Review Open Access
Copyright ©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Jul 26, 2024; 12(21): 4460-4468
Published online Jul 26, 2024. doi: 10.12998/wjcc.v12.i21.4460
Endodontic irrigants from a comprehensive perspective
Rayana Duarte Khoury, Amjad Abu Hasna, Department of Restorative Dentistry, Endodontics Division, Institute of Science and Technology, São Paulo State University, São José dos Campos 12245000, SP, Brazil
Lara Steffany de Carvalho, Department of Biosciences and Oral Diagnosis, Institute of Science and Technology, São Paulo State University, São José dos Campos 12245000, SP, Brazil
Mauro Felipe Rios do Nascimento, School of Dentistry, The National Institute of Higher Education and Postgraduate Studies Padre Gervásio-INAPÓS, Pouso Alegre 37550-121, MG, Brazil
Fadi Alhussain, School of Dentistry, Syrian Private University, Al Kiswah 877C+P2, Damascus, Syria
Amjad Abu Hasna, School of Dentistry, Universidad Espíritu Santo, Samborondón 092301, Ecuador
ORCID number: Amjad Abu Hasna (0000-0002-1112-985X).
Author contributions: Khoury RD, de Carvalho LS, do Nascimento MFR, Alhussain F, and Abu Hasna A developed the concept and methodology; Khoury RD, de Carvalho LS, do Nascimento MFR, and Alhussain F performed the analysis and investigation; Khoury RD and Abu Hasna A wrote the original draft of the manuscript and supervised the study.
Conflict-of-interest statement: The authors have no conflicts of interest to declare.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Amjad Abu Hasna, DDS, MSc, PhD, Assistant Professor, Department of Restorative Dentistry, Endodontics Division, Institute of Science and Technology, São Paulo State University, Av. Engenheiro Francisco José Longo, 777 Jardim São Dimas, São José dos Campos 12245000, São Paulo, Brazil. d.d.s.amjad@gmail.com
Received: December 20, 2023
Revised: May 6, 2024
Accepted: June 3, 2024
Published online: July 26, 2024
Processing time: 192 Days and 7.9 Hours

Abstract

This review article explores the fundamental principles of modern endodontics with a focus on root canal cleaning and shaping. It reviews commonly used endodontic irrigant, namely sodium hypochlorite (NaOCl), herbal extracts, chlorhexidine (CHX), and chelating agents, highlighting their properties, applications, and potential drawbacks. NaOCl, a key antimicrobial agent, demonstrates effectiveness against various microorganisms but poses challenges such as high cytotoxicity. Herbal extracts, gaining recognition in endodontics, present an alternative with potential advantages in preserving dentin integrity. CHX, known for its broad-spectrum antimicrobial activity, is discussed in both liquid and gel formulations, emphasizing its role in reducing smear layer formation and preserving hybrid layer durability. Chelating agents, specifically ethylenediaminetetraacetic acid and citric acid, play a vital role in removing the smear layer, enhancing dentin permeability, and facilitating the penetration of antimicrobial agents. The review article underscores the importance of careful application and consideration of each irrigant's properties to ensure safe and effective endodontic procedures. It serves as a valuable guide for clinicians in selecting appropriate irrigants based on specific treatment requirements.

Key Words: Root canal irrigants, Sodium hypochlorite, Chlorhexidine, Chelating agents, Plant extracts

Core Tip: To increase the effectiveness of mechanical preparation and bacterial removal, irrigation is necessary. The dentist must be familiar with their different modes of action, indications, advantages, and disadvantages. This article provides an overview of the characteristics of the main endodontic irrigants for the professional class. The primary irrigants used in the field of endodontics include sodium hypochlorite, chlorhexidine, ethylenediaminetetraacetic acid, tetracycline antibiotics, TetraClean, calcium hydroxide, distilled water, and herbal irrigants. It was concluded that none of these irrigants are ideal, making it necessary to evaluate each case individually for their use and conduct further research to identify the best candidate.



INTRODUCTION

Schilder is credited with establishing the fundamental principles of modern endodontics, focusing primarily on two essential elements: “cleaning” and “shaping.” The process of shaping the root canal system serves a dual purpose of both cleaning and disinfection. This preparatory step is pivotal for ensuring effective three-dimensional filling with obturating materials[1]. The concept of cleaning stands as the paramount objective in root canal treatment, adapting to the specific condition of the pulp[2]. In instances of vital pulp diseases, the primary objective is the removal and cleaning of inflamed tissues. Conversely, in cases of necrotic pulp diseases, the goal extends to the removal, cleaning, and disinfection of necrotic tissues[3].

Achieving this cleanliness involves the use of mechanical instruments, which not only shape the root canal system but also mechanically remove bacteria and their by-products. Simultaneously, endodontic irrigants are employed to lubricate the root canal system, dissolve organic tissues, and, most importantly, to clean and disinfect the canal[4-11].

In this review article, we provide a concise summary of the most employed endodontic irrigants. These solutions play a pivotal role in achieving the high standard of cleanliness required in modern endodontic procedures, underscoring their critical importance in the field.

SODIUM HYPOCHLORITE

Sodium hypochlorite (NaOCl) is obtained through the electrolysis of sodium chloride, with its relative value determined by the chlorine content released, known as active chlorine[12,13]. It is classified as a halogenated compound, it can be found in a series of products, containing varying concentrations and additives (Table 1).

Table 1 Sodium hypochlorite types and concentrations.
Solution
Concentration
Parts per million
Dakin's solution0.5% NaOCl solutionEquivalent to 5000 ppm, and is neutralized with boric acid to bring the pH close to neutral
Dausfrene solution0.5% NaOCl solutionEquivalent to 5000 ppm, that has been neutralized using sodium bicarbonate
Milton's solution1% NaOCl solutionEquivalent to 10000 ppm, that is stabilized with 16% sodium chloride
Labarraque Liqueur2.5% NaOCl solutionEquivalent to 25000 ppm
Chlorinated soda4%-6% NaOCl solutionEquivalent to 40000-60000 ppm
Sanitary water2%-2.5% NaOCl solutionEquivalent to 20000-25000 ppm

Numerous studies have provided substantial evidence supporting the antimicrobial effectiveness of NaOCl against a diverse range of microorganisms commonly found in the oral cavity such as Escherichia coli[14], Enterococcus faecalis[15], different anaerobic bacteria[16,17], and Candida albicans[18]. In addition, it is also effective against microorganisms’ endotoxins including lipopolysaccharides and lipoteichoic acid[4,11,19,20], and against matrix metalloproteinases (MMPs)[5]. While there may be ongoing debates regarding the exact mechanisms of its antimicrobial activity, the prevailing theory suggests that active chlorine hinders enzymatic processes, disrupts metabolic activities, and ultimately results in cell death[21]. This multifaceted evidence underscores the valuable role of NaOCl as a potent antimicrobial agent in oral healthcare.

