025; 15(1): 38.     CrossRef
  • Chitosan’s Ability to Remove the Smear Layer—A Systematic Review of Ex Vivo Studies
    Ana Ferreira-Reguera, Inês Ferreira, Irene Pina-Vaz, Benjamín Martín-Biedma, José Martín-Cruces
    Medicina.2025; 61(1): 114.     CrossRef
  • Nanoparticles modified bioceramic sealers on solubility, antimicrobial efficacy, pushout bond strength and marginal adaptation at apical-third of canal dentin
    Basil Almutairi, Fahad Alkhudhairy
    PeerJ.2025; 13: e18840.     CrossRef
  • Optimization of chitosan nanoparticle dentin pretreatment with different concentrations and application times to improve bonding at resin-dentin interface
    Rinki Meher, Rashmi Rekha Mallick, Priyanka Sarangi, Amit Jena, Shradha Suman, Gaurav Sharma
    Journal of Conservative Dentistry and Endodontics.2025; 28(3): 248.     CrossRef
  • Comparison of penetration depth of chitosan, zinc oxide, and silica-doped titanium novel nanoparticle irrigant solutions – A confocal laser scanning microscopic in vitro study
    Sree Laksmi Bademela, T. B. V. G. Raju, Krishna Prasad Parvathaneni, Abitha Seshadri, Nadimpalli Mahendra Varma, Gowtam Dev Dondapati
    Endodontology.2024; 36(3): 280.     CrossRef
  • Combined use of XP-Endo Finisher and different chelating agents on the smear layer
    Meenu Elizabeth Saju, Ramya Raghu, Ashish Shetty, Lekha Santhosh, Subhashini Rajasekhara, Priya C. Yadav
    Endodontology.2024;[Epub]     CrossRef
  • Therapeutic efficacy of chitosan-based hybrid nanomaterials to treat microbial biofilms and their infections – A review
    Anisha Salim, Palanivel Sathishkumar
    International Journal of Biological Macromolecules.2024; 283: 137850.     CrossRef
  • Local and systemic adverse effects of nanoparticles incorporated in dental materials- a critical review
    Harini Karunakaran, Jogikalmat Krithikadatta, Mukesh Doble
    The Saudi Dental Journal.2024; 36(1): 158.     CrossRef
  • Effect of final irrigation protocols with chitosan nanoparticle and genipin on dentine against collagenase degradation: An ex‐vivo study
    S. N. Şengül, S. Ozturk, K. Ulubayram, N. Pekel Bayramgil, S. Kucukkaya Eren
    International Endodontic Journal.2024; 57(4): 477.     CrossRef
  • Application of Nanomaterials in Endodontics
    Farzaneh Afkhami, Yuan Chen, Laurence J. Walsh, Ove A. Peters, Chun Xu
    BME Frontiers.2024;[Epub]     CrossRef
  • Evaluation of the Effect of Chitosan-Based Irrigation Solutions on the Bond Strength of Mineral Trioxide Aggregate to Bulk-Fill Composite
    Arzu Şahin Mantı, Bağdagül Helvacıoğlu Kıvanç
    Journal of Functional Biomaterials.2024; 15(12): 370.     CrossRef
  • In vitro analysis of compressive strength of root dentin on application of intracanal medicaments for different time periods
    Kushal Kumar Ghosh, Sayantan Mukherjee, Paromita Mazumdar, Sahil Ali, Lovely Das
    Journal of Conservative Dentistry and Endodontics.2024; 27(12): 1289.     CrossRef
  • The comparative of chitosan and chitosan nanoparticle versus ethylenediaminetetraacetic acid on the smear layer removal: A systematic review and meta‐analysis of in vitro study
    Hasan İlhan, Elif Bahar Cakici, Fatih Cakici
    Microscopy Research and Technique.2024; 87(2): 181.     CrossRef
