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<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Mater.</journal-id>
<journal-title>Frontiers in Materials</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Mater.</abbrev-journal-title>
<issn pub-type="epub">2296-8016</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">747169</article-id>
<article-id pub-id-type="doi">10.3389/fmats.2021.747169</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Materials</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>The Improvement in Surface Properties of Metallic Implant <italic>via</italic> Magnetron Sputtering: Recent Progress and Remaining Challenges</article-title>
<alt-title alt-title-type="left-running-head">Akhtar et&#x20;al.</alt-title>
<alt-title alt-title-type="right-running-head">Radio Frequency Magnetron Sputtering</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Akhtar</surname>
<given-names>Memoona</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1235234/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Uzair</surname>
<given-names>Syed Ahmed</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Rizwan</surname>
<given-names>Muhammad</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1419296/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Ur Rehman</surname>
<given-names>Muhammad Atiq</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/344761/overview"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Materials Science and Engineering, Institute of Space Technology</institution>, <addr-line>Islamabad</addr-line>, <country>Pakistan</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>School of Materials Science and Engineering, Northwestern Polytechnical University</institution>, <addr-line>Xi&#x2019;an</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Metallurgical Engineering, Faculty of Chemical and Process Engineering, NED University of Engineering and Technology</institution>, <addr-line>Karachi</addr-line>, <country>Pakistan</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1126529/overview">Asma Tufail Shah</ext-link>, COMSATS University Islamabad, Lahore Campus, Pakistan</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/257925/overview">Rajendra Kumar Singh</ext-link>, Institute of Tissue Regeneration Engineering (ITREN), South Korea</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1552134/overview">Muhammad Awais</ext-link>, Taibah University, Saudi Arabia</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Muhammad Rizwan, <email>materialist.riz@gmail.com</email>; Muhammad Atiq Ur Rehman, <email>atique1.1@hotmail.com</email>
</corresp>
<fn fn-type="other">
<p>This article was submitted to Biomaterials, a section of the journal Frontiers in Materials</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>14</day>
<month>01</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>8</volume>
<elocation-id>747169</elocation-id>
<history>
<date date-type="received">
<day>25</day>
<month>07</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>13</day>
<month>12</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2022 Akhtar, Uzair, Rizwan and Ur Rehman.</copyright-statement>
<copyright-year>2022</copyright-year>
<copyright-holder>Akhtar, Uzair, Rizwan and Ur Rehman</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these&#x20;terms.</p>
</license>
</permissions>
<abstract>
<p>Bioceramic coatings on metallic implants provide a wear-resistant and biocompatible layer, that own ability to develop bone-like apatite in physiological environments to ensure bonding with hard tissues. These bioceramics primarily belong to Calcium Phosphates (CaPs), bioactive glasses, and glass-ceramics. Several techniques are used to deposit these coatings such as; electrophoretic deposition (EPD), plasma spray (PS), and Radio frequency magnetron sputtering (RFMS). Most of these techniques require a high-temperature operation or sintering treatment. This causes either thermal decomposition of bioceramic or results in delamination and cracking of the bioceramic coating due to differences in thermal expansion behavior of metals and bioceramics. RFMS is primarily carried out either at room temperature. However, annealing is performed or substrate is heated at various temperatures &#x223c;400&#x2013;1,200&#xb0;C for 2 or 4&#xa0;h under dry argon (very low temperature compared to other techniques) to ensure crystallization of bioceramics and improve coating adhesion. Chemical composition stability and excellent surface finish are the premium features of RFMS, due to less heat involvement. Moreover, RFMS has the unique ability to develop one-unit/ multilayered composite coatings and the flexibility of <italic>in-situ</italic> reactions to yield oxides and nitrides. Single or multiple targets can be employed with the insertion of Oxygen and Nitrogen to yield versatile coatings. Due to this attractive set of features RFMS has a strong potential in the field of bioceramic coatings. In recent years, several multifunctional bioceramic coatings have been deposited on metallic substrates using RFMS for biomedical applications. This review focuses on the recent efforts made in order to deposit multifunctional bioceramic RFMS coatings with surface characteristics necessary for biomedical applications and highlights future directions for the improved biological performance of RFMS bioceramic coatings.</p>
</abstract>
<kwd-group>
<kwd>bioceramics (BC)</kwd>
<kwd>calcium phosphates (CaPs)</kwd>
<kwd>magnetron sputtering</kwd>
<kwd>composite coatings thickness</kwd>
<kwd>biocompatibile</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>The demand for biomaterials is increasing day by day to address the needs of an aging population. These biomedical materials are beneficial for physically disordered people as a result of an injury or any natural disease (e.g., thyroidal disorder, bone cancer, etc.) (<xref ref-type="bibr" rid="B81">Pawlik et&#x20;al., 2019</xref>; <xref ref-type="bibr" rid="B74">Pandey et&#x20;al., 2020</xref>). In this connection, bone implants (either orthopedic or dentistry) are the most prevalent use of such materials in the human body. Other aspects that contribute to increased implant surgery include bone weakening (osteoporosis), trauma, and inflammation in bone joints (osteoarthritis) (<xref ref-type="bibr" rid="B13">Bellucci et&#x20;al., 2012</xref>; <xref ref-type="bibr" rid="B110">Ur Rehman et&#x20;al., 2017</xref>).</p>
<p>A fact is that about 2.8 million cases of bone repair are performed annually worldwide. According to reports, hip replacements and knee arthroplasties are expected to increase by 174 and 673%, respectively, from their current levels by 2030 (<xref ref-type="bibr" rid="B14">Bellucci et&#x20;al., 2013</xref>). The anticipation of such a huge demand for biomaterials in the coming years has sparked the interest of scientists and researchers from all around the world (<xref ref-type="bibr" rid="B62">Liu et&#x20;al., 2019</xref>; <xref ref-type="bibr" rid="B2">Ahmed et&#x20;al., 2020</xref>; <xref ref-type="bibr" rid="B3">Ahmed and Rehman, 2020</xref>).</p>
<p>Bone-related implants once implanted, serve as a medium for contact and interaction with the surrounding cells and tissues. Therefore, selecting bone biomaterials is an important step in creating optimal bone implants (<xref ref-type="bibr" rid="B120">Zhang et&#x20;al., 2014</xref>). In general, bone implants are selected based on their inherent biocompatibility, biodegradability, and mechanical characteristics, as well as cell behavior. In addition, hydrophobicity, molecular weight, and physicochemical properties are also crucial (<xref ref-type="bibr" rid="B27">Chopplet and Theirry, 2020</xref>; <xref ref-type="bibr" rid="B71">Nawaz and Ur Rehman, 2021</xref>).</p>
<p>Bioceramics, polymers, and biomedical metals are commonly studied materials for bone-related implants. Bioceramics are brittle with poor fracture toughness, inadequate mechanical strength, and a high elastic modulus compared to the cortical bone. In contrast to this, polymers&#x2019; mechanical strength and elastic modulus are much lower than that of the cortical bone, which limits their application in weight-bearing sites. Therefore, metals are preferred for load-bearing implant applications (<xref ref-type="bibr" rid="B66">Manivasagam et&#x20;al., 2010</xref>; <xref ref-type="bibr" rid="B70">Nawaz et&#x20;al., 2020</xref>). Biomaterials are utilized in various parts of the human body as implants, as shown in <xref ref-type="fig" rid="F1">Figure&#x20;1</xref>.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Various parts of the human body where biomaterials are used as implants Adapted from (<xref ref-type="bibr" rid="B74">Pandey et&#x20;al., 2020</xref>).</p>
</caption>
<graphic xlink:href="fmats-08-747169-g001.tif"/>
</fig>
<p>Metals for biomedical applications offer better structural functions than ceramic and polymer-based biomaterials; this is because metals exhibit excellent mechanical biocompatibility (young modulus, toughness, etc.), high strength, and lower densities which are essential requirements for load-bearing implant applications. Metals can replace unhealthy natural parts or repair various organs of the human body for a long time. The use of metal-made implants was primarily established by the need to repair bone, and then their use for orthopedic purposes was expanded along with the use of short-term pins and screws, followed by the use of permanent implants for total joint replacement (<xref ref-type="bibr" rid="B42">Gao et&#x20;al., 2017</xref>).</p>