NaOCl possesses remarkable properties in the context of root canal treatment. It demonstrates a unique functionality in that it not only exhibits the capacity to dissolve organic tissues within the root canal, such as pulp tissue and collagen[10,22], but also serves as an effective lubricating agent within the canal. This lubricating action enables the mechanical removal of debris and other contaminants from the canal, contributing to a more thorough cleaning process[23]. Furthermore, NaOCl exhibits an interesting characteristic in terms of its pH (potential of hydrogen). Initially, it is alkaline in nature, which can be beneficial for its antimicrobial and tissue-dissolving properties. However, over time, its alkalinity gradually diminishes[24]. This dynamic pH change over the course of treatment may have implications for its overall effectiveness and the evolving chemical environment within the root canal.

Nonetheless, it is crucial to acknowledge the drawbacks associated with the use of NaOCl. Notably, NaOCl exhibits high cytotoxicity and relative genotoxicity[17,25,26], which are both are related to its concentration[27]. Furthermore, its ability to dissolve organic tissues can lead to the distortion of dentin collagen, ultimately resulting in reduced bond strength within the dentin-resin system[28]. This effect can have implications for the overall mechanical properties of root canal-treated teeth, potentially leading to compromised structural integrity[29]. These considerations underscore the importance of careful and precise application of NaOCl in endodontic procedures to mitigate these potential disadvantages.

It is worth mentioning that the NaOCl concentration has effect on its efficacy, in which lower concentrations (0.5%-1%) are indicated in biopulpectomy and pulpotomy; however, higher concentrations (2.5% and higher) are indicated for necropulpectomy as in periapical periodontitis and periapical abscess[30,31]. These indications are highly attributed to its antimicrobial, anti-endotoxin, and organic tissue capacity, in addition to its biocompatibility[4,5,10], in which lower concentrations are safer for tissues and have a lower risk of irritation or chemical burns but are less effective in dissolving organic matter, and require a longer exposure time[32]. Conversely, higher concentrations are more effective in dissolving organic matter and disinfecting the canal, but have a higher risk of tissue irritation and potential for damage to surrounding structures if not used cautiously[32].

HERBAL EXTRACTS

The integration of herbal extracts, or phytotherapy, in dentistry is steadily gaining recognition[33] particularly within the specialized domain of endodontics[34]. Different extracts of herbal medicine were introduced to be used as endodontic irrigants or intracanal medications[35,36] primarily due to their demonstrated antimicrobial properties and biocompatibility[37]. This highlights the growing recognition of herbal remedies in dental care, especially within endodontics, due to their potential therapeutic benefits. Still, most of the reported studies have been performed as laboratorial research not in vitro or even in vivo studies.

Numerous in tooth model studies have indicated herbal medicines extracts as endodontic irrigants. Artocarpus lakoocha (monkey jack or monkey fruit) extract might be a useful alternative for antimicrobial medication in endodontic treatment because of its efficacy against E. faecalis[38]. In addition, Allium sativum (garlic) extract is as effective as 5.25% NaOCl, and more biocompatible with good dentinal penetration property[39]. Similarly, Camellia sinensis (green tea) extract is indicated as a potential antimicrobial root canal irrigant because of its antimicrobial action against E. faecalis[40].

Furthermore, numerous laboratory studies have also supported the use of herbal medicine extracts as endodontic irrigants. These include extracts from S. officinalis, Glycyrrhiza glabra (liquorice), Brazilian green propolis, Rosmarinus officinalis (Rosemary), Pfaffia paniculata (Brazilian ginseng), Hamamelis virginiana (American witch-hazel), Stryphnodendron barbatiman (Stryphnodendron), Gymnema sylvestre (Gurmar), Curcuma longa (turmeric), Persea americana (avocado), and others[36,41-45].

While the efficacy of herbal medicine extracts has been established and several extracts have been identified for their safety, ease of use, extended shelf life, affordability, and limited microbial resistance[46,47], it is important to note that certain studies have suggested caution regarding their use as the primary irrigant for canal disinfection[48]. Unless subjected to thorough preclinical and clinical testing, as well as evaluations of potential interactions with other materials[49], the adoption of herbal extracts as main irrigants should be approached with careful consideration.

Nonetheless, it is essential to acknowledge that the capacity of these herbal irrigants in removing the smear layer is relatively lower compared to chelating agents such as ethylenediaminetetraacetic acid (EDTA) and tetracycline antibiotics (MTAD, a combination of a tetracycline isomer, an acid, and a detergent)[50,51]. However, certain studies have reported that natural irrigants can effectively remove the smear layer while causing minimal harm to the mechanical and chemical properties of radicular dentin in contrast to synthetic agents, as they have a less detrimental impact on dentin's mechanical properties[52]. This underlines the potential advantages of natural irrigants in preserving dentin integrity, despite their less robust smear layer removal compared to their synthetic counterparts, suggesting that herbal irrigants may offer unique advantages, encouraging further exploration of their potential in improving endodontic treatments.

CHLORHEXIDINE

Chlorhexidine (CHX) has been extensively utilized in the field of endodontics as a substance for irrigation or as a medicament within the root canal. This is due to its possession of a broad spectrum of antimicrobial activity, as well as its ability to sustain residual antimicrobial activity. Moreover, CHX exhibits a lower level of cytotoxicity compared to NaOCl while still demonstrating effective clinical performance, lubricating properties, and rheological action. The gel presentation of CHX aids in suspending debris and it also acts as an inhibitor of metalloproteinase. Additionally, CHX is known for its chemical stability, lack of staining on fabric, lack of odor, and water solubility, among other notable properties[53].

The structure of the compound consists of two symmetric 4-cholorophenyl rings and two biguanide groups, connected by a central hexamethylene chain[54]. In the context of endodontic applications, CHX can be utilized either in a liquid form or as a gel. The CHX gel formulation consists of a gel base containing 1% natrosol, a hydroxyethylcellulose, with a range from 6 to 9 and CHX gluconate, in an optimal pH range of 5.5 to 7.0. Natrosol gel is a biocompatible carbon polymer[55], that is a water-soluble substance, and therefore can be easily removed from the root canal with a final flush of distilled water[56,57].

The CHX gel provides lubrication to the walls of the root canal, minimizing friction between the file and the dentin surface. This, in turn, eases the instrumentation process and lowers the chances of instrument breakage within the canal. Moreover, by aiding in instrumentation, the CHX gel enhances the removal of organic tissues, addressing its inability to dissolve them[56,57]. Another advantage of CHX gel is the reduction of smear layer formation[57], which does not occur with the liquid form. CHX gel maintains almost all the dentinal tubules open because its viscosity keeps the debris in suspension (rheological action), reducing smear layer formation. Furthermore, the gel formulation may keep the “active principle” of CHX in contact with the microorganisms for a longer time, inhibiting their growth[58].

