Maria T P Albuquerque1, Stuart J Ryan2, Eliseu A Münchow3, Maria M Kamocka4, Richard L Gregory5, Marcia C Valera6, Marco C Bottino7. 1. Division of Dental Biomaterials, Department of Restorative Dentistry, Indiana University School of Dentistry, Indianapolis, Indiana; Division of Nephrology, Indiana University School of Dentistry, Indianapolis, Indiana. 2. Division of Dental Biomaterials, Department of Restorative Dentistry, Indiana University School of Dentistry, Indianapolis, Indiana. 3. Division of Dental Biomaterials, Department of Restorative Dentistry, Indiana University School of Dentistry, Indianapolis, Indiana; Department of Oral Biology, Indiana University School of Dentistry, Indianapolis, Indiana. 4. Graduate Program in Restorative Dentistry (Endodontics), Universidade Estadual Paulista, São José dos Campos Dental School, São José dos Campos, São Paulo, Brazil. 5. Department of Operative Dentistry, Federal University of Pelotas (UFPEL), School of Dentistry, Pelotas, Rio Grande do Sul, Brazil. 6. Division of Nephrology, Indiana University School of Dentistry, Indianapolis, Indiana. 7. Division of Dental Biomaterials, Department of Restorative Dentistry, Indiana University School of Dentistry, Indianapolis, Indiana. Electronic address: mbottino@iu.edu.
Abstract
INTRODUCTION: Actinomyces naeslundii has been recovered from traumatized permanent teeth diagnosed with necrotic pulps. In this work, a triple antibiotic paste (TAP)-mimic scaffold is proposed as a drug-delivery strategy to eliminate A. naeslundii dentin biofilm. METHODS: Metronidazole, ciprofloxacin, and minocycline were added to a polydioxanone (PDS) polymer solution and spun into fibrous scaffolds. Fiber morphology, mechanical properties, and drug release were investigated by using scanning electron microscopy, microtensile testing, and high-performance liquid chromatography, respectively. Human dentin specimens (4 × 4 × 1 mm(3), n = 4/group) were inoculated with A. naeslundii (ATCC 43146) for 7 days for biofilm formation. The infected dentin specimens were exposed to TAP-mimic scaffolds, TAP solution (positive control), and pure PDS (drug-free scaffold). Dentin infected (7-day biofilm) specimens were used for comparison (negative control). Confocal laser scanning microscopy was done to determine bacterial viability. RESULTS: Scaffolds displayed a submicron mean fiber diameter (PDS = 689 ± 312 nm and TAP-mimic = 718 ± 125 nm). Overall, TAP-mimic scaffolds showed significantly (P ≤ .040) lower mechanical properties than PDS. Within the first 24 hours, a burst release for all drugs was seen. A sustained maintenance of metronidazole and ciprofloxacin was observed over 4 weeks, but not for minocycline. Confocal laser scanning microscopy demonstrated complete elimination of all viable bacteria exposed to the TAP solution. Meanwhile, TAP-mimic scaffolds led to a significant (P < .05) reduction in the percentage of viable bacteria compared with the negative control and PDS. CONCLUSIONS: Our findings suggest that TAP-mimic scaffolds hold significant potential in the eradication/elimination of bacterial biofilm, a critical step in regenerative endodontics.