  • Final Irrigant Temoporfin, Femtosecond Laser, and Chitosan Nanoparticles on Extrusion Bond Strength of Glass Fiber Post, Microhardness, and Modulus of Elasticity of Canal Dentin
    Lujain Ibrahim N. Aldosari
    Journal of Biomaterials and Tissue Engineering.2024; 14(2): 78.     CrossRef
  • Comparative analysis of an epoxy resin-based and a premixed calcium silicate-based sealer’s push-out bond strength with and without incorporation of chitosan nanoparticles: An in vitro investigation
    S. Harishma, K. B. Jeyalakshmi, K. Shibani Shetty, S. Harshini
    Journal of Conservative Dentistry and Endodontics.2024; 27(9): 970.     CrossRef
  • Chitosan: A Versatile Biomaterial Revolutionizing Endodontic Therapy
    Akash Thakare, Shweta Sedani, Simran Kriplani , Aditya Patel, Utkarsh Umre
    Cureus.2024;[Epub]     CrossRef
  • Evaluation of the Effect of Farnesol and/or Chitosan as a Final Irrigation on Enterococcus faecalis Biofilm; An In-vitro Study
    Ardavan Moinafshar, Hanieh Paik, Rashid Ramazanzadeh, Amjad Ahmadi, Mohammad Rastegar Khosravi
    Scientific Journal of Kurdistan University of Medical Sciences.2024; 29(1): 85.     CrossRef
  • Bionanomaterials an emerging field of nanotechnology
    A.R. Shelin, S. Meenakshi
    Archives of Materials Science and Engineering.2023; 121(1): 33.     CrossRef
  • Bonding of chitosan and nanochitosan modified universal adhesive to dentin
    Yasmin Ezz El-Din, Ahmed El-Banna, Tarek Salah Hussein
    International Journal of Adhesion and Adhesives.2023; 125: 103432.     CrossRef
  • Nanoparticles and Their Antibacterial Application in Endodontics
    Nicoletta Capuano, Alessandra Amato, Federica Dell’Annunziata, Francesco Giordano, Veronica Folliero, Federica Di Spirito, Pragati Rajendra More, Anna De Filippis, Stefano Martina, Massimo Amato, Massimiliano Galdiero, Alfredo Iandolo, Gianluigi Franci
    Antibiotics.2023; 12(12): 1690.     CrossRef
  • In vitro techniques for evaluating smear layer removal by root canal irrigants: a literature review
    Luis Hernán Carrillo Varguez, Aracely Serrano-Medina, Eduardo Alberto López Maldonado, Eustolia Rodríguez Velázquez, José Manuel Cornejo-Bravo
    Horizon Interdisciplinary Journal.2023; 1(2): 58.     CrossRef
  • Applicability of a Natural Nano-derivative as a Mouth Rinse on Salivary pH and S. mutans Count: An Ex Vivo Study
    Raja S Prathigudupu, Deepthi N Gavarraju, Sai S Kallam, Sai Sankar J Avula, Chaitanya M Sattenapalli, Amrutha Valli Audipudi
    World Journal of Dentistry.2023; 14(3): 207.     CrossRef
  • Nanopartículas antimicrobianas en endodoncia: Revisión narrativa
    Gustavo Adolfo Tovar Rangel , Fanny Mildred González Sáenz , Ingrid Ximena Zamora Córdoba , Lina María García Zapata
    Revista Estomatología.2023;[Epub]     CrossRef
  • Quantification of Calcium Ions From the Irrigants Activated With Erbium-Doped Yttrium Aluminum Garnet (Er:YAG) Laser in the Root Dentin: An In Vitro Atomic Absorption Spectrophotometer Study
    Dhanalakshmi P, Kiran Kumar N, K Rashmi, Biji Brigit, Shwetha R S, Sourabh T J
    Cureus.2023;[Epub]     CrossRef
  • Evaluation of chelating effect of chitosan as intracanal lubricant and an irrigant on smear layer removal – An in-vitro scanning electron microscope study
    Thati Jyotsnanjali, M. A. Ranjini, G. R. Krishna Kumar, D. V. Swapna, S. N. Joshi, Roopa R. Nadig
    Endodontology.2023; 35(3): 254.     CrossRef