The pH-dependent nature of the antimicrobial activity of CHX is observed, with the optimal range falling between 5.5 and 7.0, encompassing the pH values characteristic of body surfaces and tissues. At physiological pH levels, CHX undergoes dissociation, resulting in the release of the positively charged CH component. The ability of the CHX molecule to penetrate bacterial cells and exert toxic effects is facilitated by the interaction between the positively charged molecule and the negatively charged phosphate groups present on the bacterial cell wall[59]. Consequently, the antimicrobial activity of CHX is independent of its pH, which remains within the range of 5.5 to 7.0.

In terms of its range of activity, CHX exhibits a broad spectrum of antimicrobial properties and demonstrates effectiveness against both Gram-positive and Gram-negative bacteria, as well as facultative and strict anaerobes[57,58,60-68], yeast, and fungi, particularly Candida albicans[58,69-71]. Furthermore, it demonstrates activity against certain viruses such as respiratory viruses, herpes, cytomegalovirus, and human immunodeficiency virus, while remaining inactive against bacterial spores when at room temperature[72,73].

One of the primary benefits of CHX is associated with its antimicrobial substantivity. The cations with a positive charge that CHX emits can adhere to dentin and hinder the establishment of microorganisms on the dentin surface for a duration that extends beyond the actual application period[74], thereby sustaining an extended period of antimicrobial efficacy for multiple hours[53].

CHX has the ability to preserve the durability of the hybrid layer and adhesive strength both in vitro and in vivo[75,76]. This is likely attributed to its effectiveness as an MMP inhibitor[77], leading to reduced degradation of collagen fibrils in the hybrid layer and sub-hybrid layer. This notable property is relevant because the gradual deterioration of the integrity of resin-dentin bonds over time is often linked to the breakdown of exposed collagen fibrils within inadequately infiltrated hybrid layers[78]. This breakdown is associated with an endogenous proteolytic process, primarily involving the action of MMPs present in dentin[79].

CHX has been recommended as an irrigant alternative to NaOCl, especially because of its broad-spectrum antimicrobial action, substantivity and low toxicity[80]. However, CHX's incapacity of tissue dissolution has been pointed out as its major disadvantage. Some attempts have been made to assess the ability of CHX to dissolve organic matter, and the findings indicate that neither the aqueous solution nor the gel formulations of this substance were effective in dissolving pulp tissues[81,82]. In this context, it has been recommended to combine NaOCl and CHX to amplify their antimicrobial efficacy. The benefit of concluding the procedure with a CHX final rinse lies in the sustained antimicrobial activity attributable to CHX substantivity[83]. On the other hand, when NaOCl is combined with CHX, it produces an orange-brown precipitate, forming a chemical smear layer that envelops dentinal tubules and could potentially disrupt the sealing of the root filling[56,84]. Moreover, this precipitate alters the tooth color[85], and exhibits cytotoxicity[86]. Hence, it is crucial to eliminate any remnants of the substances employed within the root canals through intermediate flushes with distilled water to prevent interactions between them.

CHELATING AGENTS

The instrumentation of the root canal walls leads to the formation of a smear layer[87], which consists of both inorganic and organic components such as dentin filings, remnants of odontoblastic processes, pulp tissue and in circumstances where root canals are infected, bacteria[88,89]. The presence of the smear layer poses a hindrance to effective disinfection by preventing the penetration of antimicrobial agents such as NaOCl, calcium hydroxide and other intracanal medicaments into the dentinal tubules[90]. Furthermore, if not removed, the smear layer has the potential to interfere with the seal between the filling material and the root canal wall, thus compromising the success of endodontic treatment[88,91].

Although NaOCl appears to be the most appropriate endodontic irrigant, when used alone, it is ineffective in smear layer removal as it cannot dissolve inorganic dentin particles[92]. In addition, calcifications hindering mechanical preparation are frequently encountered in the canal system. In this context, the use of demineralizing agents has been recommended as adjuvants in root canal therapy. Chelators such as EDTA[93] and citric acid[94] are highly efficient in chemically softening the root canal dentin and dissolving the smear layer, increasing the dentin permeability[95].

The most common chelating solutions are based on EDTA which functions through the establishment of a steadfast compound with calcium ions. Upon the binding of all accessible ions, a state of equilibrium materializes, thereby precluding any subsequent disintegration. Using gravimetrical analyses, Schilder[1,96] demonstrated that the properties of EDTA exhibited a self-limiting nature. This restriction is believed to be attributed to alterations in pH during the demineralization process of dentine. Under neutral circumstances, most chelators possess a pH in close proximity to the neutral benchmark, with 99% of the EDTA existing in the form of EDTAHNa3. The process of calcium removal from the dentine by hydrogen leads to a subsequent decline in pH. Due to the liberation of acid, the efficacy of EDTA decreases over time; conversely, the interaction of the acid with hydroxyapatite influences the solubility of dentine.

Although the antiseptic capacity of EDTA irrigant is relatively limited[97], it is significantly superior to saline in the reduction of intracanal microbiota[98]. This phenomenon can be attributed to its capability to detach biofilms that are adhered to the root canal walls[99]. While a randomized clinical trial has yet to demonstrate this, there is a consensus that utilizing an alternating irrigation regimen of NaOCl and EDTA may prove to be more effective in reducing bacterial loads in root canal systems than using NaOCl alone[100].

Antimicrobial agents, such as quaternary ammonium compounds (EDTAC)[101] or MTAD[102], have been incorporated into EDTA and citric acid irrigants, respectively, to enhance their ability to combat microorganisms. Nonetheless, the clinical significance of this practice remains uncertain. Although EDTAC exhibits comparable efficacy in removing smears compared to EDTA, it possesses a higher degree of causticity[97]. In the case of MTAD, bacteria isolated from root canals frequently exhibit resistance to tetracycline[103]. In general, the use of antibiotics, as opposed to biocides like hypochlorite or CHX, seems unjustifiable, as the former were primarily developed for systemic administration rather than localized wound debridement. Furthermore, antibiotics have a much narrower range of effectiveness compared to the latter[104].

One essential aspect regarding the currently accessible irrigation solutions, particularly EDTA and citric acid, is their powerful interaction with NaOCl[105]. Both citric acid and EDTA promptly diminish the chlorine readily available in the solution, thus rendering the NaOCl irrigant ineffective against bacteria and necrotic tissue[101]. Hence, the combination of citric acid or EDTA with NaOCl must be strictly avoided. The substances employed for disinfecting infected canals should be administered in a manner that enables them to fully exploit their potential on their intended targets within the root canal, rather than exerting an influence on one another.

Thus, it is crucial to employ a NaOCl solution during the instrumentation process, without incorporating any modifications such as the addition of EDTA or citric acid. It is essential to ensure that the canals are consistently filled with NaOCl, as this will effectively extend the duration of the irrigant's activity. In the intervals between instrument usage, it is recommended to irrigate the root canals using substantial quantities of the hypochlorite solution. Once the shaping procedure has been successfully executed, the root canals can be thoroughly cleansed by means of an aqueous solution containing EDTA or citric acid.