INTRODUCTION:Actinomyces naeslundii has been recovered from traumatized permanent teeth diagnosed with necrotic pulps. In this work, a triple antibiotic paste (TAP)-mimic scaffold is proposed as a drug-delivery strategy to eliminate A. naeslundii dentin biofilm. METHODS:Metronidazole, ciprofloxacin, and minocycline were added to a polydioxanone (PDS) polymer solution and spun into fibrous scaffolds. Fiber morphology, mechanical properties, and drug release were investigated by using scanning electron microscopy, microtensile testing, and high-performance liquid chromatography, respectively. Human dentin specimens (4 × 4 × 1 mm(3), n = 4/group) were inoculated with A. naeslundii (ATCC 43146) for 7 days for biofilm formation. The infected dentin specimens were exposed to TAP-mimic scaffolds, TAP solution (positive control), and pure PDS (drug-free scaffold). Dentin infected (7-day biofilm) specimens were used for comparison (negative control). Confocal laser scanning microscopy was done to determine bacterial viability. RESULTS: Scaffolds displayed a submicron mean fiber diameter (PDS = 689 ± 312 nm and TAP-mimic = 718 ± 125 nm). Overall, TAP-mimic scaffolds showed significantly (P ≤ .040) lower mechanical properties than PDS. Within the first 24 hours, a burst release for all drugs was seen. A sustained maintenance of metronidazole and ciprofloxacin was observed over 4 weeks, but not for minocycline. Confocal laser scanning microscopy demonstrated complete elimination of all viable bacteria exposed to the TAP solution. Meanwhile, TAP-mimic scaffolds led to a significant (P < .05) reduction in the percentage of viable bacteria compared with the negative control and PDS. CONCLUSIONS: Our findings suggest that TAP-mimic scaffolds hold significant potential in the eradication/elimination of bacterial biofilm, a critical step in regenerative endodontics.
Authors: Juliana Y Nagata; Adriana J Soares; Francisco J Souza-Filho; Alexandre A Zaia; Caio C R Ferraz; José F A Almeida; Brenda P F A Gomes Journal: J Endod Date: 2014-04-29 Impact factor: 4.171
Authors: M C Bottino; K Kamocki; G H Yassen; J A Platt; M M Vail; Y Ehrlich; K J Spolnik; R L Gregory Journal: J Dent Res Date: 2013-09-20 Impact factor: 6.116
Authors: Ronald Ordinola-Zapata; Clovis M Bramante; Paloma Gagliardi Minotti; Bruno Cavalini Cavenago; Roberto Brandão Garcia; Norberti Bernardineli; David E Jaramillo; Marco A Hungaro Duarte Journal: J Endod Date: 2012-11-10 Impact factor: 4.171
Authors: Marco C Bottino; Ghaeth H Yassen; Jeffrey A Platt; Nawaf Labban; L Jack Windsor; Kenneth J Spolnik; Ana H A Bressiani Journal: J Tissue Eng Regen Med Date: 2013-03-08 Impact factor: 3.963
Authors: Maria Tereza P Albuquerque; Joshua D Evans; Richard L Gregory; Marcia C Valera; Marco C Bottino Journal: Clin Oral Investig Date: 2015-08-29 Impact factor: 3.573
Authors: Misako Nakashima; Koichiro Iohara; Marco C Bottino; Ashraf F Fouad; Jacques E Nör; George T-J Huang Journal: Tissue Eng Part B Rev Date: 2019-01-09 Impact factor: 6.389
Authors: Divya Pankajakshan; Maria T P Albuquerque; Joshua D Evans; Malgorzata M Kamocka; Richard L Gregory; Marco C Bottino Journal: J Endod Date: 2016-10 Impact factor: 4.171
Authors: Julian M Sotomil; Eliseu A Münchow; Divya Pankajakshan; Kenneth J Spolnik; Jessica A Ferreira; Richard L Gregory; Marco C Bottino Journal: J Endod Date: 2019-09-18 Impact factor: 4.171
Authors: Juliana S Ribeiro; Eliseu A Münchow; Ester A Ferreira Bordini; Wellington Luiz de Oliveira da Rosa; Marco C Bottino Journal: J Endod Date: 2020-09 Impact factor: 4.171
Authors: Marco C Bottino; Maria T P Albuquerque; Asma Azabi; Eliseu A Münchow; Kenneth J Spolnik; Jacques E Nör; Paul C Edwards Journal: J Biomed Mater Res B Appl Biomater Date: 2018-10-03 Impact factor: 3.368