  • Assessment of the Effectiveness of Two Different Dentin Biomodifiers on Shear Bond Strength of Dentin and Resin Interface: A Comparative Study
    Narendra V Penumatsa, AlWaleed Abushanan, Uthman S Uthman, Abdulhamid Al Ghwainem, Adel S Alqarni, Abdulfatah Alazmah
    World Journal of Dentistry.2023; 14(1): 16.     CrossRef
  • Scanning electron microscopy evaluation of smear layer removal using ethylenediaminetetraacetic acid, etidronic acid, and chitosan nanoparticle solution as root canal irrigants
    Sunheri Bajpe, Chitharanjan Shetty, Aditya Shetty, Gurmeen Kaur, Shalin Ann Saji, Chandra Prabha
    Endodontology.2023; 35(1): 48.     CrossRef
  • Green fabrication of chitosan nanoparticles using Lavendula angustifolia, optimization, characterization and in‑vitro antibiofilm activity
    Noura El-Ahmady El-Naggar, Marwa Eltarahony, Elsayed E. Hafez, Shimaa I. Bashir
    Scientific Reports.2023;[Epub]     CrossRef
  • Nanobiotechnology: Synthesis components and a few approaches for controlling plant diseases
    Malavika Ram A K, Ramji Singh, Meenakshi Rana, S.A. Dwivedi, Kshitij Parmar, Abha Sharma, Chitranjan Kumar, Vineeta Pandey, Vikash Kumar, Shashank Mishra, Ajay Tomar
    Plant Nano Biology.2023; 4: 100038.     CrossRef
  • Physicochemical and biological properties of a biostimulating membrane (BBio) for pulp capping
    Natalino Lourenço Neto, Luciana Lourenço Ribeiro Vitor, Silgia Aparecida da Costa, Sirlene Maria da Costa, Thiago Cruvinel, Thais Marchini Oliveira, Rodrigo Cardoso Oliveira, Maria Aparecida Andrade Moreira Machado
    Materials Letters.2022; 308: 131186.     CrossRef
  • In Vitro Study of Irrigation solution of Chitosan Nanoparticles to Inhibit the Adhesion and Biofilm Formation of Enterococcus faecalis in the Root Canal
    Imelda Darmawi, Trimurni Abidin, Harry Agusnar, Basri A. Gani
    Research Journal of Pharmacy and Technology.2022; : 2691.     CrossRef
  • Nanoparticles in Endodontics Disinfection: State of the Art
    Xavier Roig-Soriano, Eliana B. Souto, Firas Elmsmari, Maria Luisa Garcia, Marta Espina, Fernando Duran-Sindreu, Elena Sánchez-López, Jose Antonio González Sánchez
    Pharmaceutics.2022; 14(7): 1519.     CrossRef
  • An In Vitro Study Comparing the Antimicrobial Efficacy of 0.2% Chitosan, 3% Sodium Hypochlorite, 2% Chlorhexidine against Enterococcus faecalis, Alone and in Conjunction with Diode Laser
    Sameer Makkar, Tamanpreet Kaur, Pallavi Goel, Virat Galhotra, Jatinder Mohan, Neetu Bala
    International Journal of Clinical Pediatric Dentistry.2022; 15(1): 109.     CrossRef
  • Chitosan-Based Carbon Dots with Applied Aspects: New Frontiers of International Interest in a Material of Marine Origin
    Angel M. Villalba-Rodríguez, Reyna Berenice González-González, Manuel Martínez-Ruiz, Elda A. Flores-Contreras, María Fernanda Cárdenas-Alcaide, Hafiz M. N. Iqbal, Roberto Parra-Saldívar
    Marine Drugs.2022; 20(12): 782.     CrossRef
  • The Effect of Final Irrigation Protocols on the Apical Sealing Ability of Epoxy Resin-based and Bioceramic-based Root Canal Sealers
    Anan Medhat, Angie Ghoneim, Nehal Nabil Roshdy
    Open Access Macedonian Journal of Medical Sciences.2022; 10(D): 458.     CrossRef
  • Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria
    Ziliang Zhou, Yanyan Yang, Lu He, Junmei Wang, Jie Xiong