Generally, each canal is flushed for a minimum of one minute using a volume of 5 to 10 mL of the chelator irrigant. It is important to exercise caution, as extended exposure to potent chelators like EDTA could potentially compromise the integrity of the root dentin[106]. This is because the hardness and elastic modulus of dentin are influenced by the mineral composition of the dentin[107]. Following the procedure to remove smear layer, a concluding rinse with an antiseptic solution seems to offer advantages[108]. The choice of the ultimate irrigant is contingent upon the subsequent step in treatment, specifically whether an intervisit dressing is intended.

In this communication, we intended to provide a simple exposition of root canal irrigants that are cost-effective materials and currently accessible to the clinician. It is important to note that this does not preclude the existence of other biologically acceptable options for cleansing root canal systems. Nevertheless, it is crucial for the reader to acknowledge the tendency for novel concepts to be excessively praised in preliminary investigations, in contrast to the established benchmark[102].

CONCLUSION

This review concludes by highlighting the importance of selecting appropriate root canal irrigants based on their properties and applications. It emphasizes the need for careful consideration and precise application of these irrigants to ensure effective and safe endodontic procedures. The information presented serves as a guide for clinicians in choosing irrigants that meet the specific requirements of root canal treatments.

Footnotes

Provenance and peer review: Invited article; Externally peer reviewed.

Peer-review model: Single blind

Specialty type: Medicine, research and experimental

Country of origin: Brazil

Peer-review report’s classification

Scientific Quality: Grade D

Novelty: Grade D

Creativity or Innovation: Grade C

Scientific Significance: Grade C

P-Reviewer: Rifaat S, Saudi Arabia S-Editor: Liu H L-Editor: Filipodia P-Editor: Zheng XM

