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      Silicalite-1 Layers as a Biocompatible Nano- and Micro-Structured Coating: An In Vitro Study on MG-63 Cells

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          Abstract

          Silicalite-1 is a purely siliceous form of zeolite, which does not contain potentially harmful aluminum in its structure as opposed to ZSM-5 aluminosilicate types of zeolite. This paper reports on a study of a silicalite-1 film, deposited on a silicon Si(100) substrate, as a potential anti-corrosive and biocompatible coating for orthopaedic implants. Silicalite-1 film was prepared in situ on the surface of Si(100) wafers using a reaction mixture of tetrapropyl-ammonium hydroxide (TPAOH), tetraethyl-orthosilicate (TEOS), and diH 2O. The physico-chemical properties of the obtained surface were characterized by means of X-ray photoelectron spectroscopy, water contact angle measurement, atomic force microscopy, and scanning electron microscopy. The biocompatibility was assessed by interaction with the MG-63 cell line (human osteosarcoma) in terms of cell adhesion, morphology, proliferation, and viability. The synthesized silicalite-1 film consisted of two layers ( b - and a, b -oriented crystals) creating a combination of micro- and nano-scale surface morphology suitable for cell growth. Despite its hydrophobicity, the silicalite-1 film increased the number of initially adhered human osteoblast-like MG-63 cells and the proliferation rate of these cells. The silicalite-1 film also improved the cell viability in comparison with the reference Si(100) substrate. It is therefore a promising candidate for coating of orthopaedic implants.

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          Most cited references33

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          Silicalite, a new hydrophobic crystalline silica molecular sieve

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            Long-term implant fixation and stress-shielding in total hip replacement.

            D R Sumner (2015)
            Implant fixation implies a strong and durable mechanical bond between the prosthetic component and host skeleton. Assuming the short-term impediments to implant fixation are successfully addressed and that longer-term issues such as late infection and mechanical failure of the components are avoided, the biological response of the host tissue to the presence of the implant is critical to long-term success. In particular, maintenance of adequate peri-prosthetic bone stock is a key factor. Two major causes of bone loss in the supporting bone are adverse bone remodeling in response to debris shed from the implant and stress-shielding. Here, I review some of the major lessons learned from studying stress-shielding-induced bone loss. It is well known that stress-shielding can be manipulated by altering implant design, but less well appreciated that the development of bone anabolic agents may make it possible to reduce the severity of stress-shielding and the associated bone loss by augmenting the host skeleton through the use of locally or systemically delivered agents. In most cases, mechanical, material and biological factors do not act in isolation, emphasizing that it is often not possible to optimize all boundary conditions.
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              The effects on bone cells of metal ions released from orthopaedic implants. A review.

              The increasing use of orthopedic implants and, in particular, of hip and knee joint replacements for young and active patients, has stimulated interest and concern regarding the chronic, long-term effects of the materials used. This review focuses on the current knowledge of the adverse biologic reactions to metal particles released from orthopaedic implants in vivo and in vitro. More specifically, the purpose of this article is to provide an overview of the current literature about the adverse effects of metal particles on bone cells and peri-implant bone.
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                Author and article information

                Journal
                Materials (Basel)
                Materials (Basel)
                materials
                Materials
                MDPI
                1996-1944
                31 October 2019
                November 2019
                : 12
                : 21
                : 3583
                Affiliations
                [1 ]Institute of Physiology of the Czech Academy of Sciences, v.v.i., Videnska 1083, 142 20 Prague 4, Czech Republic; martina.doubkova@ 123456fgu.cas.cz (M.D.); lucie.bacakova@ 123456fgu.cas.cz (L.B.)
                [2 ]Second Faculty of Medicine, Charles University, V Uvalu 84, 150 06 Prague 5, Czech Republic
                [3 ]J. Heyrovsky Institute of Physical Chemistry of the Czech Academy of Sciences, v.v.i., Dolejskova 3, 182 23 Prague 8, Czech Republic; ivan.jirka@ 123456jh-inst.cas.cz
                [4 ]Institute of Complex Systems, Faculty of Fisheries and Protection of Waters, University of South Bohemia in Ceske Budejovice, Zamek 136, 373 33 Nove Hrady, Czech Republic; brezinavita@ 123456gmail.com
                Author notes
                Author information
                https://orcid.org/0000-0002-4955-4093
                https://orcid.org/0000-0001-9725-8048
                https://orcid.org/0000-0002-0222-4855
                Article
                materials-12-03583
                10.3390/ma12213583
                6862472
                31683581
                350f765c-f617-40da-a1b4-4bab25427e75
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 11 October 2019
                : 29 October 2019
                Categories
                Article

                silicalite-1,zeolite,coating,mg-63 cells,osteoblasts,biocompatibility

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