<p>As far as biometals are concerned currently, load-bearing bone implants are manufactured using Stainless steels (SS), Co or Ti-based alloys. Apart from the advantage of strength, these alloys contain some toxic metallic ions (e.g., Ni, Cr, and V) which are responsible for biocompatibility complications. Moreover, elastic moduli of these metals are much higher as compared to the cortical bone which results in stress shielding effect. Further, the need for revision surgery is also a concern with metallic implants. These metals are non-bioresorbable, meaning they will remain in the body indefinitely. On the other hand, biodegradable metals, mainly including Mg, Zn, Fe, and their alloys, are considered potential load-bearing bone biomaterials (<xref ref-type="bibr" rid="B10">Barati Darband et&#x20;al., 2017</xref>). Among these, Mg and its alloys have attracted the most attention because their Young&#x2019;s moduli and densities are closer to those of cortical bone. They can effectively relieve the stress-shielding effect and curse of revisionary surgery due to their degradability. <xref ref-type="fig" rid="F2">Figure&#x20;2</xref> demonstrates that how biomedical materials are being revolutionized during the last 7&#xa0;decades (<xref ref-type="bibr" rid="B117">Yang et&#x20;al., 2020</xref>). The story of biomedical material started with the metallic implants where the focus was to meet the mechanical compatibility. The second-generation biomedical materials were bioactive and can form a robust bond with the natural tissue. Thus, the second generation introduces the concept of bioceramics. Although, the bioceramics presented poor mechanical properties. Yet, their favorable degradation kinetics revolutionize the biomedical industry. Finally, the third generation introduces the concept of bone tissue engineering and the possibility to repair the defective tissues. Furthermore, the concept of a targeted drug delivery system further improved the performance of biomedical materials (<xref ref-type="bibr" rid="B72">Nimbalkar et&#x20;al., 2020</xref>).</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Evolution of three generations of biomaterials over the last 70&#xa0;years.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g002.tif"/>
</fig>
<p>This review paper summarizes the recent developments in the field of bioceramic coatings highlighting the importance of the coatings obtained <italic>via</italic> magnetron sputtering. Various types of bioceramic coatings including hydroxyapatite (HA), calcium phosphate (CaP), bioactive glasses (BGs), etc. are discussed. We highlighted the advantages and challenges associated with each type of coatings by collecting the data from the available literature. Finally, concluding remarks and future prospect is presented.</p>
</sec>
<sec id="s2">
<title>Need of Bioceramic Coatings</title>
<p>The physiological environment contains a relatively higher concentration of chloride ions at relatively higher humidity. Thus, the metallic implants corrode in the human body leading to the leaching of unwanted toxic metal ions. Therefore, the performance of current orthopedic implants and prosthesis components composed of metallic biomaterials is relatively limited (<xref ref-type="bibr" rid="B109">Ur Rehman et&#x20;al., 2020</xref>). The strategies for functionalizing metallic implant surfaces through changes in the material&#x2019;s surface composition, structure, and morphology while maintaining mechanical qualities are needed. As a result, dental and orthopedic implants will have considerably improved performance and service life. Owing to their superior osteoconductive capabilities and high chemical stability, bioceramic coatings appear to be the option for the functionalization of implants that are in direct contact with bone. In particular, the following are some necessary aspects that justify the fact that why bioceramic coatings are vital for a metallic implant (<xref ref-type="bibr" rid="B84">Prasad et&#x20;al., 2017</xref>).<list list-type="simple">
<list-item>
<p>a) Biocompatibility</p>
</list-item>
</list>
</p>
<p>Human blood and bone tissue come into close contact with the implant material being employed. The human body may be affected by two types of unfavorable changes. The unfavorable alterations are as follows: the first is a change in the genome&#x2019;s DNA (i.e.,&#x20;genotoxic), and the second is cell damage (i.e.,&#x20;cytotoxic). To avoid these undesirable effects the higher biocompatible bioceramic coatings (e.g., HA or calcium phosphates) are very useful for metallic implant surfaces (<xref ref-type="bibr" rid="B113">Wegst et&#x20;al., 2015</xref>).<list list-type="simple">
<list-item>
<p>b) Osseointegration</p>
</list-item>
</list>
</p>
<p>Osseointegration refers to the capacity of an implant&#x2019;s surface to integrate with surrounding bone and tissues. Bioceramics [such as HA and biphasic Calcium Phosphate (BCP)] have a high ability to form osseous tissues which assist bone formation (<xref ref-type="bibr" rid="B97">Rizwan et&#x20;al., 2017</xref>).<list list-type="simple">
<list-item>
<p>c) Corrosion resistance</p>
</list-item>
</list>
</p>
<p>Implant corrosion is a serious and concerning problem. It emerges as a consequence of metal implants exposure to chloride ions and protein in human blood. The metallic implant conducts an oxidation reaction, which yields metallic ions. The formation of a thin and adhesive layer of bioceramic on the surface of the implant will preserve the metal substrate and ultimately enhance the corrosion resistance (<xref ref-type="bibr" rid="B64">Mahapatro and Arshanapalli, 2017</xref>).<list list-type="simple">
<list-item>
<p>d) Drug delivery</p>
</list-item>
</list>
</p>
<p>Porous bioceramic coatings may be employed to deliver drugs, growth factors and proteins at a controlled rate (<xref ref-type="bibr" rid="B104">Singh et&#x20;al., 2015</xref>). Nano-featured coatings exhibit enhanced ability of controlled drug delivery due to larger surface area (<xref ref-type="bibr" rid="B76">Patel et&#x20;al., 2012</xref>; <xref ref-type="bibr" rid="B78">Patel et&#x20;al., 2014b</xref>). Antibiotics are particularly loaded in bioceramic coatings on metallic implants, to resist surgical site and hospital acquired infections. <xref ref-type="bibr" rid="B76">Patel et&#x20;al., 2012</xref> has reported the loading of ampicillin (a well-known antibiotic) on Chitosan&#x2013;nanobioactive glass coating. In a similar work, (<xref ref-type="bibr" rid="B80">Patel et&#x20;al., 2016</xref>) has studied the drug (dexamethasone phosphate) delivery potential of mesoporous silica-shelled hydroxyapatite nanoparticles and chitosan composite layer.<list list-type="simple">
<list-item>
<p>e) Microbial resistance</p>
</list-item>
</list>
</p>
<p>The usage of implants with antibacterial characteristics, as well as superior mechanical and physical-chemical properties and strong bond bonding, is the latest medical trend. Cu and Ag have been utilized to improve the antibacterial characteristics of materials over the years. Despite their capabilities, such coating materials have significant disadvantages like cytotoxicity and harmful long-term effects. In this scenario, bioceramic coatings (such as bioglass and zirconia-based ceramics) might be a good choice (<xref ref-type="bibr" rid="B13">Bellucci et&#x20;al., 2012</xref>).</p>
</sec>
<sec id="s3">
<title>Bioceramic Coating Techniques</title>
<p>Ceramic-based films have been employed for therapeutic purposes in orthopedics (<xref ref-type="bibr" rid="B26">Choi et&#x20;al., 2018</xref>). Most of the research for biomedical implants is influenced by this philosophy. Biopolymers like peptides, polysaccharides, as well as triglycerides are used to construct support as well as shielding for a calcified structure such as shell, bone, even teeth (<xref ref-type="bibr" rid="B61">Liu et&#x20;al., 2004</xref>). Biopolymers are also reported to regulate growth rate, phase composition, crystal volume, as well as crystalline alignment of biomineralization. Nature&#x2019;s technique of hard tissue synthesis is progressively being imitated by replicating organic resorption activities as well as practicing their tactics to enhance the properties and performance of bioceramic surfaces (<xref ref-type="bibr" rid="B65">Mali et&#x20;al., 2016</xref>). Template-mediated self-organization is being used to build solution-based coating processes that imitate biological resorption paths. Regulated crystalline nucleation and regulated phase formation are required for the optimal implementation of such approaches (<xref ref-type="bibr" rid="B90">Qaid et&#x20;al., 2019</xref>). Uniform coatings are being deposited to practically any material using such procedures (<xref ref-type="bibr" rid="B38">Fathi et&#x20;al., 2003</xref>). Osteoinductive entities, like the non-collagen extracellular matrix (ECM), proteins, osteocalcin, osteonectin, osteopontin, or cytokines, including components of recombinant human bone morphogenetic protein (rhBMP), can be incorporated into biomimmetically deposited coatings to stimulate potent osteoinductivity. Biomimetic carbonated hydroxyapatite development (<xref ref-type="bibr" rid="B46">Hamdi et&#x20;al., 2019</xref>).</p>