References
1.  Schilder H. Cleaning and shaping the root canal. Dent Clin North Am. 1974;18:269-296.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Estrela C, Holland R, Estrela CR, Alencar AH, Sousa-Neto MD, Pécora JD. Characterization of successful root canal treatment. Braz Dent J. 2014;25:3-11.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 119]  [Cited by in F6Publishing: 129]  [Article Influence: 16.1]  [Reference Citation Analysis (0)]
3.  Siqueira Junior JF, Rôças IDN, Marceliano-Alves MF, Pérez AR, Ricucci D. Unprepared root canal surface areas: causes, clinical implications, and therapeutic strategies. Braz Oral Res. 2018;32:e65.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 50]  [Article Influence: 8.3]  [Reference Citation Analysis (0)]
4.  Abu Hasna A, Pereira Da Silva L, Pelegrini FC, Ferreira CLR, de Oliveira LD, Carvalho CAT. Effect of sodium hypochlorite solution and gel with/without passive ultrasonic irrigation on Enterococcus faecalis, Escherichia coli and their endotoxins. F1000Res. 2020;9:642.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13]  [Cited by in F6Publishing: 18]  [Article Influence: 4.5]  [Reference Citation Analysis (0)]
5.  Carvalho CAT, Hasna AA, Carvalho AS, Vilela PDGF, Ramos LP, Valera MC, Oliveira LD. Clinical Study of Sodium Hypochlorite, Polymyxin B And Limewater Effect on MMP-3,-8,-9 In Apical Periodontitis. Braz Dent J. 2020;31:116-121.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 9]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
6.  Abu Hasna A, Ungaro DMT, de Melo AAP, Yui KCK, da Silva EG, Martinho FC, Gomes APM. Nonsurgical endodontic management of dens invaginatus: a report of two cases. F1000Res. 2019;8:2039.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 6]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
7.  Abu Hasna A, Khoury RD, Toia CC, Gonçalves GB, de Andrade FB, Talge Carvalho CA, Ribeiro Camargo CH, Carneiro Valera M. In vitro Evaluation of the Antimicrobial Effect of N-acetylcysteine and Photodynamic Therapy on Root Canals Infected with Enterococcus faecalis. Iran Endod J. 2020;15:236-245.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 2]  [Reference Citation Analysis (0)]
8.  Abu Hasna A, Ferrari CH, Talge Carvalho CA. Endodontic treatment of a large periapical cyst with the aid of antimicrobial photodynamic therapy - Case report. BDS. 2019;22:561-568.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 7]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
9.  Ribeiro Camargo CH, Bittencourt TS, Hasna AA, Palo RM, Talge Carvalho CA, Valera MC. Cyclic fatigue, torsional failure, and flexural resistance of rotary and reciprocating instruments. J Conserv Dent. 2020;23:364-369.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 8]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
10.  Abu Hasna A, Monteiro JB, Abreu RT, Camillo W, Nogueira Matuda AG, de Oliveira LD, Pucci CR, Carvalho CAT. Effect of Passive Ultrasonic Irrigation over Organic Tissue of Simulated Internal Root Resorption. Int J Dent. 2021;2021:3130813.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
11.  Oliveira LD, Oliveira FE, Hatje BA, Valera MC, Carvalho CAT, Hasna AA. Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production. Braz Dent J. 2022;33:36-43.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
12.  Hoover CP. Laboratory Section: Electrolytic production of sodium hypochlorite. J Am Public Health Assoc. 1911;1:114-117.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 1]  [Article Influence: 0.0]  [Reference Citation Analysis (0)]
13.  Askenaizer D. Drinking Water Quality and Treatment. Encyclopedia of Physical Science and Technology. 2003;.  [PubMed]  [DOI]  [Cited in This Article: ]
14.  Prat R, Nofre C, Cier A. [Effects of sodium hypochlorite, ozone and ionizing radiations on the pyrimidine constituants of Escherichia coli]. Ann Inst Pasteur (Paris). 1968;114:595-607.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Siqueira JF Jr, Machado AG, Silveira RM, Lopes HP, de Uzeda M. Evaluation of the effectiveness of sodium hypochlorite used with three irrigation methods in the elimination of Enterococcus faecalis from the root canal, in vitro. Int Endod J. 1997;30:279-282.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13]  [Cited by in F6Publishing: 49]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
16.  Giardino L, Savoldi E, Ambu E, Rimondini R, Palezona A, Debbia EA. Antimicrobial effect of MTAD, Tetraclean, Cloreximid, and sodium hypochlorite on three common endodontic pathogens. Indian J Dent Res. 2009;20:391.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 13]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
17.  Abu Hasna A, Theodoro AL, Pereira LM, Ramos LP, Campos TMB, Ala Rachi M, Al-Nahalwi T, de Oliveira LD, Carvalho CAT. Antimicrobial Action, Genotoxicity, and Morphological Analysis of Three Calcium Silicate-Based Cements. Biomed Res Int. 2022;2022:2155226.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 2]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
18.  Valera MC, Silva KC, Maekawa LE, Carvalho CA, Koga-Ito CY, Camargo CH, Lima RS. Antimicrobial activity of sodium hypochlorite associated with intracanal medication for Candida albicans and Enterococcus faecalis inoculated in root canals. J Appl Oral Sci. 2009;17:555-559.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 24]  [Cited by in F6Publishing: 31]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
19.  Valera MC, Maekawa LE, Chung A, Cardoso FG, Oliveira LD, Oliveira CL, Carvalho CA. The effect of sodium hypochlorite and ginger extract on microorganisms and endotoxins in endodontic treatment of infected root canals. Gen Dent. 2014;62:25-29.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Maekawa LE, Valera MC, Oliveira LD, Carvalho CA, Koga-Ito CY, Jorge AO. In vitro evaluation of the action of irrigating solutions associated with intracanal medications on Escherichia coli and its endotoxin in root canals. J Appl Oral Sci. 2011;19:106-112.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 20]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
21.  Estrela C, Estrela CR, Barbin EL, Spanó JC, Marchesan MA, Pécora JD. Mechanism of action of sodium hypochlorite. Braz Dent J. 2002;13:113-117.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 323]  [Cited by in F6Publishing: 306]  [Article Influence: 14.6]  [Reference Citation Analysis (0)]
22.  Naenni N, Thoma K, Zehnder M. Soft tissue dissolution capacity of currently used and potential endodontic irrigants. J Endod. 2004;30:785-787.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 160]  [Cited by in F6Publishing: 167]  [Article Influence: 8.4]  [Reference Citation Analysis (0)]
23.  Baratto-Filho F, de Carvalho JR Jr, Fariniuk LF, Sousa-Neto MD, Pécora JD, da Cruz-Filho AM. Morphometric analysis of the effectiveness of different concentrations of sodium hypochlorite associated with rotary instrumentation for root canal cleaning. Braz Dent J. 2004;15:36-40.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23]  [Cited by in F6Publishing: 24]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
24.  Dos Santos Pereira SR, Pereira TC, Meccatti VM, De Carvalho LS, Coser Bridi E, De Oliveira LD, Abu Hasna A. Avaliação do potencial de hidrogénio (PH) em três momentos diferentes antes do prazo de validade do hipoclorito de sódio. RECIMA21. 2023;4:e453110.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
25.  Marins JS, Sassone LM, Fidel SR, Ribeiro DA. In vitro genotoxicity and cytotoxicity in murine fibroblasts exposed to EDTA, NaOCl, MTAD and citric acid. Braz Dent J. 2012;23:527-533.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 32]  [Cited by in F6Publishing: 36]  [Article Influence: 3.0]  [Reference Citation Analysis (0)]
26.  Teixeira PA, Coelho MS, Kato AS, Fontana CE, Bueno CE, Pedro-Rocha DG. Cytotoxicity assessment of 1% peracetic acid, 2.5% sodium hypochlorite and 17% EDTA on FG11 and FG15 human fibroblasts. Acta Odontol Latinoam. 2018;31:11-15.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Demenech LS, Tomazinho FSF, Baratto-Filho F, Brancher JA, Pereira LF, Gabardo MCL. Biocompatibility of the 8.25% sodium hypochlorite irrigant solution in endodontics: An in vivo study. Microsc Res Tech. 2021;84:1506-1512.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
28.  Martinho FC, Carvalho CA, Oliveira LD, de Lacerda AJ, Xavier AC, Augusto MG, Zanatta RF, Pucci CR. Comparison of different dentin pretreatment protocols on the bond strength of glass fiber post using self-etching adhesive. J Endod. 2015;41:83-87.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 34]  [Cited by in F6Publishing: 40]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
