A comparative evaluation of the efficacy of Citric Acid, Ethylene Diamine Tetra Acetic Acid (EDTA) and Tetracycline Hydrochloride as root biomodification agents: An in vitro SEM study
{"title":"A comparative evaluation of the efficacy of Citric Acid, Ethylene Diamine Tetra Acetic Acid (EDTA) and Tetracycline Hydrochloride as root biomodification agents: An in vitro SEM study","authors":"H. Grover, A. Yadav, Prashant Nanda","doi":"10.5681/JPID.2011.014","DOIUrl":null,"url":null,"abstract":"Aim: To compare the efficacy of Citric Acid, Ethylenediaminetetraacetic Acid (EDTA), and Tetracycline Hydrochloride as root biomodification agents. Materials and Method: 15 freshly extracted teeth were used for the study. The teeth were root planed and specimens obtained from the cervical 2/3 rd of the root. Each tooth root provided four specimens to be treated by the control (Saline), Citric Acid, EDTA and Tetracycline Hydrochloride, for a total of three minutes using the passive burnishing technique. The specimens were then observed under a scanning electron microscope (SEM). The specimens were evaluated for presence or absence of smear layer, total number of tubules visible, number of patent tubules and diameter of patent tubules. Statistical analysis was performed using “Paired t test”. Results: All the three test groups effectively removed the smear layer in comparison to the control. The number of patent tubules present in the Citric Acid and EDTA test groups was significantly higher than those in the Tetracycline Hydrochloride test group. However, the average diameter of the patent tubules was greater in the Tetracycline Hydrochloride group compared with Citric Acid and EDTA groups. Conclusion: All three agents appeared to be equally effective as root biomodification agents. However, in clinical practice EDTA might be more beneficial owing to its neutral pH and high efficacy in removing the smear layer and opening the dentinal tubules.","PeriodicalId":13857,"journal":{"name":"International Journal of Contemporary Dentistry","volume":"100 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2011-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Contemporary Dentistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5681/JPID.2011.014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Aim: To compare the efficacy of Citric Acid, Ethylenediaminetetraacetic Acid (EDTA), and Tetracycline Hydrochloride as root biomodification agents. Materials and Method: 15 freshly extracted teeth were used for the study. The teeth were root planed and specimens obtained from the cervical 2/3 rd of the root. Each tooth root provided four specimens to be treated by the control (Saline), Citric Acid, EDTA and Tetracycline Hydrochloride, for a total of three minutes using the passive burnishing technique. The specimens were then observed under a scanning electron microscope (SEM). The specimens were evaluated for presence or absence of smear layer, total number of tubules visible, number of patent tubules and diameter of patent tubules. Statistical analysis was performed using “Paired t test”. Results: All the three test groups effectively removed the smear layer in comparison to the control. The number of patent tubules present in the Citric Acid and EDTA test groups was significantly higher than those in the Tetracycline Hydrochloride test group. However, the average diameter of the patent tubules was greater in the Tetracycline Hydrochloride group compared with Citric Acid and EDTA groups. Conclusion: All three agents appeared to be equally effective as root biomodification agents. However, in clinical practice EDTA might be more beneficial owing to its neutral pH and high efficacy in removing the smear layer and opening the dentinal tubules.