    Journal of Materials Science: Materials in Medicine.2022;[Epub]     CrossRef
  • Evaluation of Free Available Chlorine of Sodium Hypochlorite When Admixed with 0.2% Chitosan: A Preliminary Study
    Rupali Karale, Nithin K Shetty, Prashanth Bytarahosalli Rajachar, Mythreyee S Vidhya, Vinay Kumar Govindaraju
    The Journal of Contemporary Dental Practice.2022; 22(10): 1171.     CrossRef
  • Effect of chitosan irrigant solutions on the release of bioactive proteins from root dentin
    Sara Quijano-Guauque, Lilia J. Bernal-Cepeda, Félix G. Delgado, Jaime E. Castellanos, Claudia García-Guerrero
    Clinical Oral Investigations.2022; 27(2): 691.     CrossRef
  • Chemical and morphological characterization of self-etch primers incorporated with nanochitosan
    Pâmella Coelho Dias, Isabela Barbosa Quero, Juliana Jendiroba Faraoni, Regina Guenka Palma-Dibb
    International Journal of Adhesion and Adhesives.2022; 118: 103215.     CrossRef
  • The effects of different root canal irrigation protocols and artificial aging procedures on the bond strength between dentin and hybrid ceramic posts
    Celalettin Topbaş, Şevki Çınar, Bike Altan, Dursun Ali Şirin, Mehmet Ali Fildişi
    BMC Oral Health.2022;[Epub]     CrossRef
  • Effect of two different concentrations of chitosan irrigation on smear layer removal during root canal treatment
    Doaa M. Abd El-latif, Abeer M. Darrag, Dalia A. Sherif
    Tanta Dental Journal.2022; 19(4): 204.     CrossRef
  • Impact of Dentin Conditioning and Sealer Modification With Chitosan-Hydroxyapatite Nanocomplexes on the Antibacterial and Mechanical Characteristics of Root Dentin
    Aldo del Carpio-Perochena, Eric Nicholson, Chandra Veer Singh, Josette Camilleri, Anil Kishen
    Journal of Endodontics.2022; 48(10): 1319.     CrossRef
  • Assessment of Antimicrobial Efficacy of Nano Chitosan, Chlorhexidine, Chlorhexidine/Nano Chitosan Combination versus Sodium Hypochlorite Irrigation in Patients with Necrotic Mandibular Premolars: A Randomized Clinical Trial
    Maha Nasr, Alaa Diab, Nehal Roshdy, Amira Farouk
    Open Access Macedonian Journal of Medical Sciences.2021; 9(D): 235.     CrossRef
  • Enhanced visualization of the root canal morphology using a chitosan-based endo-radiopaque solution
    Shashirekha Govind, Amit Jena, Satabdi Pattanaik, Mahaprasad Anarasi, Satyajit Mohapatra, Vinay Shivagange
    Restorative Dentistry & Endodontics.2021;[Epub]     CrossRef
  • Chitosan-Based Biomaterial, Calcium Hydroxide and Chlorhexidine for Potential Use as Intracanal Medication
    Bruna de Siqueira Nunes, Rosana Araújo Rosendo, Abrahão Alves de Oliveira Filho, Marcus Vinícius Lia Fook, Wladymyr Jefferson Bacalhau de Sousa, Rossemberg Cardoso Barbosa, Hermano de Vasconcelos Pina, João Emídio da Silva Neto, Solomon Kweku Sagoe Amoah,
    Materials.2021; 14(3): 488.     CrossRef
  • Nanostructures as Targeted Therapeutics for Combating Oral Bacterial Diseases
    Shima Afrasiabi, Nasim Chiniforush, Hamid Reza Barikani, Alireza Partoazar, Ramin Goudarzi
    Biomedicines.2021; 9(10): 1435.     CrossRef
  • Microbiological Aspects of Root Canal Infections and Disinfection Strategies: An Update Review on the Current Knowledge and Challenges
    Jasmine Wong, Daniel Manoil, Peggy Näsman, Georgios N. Belibasakis, Prasanna Neelakantan