29.  Rath PP, Yiu CKY, Matinlinna JP, Kishen A, Neelakantan P. The effect of root canal irrigants on dentin: a focused review. Restor Dent Endod. 2020;45:e39.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 25]  [Article Influence: 6.3]  [Reference Citation Analysis (0)]
30.  Xu H, Ye Z, Zhang A, Lin F, Fu J, Fok ASL. Effects of concentration of sodium hypochlorite as an endodontic irrigant on the mechanical and structural properties of root dentine: A laboratory study. Int Endod J. 2022;55:1091-1102.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 11]  [Reference Citation Analysis (0)]
31.  Mokhtari H, Milani AS, Zand V, Shakuie S, Nazari L. The effect of different concentrations and temperatures of sodium hypochlorite irrigation on pain intensity following endodontic treatment of mandibular molars with irreversible pulpitis: A randomized, double-blind clinical trial. Clin Exp Dent Res. 2023;9:859-867.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Reference Citation Analysis (0)]
32.  Chung I, Ryu H, Yoon SY, Ha JC. Health effects of sodium hypochlorite: review of published case reports. Environ Anal Health Toxicol. 2022;37:e2022006-e2022000.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 5]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
33.  Al-Abdullah A, Edris S, Abu Hasna A, de Carvalho LS, Al-Nahlawi T. The Effect of Aloe vera and Chlorhexidine as Disinfectants on the Success of Selective Caries Removal Technique: A Randomized Controlled Trial. Int J Dent. 2022;2022:9474677.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
34.  Li TT, Xia WW. [Development of research on the application of traditional Chinese herbal drugs in root canal disinfection]. Zhong Xi Yi Jie He Xue Bao. 2008;6:311-315.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 1]  [Article Influence: 0.1]  [Reference Citation Analysis (0)]
35.  Noushad MC, Balan B, Basheer S, Usman SB, Muhammed Askar MK. Antimicrobial Efficacy of Different Natural Extracts Against Persistent Root Canal Pathogens: An In vitro Study. Contemp Clin Dent. 2018;9:177-181.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
36.  Domingues N, Ramos LP, Pereira LM, do Rosário Estevam Dos Santos PB, Scorzoni L, Pereira TC, Abu Hasna A, Carvalho CAT, de Oliveira LD. Antimicrobial action of four herbal plants over mixed-species biofilms of Candida albicans with four different microorganisms. Aust Endod J. 2023;49:262-271.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Reference Citation Analysis (0)]
37.  Badr AE, Omar N, Badria FA. A laboratory evaluation of the antibacterial and cytotoxic effect of Liquorice when used as root canal medicament. Int Endod J. 2011;44:51-58.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 37]  [Article Influence: 2.6]  [Reference Citation Analysis (0)]
38.  Teanpaisan R, Ruangkiatkul P, Thammasitboon K, Puripattanavong J, Faroongsarng D. Effectiveness of Artocarpus lakoocha extract, poloxamer 407, on Enterococcus faecalis in vitro. J Investig Clin Dent. 2013;4:219-224.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
39.  Birring OJ, Viloria IL, Nunez P. Anti-microbial efficacy of Allium sativum extract against Enterococcus faecalis biofilm and its penetration into the root dentin: An in vitro study. Indian J Dent Res. 2015;26:477-482.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 8]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
40.  Ramezanali F, Samimi S, Kharazifard M, Afkhami F. The in Vitro Antibacterial Efficacy of Persian Green Tea Extract as an Intracanal Irrigant on Enterococcus faecalis Biofilm. Iran Endod J. 2016;11:304-308.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
41.  Santos TDSA, Meccatti VM, Pereira TC, Marcucci MC, Hasna AA, Valera MC, de Oliveira LD, Carvalho CAT. Antibacterial Effect of Combinations of Salvia officinalis and Glycyrrhiza glabra Hydroalcoholic Extracts against Enterococcus spp. Coatings. 2023;13:1579.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
42.  de Sá Assis MA, de Paula Ramos L, Abu Hasna A, de Queiroz TS, Pereira TC, Nagai de Lima PM, Berretta AA, Marcucci MC, Talge Carvalho CA, de Oliveira LD. Antimicrobial and Antibiofilm Effect of Brazilian Green Propolis Aqueous Extract against Dental Anaerobic Bacteria. Molecules. 2022;27.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
43.  Meccatti VM, Figueiredo-Godoi LMA, Pereira TC, de Lima PMN, Abu Hasna A, Senna LB, Marcucci MC, Junqueira JC, de Oliveira LD. The biocompatibility and antifungal effect of Rosmarinus officinalis against Candida albicans in Galleria mellonella model. Sci Rep. 2022;12:15611.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 3]  [Reference Citation Analysis (0)]
44.  Marques Meccatti V, de Souza Moura L, Guerra Pinto J, Ferreira-Strixino J, Abu Hasna A, Alves Figueiredo-Godoi LM, Campos Junqueira J, Marcucci MC, de Paula Ramos L, Carvalho CAT, Pucci CR, de Oliveira LD. Curcuma longa L. Extract and Photodynamic Therapy are Effective against Candida spp. and Do Not Show Toxicity In Vivo. Int J Dent. 2022;2022:5837864.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 2]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
45.  Dos Santos Liberato SF, da Cruz Vegian MR, Abu Hasna A, de Alvarenga JA, Dos Santos JG, Tini ÍRP, Amêndola I, Junqueira JC, de Oliveira LD. Antibiofilm action of Persea americana glycolic extract over Acinetobacter baumannii and absence of toxicity in Galleria mellonella. J Complement Integr Med. 2022;19:905-911.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 5]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
46.  Mittal R, Rathee G, Tandan M. Evaluation of Antimicrobial Efficacy of Commercially Available Herbal Products as Irrigants and Medicaments in Primary Endodontic Infections: In Vivo Study. World J Dent. 2021;11:488-493.  [PubMed]  [DOI]  [Cited in This Article: ]
47.  Kale PP, Raut AW. A proposed classification system for herbal endodontic irrigants. J Conserv Dent. 2021;24:293-295.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 4]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
48.  Teja KV, Janani K, Srivastava KC, Shrivastava D, Jose J, Marya A, Karobari MI. Comparison of Herbal Agents with Sodium Hypochlorite as Root Canal Irrigant: A Systematic Review of In Vitro Studies. Evid Based Complement Alternat Med. 2021;2021:8967219.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 12]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
49.  Karobari MI, Adil AH, Assiry AA, Basheer SN, Noorani TY, Pawar AM, Marya A, Messina P, Scardina GA. Herbal Medications in Endodontics and Its Application-A Review of Literature. Materials (Basel). 2022;15.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Reference Citation Analysis (0)]
50.  Balto H, Salama F, Al-Mofareh S, Al-Yahya F. Evaluation of different irrigating solutions on smear layer removal of primary root dentin. J Contemp Dent Pract. 2015;16:187-191.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 4]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
51.  Mukherjee M, Kalita T, Barua P, Barman A, Thonai S, Mahanta P Sr, Medhi H. Efficacy of Smear Layer Removal of Human Teeth Root Canals Using Herbal and Chemical Irrigants: An In Vitro Study. Cureus. 2023;15:e40467.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
52.  Cecchin D, Soares Giaretta V, Granella Cadorin B, Albino Souza M, Vidal CMP, Paula Farina A. Effect of synthetic and natural-derived novel endodontic irrigant solutions on mechanical properties of human dentin. J Mater Sci Mater Med. 2017;28:141.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 19]  [Cited by in F6Publishing: 19]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
53.  Mohammadi Z, Abbott PV. The properties and applications of chlorhexidine in endodontics. Int Endod J. 2009;42:288-302.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 238]  [Cited by in F6Publishing: 237]  [Article Influence: 15.8]  [Reference Citation Analysis (0)]
54.  Greenstein G, Berman C, Jaffin R. Chlorhexidine. An adjunct to periodontal therapy. J Periodontol. 1986;57:370-377.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 121]  [Cited by in F6Publishing: 112]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
55.  Miyamoto T, Takahashi S, Ito H, Inagaki H, Noishiki Y. Tissue biocompatibility of cellulose and its derivatives. J Biomed Mater Res. 1989;23:125-133.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 294]  [Cited by in F6Publishing: 212]  [Article Influence: 6.1]  [Reference Citation Analysis (0)]