<p>
<italic>Biomimetics</italic> is a new era material science topic that probes deep into the secrets about how Nature&#x2019;s route functions and explores the elements of science engineering, to imitate therapeutic products (<xref ref-type="bibr" rid="B114">Wu et&#x20;al., 2020</xref>). To deposit biomimetic carbonated hydroxyapatite, substrates are placed in simulated body fluid (SBF)/ Hank&#x2019;s mixture for many weeks at 37&#xb0;C. This procedure results in the creation of a bone-like bioactive layer upon this substrate. This process is used to make nebulous or amorphous-crystalline Ca-P coats of 1&#x2013;5&#xa0;mm thickness (<xref ref-type="bibr" rid="B118">Zafar et&#x20;al., 2018</xref>). As the substrates are completely immersed in the solution, even those samples having complex geometries can still be coated with such a method (<xref ref-type="bibr" rid="B48">Heimann and Lehmann</xref>). For example, Ti implants are commonly employed as templates for biomimetic deposition, yet such implantation was annealed (to improve the adherence and crystallinity of biomimetic apatite layer) before final usage (<xref ref-type="bibr" rid="B123">Zhou et&#x20;al., 2019</xref>). The most significant feature of this technique is its ability to deposit bone-like apatite at almost room temperature. Complex structures can be coated by such techniques. This technique has some limitations, such as it consumes time and necessitates replenishing continuously to ensure constant ionic concentration and pH. (<xref ref-type="bibr" rid="B22">Campbell, 2003</xref>).</p>
<sec id="s3-1">
<title>Electrochemical Deposition Technique</title>
<p>Low-temperature production, as well as precise control of coating thickness through deposition parameters, are two advantages of the electrochemical deposition (ECD) (<xref ref-type="bibr" rid="B48">Heimann and Lehmann</xref>). A three-electrode assembly soaked in an electrolytic cell as well as coupled to an electrical device is generally used in this method (<xref ref-type="bibr" rid="B23">Chatterjee et&#x20;al., 2019</xref>). A titanium/magnesium alloy cathode (implant material serves as a working electrode while an Ag/AgCl reference electrode acts as a reference electrode in the presence of a platinum reference electrode. For the deposition of CaPs a calcium ion (Ca<sup>2&#x2b;</sup>) carrier, like calcium dihydrogen phosphate or calcium acetate, along with a phosphate ion (PO<sub>4</sub>
<sup>2<bold>&#x2212;</bold>
</sup>) carrier (including calcium or sodium dihydrogen phosphate, or sodium glycerophosphate) are widely used in electrolytic solutions (<xref ref-type="bibr" rid="B83">Pina et&#x20;al., 2018</xref>). In ECD, the pH of the solution, current density, the electrolyte temperature, and the ionic strength derive the type as well as stoichiometric calculations of calcium phosphate deposited at the cathode (<xref ref-type="bibr" rid="B40">Furko et&#x20;al., 2016a</xref>). Electrolytic deposition of calcium phosphate coating in the continuous current mode is restricted to current densities. Combination strategies, such as the utilization of pulsed currents and the insertion of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) into electrolytic solution are being recommended to fix this issue (<xref ref-type="bibr" rid="B73">Oh et&#x20;al., 2006</xref>).</p>
</sec>
<sec id="s3-2">
<title>Electrophoretic Deposition</title>
<p>The mechanism of electro-kinetic motion of colloidal particulates in the presence of an electric field is known as (EPD) (<xref ref-type="bibr" rid="B95">Riau et&#x20;al., 2016</xref>). It is a robust minimum material-processing approach for fabricating various combinations of biopolymer and bioceramics, for example, hydroxyapatite/chitosan, hydroxyapatite/poly (-caprolactone) coatings, carbon nanotubes (CNTs)/chitosan, etc (<xref ref-type="bibr" rid="B82">Pezzotti, 2021</xref>). It&#x2019;s a wet deposition process that uses colloidal ceramics. It has the potential of depositing homogeneous coatings on complex-shaped substrates while consuming minimal material. The deposition rate, crystallite size, as well as thicknesses of the deposited coatings, can all be adjusted by adjusting the suspensions as well as applied electric field values (<xref ref-type="bibr" rid="B41">Furko et&#x20;al., 2016b</xref>)<italic>.</italic> EPD is a cost-effective process that led to, homogeneous coatings with the controlled morphology and composition (<xref ref-type="bibr" rid="B32">Das and Shukla, 2019</xref>). The costings thickness obtained <italic>via</italic> EPD varies from few nanometers to few micrometers. The coating thickness can be manipulated by varying the deposition voltage and deposition time. Co-EPD of composite from single suspension is a challenging task. Furthermore, EPD is affected by the minor changes in deposition parameters, i.e.,&#x20;applied electric field, pH, temperature, humidity, etc. The major concern with the EPD is relatively low adhesion between the coatings and the substrate (<xref ref-type="bibr" rid="B49">Heimann, 2013</xref>).</p>
</sec>
<sec id="s3-3">
<title>Plasma Techniques</title>
<p>Plasma Electrolytic oxidation (PEO), also known as micro-arc oxidation (MAO) develops an adherent porous coating layer on valve metals through oxidation beyond the breakdown potential (<xref ref-type="bibr" rid="B45">Gul et&#x20;al., 2019</xref>). In the process of MAO, ions from valve metals combine with anions in the electrolyte by traveling far from the metallic surface, whereas oxygen travels concurrently towards the substrate as a result of a strong electric field. This yields in the development of a porous oxide layer, and during the process it can incorporate ions/particles present in the electrolyte inside the ceramic layer (<xref ref-type="bibr" rid="B63">Love et&#x20;al., 2013</xref>). Under the influence of a strong electric field, collisions between traveling atoms and ions cause local heating (Joule heating) as a result of the strong electrical resistance of the oxide layer. Several ceramics incorporated MAO layers have been developed in recent years through particle suspension in the electrolyte (<xref ref-type="bibr" rid="B106">Su et&#x20;al., 2019</xref>). Hydroxyapatite and other CaPs have been incorporated to improve biological performance, while SiC, ZrO<sub>2,</sub> and other high hardness ceramics have been employed to improve the wear resistance of MAO layers. The autosintering nature of the MAO technique makes it an extremely attractive technique to deposit bioceramics. However, it has an inherent limitation of applying to only valve metals (<xref ref-type="bibr" rid="B38">Fathi et&#x20;al., 2003</xref>). Due to benefits including procedure efficiency, high deposition kinetics, minimal substrate temperature, as well as sustainability, plasma spraying is the most commonly used technology for preparing coatings for load-bearing prostheses. Bioinert, as well as bioactive coatings, can be deposited in a cost-effective manner using this set of techniques (<xref ref-type="bibr" rid="B54">Kaur et&#x20;al., 2019</xref>), Through this method, 30&#x2013;300&#xa0;mm, thick, non&#x2014;homogeneous HAp coatings with significant deposition potential are produced. The coatings produced are wear and corrosion-resistant. In certain circumstances, an adhesive strength of more than 15&#xa0;MPa may be achieved (<xref ref-type="bibr" rid="B4">Alagarsamy et&#x20;al., 2020</xref>). Heat causes degradation of the bioceramics. Moreover, major limitations of plasma spray techniques include thickness inhomogeneity, inadequate crystallinity, line-of-sight nature, as well as minimal adhesion strength to metallic surfaces. Rapid depressurization causes fractures in the coating (<xref ref-type="bibr" rid="B7">Arcos et&#x20;al., 2009</xref>). Plasma-sprayed coated prostheses demonstrate an obvious advantage of owing greater surface area, which leads to improved osseointegration <italic>in vivo</italic> (<xref ref-type="bibr" rid="B9">Bansal et&#x20;al., 2020</xref>).</p>
</sec>
<sec id="s3-4">
<title>Radio Frequency Magnetron Sputtering</title>
<p>RF magnetron sputtering, unlike many other technologies, permits coating to be deposited upon the surface of metallic implants, ceramics, or even polymeric materials (<xref ref-type="bibr" rid="B89">Qadir et&#x20;al., 2019</xref>; <xref ref-type="bibr" rid="B16">Bociaga et&#x20;al., 2016</xref>). In the sputtering process, the material needs to be deposited (target) serves as a cathode, and receives a bombardment of high-energy ions (<xref ref-type="bibr" rid="B17">Bociaga et&#x20;al., 2019</xref>). These ions are produced as a result of plasma generation from Ar Bombardment, causes the target to erode (sputter) and the eroded atoms deposit onto the substrate (<xref ref-type="bibr" rid="B19">Bolbasov et&#x20;al., 2018</xref>; <xref ref-type="bibr" rid="B30">Das and Shukla, 2020b</xref>). This conventional sputtering exhibits slower deposition rates, higher substrate heating, and limited plasma ionization efficiency (<xref ref-type="bibr" rid="B102">Shukla et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B87">Prosolov et&#x20;al., 2017</xref>). These limitations of conventional sputtering have been counterbalanced by magnetron sputtering, which carries a set of permanent magnets under the target resulting in enhanced plasma and increased deposition rate (<xref ref-type="bibr" rid="B89">Qadir et&#x20;al., 2019</xref>; <xref ref-type="bibr" rid="B16">Bociaga et&#x20;al., 2016</xref>).</p>
