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Maleic acid as a root canal irrigant- a scoping review
Tanya Kapur1, Edlin Glane Mathias2, Sonia Gupta3
1Department of Conservative Dentistry and Endodontics, Manipal College of Dental Sciences, Manipal, Manipal Academy of Higher Education, Manipal, Karnataka, India. tanyakapur9@gmail.com.
Maleic acid (MA) effectively removes smear layer in root canal therapy, especially in the apical third, offering better adhesion and regeneration potential than ethylenediaminetetraacetic acid (EDTA). Controlled application is key to minimize risks.
Area of Science:
- Endodontics
- Dental Materials Science
- Biomaterials
Background:
- Root canal treatment (RCT) necessitates effective smear layer removal for optimal sealing and reduced microbial contamination.
- Ethylenediaminetetraacetic acid (EDTA) is a common chelator but has limitations, particularly in the apical root canal regions.
- Maleic acid (MA) is emerging as a promising alternative due to its demineralizing and adhesion-promoting properties.
Purpose of the Study:
- To evaluate maleic acid's efficacy in root canal therapy.
- Emphasis on smear layer removal, antimicrobial activity, dentin interactions, and dental material compatibility.
Main Methods:
- Systematic review adhering to PRISMA-ScR guidelines.
- Searched major databases (PubMed, Scopus, Embase, Web of Science) up to October 2024.
- Included 71 studies comparing MA with other irrigants (EDTA, citric acid) based on PICO criteria.
Main Results:
- 7% MA demonstrated superior smear layer removal in the apical third compared to 17% EDTA.
- MA enhanced dentin wettability, sealer penetration, bond strength, and removal of intracanal medicaments.
- MA showed moderate antimicrobial activity alone but improved with combinations; it negatively affected dentin microhardness and calcium silicate-based materials.
Conclusions:
- Maleic acid (MA) offers superior apical smear layer removal and advantages in adhesion and regeneration.
- Controlled application (1-3 min) is recommended to balance benefits and risks.
- MA is a promising, less cytotoxic alternative to EDTA, requiring standardized protocols and in vivo validation for clinical integration.
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