56.  Vivacqua-Gomes N, Ferraz CC, Gomes BP, Zaia AA, Teixeira FB, Souza-Filho FJ. Influence of irrigants on the coronal microleakage of laterally condensed gutta-percha root fillings. Int Endod J. 2002;35:791-795.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 75]  [Cited by in F6Publishing: 83]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
57.  Ferraz CC, Gomes BP, Zaia AA, Teixeira FB, Souza-Filho FJ. In vitro assessment of the antimicrobial action and the mechanical ability of chlorhexidine gel as an endodontic irrigant. J Endod. 2001;27:452-455.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 136]  [Cited by in F6Publishing: 148]  [Article Influence: 6.4]  [Reference Citation Analysis (0)]
58.  Vianna ME, Gomes BP, Berber VB, Zaia AA, Ferraz CC, de Souza-Filho FJ. In vitro evaluation of the antimicrobial activity of chlorhexidine and sodium hypochlorite. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004;97:79-84.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 188]  [Cited by in F6Publishing: 212]  [Article Influence: 10.6]  [Reference Citation Analysis (0)]
59.  Lindskog S, Pierce AM, Blomlöf L. Chlorhexidine as a root canal medicament for treating inflammatory lesions in the periodontal space. Endod Dent Traumatol. 1998;14:186-190.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 29]  [Cited by in F6Publishing: 33]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
60.  Gomes BP, Ferraz CC, Vianna ME, Berber VB, Teixeira FB, Souza-Filho FJ. In vitro antimicrobial activity of several concentrations of sodium hypochlorite and chlorhexidine gluconate in the elimination of Enterococcus faecalis. Int Endod J. 2001;34:424-428.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 283]  [Cited by in F6Publishing: 287]  [Article Influence: 12.5]  [Reference Citation Analysis (0)]
61.  Fardal O, Turnbull RS. A review of the literature on use of chlorhexidine in dentistry. J Am Dent Assoc. 1986;112:863-869.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 165]  [Cited by in F6Publishing: 171]  [Article Influence: 4.5]  [Reference Citation Analysis (0)]
62.  Delany GM, Patterson SS, Miller CH, Newton CW. The effect of chlorhexidine gluconate irrigation on the root canal flora of freshly extracted necrotic teeth. Oral Surg Oral Med Oral Pathol. 1982;53:518-523.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 92]  [Cited by in F6Publishing: 99]  [Article Influence: 2.4]  [Reference Citation Analysis (0)]
63.  Greenstein G. Povidone-iodine's effects and role in the management of periodontal diseases: a review. J Periodontol. 1999;70:1397-1405.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 33]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
64.  Siqueira JF Jr, de Uzeda M. Disinfection by calcium hydroxide pastes of dentinal tubules infected with two obligate and one facultative anaerobic bacteria. J Endod. 1996;22:674-676.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 116]  [Cited by in F6Publishing: 116]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
65.  Onçag O, Cogulu D, Uzel A. Efficacy of various intracanal medicaments against Enterococcus faecalis in primary teeth: an in vivo study. J Clin Pediatr Dent. 2006;30:233-237.  [PubMed]  [DOI]  [Cited in This Article: ]
66.  Onçağ O, Hoşgör M, Hilmioğlu S, Zekioğlu O, Eronat C, Burhanoğlu D. Comparison of antibacterial and toxic effects of various root canal irrigants. Int Endod J. 2003;36:423-432.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 95]  [Cited by in F6Publishing: 104]  [Article Influence: 5.0]  [Reference Citation Analysis (0)]
67.  Dametto FR, Ferraz CC, Gomes BP, Zaia AA, Teixeira FB, de Souza-Filho FJ. In vitro assessment of the immediate and prolonged antimicrobial action of chlorhexidine gel as an endodontic irrigant against Enterococcus faecalis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;99:768-772.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 79]  [Cited by in F6Publishing: 79]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
68.  Basrani B, Lemonie C. Chlorhexidine gluconate. Aust Endod J. 2005;31:48-52.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 54]  [Cited by in F6Publishing: 48]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
69.  Sena NT, Gomes BP, Vianna ME, Berber VB, Zaia AA, Ferraz CC, Souza-Filho FJ. In vitro antimicrobial activity of sodium hypochlorite and chlorhexidine against selected single-species biofilms. Int Endod J. 2006;39:878-885.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 81]  [Cited by in F6Publishing: 76]  [Article Influence: 4.2]  [Reference Citation Analysis (0)]
70.  Ferraz CC, Gomes BP, Zaia AA, Teixeira FB, Souza-Filho FJ. Comparative study of the antimicrobial efficacy of chlorhexidine gel, chlorhexidine solution and sodium hypochlorite as endodontic irrigants. Braz Dent J. 2007;18:294-298.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 40]  [Cited by in F6Publishing: 47]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
71.  Ferguson DB, Marley JT, Hartwell GR. The effect of chlorhexidine gluconate as an endodontic irrigant on the apical seal: long-term results. J Endod. 2003;29:91-94.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 21]  [Cited by in F6Publishing: 21]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
72.  Gomes BP, Vianna ME, Matsumoto CU, Rossi Vde P, Zaia AA, Ferraz CC, Souza Filho FJ. Disinfection of gutta-percha cones with chlorhexidine and sodium hypochlorite. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:512-517.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 52]  [Cited by in F6Publishing: 60]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
73.  Siqueira JF Jr, da Silva CH, Cerqueira M das D, Lopes HP, de Uzeda M. Effectiveness of four chemical solutions in eliminating Bacillus subtilis spores on gutta-percha cones. Endod Dent Traumatol. 1998;14:124-126.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 39]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
74.  Athanassiadis B, Abbott PV, Walsh LJ. The use of calcium hydroxide, antibiotics and biocides as antimicrobial medicaments in endodontics. Aust Dent J. 2007;52:S64-S82.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 177]  [Cited by in F6Publishing: 182]  [Article Influence: 10.7]  [Reference Citation Analysis (0)]
75.  Carrilho MR, Carvalho RM, de Goes MF, di Hipólito V, Geraldeli S, Tay FR, Pashley DH, Tjäderhane L. Chlorhexidine preserves dentin bond in vitro. J Dent Res. 2007;86:90-94.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 269]  [Cited by in F6Publishing: 268]  [Article Influence: 15.8]  [Reference Citation Analysis (0)]
76.  Hebling J, Pashley DH, Tjäderhane L, Tay FR. Chlorhexidine arrests subclinical degradation of dentin hybrid layers in vivo. J Dent Res. 2005;84:741-746.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 352]  [Cited by in F6Publishing: 333]  [Article Influence: 18.5]  [Reference Citation Analysis (0)]
77.  Gendron R, Grenier D, Sorsa T, Mayrand D. Inhibition of the activities of matrix metalloproteinases 2, 8, and 9 by chlorhexidine. Clin Diagn Lab Immunol. 1999;6:437-439.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 336]  [Cited by in F6Publishing: 323]  [Article Influence: 12.9]  [Reference Citation Analysis (0)]
78.  Wang Y, Spencer P. Hybridization efficiency of the adhesive/dentin interface with wet bonding. J Dent Res. 2003;82:141-145.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 243]  [Cited by in F6Publishing: 225]  [Article Influence: 10.7]  [Reference Citation Analysis (0)]
79.  Santos J, Carrilho M, Tervahartiala T, Sorsa T, Breschi L, Mazzoni A, Pashley D, Tay F, Ferraz C, Tjäderhane L. Determination of matrix metalloproteinases in human radicular dentin. J Endod. 2009;35:686-689.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 78]  [Cited by in F6Publishing: 64]  [Article Influence: 4.3]  [Reference Citation Analysis (0)]
80.  Jeansonne MJ, White RR. A comparison of 2.0% chlorhexidine gluconate and 5.25% sodium hypochlorite as antimicrobial endodontic irrigants. J Endod. 1994;20:276-278.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 245]  [Cited by in F6Publishing: 233]  [Article Influence: 7.8]  [Reference Citation Analysis (0)]
81.  Marley JT, Ferguson DB, Hartwell GR. Effects of chlorhexidine gluconate as an endodontic irrigant on the apical seal: short-term results. J Endod. 2001;27:775-778.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 14]  [Cited by in F6Publishing: 14]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