    Frontiers in Oral Health.2021;[Epub]     CrossRef
  • Nanomaterials Application in Endodontics
    Wojciech Zakrzewski, Maciej Dobrzyński, Anna Zawadzka-Knefel, Adam Lubojański, Wojciech Dobrzyński, Mateusz Janecki, Karolina Kurek, Maria Szymonowicz, Rafał Jakub Wiglusz, Zbigniew Rybak
    Materials.2021; 14(18): 5296.     CrossRef
  • Preparation and application of chitosan biomaterials in dentistry
    Chenxi Zhang, Didi Hui, Colin Du, Huan Sun, Wei Peng, Xiaobing Pu, Zhengyong Li, Jianxun Sun, Changchun Zhou
    International Journal of Biological Macromolecules.2021; 167: 1198.     CrossRef
  • The Potential Translational Applications of Nanoparticles in Endodontics
    Jasmine Wong, Ting Zou, Angeline Hui Cheng Lee, Chengfei Zhang
    International Journal of Nanomedicine.2021; Volume 16: 2087.     CrossRef
  • Chitosan Enhances the Anti-Biofilm Activity of Biodentine against an Interkingdom Biofilm Model
    Sumaya Abusrewil, Jason L. Brown, Christopher Delaney, Mark C. Butcher, Mohammed Tiba, J. Alun Scott, Gordon Ramage, William McLean
    Antibiotics.2021; 10(11): 1317.     CrossRef
  • Evaluation of Anti-Biofilm Activity of Mouthrinses Containing Tannic Acid or Chitosan on Dentin In Situ
    Anton Schestakow, Moritz S. Guth, Tobias A. Eisenmenger, Matthias Hannig
    Molecules.2021; 26(5): 1351.     CrossRef
  • An All-inclusive Estimation of Antibacterial and Antifungal Efficiencies of Propolis and Cetrimide Root Canal Irrigants against Enterococcus faecalis and Candida albicans: An In vitro (Original Research) Study
    Sumita Giri Nishad
    Journal of Research and Advancement in Dentistry.2021; 12(5): 185.     CrossRef
  • Carbohydrate-containing nanoparticles as vaccine adjuvants
    Xinyuan Zhang, Zhigang Zhang, Ningshao Xia, Qinjian Zhao
    Expert Review of Vaccines.2021; 20(7): 797.     CrossRef
  • RANDOMIZED CLINICAL TRIAL OF ANTIMICROBIAL EFFICACY OF TWO HERBAL PRODUCTS AS ROOT CANAL IRRIGANTS IN PRIMARY ENDODONTIC INFECTIONS.
    Sonam Dhall, Rakesh Mittal, Monika Tandan
    Journal of Indian Dental Association.2021;[Epub]     CrossRef
  • Preparation methods and applications of chitosan nanoparticles; with an outlook toward reinforcement of biodegradable packaging
    Murat Yanat, Karin Schroën
    Reactive and Functional Polymers.2021; 161: 104849.     CrossRef
  • Effect of the Incorporation of Chitosan and TiO2 Nanoparticles on the Shear Bond Strength of an Orthodontic Adhesive: An In Vitro Study
    Fahimeh Farzanegan, Hooman Shafaee, Majid Darroudi, Abdolrasoul Rangrazi
    Journal of Advanced Oral Research.2021; 12(2): 261.     CrossRef
  • Antibacterial effect of hyaluronan/chitosan nanofilm in the initial adhesion of Pseudomonas aeruginosa wild type, and IV pili and LPS mutant strains
    Jacobo Hernandez-Montelongo, Gianlucca G. Nicastro, Thays de O. Pereira, Mariana Zavarize, Marisa M. Beppu, Waldemar A.A. Macedo, Regina L. Baldini, Monica A. Cotta
    Surfaces and Interfaces.2021; 26: 101415.     CrossRef
  • Randomized Clinical Trial of Antimicrobial Effi cacy of two Herbal Products as Root Canal Irrigants in Primary Endodontic Infections
    Sonam Dhall, Rakesh Mittal, Monika Tandan
    Journal of Indian Dental Association.2021;[Epub]     CrossRef
  • Comparative Evaluation Of Fracture Resistance Of Root Dentin To Different Intracanal Medicaments: In-Vitro Study
