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      Controlled drug delivery and cell adhesion for bone tissue regeneration by Keplerate polyoxometalate (Mo 132)/metronidazole/PMMA scaffolds

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          Abstract

          The aim of this study is to fabricate a new scaffold appropriate for tissue regeneration with antimicrobial activity and ability of controlled drug delivery. In this regard, scaffold nanofibers were produced using poly (methyl methacrylate) (PMMA), Mo 132 as a Keplerate polyoxometalate and metronidazole. The final scaffolds, obtained by electrospinning, represent the intrinsic features including exceptional doubling tensile strength, high hydrophilicity (126 ± 5.2° to 83.9 ± 3.2° for contact angle and 14.18 ± 0.62% to 35.62 ± 0.24% for water uptake), proper bioactivity and cell adhesion. Moreover, the addition of Mo 132 and metronidazole enhances the biodegradation rate of resulted scaffolds compared to the pure PMMA membrane. The controlled release of metronidazole over 14 days efficiently inhibits the colonization of anaerobic microorganisms. Overall, the results demonstrate high potential of Mo 132 and metronidazole-loaded PMMA scaffold for guided bone regeneration/guided tissue regeneration.

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          How useful is SBF in predicting in vivo bone bioactivity?

          The bone-bonding ability of a material is often evaluated by examining the ability of apatite to form on its surface in a simulated body fluid (SBF) with ion concentrations nearly equal to those of human blood plasma. However, the validity of this method for evaluating bone-bonding ability has not been assessed systematically. Here, the history of SBF, correlation of the ability of apatite to form on various materials in SBF with their in vivo bone bioactivities, and some examples of the development of novel bioactive materials based on apatite formation in SBF are reviewed. It was concluded that examination of apatite formation on a material in SBF is useful for predicting the in vivo bone bioactivity of a material, and the number of animals used in and the duration of animal experiments can be reduced remarkably by using this method.
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            Polyoxometalate clusters, nanostructures and materials: from self assembly to designer materials and devices.

            Polyoxometalates represent a diverse range of molecular clusters with an almost unmatched range of physical properties and the ability to form structures that can bridge several length scales. The new building block principles that have been discovered are beginning to allow the design of complex clusters with desired properties and structures and several structural types and novel physical properties are examined. In this critical review the synthetic and design approaches to the many polyoxometalate cluster types are presented encompassing all the sub-types of polyoxometalates including, isopolyoxometalates, heteropolyoxometalates, and reduced molybdenum blue systems. As well as the fundamental structure and bonding aspects, the final section is devoted to discussing these clusters in the context of contemporary and emerging interdisciplinary interests from areas as diverse as anti-viral agents, biological ion transport models, and materials science.
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              Polyoxometalates in Medicine.

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                Author and article information

                Contributors
                yadollahi@chem.ui.ac.ir , yadollahi.b@gmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                24 August 2022
                24 August 2022
                2022
                : 12
                : 14443
                Affiliations
                [1 ]GRID grid.411750.6, ISNI 0000 0001 0454 365X, Department of Chemistry, , University of Isfahan, ; Isfahan, 81746-73441 Iran
                [2 ]GRID grid.411750.6, ISNI 0000 0001 0454 365X, Department of Biotechnology, Faculty of Biological Science and Technology, , University of Isfahan, ; Isfahan, 81746-73441 Iran
                Article
                18622
                10.1038/s41598-022-18622-w
                9402948
                36002474
                ee85e2a8-f2c1-4f72-b8e8-8ba9a8eac8a3
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 6 July 2022
                : 16 August 2022
                Categories
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                © The Author(s) 2022

                Uncategorized
                drug discovery,molecular medicine,chemistry
                Uncategorized
                drug discovery, molecular medicine, chemistry

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