82.  Okino LA, Siqueira EL, Santos M, Bombana AC, Figueiredo JA. Dissolution of pulp tissue by aqueous solution of chlorhexidine digluconate and chlorhexidine digluconate gel. Int Endod J. 2004;37:38-41.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 93]  [Cited by in F6Publishing: 97]  [Article Influence: 4.9]  [Reference Citation Analysis (0)]
83.  Mallya L, Shenoy R, Mala K, Shenoy S. Evaluation of the antimicrobial efficacy of 20% Punica granatum, 0.2% chlorhexidine gluconate, and 2.5% sodium hypochlorite used alone or in combinations against Enterococcus faecalis: An in-vitro study. J Conserv Dent. 2019;22:367-370.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 5]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
84.  Do Prado M, Simão RA, Gomes BP. Evaluation of different irrigation protocols concerning the formation of chemical smear layer. Microsc Res Tech. 2013;76:196-200.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 17]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
85.  Akisue E, Tomita VS, Gavini G, Poli de Figueiredo JA. Effect of the combination of sodium hypochlorite and chlorhexidine on dentinal permeability and scanning electron microscopy precipitate observation. J Endod. 2010;36:847-850.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 45]  [Cited by in F6Publishing: 52]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
86.  Burkhardt-Holm P, Oulmi Y, Schroeder A, Storch V, Braunbeck T. Toxicity of 4-chloroaniline in early life stages of zebrafish (Danio rerio): II. Cytopathology and regeneration of liver and gills after prolonged exposure to waterborne 4-chloroaniline. Arch Environ Contam Toxicol. 1999;37:85-102.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 41]  [Cited by in F6Publishing: 41]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
87.  McComb D, Smith DC, Beagrie GS. The results of in vivo endodontic chemomechanical instrumentation--a scanning electron microscopic study. J Br Endod Soc. 1976;9:11-18.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 57]  [Cited by in F6Publishing: 54]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
88.  Mader CL, Baumgartner JC, Peters DD. Scanning electron microscopic investigation of the smeared layer on root canal walls. J Endod. 1984;10:477-483.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 208]  [Cited by in F6Publishing: 187]  [Article Influence: 4.7]  [Reference Citation Analysis (0)]
89.  Meryon SD, Tobias RS, Jakeman KJ. Smear removal agents: a quantitative study in vivo and in vitro. J Prosthet Dent. 1987;57:174-179.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 46]  [Cited by in F6Publishing: 43]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
90.  Baumgartner JC, Mader CL. A scanning electron microscopic evaluation of four root canal irrigation regimens. J Endod. 1987;13:147-157.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 333]  [Cited by in F6Publishing: 357]  [Article Influence: 9.6]  [Reference Citation Analysis (0)]
91.  Saunders WP, Saunders EM. The effect of smear layer upon the coronal leakage of gutta-percha fillings and a glass ionomer sealer. Int Endod J. 1992;25:245-249.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 67]  [Cited by in F6Publishing: 71]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
92.  Lester KS, Boyde A. Scanning electron microscopy of instrumented, irrigated and filled root canals. Br Dent J. 1977;143:359-367.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 64]  [Cited by in F6Publishing: 66]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
93.  Hülsmann M, Heckendorff M, Lennon A. Chelating agents in root canal treatment: mode of action and indications for their use. Int Endod J. 2003;36:810-830.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 269]  [Cited by in F6Publishing: 309]  [Article Influence: 14.7]  [Reference Citation Analysis (0)]
94.  Loel DA. Use of acid cleanser in endodontic therapy. J Am Dent Assoc. 1975;90:148-151.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 46]  [Cited by in F6Publishing: 47]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
95.  Machado R, Garcia LDFR, da Silva Neto UX, Cruz Filho AMD, Silva RG, Vansan LP. Evaluation of 17% EDTA and 10% citric acid in smear layer removal and tubular dentin sealer penetration. Microsc Res Tech. 2018;81:275-282.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 19]  [Cited by in F6Publishing: 22]  [Article Influence: 3.1]  [Reference Citation Analysis (0)]
96.  Gopikrishna V, Venkateshbabu N, Krithikadatta J, Kandaswamy D. Evaluation of the effect of MTAD in comparison with EDTA when employed as the final rinse on the shear bond strength of three endodontic sealers to dentine. Aust Endod J. 2011;37:12-17.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 9]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
97.  Patterson SS. In vivo and in vitro studies of the effect of the disodium slat of ethylenediamine tetra-acetate on human dentine and its endodontic implications. Oral Surg Oral Med Oral Pathol. 1963;16:83-103.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 80]  [Cited by in F6Publishing: 82]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
98.  Yoshida T, Shibata T, Shinohara T, Gomyo S, Sekine I. Clinical evaluation of the efficacy of EDTA solution as an endodontic irrigant. J Endod. 1995;21:592-593.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 39]  [Cited by in F6Publishing: 41]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
99.  Liu F, Hansra S, Crockford G, Köster W, Allan BJ, Blondeau JM, Lainesse C, White AP. Tetrasodium EDTA Is Effective at Eradicating Biofilms Formed by Clinically Relevant Microorganisms from Patients' Central Venous Catheters. mSphere. 2018;3.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 23]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
100.  Bystrom A, Sundqvist G. The antibacterial action of sodium hypochlorite and EDTA in 60 cases of endodontic therapy. Int Endod J. 1985;18:35-40.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 528]  [Cited by in F6Publishing: 495]  [Article Influence: 12.7]  [Reference Citation Analysis (0)]
101.  Zehnder M, Schmidlin P, Sener B, Waltimo T. Chelation in root canal therapy reconsidered. J Endod. 2005;31:817-820.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 171]  [Cited by in F6Publishing: 184]  [Article Influence: 9.7]  [Reference Citation Analysis (0)]
102.  Torabinejad M, Khademi AA, Babagoli J, Cho Y, Johnson WB, Bozhilov K, Kim J, Shabahang S. A new solution for the removal of the smear layer. J Endod. 2003;29:170-175.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 293]  [Cited by in F6Publishing: 318]  [Article Influence: 15.1]  [Reference Citation Analysis (0)]
103.  Dahlén G, Samuelsson W, Molander A, Reit C. Identification and antimicrobial susceptibility of enterococci isolated from the root canal. Oral Microbiol Immunol. 2000;15:309-312.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 132]  [Cited by in F6Publishing: 137]  [Article Influence: 5.7]  [Reference Citation Analysis (0)]
104.  McDonnell G, Russell AD. Antiseptics and disinfectants: activity, action, and resistance. Clin Microbiol Rev. 1999;12:147-179.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3207]  [Cited by in F6Publishing: 2629]  [Article Influence: 105.2]  [Reference Citation Analysis (0)]
105.  Baumgartner JC, Ibay AC. The chemical reactions of irrigants used for root canal debridement. J Endod. 1987;13:47-51.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 57]  [Cited by in F6Publishing: 53]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
106.  Calt S, Serper A. Time-dependent effects of EDTA on dentin structures. J Endod. 2002;28:17-19.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 282]  [Cited by in F6Publishing: 277]  [Article Influence: 12.6]  [Reference Citation Analysis (0)]
107.  Angker L, Swain MV, Kilpatrick N. Characterising the micro-mechanical behaviour of the carious dentine of primary teeth using nano-indentation. J Biomech. 2005;38:1535-1542.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 49]  [Cited by in F6Publishing: 50]  [Article Influence: 2.6]  [Reference Citation Analysis (0)]
108.  Yamada RS, Armas A, Goldman M, Lin PS. A scanning electron microscopic comparison of a high volume final flush with several irrigating solutions: Part 3. J Endod. 1983;9:137-142.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 331]  [Cited by in F6Publishing: 327]  [Article Influence: 8.0]  [Reference Citation Analysis (0)]