<p>RF-sputtered coatings exhibit bioceramic composition control, spatial homogeneity, as well as the capacity to coat implants with complex shapes owing to good adherence (<xref ref-type="bibr" rid="B46">Hamdi et&#x20;al., 2019</xref>). Coatings created by RF magnetron sputtering (a plasma-chemical technique) are often amorphous and therefore require a moderate temperature annealing to impart crystallinity (<xref ref-type="bibr" rid="B55">Kozelskaya et&#x20;al., 2018</xref>; <xref ref-type="bibr" rid="B21">Calderon Velasco et&#x20;al., 2016</xref>). With its faster deposition potential, magnetron sputtering is far more favorable than other sputtered processes, (<xref ref-type="bibr" rid="B98">Safavi et&#x20;al., 2020</xref>). It also has excellent substrate adherence and can coat complicated pieces with greater ease than other sputtering processes (<xref ref-type="bibr" rid="B85">Prosolov K. A. et&#x20;al., 2019</xref>). Efficient, productivity high reproducibility, ability to coat samples with 3D symmetry, and low internal stresses are the major advantages of this technique (<xref ref-type="bibr" rid="B21">Calderon Velasco et&#x20;al., 2016</xref>). <xref ref-type="table" rid="T1">Table&#x20;1</xref> illustrates different bioceramic coating techniques showing their pros and cons. <xref ref-type="fig" rid="F3">Figure&#x20;3</xref> shows the different technologies available to deposit bioceramic coatings.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Summary of the advantages and disadvantages of bioceramic coatings.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Advantages</th>
<th align="center">Disadvantages</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Resistance to bio corrosion</td>
<td align="left">Wear products may interact with the biological systems. (Mechanical properties and wear behaviour of alumina/tricalcium phosphate/titania ceramics as coating for orthopedic implant) (<xref ref-type="bibr" rid="B8">Avcu et&#x20;al., 2018</xref>; <xref ref-type="bibr" rid="B109">Ur Rehman et&#x20;al., 2020</xref>)</td>
</tr>
<tr>
<td align="left">Bioactivity (Electrophoretic coatings of hydroxyapatite with various nanocrystal Shapes)</td>
<td align="left">Poor adhesion (Prediction of cyclic delamination lives of plasma-sprayed hydroxyapatite coating on Ti&#x2013;6Al&#x2013;4V substrates with considering wear and dissolutions) (<xref ref-type="bibr" rid="B79">Patel et&#x20;al., 2019</xref>)</td>
</tr>
<tr>
<td align="left">Biocompatibility (&#x201c;Hard&#x201d; ceramics for &#x201c;Soft&#x201d; tissue engineering: Paradox or opportunity?)</td>
<td align="left">
<xref ref-type="bibr" rid="B78">Patel et&#x20;al. (2014b)</xref>
</td>
</tr>
<tr>
<td align="left">Drug delivery (Nanostructured Biointerfacing of Metals with Carbon Nanotube/Chitosan Hybrids by Electrodeposition for Cell Stimulation and Therapeutics Delivery)</td>
<td align="left">
<xref ref-type="bibr" rid="B77">Patel et&#x20;al. (2014a)</xref>
</td>
</tr>
<tr>
<td align="left">(Resistance to the release of undesirable metallic ions such as Ti, Al and Ni)</td>
<td align="left">
<xref ref-type="bibr" rid="B8">Avcu et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">Antibacterial character (Physico-chemical and antimicrobial properties of Ag/Ta<sub>2</sub>O<sub>5</sub> nanocomposite coatings)</td>
<td align="left">
<xref ref-type="bibr" rid="B80">Patel et&#x20;al. (2016)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>
<bold>(A,B)</bold> SEM Surface morphology of Ti6Al4V 3D-lattice structures generated by additive manufacturing with HA coating. Adapted from (<xref ref-type="bibr" rid="B28">Chudinova et&#x20;al., 2016</xref>). Reproduced with permission from IOP Publishing (United&#x20;Kingdom) <bold>(C)</bold> Surface roughness (Ra) variation with the change in coating thickness and, <bold>(D)</bold> variation in contact angle (measure by using SBF drop) with the change in the thickness of the coatings. Adapted from (<xref ref-type="bibr" rid="B12">Behera et&#x20;al., 2018</xref>). Reproduced with the permission from Journal of Elsevier.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g003.tif"/>
</fig>
</sec>
</sec>
<sec id="s4">
<title>The Current State of the Art in RF Magnetron Sputtered Bioceramic Coatings</title>
<p>Bioceramics are deposited on metals using different techniques. The earlier section discusses the merits and demerits of each coating technique. This section summarizes the recent developments related to the deposition of bioceramics using RF Magnetron sputtering. Ti and its alloys due to their excellent biocompatibility and good corrosion resistance are primarily materials of choice for bone and dental implants (<xref ref-type="bibr" rid="B51">Ibrahim et&#x20;al., 2017</xref>). However, like other metals, these alloys also lack bioactivity. To impart bioactivity and enhance biological performance, bioceramic coatings are being developed on the surface of these alloys. Due to the proven performance of Ti and its alloys as implant materials, the highest share of RF magnetron sputtering bioceramic coatings has been received by them. Researchers have reported the ability of RF magnetron sputtering to deposit a thick layer (millimeter range) of adherent bioceramics on pure (<xref ref-type="bibr" rid="B52">Ivanova et&#x20;al., 2018</xref>) developed HA coating on Ti with preferred orientation along all three axes and evaluated the mechanical behavior of the coatings concerning orientation. A novel approach of water added into the working chamber of RF magnetron sputtering was used in this study to compensate for OH<sup>&#x2212;</sup> group loss during processing.</p>
<p>Among Ti alloys, Ti6Al4V (TC4) has received the highest research interest related to RF magnetron sputtering of bioceramics, as it is the most widely employed Ti alloy for the production of biomedical implants and surgical tools. RF magnetron sputtering has also been reported to successfully deposit HA-based coatings on porous scaffolds of TC4 alloy (<xref ref-type="bibr" rid="B24">Chernozem et&#x20;al., 2017</xref>). Apart from pristine HA ion-substituted HA (which is known to further enhance biocompatibility) and Biphasic calcium phosphate (BCP) have also been deposited onto TC4 alloy using RF magnetron sputtering (<xref ref-type="bibr" rid="B12">Behera et&#x20;al., 2018</xref>; <xref ref-type="bibr" rid="B86">Prosolov et&#x20;al., 2018</xref>). Along with biocompatible coatings antimicrobial layers based on metallic ion containing bioceramics have also been deposited using RF magnetron sputtering. Zn-substituted HA, which exhibits antibacterial behavior along with improved osteointegration was deposited using RF magnetron sputtering with the heated substrate (<xref ref-type="bibr" rid="B44">Graziani et&#x20;al., 2017</xref>). Substrate heating at 400&#xb0;C resulted in completely crystallized Zn-substituted HA deposition with columnar morphology. Similar findings from different researchers suggest that controlled heating of the substrate can improve the crystallinity of the bioceramic coatings. (<xref ref-type="bibr" rid="B59">Lenis et&#x20;al., 2019</xref>) has reported the deposition of homogenous crack-free BCP with prolonged (up to 8&#xa0;h) RF magnetron sputtering. Relatively newer Ti alloy (Ti&#x2013;35Nb&#x2013;10Zr) is also a good candidate for potential biomedical applications. Si-HA layer was also shown to be successfully synthesized on this alloy using RF magnetron sputtering to favor enhanced osseointegration as an orthopedic implant. <xref ref-type="fig" rid="F3">Figure&#x20;3A</xref> shows the SEM image depicting a fairly uniform morphology. <xref ref-type="fig" rid="F3">Figure&#x20;3B</xref> shows the bilayer structure of TiN and HA layer deposited on Ti substrate. The coating was uniform throughout the substrate surface. The inset of <xref ref-type="fig" rid="F3">Figure&#x20;3B</xref> confirms the presence of Ca and P in the top layer. <xref ref-type="fig" rid="F3">Figure&#x20;3C</xref> shows that the average roughness (Ra) increases with the increase in the coating thickness. Thus, it is possible to tune the surface topography as a function of coating thickness to achieve roughness values suitable for bone regeneration applications (<xref ref-type="bibr" rid="B111">Ure&#xf1;a et&#x20;al., 2018</xref>). Another important aspect of the biomedical coating is wettability. The surface should promote the protein attachment owe to the favorable surface chemistry, wettability, and topography (<xref ref-type="bibr" rid="B57">Lee et&#x20;al., 2013</xref>; <xref ref-type="bibr" rid="B94">Rehman et&#x20;al., 2019</xref>). Since magnetron sputtering has shown the potential to improve the surface wettability as the function of coating thickness and surface chemistry (<xref ref-type="bibr" rid="B53">Jeong et&#x20;al., 2016</xref>). <xref ref-type="fig" rid="F3">Figure&#x20;3D</xref> shows that the SBF contact angle decreases with the increase in the coating thickness. The increase in coating thickness means more HA deposition and subsequently leading to mildly hydrophilic character, which in turn is suitable for the initial protein attachment (<xref ref-type="bibr" rid="B20">Bumgardner et&#x20;al., 2003</xref>; <xref ref-type="bibr" rid="B68">Menzies and Jones, 2010</xref>; <xref ref-type="bibr" rid="B37">Farris et&#x20;al., 2011</xref>).</p>