    Anita Sanap-Tandale, Nikhil Borse, Kunal Kunjir, Karan Bhargava
    Annals of Dental Specialty.2021; 9(2): 86.     CrossRef
  • Engineering Polymeric Nanosystems against Oral Diseases
    Valeria Mercadante, Edoardo Scarpa, Valeria De Matteis, Loris Rizzello, Alessandro Poma
    Molecules.2021; 26(8): 2229.     CrossRef
  • Chelation capability of chitosan and chitosan derivatives: Recent developments in sustainable corrosion inhibition and metal decontamination applications
    Chandrabhan Verma, M.A. Quraishi
    Current Research in Green and Sustainable Chemistry.2021; 4: 100184.     CrossRef
  • Comparative effects of final canal irrigation with chitosan and EDTA
    Polliana Vilaça Silva Antunes, Luis Eduardo Souza Flamini, Jardel Francisco Mazzi Chaves, Ricardo Gariba Silva, Antonio Miranda da Cruz Filho
    Journal of Applied Oral Science.2020;[Epub]     CrossRef
  • Antibacterial property of chitosan against E. faecalis standard strain and clinical isolates
    Apimon SUPOTNGARMKUL, Anchana PANICHUTTRA, Chootima RATISOONTORN, Mettachit NAWACHINDA, Oranart MATANGKASOMBUT
    Dental Materials Journal.2020; 39(3): 456.     CrossRef
  • Polymeric and inorganic nanoscopical antimicrobial fillers in dentistry
    Pooyan Makvandi, Jun Ting Gu, Ehsan Nazarzadeh Zare, Behnaz Ashtari, Arash Moeini, Franklin R. Tay, Li-na Niu
    Acta Biomaterialia.2020; 101: 69.     CrossRef
  • A chitosan-based irrigant improves the dislocation resistance of a mineral trioxide aggregate-resin hybrid root canal sealer
    Esin Ozlek, Priti Pragati Rath, Anil Kishen, Prasanna Neelakantan
    Clinical Oral Investigations.2020; 24(1): 151.     CrossRef
  • Detection, treatment and prevention of endodontic biofilm infections: what’s new in 2020?
    Sumaya Abusrewil, Om Alkhir Alshanta, Khawlah Albashaireh, Saeed Alqahtani, Christopher J. Nile, James Alun Scott, William McLean
    Critical Reviews in Microbiology.2020; 46(2): 194.     CrossRef
  • Cytotoxicity of Chelating Agents Used In Endodontics and Their Influence on MMPs of Cell Membranes
    Kellin Pivatto, Fabio Luis Miranda Pedro, Orlando Aguirre Guedes, Adriana Fernandes da Silva, Evandro Piva, Thiago Machado Pereira, Welligton Luiz de Oliveira da Rosa, Alvaro Henrique Borges
    Brazilian Dental Journal.2020; 31(1): 32.     CrossRef
  • The Effect of Chitosan Nanoparticle as A Final Irrigation Solution on The Smear Layer Removal, Micro-hardness and Surface Roughness of Root Canal Dentin
    Diatri Nari Ratih, Raras Ajeng Enggardipta, Aqilla Tiara Kartikaningtyas
    The Open Dentistry Journal.2020; 14(1): 19.     CrossRef
  • Time-Dependent Effect of Chitosan Nanoparticles as Final Irrigation on the Apical Sealing Ability and Push-Out Bond Strength of Root Canal Obturation
    Diatri Nari Ratih, Nikita Ika Sari, Pribadi Santosa, Nofa Mardia Ningsih Kaswati
    International Journal of Dentistry.2020; 2020: 1.     CrossRef
  • Targeting tuberculosis infection in macrophages using chitosan oligosaccharide nanoplexes
    Uday Koli, Kayzad Nilgiriwala, Kalpana Sriraman, Ratnesh Jain, Prajakta Dandekar
    Journal of Nanoparticle Research.2019;[Epub]     CrossRef
  • Application of Antimicrobial Nanoparticles in Dentistry
    Wenjing Song, Shaohua Ge
    Molecules.2019; 24(6): 1033.     CrossRef
