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Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation

BACKGROUND AND OBJECTIVE: Povidone-iodine [polyvinylpyrrolidone-iodine complex (PVP-I)] is a broad-spectrum antimicrobial agent, frequently used in dentistry. In this study we investigated the short- and longterm effects on osteoblast number, viability, and function after short exposure to PVP-I wit...

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Autores principales: Schmidlin, P.R, Imfeld, T, Sahrmann, P, Tchouboukov, A, Weber, F.E
Formato: Texto
Lenguaje:English
Publicado: Bentham Open 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776307/
https://www.ncbi.nlm.nih.gov/pubmed/19915721
http://dx.doi.org/10.2174/1874210600903010208
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author Schmidlin, P.R
Imfeld, T
Sahrmann, P
Tchouboukov, A
Weber, F.E
author_facet Schmidlin, P.R
Imfeld, T
Sahrmann, P
Tchouboukov, A
Weber, F.E
author_sort Schmidlin, P.R
collection PubMed
description BACKGROUND AND OBJECTIVE: Povidone-iodine [polyvinylpyrrolidone-iodine complex (PVP-I)] is a broad-spectrum antimicrobial agent, frequently used in dentistry. In this study we investigated the short- and longterm effects on osteoblast number, viability, and function after short exposure to PVP-I with and without additional bone-morphogenetic protein-2 (BMP-2). MATERIAL AND METHODS: Confluent osteoblast-like cell line (MC3T3-E1, subclone 24) cultures were exposed to pure PVP-I solution (7.7 mg/ml) and dilutions of 1:10, 1:100 and 1:1000 for 10 seconds and washed with phosphate buffer solution. Cell proliferation and viability was determined by MTT and differentiation status by alkaline phosphatase (ALP) activity 6 days after initial plating. In a separate experiment, long-term cell proliferation, viability and function were assessed 4 weeks after PVP-I treatment by MTT and deposited calcium using an Alizarin-red staining test. RESULTS: PVP-I decreased ALP activity substantially. Stimulation by BMP-2 recovered ALP activity to near control levels at 1:100 and 1:1000 dilutions of PVP-I. The MTT assay showed reduced proliferation of the preosteoblastic cells for all treatments, irrespective whether BMP-2 was used or not. Only at PVP-I dilutions of 1:1000 proliferation rate was back to normal levels (95.6±2.4 %). No adverse long-term effect of PVP-I on mineralization of the extracellular matrix (Alizarinred) for dilutions higher than 1:100 was observed. Interestingly, undiluted and 1:10 diluted PVP-I even showed a significant increase in mineral deposition, especially in the presence of BMP-2. CONCLUSION: Short-time application of PVP-I in concentrations of 1:10 and higher lead to decreased viability and impaired differentiation. However, surviving cells showed good recovery and mineralization potential.
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spelling pubmed-27763072009-11-14 Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation Schmidlin, P.R Imfeld, T Sahrmann, P Tchouboukov, A Weber, F.E Open Dent J Article BACKGROUND AND OBJECTIVE: Povidone-iodine [polyvinylpyrrolidone-iodine complex (PVP-I)] is a broad-spectrum antimicrobial agent, frequently used in dentistry. In this study we investigated the short- and longterm effects on osteoblast number, viability, and function after short exposure to PVP-I with and without additional bone-morphogenetic protein-2 (BMP-2). MATERIAL AND METHODS: Confluent osteoblast-like cell line (MC3T3-E1, subclone 24) cultures were exposed to pure PVP-I solution (7.7 mg/ml) and dilutions of 1:10, 1:100 and 1:1000 for 10 seconds and washed with phosphate buffer solution. Cell proliferation and viability was determined by MTT and differentiation status by alkaline phosphatase (ALP) activity 6 days after initial plating. In a separate experiment, long-term cell proliferation, viability and function were assessed 4 weeks after PVP-I treatment by MTT and deposited calcium using an Alizarin-red staining test. RESULTS: PVP-I decreased ALP activity substantially. Stimulation by BMP-2 recovered ALP activity to near control levels at 1:100 and 1:1000 dilutions of PVP-I. The MTT assay showed reduced proliferation of the preosteoblastic cells for all treatments, irrespective whether BMP-2 was used or not. Only at PVP-I dilutions of 1:1000 proliferation rate was back to normal levels (95.6±2.4 %). No adverse long-term effect of PVP-I on mineralization of the extracellular matrix (Alizarinred) for dilutions higher than 1:100 was observed. Interestingly, undiluted and 1:10 diluted PVP-I even showed a significant increase in mineral deposition, especially in the presence of BMP-2. CONCLUSION: Short-time application of PVP-I in concentrations of 1:10 and higher lead to decreased viability and impaired differentiation. However, surviving cells showed good recovery and mineralization potential. Bentham Open 2009-10-16 /pmc/articles/PMC2776307/ /pubmed/19915721 http://dx.doi.org/10.2174/1874210600903010208 Text en © Schmidlin et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Schmidlin, P.R
Imfeld, T
Sahrmann, P
Tchouboukov, A
Weber, F.E
Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation
title Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation
title_full Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation
title_fullStr Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation
title_full_unstemmed Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation
title_short Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation
title_sort effect of short-time povidone-iodine application on osteoblast proliferation and differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776307/
https://www.ncbi.nlm.nih.gov/pubmed/19915721
http://dx.doi.org/10.2174/1874210600903010208
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