<p>In conventional RF-magnetron sputtering, it&#x2019;s not possible to incorporate controlled porosity (<xref ref-type="bibr" rid="B33">Dorozhkin, 2012</xref>). Chernozem et&#x20;al. (<xref ref-type="bibr" rid="B24">Chernozem et&#x20;al., 2017</xref>) introduced a unique strategy to control porosity in the HA layer by growing vertically aligned TiO<sub>2</sub> nanotubes through anodization of Ti and then covering it with HA through RF-magnetron sputtering. RF-magnetron sputtering can accommodate simple reactions as well to prepare oxides and nitrides through the introduction of Oxygen or Nitrogen gases in the sputtering chamber (<xref ref-type="bibr" rid="B5">Alias et&#x20;al., 2020</xref>). <xref ref-type="bibr" rid="B91">Qi et&#x20;al. (2019)</xref> synthesized a TiN-HA composite (two targets, i.e.,&#x20;Ti and HA) layer on TC4 alloy through reactive magnetron sputtering. TiN interlayer was used to improve the adhesion of HA. Using a similar strategy. HA-based composite layer with TiO<sub>2</sub> and TiN interlayers have also been reported by introducing O and N gases in the sputtering chamber (<xref ref-type="bibr" rid="B92">Quirama et&#x20;al., 2017</xref>). Apart from CaP based bioceramics other bioactive ceramics have also been reported to be magnetron sputtered. Hopeite is hydrated zinc phosphate which is a bioactive ceramic and commonly used as a coating on dental implants (<xref ref-type="bibr" rid="B50">Herschke et&#x20;al., 2006</xref>). (<xref ref-type="bibr" rid="B30">Das and Shukla, 2020b</xref>) reported a hopeite-based bioactive layer on TC4 alloy using RF-magnetron sputtering. <xref ref-type="fig" rid="F4">Figure&#x20;4A</xref> shows the SEM image of hopeite coated sample subsequent to tensile pull-out test. <xref ref-type="fig" rid="F4">Figure&#x20;4B</xref> demonstrated the adhesion strength of the coatings as a factor of distance as well as deposit temperature. It was suggested that the increase in the coating temperature led to the increase in the adhesion strength, as indicated by the increase in the critical load (<xref ref-type="fig" rid="F4">Figure&#x20;4B</xref>). <xref ref-type="fig" rid="F4">Figure&#x20;4C</xref> depicted the strain change of the (002) as well as (300) planes of the HA coatings placed in an Ar &#x2b; 10% H<sub>2</sub>O atmosphere. <xref ref-type="fig" rid="F4">Figure&#x20;4D</xref> shows the Raman spectra of HA monolayer and TiN/TiO<sub>2</sub>/HA trilayers. The tri-layer coating system shows the shifting of the peaks associated with the HA. Thus, indicating the possible chemical interaction between the different layer. The strong chemical linkage between the different layer will lead to the increase in the adhesion strength between the coating layer. Thus, the coatings obtained <italic>via</italic> RF magnetron sputtering can lead to the coatings with the better mechanical and surface properties for the orthopedic and dental applications.</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>
<bold>(A)</bold> Scanning electron microscopy images of hopeite coated sample after the tensile pull-out test. Adapted from (<xref ref-type="bibr" rid="B30">Das and Shukla, 2020b</xref>). Reproduced with permission from Transactions of the Institute of Metal Finishing <bold>(B)</bold> As a factor of distance as well as deposit temperature, the load capacity (critical load) of the coatings were evaluated. Adapted from (<xref ref-type="bibr" rid="B59">Lenis et&#x20;al., 2019</xref>). Reproduced with the permission from Elsevier <bold>(C)</bold> Depicted the strain change of the (002) as well as (300) plans of the HA coatings placed in an Ar &#x2b; 10% H<sub>2</sub>O atmosphere. Adapted from (<xref ref-type="bibr" rid="B52">Ivanova et&#x20;al., 2018</xref>). Reproduced with the permission from Elsevier <bold>(D)</bold> Raman spectra of HA monolayer and TiN/TiO<sub>2</sub>/HA. Adapted from (<xref ref-type="bibr" rid="B92">Quirama et&#x20;al., 2017</xref>). Reproduced with permission from Elsevier.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g004.tif"/>
</fig>
<p>Magnesium-based alloys are under research focus in recent years due to their comparable young modulus with bones, lower density, and biodegradability (<xref ref-type="bibr" rid="B122">Zheng et&#x20;al., 2014</xref>). The primary limitation of these alloys is their fast dissolution rate in physiological environments (<xref ref-type="bibr" rid="B10">Barati Darband et&#x20;al., 2017</xref>). To improve dissolution behavior and improve biocompatibility bioceramic coatings have been developed on these alloys. Bita et. al. (2016) exploited RF magnetron sputtering to achieve the adherence of HA and BG on biodegradable prosthetic magnesium&#x2013;calcium (Mg-Ca) alloy. According to the study, a post-deposition tempering approach at 500&#xb0;C/1&#xa0;h in the air is sufficient to trigger the crystallization of a 1&#xa0;&#xb5;m thick layer. <xref ref-type="fig" rid="F5">Figures 5A,B</xref> presents a comparison of oxides content of bioactive glasses Cohesion/ adhesion pull-out strength higher than the minimum acceptable value defined in ISO 13779-2 (standard regulating the manufacturing of superior load-bearing implant type) were obtained using all varieties of sputtered HA as well as BG layers. Mg alloy AZ91 has also been evaluated for the <italic>in&#x20;vitro</italic> biological performance after the deposition of RF magnetron sputtered HA (<xref ref-type="bibr" rid="B107">Surmeneva et&#x20;al., 2019</xref>). A homogeneous and pore-free HA coating was developed using RF magnetron sputtering with a substrate bias of &#x2212;25 and a substrate bias of &#x2212;100&#xa0;V, followed by post-deposition annealing. &#x2013;100&#xa0;V bias substrate yielded a better surface for bone marrow stromal cells (BMSCs) proliferation and decreased dissolution of Mg ions. The negative biasing of the metallic substrate is an attractive research direction to overcome the inherent inability of RF magnetron sputtering to deposit porous layers.</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>
<bold>(A,B)</bold> Oxide concentration (mol%) of BG target materials with RF-MS deposited coatings are compared in histograms. Adapted from (<xref ref-type="bibr" rid="B15">Bita et&#x20;al., 2016</xref>). Reproduced with the permission from Journal of Adhesion Science and Technology.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g005.tif"/>
</fig>
<p>RF magnetron sputtering owns a unique ability to deposit bioceramic layers to yield composite coatings in a single step, as well as they can be employed as a subsequent step after any other coating technique. For single-step composite coatings, two strategies may be employed. One target with desired composite&#x2019;s content may be prepared or multiple targets can be used (<xref ref-type="bibr" rid="B6">Alias et&#x20;al., 2019</xref>) and (<xref ref-type="bibr" rid="B6">Alias et&#x20;al., 2019</xref>). Behera et&#x20;al deposited TiO<sub>2</sub>-BCP layer on TC4 alloy by synthesizing a single target with varying content of each bioceramic. <xref ref-type="fig" rid="F6">Figure&#x20;6A</xref> shows the SEM image of anodized Ti surface and <xref ref-type="fig" rid="F6">Figure&#x20;6B</xref> shows the SEM image from side one to show the aspect ratio TiO<sub>2</sub> nanotubes. <xref ref-type="fig" rid="F6">Figure&#x20;6C</xref> shows variation in the surface wettability with the change in the composition of two-layer, i.e.,&#x20;TiO<sub>2</sub>-BCP content in the coatings. It was shown that the increase in the TiO<sub>2</sub> content from 0&#x2212;50% induces hydrophilic character. Thus, the increase in TiO<sub>2</sub> content is beneficial in achieving contact angle values suitable for bone regeneration applications (<xref ref-type="bibr" rid="B20">Bumgardner et&#x20;al., 2003</xref>). The best compromise of adhesion strength and biological performance was achieved at equivalent amounts of BCP and TiO<sub>2</sub> (in target). Furthermore, multilayered coatings with separate targets (Ag and HA) were also prepared for orthopedic and dental applications.</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption>
<p>
<bold>(A,B)</bold> Scanning electron microscopy of upper and side overview respectively of calcium phosphate coated with titania synthesized at 60&#xa0;V for 30&#xa0;min of electrochemical anodization in an electrolyte after annealing. Adapted from (<xref ref-type="bibr" rid="B24">Chernozem et&#x20;al., 2017</xref>). Reproduced with the permission from Elsevier <bold>(C)</bold> Wettability results of 100 BCP, 25 TiO<sub>2</sub>-BCP, and 50 TiO<sub>2</sub>-BCP films with and without annealing. Adapted from (<xref ref-type="bibr" rid="B11">Behera et&#x20;al., 2020</xref>). Reproduced with permission from Elsevier.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g006.tif"/>
</fig>
<p>