  • Assessment of antibacterial activity of 2.5% NaOCl, chitosan nano-particles against Enterococcus faecalis contaminating root canals with and without diode laser irradiation: an in vitro study
    Nehal Nabil Roshdy, Engy M. Kataia, Neveen A. Helmy
    Acta Odontologica Scandinavica.2019; 77(1): 39.     CrossRef
  • In Vitro Antimicrobial Effect of Bioadhesive Oral Membrane with Chlorhexidine Gel
    Annelyze Podolan Kloster, Natalino Lourenço Neto, Silgia Aparecida da Costa, Thais Marchini Oliveira, Rodrigo Cardoso de Oliveira, Maria Aparecida Andrade Moreira Machado
    Brazilian Dental Journal.2018; 29(4): 354.     CrossRef
  • How to improve root canal filling in teeth subjected to radiation therapy for cancer
    Fabiana de Góes Paiola, Fabiane Carneiro Lopes, Jardel Francisco Mazzi-Chaves, Rodrigo Dantas Pereira, Harley Francisco Oliveira, Alexandra Mussolino de Queiroz, Manoel Damião de Sousa-Neto
    Brazilian Oral Research.2018;[Epub]     CrossRef
  • Assessment of toxicity and oxidative DNA damage of sodium hypochlorite, chitosan and propolis on fibroblast cells
    Zeliha Uğur Aydin, Kerem Engin Akpinar, Ceylan Hepokur, Demet Erdönmez
    Brazilian Oral Research.2018;[Epub]     CrossRef
  • Recent developments in the use of nanoparticles for treatment of biofilms
    Chendong Han, Nicholas Romero, Stephen Fischer, Julia Dookran, Aaron Berger, Amber L. Doiron
    Nanotechnology Reviews.2017; 6(5): 383.     CrossRef
  • Assessment of the Amount of Calcium Ions Released after the use of Different Chelating Agents and Agitation Protocols
    Fábio Luis Miranda Pedro, Laura Maria Amorim Santana Costa, Gilberto Siebert Filho, Orlando Aguirre Guedes, Thiago Machado Pereira, Alvaro Henrique Borges
    The Open Dentistry Journal.2017; 11(1): 133.     CrossRef
  • Wettability and surface morphology of eroded dentin treated with chitosan
    Mirian Saavedra Ururahy, Fabiana Almeida Curylofo-Zotti, Rodrigo Galo, Lucas Fabricio Bahia Nogueira, Ana Paula Ramos, Silmara Aparecida Milori Corona
    Archives of Oral Biology.2017; 75: 68.     CrossRef
  • Biophysical and biological characterization of intraoral multilayer membranes as potential carriers: A new drug delivery system for dentistry
    Mariana dos Santos Silva, Natalino Lourenço Neto, Silgia Aparecida da Costa, Sirlene Maria da Costa, Thais Marchini Oliveira, Rodrigo Cardoso de Oliveira, Maria Aparecida Andrade Moreira Machado
    Materials Science and Engineering: C.2017; 71: 498.     CrossRef
  • Antibacterial Properties of Chitosan Nanoparticles and Propolis Associated with Calcium Hydroxide against Single- and Multispecies Biofilms: An In Vitro and In Situ Study
    Aldo del Carpio-Perochena, Anil Kishen, Rafael Felitti, Anjali Y. Bhagirath, Manoj R. Medapati, Christopher Lai, Rodrigo S. Cunha
    Journal of Endodontics.2017; 43(8): 1332.     CrossRef
  • Analysis of the shelf life of chitosan stored in different types of packaging, using colorimetry and dentin microhardness
    Antonio Miranda da Cruz-Filho, Angelo Rafael de Vito Bordin, Luis Eduardo Souza-Flamini, Débora Fernandes da Costa Guedes, Paulo César Saquy, Ricardo Gariba Silva, Jesus Djalma Pécora
    Restorative Dentistry & Endodontics.2017; 42(2): 87.     CrossRef
  • Does nanobiotechnology create new tools to combat microorganisms?
