Pectin as a Biomaterial in Regenerative Endodontics—Assessing Biocompatibility and Antibacterial Efficacy against Common Endodontic Pathogens: An In Vitro Study

Author:

Abdelgawad Raghda Magdy12ORCID,Damé-Teixeira Nailê13ORCID,Gurzawska-Comis Katarzyna4,Alghamdi Arwa15,Mahran Abeer H.6ORCID,Elbackly Rania7,Do Thuy1ORCID,El-Gendy Reem18

Affiliation:

1. Division of Oral Biology, Leeds School of Dentistry, St. James University Hospital, University of Leeds, Leeds LS9 7TF, UK

2. Department of Endodontics, Faculty of Dentistry, Assiut University, Assiut 83523, Egypt

3. Department of Dentistry, School of Health Sciences, University of Brasilia, Brasilia 70910-900, Brazil

4. Oral Surgery, Life Course and Medical Science, Liverpool L8 7SS, UK

5. Oral Biology Department, Faculty of Dentistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia

6. Department of Endodontics, Faculty of Dentistry, Ain Shams University, Cairo 11566, Egypt

7. Endodontics, Conservative Dentistry Department and Tissue Engineering Laboratories, Faculty of Dentistry, Alexandria University, Alexandria 21527, Egypt

8. Department of Oral Pathology, Faculty of Dentistry, Suez Canal University, Ismailia 8366004, Egypt

Abstract

Regenerative endodontics (REP) is a new clinical modality aiming to regenerate damaged soft and hard dental tissues, allowing for root completion in young adults’ teeth. Effective disinfection is crucial for REP success, but commonly used antimicrobials often harm the niche dental pulp stem cells (DPSCs). To our knowledge, this is the first study to explore the biocompatibility and antimicrobial potential of pectin as a potential natural intracanal medicament for REPs. Low methoxyl commercial citrus pectin (LM) (pectin CU701, Herbstreith&Fox.de) was used in all experiments. The pectin’s antibacterial activity against single species biofilms (E. faecalis and F. nucleatum) was assessed using growth curves. The pectin’s antimicrobial effect against mature dual-species biofilm was also evaluated using confocal laser scanning microscopy (CLSM) after 30 min and 7 days of treatment. The DPSC biocompatibility with 2% and 4% w/v of the pectin coatings was evaluated using live/dead staining, LDH, and WST-1 assays. Pectin showed a concentration-dependent inhibitory effect against single-species biofilms (E. faecalis and F. nucleatum) but failed to disrupt dual-species biofilm. Pectin at 2% w/v concentration proved to be biocompatible with the HDPSCs. However, 4% w/v pectin reduced both the viability and proliferation of the DPSCs. Low concentration (2% w/v) pectin was biocompatible with the DPSCs and showed an antimicrobial effect against single-species biofilms. This suggests the potential for using pectin as an injectable hydrogel for clinical applications in regenerative endodontics.

Funder

Newton-Mosharafa Fund

Publisher

MDPI AG

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