<xref ref-type="table" rid="T2">Table&#x20;2</xref> provides an insight regarding the recent developments in the field of bioceramic coatings using RF magnetron sputtering (<xref ref-type="bibr" rid="B59">Lenis et&#x20;al., 2019</xref>).</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Different bioceramic coating techniques showing their pros and&#x20;cons.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Coating techniques</th>
<th align="center">Merits</th>
<th align="center">Demerits</th>
<th align="center">Ref</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Biomimetic coating</td>
<td align="left">Uniform coating, stimulate potent osteoinductive actions</td>
<td align="left">consumes time and necessitates replenishing, A continuous SBF pH is required</td>
<td align="left">
<xref ref-type="bibr" rid="B93">Razavi et&#x20;al. (2020)</xref>, <xref ref-type="bibr" rid="B58">Lee et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">Sol-gel method</td>
<td align="left">moderate deposition temperature, Optimizing the stoichiometric ratio of precursors allows for better compositional changes, as well as the ability to cover a variety of substrates with complicated shapes</td>
<td align="left">Minimal adherence with metallic surfaces, low reproducibility of thickness, roughness, as well as biological features</td>
<td align="left">
<xref ref-type="bibr" rid="B69">Mohammed and Hussein. (2019)</xref>, <xref ref-type="bibr" rid="B100">Sebastin and Uthirapathy. (2020)</xref>, <xref ref-type="bibr" rid="B115">Xiong et&#x20;al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left">Plasma spray coating</td>
<td align="left">High deposition rates, high efficiency, economical method, bioinert and bioactive coatings</td>
<td align="left">High deposition temperature that stimulates deposition, a paucity of thickness homogeneity, a lack of crystallization, a lack of adherence to metallic surfaces, as well as a lack of physicochemical property modulation</td>
<td align="left">
<xref ref-type="bibr" rid="B103">Singh et&#x20;al. (2021)</xref>, <xref ref-type="bibr" rid="B105">Singh et&#x20;al. (2020)</xref>
</td>
</tr>
<tr>
<td align="left">EPD</td>
<td align="left">High deposition rates, cost-effectiveness, uniform thickness, homogeneous properties</td>
<td align="left">High sintering temperature, produce cracks, cause delamination of the coatings</td>
<td align="left">
<xref ref-type="bibr" rid="B34">Drevet et&#x20;al. (2016)</xref>, <xref ref-type="bibr" rid="B121">Zhang. (2020)</xref>, <xref ref-type="bibr" rid="B79">Patel et&#x20;al. (2019)</xref> <xref ref-type="bibr" rid="B47">Heimann. (2017)</xref>, <xref ref-type="bibr" rid="B77">Patel et&#x20;al. (2014a)</xref>, <xref ref-type="bibr" rid="B104">Singh et&#x20;al. (2015)</xref>
</td>
</tr>
<tr>
<td align="left">ECD</td>
<td align="left">Low-temperature production, control of coating thickness</td>
<td align="left">restricted to current densities far below a particular threshold level, which also limits the coated content</td>
<td align="left">
<xref ref-type="bibr" rid="B119">Zeng et&#x20;al. (2016)</xref>, <xref ref-type="bibr" rid="B1">Ahmadi and Afshar. (2021)</xref>, <xref ref-type="bibr" rid="B36">Durdu et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">Micro arc oxidation</td>
<td align="left">High deposition rates, highly ionized water vapor, enhanced adhesion, possibilities to coat <italic>via</italic> metals having variation in melting points</td>
<td align="left">development of microparticles having dimension up to tens of microns, these nanoparticles having an effect on the coating property particularly with biological and tribological ones</td>
<td align="left">
<xref ref-type="bibr" rid="B90">Qaid et&#x20;al. (2019)</xref>, <xref ref-type="bibr" rid="B60">Li et&#x20;al. (2018)</xref>, <xref ref-type="bibr" rid="B35">Durdu et&#x20;al. (2017)</xref>, <xref ref-type="bibr" rid="B116">Xiong et&#x20;al. (2019)</xref>
</td>
</tr>
<tr>
<td align="left">Magnetic sputtering</td>
<td align="left">Efficient, productive, high reproducibility, coating samples with 3D symmetry, biocompatible, highly smooth, corrosion and wear-resistant, and relatively low internal stress</td>
<td align="left">Low deposition rates</td>
<td align="left">
<xref ref-type="bibr" rid="B29">Das and Shukla. (2020a)</xref>, <xref ref-type="bibr" rid="B46">Hamdi et&#x20;al. (2019)</xref>, <xref ref-type="bibr" rid="B99">Samiee et&#x20;al. (2021)</xref> <xref ref-type="bibr" rid="B25">Chioibasu et&#x20;al. (2019)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s5">
<title>Improvement in the Surface Properties <italic>via</italic> Magnetron Sputtering</title>
<p>In a recent work (<xref ref-type="bibr" rid="B75">Pantaroto et&#x20;al., 2021</xref>) used magnetron sputtering to develop various crystalline phases of TiO<sub>2</sub> on titanium substrates (CpTi). Sputtered films had an excellent mechanical adherence to the substrates and were more resistant to abrasion. The TiO<sub>2</sub> films produced measured 312&#x2013;338&#xa0;nm thick, thus, they had no effect on prosthesis adaption because a gap of 150&#xa0;nm is within approved clinical limits. <xref ref-type="fig" rid="F7">Figure&#x20;7</xref> describes the mechanism of TiO<sub>2</sub> deposition on CpTi, as this study is among the pioneering works on the deposition of TiO2 on titanium substrates using reactive RF magnetron sputtering.</p>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>Proposed mechanism of sputtered bi-phasic rutile and anatase TiO<sub>2</sub> film on the electrochemical and biological behavior of cpTi substrate. Adapted from (<xref ref-type="bibr" rid="B75">Pantaroto et&#x20;al., 2021</xref>). Reproduced with the Permission from Elsevier.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g007.tif"/>
</fig>
<p>Multilayer bioactive coatings have also been deposited using RF magnetron sputtering. (<xref ref-type="bibr" rid="B46">Hamdi et&#x20;al., 2019</xref>) deposited triple-layered (HAp/Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub>) thin film coatings on the Ti alloy substrates. The presence of interim Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub> layers aided in the improvement of HAp coating adherence to the substrate. As a corollary, HAp layers figured prominently in the surface&#x2019;s biocompatibility, whereas interim Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub> layers were used to improve the adherence of the HAp coating to the substrate along with the substrate&#x2019;s corrosion tendency. The increased porosity is associated with enhanced osseointegration by allowing bone to grow into the coatings, resulting in mechanical interlock (as shown in <xref ref-type="fig" rid="F8">Figure&#x20;8</xref>). By RF magnetron sputtering, (<xref ref-type="bibr" rid="B31">Das and Shukla, 2017</xref>) effectively produced columnar HA coatings on UNS S31254 substrate (MS). HA coatings produced on SS254 by magnetron sputtering yielded improved surface characteristics, adhesion, as well as biocompatibility of HA coatings. yield. The developed layer is well suited for possible orthopaedic implant applications due to the anhanced bioactivity, promoting better osseointegration (<xref ref-type="fig" rid="F8">Figure&#x20;8</xref>).</p>
<fig id="F8" position="float">
<label>FIGURE 8</label>
<caption>
<p>The cross-sectional SEM image of <bold>(A)</bold> Ti-6Al-4V original alloys, and <bold>(B)</bold> triplelayered (HAp/Al2O3/TiO2) thin film. Adapted from (<xref ref-type="bibr" rid="B46">Hamdi et&#x20;al., 2019</xref>). Reproduced with the permission from Elsevier. <bold>(C,D)</bold> SEM micrographs of HA-coated sample after immersion test at <bold>(A)</bold> 1,000&#xd7; and <bold>(B)</bold> 2,500&#xd7;. Adapted from (<xref ref-type="bibr" rid="B31">Das and Shukla, 2017</xref>). Reproduced with the permission of Maney Publishing.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g008.tif"/>
</fig>
<p>Along with metallic substrate RF magnetron sputtering has also been employed to coat polymeric substrates for biomedical applications (<xref ref-type="bibr" rid="B108">Tverdokhlebov et&#x20;al., 2012</xref>; <xref ref-type="bibr" rid="B43">Goreninskii et&#x20;al., 2017</xref>) examined the features of thin calcium-phosphate coatings generated on the surface of the thermoplastic copolymer of vinilidene fluoride and tetrafluoroethylene (VDF&#x2013;TeFE) by radio-frequency magnetron sputtering of a solid target constructed of hydroxyapatite. The VDF&#x2013;TeFE polymer coating&#x2019;s surface is a homogenous film made up of polymer globules of elongated ellipsoids with 1.02 and 0.71&#xa0;nm diameters. In orthopaedics and traumatology, the proposed surface modification technique can be employed to assist the adhesion and proliferation of osteogenic cells in order to manufacture implants (<xref ref-type="fig" rid="F9">Figure&#x20;9</xref>). It was shown that hydroxyapatite produced from fish scale and sputtered onto AZ31Magnesium alloy using an RF magnetron sputtering technique enhanced the stability of biodegradable alloy. The degradation rate of untreated AZ31 was calculated to be 0.021&#x20;d-1 k, however it was reduced to 20% for the 9-h coated AZ31 (i.e.,&#x20;0.016 d-1). It was also reported that the hydrophobic surfaces limit solid-liquid interfacial interactions, thus, prevent degradation.</p>
<fig id="F9" position="float">
<label>FIGURE 9</label>
<caption>