    Marlena K. Zielińska-Górska, Ewa Sawosz, Konrad Górski, André Chwalibog
    Nanotechnology Reviews.2017; 6(2): 171.     CrossRef
  • New frontiers for anti-biofilm drug development
    Suzana M. Ribeiro, Mário R. Felício, Esther Vilas Boas, Sónia Gonçalves, Fabrício F. Costa, Ramar Perumal Samy, Nuno C. Santos, Octávio L. Franco
    Pharmacology & Therapeutics.2016; 160: 133.     CrossRef
  • The effect of combined use of chitosan and PIPS on push-out bond strength of root canal filling materials
    Ugur Aydin, Fatih Aksoy, Samet Tosun, Abdul Semih Ozsevik
    Journal of Adhesion Science and Technology.2016; 30(18): 2024.     CrossRef
  • Organic Nanomaterials and Their Applications in the Treatment of Oral Diseases
    Maria Virlan, Daniela Miricescu, Radu Radulescu, Cristina Sabliov, Alexandra Totan, Bogdan Calenic, Maria Greabu
    Molecules.2016; 21(2): 207.     CrossRef
CanvasJS.com
CanvasJS.com
CanvasJS.com

  • ePub LinkePub Link
  • Cite
    CITE
    export Copy Download
    Close
    Download Citation
    Download a citation file in RIS format that can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Reference Manager.

    Format:
    • RIS — For EndNote, ProCite, RefWorks, and most other reference management software
    • BibTeX — For JabRef, BibDesk, and other BibTeX-specific software
    Include:
    • Citation for the content below
    Chelating and antibacterial properties of chitosan nanoparticles on dentin
    Restor Dent Endod. 2015;40(3):195-201.   Published online March 30, 2015
    Close
  • XML DownloadXML Download
Figure
  • 0
Related articles
Chelating and antibacterial properties of chitosan nanoparticles on dentin
Image Image
Figure 1 Representative images from the portable scanning electron microscope (×500) and confocal laser scanning microscope (×40). The irrigated pre-infection samples can be seen in images (a) - (e), and the infected samples after experimental irrigation protocols can be seen in images (f) - (j). A substantial amount of smear layer was observed when the samples were irrigated with sterile distilled water (a) and NaOCl (b). Visible dentinal tubules were seen in the samples treated with NaOCl-EDTA (c), NaOCl-EDTA-CNPs (d) and NaOCl-CNPs (e). A positive cellular viability and evident biomass were observed in the control (f), NaOCl (g) and NaOCl-EDTA (h) groups. The NaOCl-EDTA-CNPs and NaOCl-CNPs groups had decreased biomass (i) and interfered with bacterial growth (j). All bars represent 20 µm.
Figure 2 The percentage of areas with open dentinal tubules for each score (1 to 4). Having less than 10% of the area containing open dentinal tubules was scored as one, having 10 - 50% of the area containing open dentinal tubules was scored as two, having 50 - 70% of the area containing open dentinal tubules was scored as three and having more than 70% of the area containing open dentinal tubules was scored as four.*Different letters within a column depict a significant difference (p < 0.05).NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochloriteethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.
Chelating and antibacterial properties of chitosan nanoparticles on dentin

Medians (25 - 75 percentiles) of the total biovolume and the percentage of live cells of the comparisons among the groups

Total Biovolume (µm3/µm2)Percentage of live cells
Control5.0 (4.0 - 5.4)a92 (90 - 96)a
NaOCl3.9 (3.1 - 5.1)ab90 (85 - 92)a
NaOCl-EDTA3.6 (2.8 - 5.1)ab91 (87 - 94)a
NaOCl-EDTA-CNPs2.6 (0.85 - 4.4)c73 (51 - 86)b
NaOCl-CNPs2.7 (1.8 - 4.2)bc77 (60 - 83)b

*Different superscript letters in each column represent significant differences (p < 0.05).

NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochlorite-ethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.

Table 1 Medians (25 - 75 percentiles) of the total biovolume and the percentage of live cells of the comparisons among the groups

*Different superscript letters in each column represent significant differences (p < 0.05).

NaOCl, Sodium hypochlorite; NaOCl-EDTA, Sodium hypochlorite-ethylenediaminetetraacetic acid; NaOCl-EDTA-CNPs, Sodium hypochlorite-ethylenediaminetetraacetic acid-chitosan nanoparticles; NaOCl-CNPs, Sodium hypochlorite-chitosan nanoparticles.


Restor Dent Endod : Restorative Dentistry & Endodontics
Close layer
TOP Mpgyi