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Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis

BACKGROUND: Bacteria have long been recognized as the primary etiology for pulpal and periapical lesions, which necessitates the elimination of bacteria from the root canal system. In primary teeth, irrigation and debridement is the main protocol required to disinfect the canal. Biomechanical prepar...

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Autores principales: Goel, Ankit, Sinha, Abhishek, Khandeparker, Rakshit Vijay Sinai, Mehrotra, Rachit, Vashisth, Pallavi, Garg, Anuj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dentmedpub Research and Printing Co 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588793/
https://www.ncbi.nlm.nih.gov/pubmed/26464542
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author Goel, Ankit
Sinha, Abhishek
Khandeparker, Rakshit Vijay Sinai
Mehrotra, Rachit
Vashisth, Pallavi
Garg, Anuj
author_facet Goel, Ankit
Sinha, Abhishek
Khandeparker, Rakshit Vijay Sinai
Mehrotra, Rachit
Vashisth, Pallavi
Garg, Anuj
author_sort Goel, Ankit
collection PubMed
description BACKGROUND: Bacteria have long been recognized as the primary etiology for pulpal and periapical lesions, which necessitates the elimination of bacteria from the root canal system. In primary teeth, irrigation and debridement is the main protocol required to disinfect the canal. Biomechanical preparation cannot be vigorously done on the primary teeth due to anatomical barrier such as thin and flared roots. This calls for the use of an effective intracanal medication that will assist disinfection of root canal system. Aim of the study was to examine the in-vivo susceptibility of root canal bacteria to chlorhexidine (CHX) gluconate-1% gel and bioactive glass (BAG) S53P4 when used as intracanal medicaments using polymerase chain reaction (PCR). METHODOLOGY: PCR (analysis used oligonucleotide primers of Escherichia coli) was used to detect and compare the microbial load reduction after medication of 14 teeth for a week with either CHX gel - 1% or BAG S53P4. The pre and post microbial load was checked in the form of colony forming units. When analysis was done, a statistically significant difference was observed between the two groups. RESULTS: The study revealed that both medicaments caused a considerable amount of microbial load reduction. BAG S53P4 caused much more reduction than CHX 1% gel. Statistical analysis showed a significant difference between the two groups. CONCLUSION: BAG S53P4 has superior antibacterial property as compared to CHX 1% gel.
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spelling pubmed-45887932015-10-13 Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis Goel, Ankit Sinha, Abhishek Khandeparker, Rakshit Vijay Sinai Mehrotra, Rachit Vashisth, Pallavi Garg, Anuj J Int Oral Health Original Research BACKGROUND: Bacteria have long been recognized as the primary etiology for pulpal and periapical lesions, which necessitates the elimination of bacteria from the root canal system. In primary teeth, irrigation and debridement is the main protocol required to disinfect the canal. Biomechanical preparation cannot be vigorously done on the primary teeth due to anatomical barrier such as thin and flared roots. This calls for the use of an effective intracanal medication that will assist disinfection of root canal system. Aim of the study was to examine the in-vivo susceptibility of root canal bacteria to chlorhexidine (CHX) gluconate-1% gel and bioactive glass (BAG) S53P4 when used as intracanal medicaments using polymerase chain reaction (PCR). METHODOLOGY: PCR (analysis used oligonucleotide primers of Escherichia coli) was used to detect and compare the microbial load reduction after medication of 14 teeth for a week with either CHX gel - 1% or BAG S53P4. The pre and post microbial load was checked in the form of colony forming units. When analysis was done, a statistically significant difference was observed between the two groups. RESULTS: The study revealed that both medicaments caused a considerable amount of microbial load reduction. BAG S53P4 caused much more reduction than CHX 1% gel. Statistical analysis showed a significant difference between the two groups. CONCLUSION: BAG S53P4 has superior antibacterial property as compared to CHX 1% gel. Dentmedpub Research and Printing Co 2015-08 /pmc/articles/PMC4588793/ /pubmed/26464542 Text en Copyright: © Journal of International Oral Health http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Goel, Ankit
Sinha, Abhishek
Khandeparker, Rakshit Vijay Sinai
Mehrotra, Rachit
Vashisth, Pallavi
Garg, Anuj
Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis
title Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis
title_full Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis
title_fullStr Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis
title_full_unstemmed Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis
title_short Bioactive Glass S53P4 versus Chlorhexidine Gluconate as Intracanal Medicament in Primary Teeth: An In-vivo Study Using Polymerase Chain Reaction Analysis
title_sort bioactive glass s53p4 versus chlorhexidine gluconate as intracanal medicament in primary teeth: an in-vivo study using polymerase chain reaction analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588793/
https://www.ncbi.nlm.nih.gov/pubmed/26464542
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