<p>AFM images of the surface samples of the group II: <bold>(A)</bold> relief, <bold>(B)</bold> map of the distribution of the potential, <bold>(C)</bold> the image of the phase contrast. The scanning area is 10&#xa0;m &#xd7; 10&#xa0;m. Adapted from (<xref ref-type="bibr" rid="B108">Tverdokhlebov et&#x20;al., 2012</xref>). Reproduced with the permission from Elsevier. <bold>(D)</bold> Schematic illustration of HAp (target) deposition on AZ31 (substrates).</p>
</caption>
<graphic xlink:href="fmats-08-747169-g009.tif"/>
</fig>
<p>(<xref ref-type="bibr" rid="B67">Masoorianfar et&#x20;al., 2020</xref>) modified the surface of metallic implants by the addition of fluorine into HA. This fluorine substituted HA is known to enhance the dissolution resistance of HA in biological environments (<xref ref-type="bibr" rid="B96">Rizwan et&#x20;al., 2020</xref>). The higher affinity of fluorine ion, apatite layer is formed without change in size, topography and composition (<xref ref-type="fig" rid="F10">Figure&#x20;10</xref>). Degradation decreased by the incorporation of fluorine within apatite layer so, FA is considered as a potential candidate for enhanced corrosion resistance in biological environment.</p>
<fig id="F10" position="float">
<label>FIGURE 10</label>
<caption>
<p>The fluorhydroxyapatite (FA) tissue and surface manufactured thin film of FA employed in this research are shown in this diagram. Adapted from (<xref ref-type="bibr" rid="B67">Mansoorianfar et&#x20;al., 2020</xref>). Reproduced with the permission from Elsevier.</p>
</caption>
<graphic xlink:href="fmats-08-747169-g010.tif"/>
</fig>
</sec>
<sec id="s6">
<title>Concluding Remarks and Future Directions</title>
<p>The surface modification <italic>via</italic> coating process can tune the chemical, physical and biological properties of the implant material. Various coating techniques including conversion coatings, electrochemical plating, EPD, anodizing, RF magnetron sputtering are being used to develop biomedical coatings with favorable mechanical and biological characteristics (<xref ref-type="bibr" rid="B56">Kumar et&#x20;al., 2019</xref>). Magnetron sputtering is the method of choice to tune the implant surface with relatively higher thermal, mechanical, and chemical stability. The coating deposited <italic>via</italic> magnetron sputtering can yield better wear and corrosion resistance compared to the other counterparts. For example, ion-substituted calcium phosphate coatings deposited <italic>via</italic> magnetron sputtering are being widely adopted for dental and orthopedic applications owe the favorable microstructure, adhesion strength, chemical and surface properties (<xref ref-type="bibr" rid="B101">Shi et&#x20;al., 2008</xref>). Although, the magnetron sputtering requires higher capital investment. However, the running coat of the process is affordable. The coating properties can be controlled by varying the discharge power, bias voltage, deposition time, substrate temperature, and post-deposition annealing treatment.</p>
<p>The real challenge in the coating process is to develop the surface with good adhesion, strength, wettability, chemical structure, surface topography, wear resistance, electrochemical stability, antibacterial properties, and negligible cytotoxicity. It is quite challenging for any coating process to meet&#x20;all the requirements. For example, the coatings deposited <italic>via</italic> magnetron sputtering lack porosity (surface topography). Thus, the coatings developed <italic>via</italic> the magnetron sputtering process can result in poor osseointegration. The osseointegration of the coatings can be improved by changing the microstructure, surface morphology, and thickness of the coatings (<xref ref-type="bibr" rid="B99">Samiee et&#x20;al., 2021</xref>). The magnetron sputtering process requires relatively lower processing temperatures. Thus, it is possible to achieve the coatings with different percentages of crystallinity depending upon the feedstock. For example, amorphous HA coatings and ion-substituted HA were shown to improve the cell attachment compared to the crystalline HA (<xref ref-type="bibr" rid="B112">Vladescu et&#x20;al., 2018</xref>). To improve the cellular interaction of the coatings magnetron sputtering is recently being coupled with EPD. The first layer deposited <italic>via</italic> EPD creates a particular pattern on the implant surface. Later, magnetron sputtering was used to deposit mechanically and chemically robust layers. However, the topography of the first was maintained. Thus, the favorable topography resulted in improved osseointegration and cellular attachment, and proliferation. Furthermore, bilayer and tri-layer structures have also been deposited <italic>via</italic> magnetron sputtering to achieve the ideal topography for biomedical applications (<xref ref-type="bibr" rid="B56">Kumar et&#x20;al., 2019</xref>).</p>
<p>Another challenge associated with the magnetron sputtering is the longer deposition times, which restricts its commercialization. To commercialize the subject process, it is an important future direction to reduce the deposition time, i.e.,&#x20;increase the deposition rate. Future research is expected to improve the deposition kinetics of the magnetron sputtering; thus, the process is successfully translated to the clinic <xref ref-type="table" rid="T3">Table&#x20;3</xref>.</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Represents the different metallic substrates along with their characteristics.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Metallic substrates</th>
<th align="center">Percentage of materials/Parameters</th>
<th align="center">Cell type</th>
<th align="center">Production technique</th>
<th align="center">Density/ porosity/nature</th>
<th align="center">Mechanical/ chemical/ biological characteristics</th>
<th align="center">Ref</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">magnesium&#x2013;calcium (MgCa) alloys</td>
<td align="left">Mg (99.96&#xa0;wt%) and Ca (99.98&#xa0;wt%) powders</td>
<td align="center">&#x2014;</td>
<td align="left">Post-deposition tempering approach/MS</td>
<td align="left">&#x223c;1&#xa0;&#x3bc;m thick HA coating</td>
<td align="left">15&#xa0;MPa specified by the ISO 13779-2 standard, superior load-bearing implant</td>
<td align="left">
<xref ref-type="bibr" rid="B15">Bita et&#x20;al. (2016)</xref>
</td>
</tr>
<tr>
<td align="left">TiO<sub>2</sub> nanotubes in an NH<sub>4</sub>F</td>
<td align="left">Samples of Ti foil 0.4&#xa0;wt. percent solution of NH<sub>4</sub>F in 54&#xa0;ml of ethylene glycol and 5&#xa0;ml of deionised water, widths &#x3d; 2&#xa0;mm, lengths &#x3d; 50&#xa0;mm,</td>
<td align="center">&#x2014;</td>
<td align="left">electrochemical anodization process/ MS</td>
<td align="left">The NTs&#x2019; high porosity reflects an increase in elastic strain, which leads to coat degradation (H/E). thicknesses &#x3d; 0.11&#xa0;mm</td>
<td align="left">Lower modulus of elasticity as well as nanohardnesses, increased elastic indices H/E with susceptibility to plastic deformation, porous TiO<sub>2</sub> NT&#x2019;s structure resulted in increased nanohardness and a minor rise in Young&#x2019;s modulus</td>
<td align="left">
<xref ref-type="bibr" rid="B24">Chernozem et&#x20;al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left">biphasic calcium phosphate</td>
<td rowspan="2" align="left">100% BCP<break/>25% TiO<sub>2</sub>-75% BCP<break/>50% TiO<sub>2</sub>-50% BCP films</td>
<td rowspan="2" align="left">MG-63 human osteoblast-like cell line</td>
<td rowspan="2" align="left">thermal diffusion/MS</td>
<td rowspan="2" align="left">At 700&#xb0;C, crystalline structure is formed</td>
<td rowspan="2" align="left">improves implant&#x2019;s wettability, adhesion, bioactivity, as well as cytocompatibility</td>
<td rowspan="2" align="left">
<xref ref-type="bibr" rid="B11">Behera et&#x20;al. (2020)</xref>
</td>
</tr>
<tr>
<td align="left">titania composite films on Ti-6Al-4V substrate</td>
</tr>
<tr>
<td align="left">Zn substituted hydroxyapatite, TiO2</td>
<td align="left">&#x2014;</td>
<td align="left">
<italic>Vivo</italic>
</td>
<td align="left">physical vapor deposition/ MS</td>
<td align="left">amorphous</td>
<td align="left">Controllable bioresorption rate</td>
<td align="left">
<xref ref-type="bibr" rid="B86">Prosolov et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">TC4 substrates</td>
<td align="left">&#x2014;</td>
<td align="left">
<italic>Vitro</italic> (<italic>E.&#x20;coli</italic>)&#x7c;Vivo (human osteoblasts)</td>
<td align="left">post-deposition annealing/MS</td>
<td align="left">dome sharpened grains, crystalline nature</td>
<td align="left">an adhesion of 21.75 2.1&#xa0;MPa, according to tensile pullout tests, excellent osseointegration as well as antimicrobial properties</td>
<td align="left">
<xref ref-type="bibr" rid="B30">Das and Shukla, (2020b)</xref>
</td>
</tr>
<tr>
<td align="left">(HA)&#x2014;silver</td>
<td align="left">HA &#x3d; 99.99% purity<break/>Ag &#x3d; 99.9% purity dimensions &#x3d; 500&#xa0;mm &#xd7; 100&#xa0;mm &#xd7; 6&#xa0;mm</td>
<td align="center">&#x2014;</td>
<td align="left">MS</td>
<td align="left">greater crystallinity</td>
<td align="left">Hardness-7 0.4&#xa0;GPa elastic modulus &#x3d; 134&#x20;7&#xa0;GPa, the critical load of 169&#x20;5&#xa0;mN<break/>better friction coefficients with significantly reduced wear rates</td>
<td align="left">
<xref ref-type="bibr" rid="B59">Lenis et&#x20;al. (2019)</xref>
</td>
</tr>
<tr>
<td align="left">Ti, HA</td>
<td align="left">Pure Ti &#x3d; 1.5&#xa0;mm thick were used as substrates (10&#xa0;mm &#xd7; 10&#xa0;mm)</td>
<td align="center">&#x2014;</td>
<td align="left">MS</td>
<td align="left">crystallographic textured</td>
<td align="left">Nanoindendnes &#x3d; 4.7 2.0&#xa0;GPa and 4.4 2.2&#xa0;GPa elastic modulus &#x3d; 75 and 103&#xa0;GPa</td>
<td align="left">
<xref ref-type="bibr" rid="B52">Ivanova et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">TiN/TiO<sub>2</sub>/HA</td>
<td align="left">Ti target &#x3d; 9.9% pure</td>
<td align="center">&#x2014;</td>
<td align="left">reactive magnetron sputtering process, unbalanced magnetron sputtering technique</td>
<td align="left">Crystalline, adherent, HA amorphous coating</td>
<td align="left">better adhesion strength, high mechanical strength, low density, thicknesses of the deposited HA &#x3d; 0.68&#x20;&#xb1; 0.02&#xa0;&#x3bc;m TiN/TiO<sub>2</sub>/HA coatings &#x3d; 1.06&#x20;&#xb1; 0.01&#xa0;&#x3bc;m, respectively, higher wear resistance</td>
<td align="left">
<xref ref-type="bibr" rid="B92">Quirama et&#x20;al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left">HA, Ti64 scaffolds</td>
<td align="left">RF power &#x3d; 400&#xa0;W argon gas pressure &#x3d; working pressure 0.4&#xa0;Pa, base pressure 10&#x2212;4&#xa0;Pa distance between the target and substrate &#x3d; 40&#xa0;mm, specific stoichiometric composition</td>
<td align="center">&#x2014;</td>
<td align="left">RF-magnetron sputtering, Electron Beam Melting technology</td>
<td align="left">3D-lattice structures</td>
<td align="left">the coating thickness of 700&#xa0;nm, higher rate of deposition, and thermal stability provide the mechanical integrity, enhanced biocompatibility encourage bone ingrowth for improved implant stability in the body</td>
<td align="left">
<xref ref-type="bibr" rid="B28">Chudinova et&#x20;al. (2016)</xref>
</td>
</tr>
<tr>
<td align="left">magnesium alloy (AZ91). HA</td>
<td align="left">size of width &#x3d; 10 length &#x3d; 10 thickness &#x3d; 1&#xa0;mm<sup>3</sup> were used as substrates</td>
<td align="left">bone marrow stromal cells (BMSCs)</td>
<td align="left">post-deposition annealing/MS</td>
<td align="left">higher BMSCs adhesion density, crystallinity</td>
<td align="left">surface roughness &#x3d; 92 to 130&#xa0;nm over areas of 5&#xa0;&#x3bc;m<sup>2</sup> &#xd7; 5&#xa0;&#x3bc;m<sup>2</sup>, durable stable for the implantation, high dissolution rate</td>
<td align="left">
<xref ref-type="bibr" rid="B107">Surmeneva et&#x20;al. (2019)</xref>
</td>
</tr>
<tr>
<td align="left">Ti-6Al-4V alloy, TiN, HA</td>
<td align="left">partial pressure of nitrogen &#x3d; 0.08&#xa0;Pa 600&#xa0;W RF power supply (13.56&#xa0;&#x41c;Hz)</td>
<td align="center">&#x2014;</td>
<td align="left">MS</td>
<td align="left">Crystalline nature</td>
<td align="left">improved wear-resistant, the adhesion strength &#x3d; increased from 6.50&#x20;&#xb1; 0.5N to 11.70&#x20;&#xb1; 1.2N, enhances the Ti alloy&#x2019;s mechanical characteristics and electrochemical behavior, stabile surface bioactive coating. Biocompatibility, boost the surface&#x2019;s specific surface area as well as induce cell proliferation In comparison to a single TiN layer and titanium alloy, the single TiN layer has the minimum corrosion current density and the maximum corrosion potential</td>
<td align="left">
<xref ref-type="bibr" rid="B91">Qi et&#x20;al. (2019)</xref>
</td>
</tr>
<tr>
<td align="left">BCP films on Ti-6Al-4V substrate, HA and&#x2014;TCP</td>
<td align="left">RF power &#x3d; 30&#x20;W sputtering pressure &#x3d; 3102&#xa0;mbar target-to-substrate distance &#x3d; 5&#xa0;cm</td>
<td align="center">&#x2014;</td>
<td align="left">MS</td>
<td align="left">Crystalline in nature</td>
<td align="left">maximum micro-hardness as well as scratch resistance, no film splitting up to 2.3&#x20;N scratch load and no substantial delamination up to 7.8&#x20;N load, excellent adherence between BCP sheets and Ti-6Al-4V substrates</td>
<td align="left">
<xref ref-type="bibr" rid="B12">Behera et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">Ti, Ti-6Al-7Nb, and Mg-based alloy, Zn- or Cu-substituted HA</td>
<td align="left">RF magnetron source &#x3d; 13.56&#xa0;MHz, working level 50&#xa0;W per 15&#xa0;min argon gas pressure&#x3d; (base pressure 10-5&#xa0;Pa, working pressure 0.1&#xa0;Pa), deposition time &#x3d; 2.5&#xa0;h</td>
<td align="left">
<italic>Staphylococcus aureus strain</italic> 209P</td>
<td align="left">post-deposition annealing/MS</td>
<td align="left">crystalline</td>
<td align="left">Thickness (nm) Cu-HA- 1,251&#x20;&#xb1; 5% Zn-HA &#x3d; 1,241&#x20;&#xb1; 5%, enhanced osseointegration properties</td>
<td align="left">
<xref ref-type="bibr" rid="B85">Prosolov et&#x20;al. (2019a)</xref>
</td>
</tr>
<tr>
<td align="left">Si-doped HA sheets on Ti-35Nb-10Zr</td>
<td align="left">The ingots were homogenized for 24&#xa0;h at 1,000&#xb0;C in an Ar environment before being quenched in 0&#xb0;C water. 10&#xa0;mm in diameter and 2.5&#xa0;mm in thickness</td>
<td align="center">&#x2014;</td>
<td align="left">electrochemical as well as magnetron sputtering approach</td>
<td align="left">Crystalline</td>
<td align="left">larger corrosion-resistant, reduced corrosion current density, current density &#x3d; 300&#xa0;mV (I300) value of 2.23 &#xd7; 10<sup>&#x2212;7</sup> and 2.14 &#xd7; 10<sup>&#x2212;6</sup>&#xa0;A&#xa0;cm<sup>&#x2212;2</sup>, highly biocompatible for implantation</td>
<td align="left">
<xref ref-type="bibr" rid="B53">Jeong et&#x20;al. (2016)</xref>
</td>
</tr>
<tr>
<td align="left">Zn-doped calcium phosphate</td>
<td align="left">Ti samples &#x3d; 99.58 Ti, 0.12 O, 0.18 Fe, 0.07 C, 0.04 N, and 0.01&#x20;H wt% Width &#x3d; 10 Length &#x3d; 10 Thickness &#x3d; 1&#xa0;mm<sup>3</sup> size</td>
<td align="center">&#x2014;</td>
<td align="left">the GLAD technique in RF magnetron sputtering</td>
<td align="left">Crystallites</td>
<td align="left">high power density self-organized nanostructures</td>
<td align="left">
<xref ref-type="bibr" rid="B88">Prosolov et&#x20;al. (2019b)</xref>
</td>
</tr>
<tr>
<td align="left">Thin titanium coatings</td>
<td align="left">bioresorbable polymers (8%&#xa0;wt.), 1:2 (v/v) mixture of (PCL) and poly (3-hydroxybutyrate-co-3-hydroxyvalerate)</td>
<td align="left">EA.hy926 cell line)</td>
<td align="left">MS</td>
<td align="left">Crystallinity</td>
<td align="left">Better adherence, high biocompatibility, high porosity, and heterogeneity, have proangiogenic activity</td>
<td align="left">
<xref ref-type="bibr" rid="B18">Bolbasov et&#x20;al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left">Titanium coatings of hydroxyapatite targets in the neon, argon, krypton, and xenon (Xenon)</td>
<td align="left">Discs diameter &#x3d; 10&#xa0;mm thickness o &#x3d; 1&#xa0;m from Ti-6Al- 4&#xa0;V alloy sputtered target &#x3d; area 224&#xa0;cm<sup>2</sup> thickness &#x3d; 6&#xa0;mm</td>
<td align="center">&#x2014;</td>
<td align="left">MS</td>
<td align="left">Crystallinity. Xe was entirely amorphous, and the crystallinity of the coating increased as the atomic weight of the working gas increased</td>
<td align="left">poor adhesion, coating delamination at the coating-substrate interface result in a 36% drop in hardness and a 23% reduction in Young&#x2019;s modulus for coatings produced in Kr. The adherence of Xe to the substrate was excellent</td>
<td align="left">
<xref ref-type="bibr" rid="B39">Fedotkin et&#x20;al. (2019)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Although, bio-ceramics deposited <italic>via</italic> magnetron sputtering led to better bone cell attachment, proliferation, growth, osseointegration, and antibacterial properties. However, further research efforts are required to improve the biocompatibility of the deposits to realize the real benefit of excellent mechanical and chemical properties attributed to magnetron sputtering. A comprehensive understanding of the detailed chemical, morphological and structural characteristics of coatings are required. Future research directions include <italic>in vivo</italic> assessments of coatings.</p>
<p>All in all, the magnetron sputtering process led to bioactive coatings with excellent adhesion strength and corrosion resistance. Magnetron sputtering can fabricate nanostructured coatings on metallic and polymeric surfaces. Magnetron sputtering can also be a useful process to control the degradation kinetic of Mg-based alloys. Therefore, it is expected that the magnetron sputtering would broaden the spectrum of clinical applications in the coming&#x20;years.</p>
</sec>
</body>
<back>
<sec id="s7">
<title>Author Contributions</title>
<p>MA writes most sections of the original draft. SU wrote the introduction section, draw the graphics, and review the manuscript. MR wrote the magnetron sputtering section and thoroughly review the whole draft and provide feedback. MU Review the paper and write concluding remarks.</p>
</sec>
<sec sec-type="COI-statement" id="s8">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s9">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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