Biomaterials and Porous Scaffolds for Tissue Engineering and Regenerative Medicine

A special issue of Journal of Functional Biomaterials (ISSN 2079-4983). This special issue belongs to the section "Biomaterials for Tissue Engineering and Regenerative Medicine".

Deadline for manuscript submissions: 30 July 2024 | Viewed by 6740

Special Issue Editors


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Guest Editor
Department of Mechanical Engineering, The University of Hong Kong, Hong Kong, China
Interests: biomedical materials; tissue engineering; materials and systems for the controlled release of drugs/biomolecules/genes; surface engineering; nanotechnologies; electrospinning; additive manufacturing ("3D printing"); biomanufacturing
School of Mechanical Engineering, Dongguan University of Technology, Dongguan, China
Interests: 3D/4D printing; biofabrication; tissue regeneration; biomaterials; organoid
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Institute of Biomedical and Health Engineering, Shenzhen Institute of Advanced Technology (SIAT), Chinese Academy of Sciences (CAS), Shenzhen, China
Interests: biointerfaces; stimuli-responsive biomaterials; tissue engineering; biomanufacturing; electrospinning; electrospraying

Special Issue Information

Dear Colleagues,

Tissue engineering emerged more than three decades ago. It has attracted great attention because it holds great promise for solving many difficult medical problems that current treatments cannot deal with or cannot achieve satisfactory clinical outcomes for. Worldwide efforts over the past few decades have led to remarkable progresses in regenerating human body tissues such as skin, blood vessels, and bone. However, there are still great challenges in tissue engineering and regenerative medicine. Recent advances in materials science and engineering, nanoscience and nanotechnology, manufacturing technologies, biological science, clinical sciences, etc., can significantly move the field forward and greatly assist us to tackle the challenges and regenerate complex body tissues/organs such as the gastrointestinal tract, liver, and uterus.

There are different strategies for human body tissue regeneration. Many researchers have successfully used scaffold-, growth factor (GF)-, or cell-based tissue engineering for regenerating human skin, bone, articular cartilage, etc. In scaffold-based tissue engineering, scaffolds provide conducive microenvironments for cells and play vital roles for cell adhesion, proliferation, differentiation, and new tissue formation. Many biocompatible materials, including polymers, metals, ceramics, and composites/hybrids, have been used/developed as tissue engineering materials and have achieved their successes. However, different materials have their advantages and shortcomings. For example, hydrogels have seen their increasing use in the tissue engineering field because of their particular attractiveness, but they are weak materials. Strong and highly resilient hydrogels are now being investigated/developed for targeted applications by research groups in different continents. For the regeneration of a specific body tissue, the material/materials should be carefully selected and evaluated. There are also many scaffold fabrication technologies, including electrospinning and additive manufacturing (i.e., “3D printing”). Electrospinning is attractive because it can produce nanofibrous structures that mimic the extracellular matrix structure. However, there are limitations in electrospinning, so significant improvements for electrospun products are also required. 3D-printing technologies have significantly raised our ability to create complex scaffolds or cell-scaffold constructs for regenerating complex body tissues. Bioprinting has shown great promise in a number of areas, including tissue engineering. However, there many scientific and technological issues that need to be addressed for 3D printing in tissue engineering and for bioprinting. Additionally, stem cells are increasingly used in tissue engineering investigations. Again, there are fundamental and technical questions that need to be answered for their wide use in the field. Designing scaffolds and scaffold simulation (mechanical, fluidic, etc.) are gaining increasing attention with the aim to achieve the best clinical performance for scaffolds. Biomimicking scaffolds are becoming popular for tissue regeneration. Guidelines on scaffold design, which are tissue specific, should therefore be established. Even though there are already numerous investigations on cell‒scaffold interactions, scaffold‒tissue interactions, and biochemical and/or biomechanical cues on cell behaviour and tissue formation, great efforts are still needed to gain further understanding and new insights in these areas. Furthermore, developing multifunctional scaffolds that can also perform other functions (anti-inflammatory, anti-cancer, etc.) provides much wider scope for our R&D activities.

This Special Issue provides a forum for sharing new research findings and new insights in different areas mentioned above from people, both experienced workers and newcomers, involved in tissue engineering and regenerative medicine. These people include biomaterials scientists and engineers, tissue engineers, biological scientists, clinicians, and industrialists. Submissions presenting new ideas/approaches, new materials, new scaffold designs, new fabrication technologies, novel scaffolds, new testing techniques, and new assessment methods are very welcome. The materials and porous scaffolds that are presented in these submissions are/will be used for regenerating different body tissues/organs, including skin, blood vessels, bone, tendon/ligament, articular cartilage, osteochondral tissue, gastrointestinal tract, liver, uterus, etc. Articles of excellent quality in this Special Issue will be selected as Feature Papers of the Journal of Functional Biomaterials.

Prof. Dr. Min Wang
Dr. Chong Wang
Dr. Qilong Zhao
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Journal of Functional Biomaterials is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • tissue engineering
  • regenerative medicine
  • natural polymer
  • synthetic polymer
  • hydrogel
  • metal
  • ceramic
  • composite
  • hybrid
  • porous scaffold
  • scaffold design
  • biomimicking
  • graded scaffold
  • multifunctional scaffold
  • cell‒scaffold construct
  • scaffold fabrication
  • electrospinning
  • 3D printing
  • bioprinting
  • structure
  • performance
  • biodegradation
  • scaffold simulation
  • biochemical cue
  • biomechanical cue
  • bioreactor
  • mature cell
  • stem cell
  • cell‒scaffold interaction
  • scaffold‒tissue interaction
  • in vitro evaluation
  • in vivo evaluation

Published Papers (4 papers)

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Research

22 pages, 6821 KiB  
Article
Design of Laser Activated Antimicrobial Porous Tricalcium Phosphate-Hydroxyapatite Scaffolds for Orthopedic Applications
by Emil Filipov, Ridvan Yildiz, Anna Dikovska, Lamborghini Sotelo, Tharun Soma, Georgi Avdeev, Penka Terziyska, Silke Christiansen, Anne Leriche, Maria Helena Fernandes and Albena Daskalova
J. Funct. Biomater. 2024, 15(2), 36; https://0-doi-org.brum.beds.ac.uk/10.3390/jfb15020036 - 30 Jan 2024
Viewed by 1421
Abstract
The field of bone tissue engineering is steadily being improved by novel experimental approaches. Nevertheless, microbial adhesion after scaffold implantation remains a limitation that could lead to the impairment of the regeneration process, or scaffold rejection. The present study introduces a methodology that [...] Read more.
The field of bone tissue engineering is steadily being improved by novel experimental approaches. Nevertheless, microbial adhesion after scaffold implantation remains a limitation that could lead to the impairment of the regeneration process, or scaffold rejection. The present study introduces a methodology that employs laser-based strategies for the development of antimicrobial interfaces on tricalcium phosphate–hydroxyapatite (TCP-HA) scaffolds. The outer surfaces of the ceramic scaffolds with inner porosity were structured using a femtosecond laser (λ = 800 nm; τ = 70 fs) for developing micropatterns and altering local surface roughness. The pulsed laser deposition of ZnO was used for the subsequent functionalization of both laser-structured and unmodified surfaces. The impact of the fs irradiation was investigated by Raman spectroscopy and X-ray diffraction. The effects of the ZnO-layered ceramic surfaces on initial bacterial adherence were assessed by culturing Staphylococcus aureus on both functionalized and non-functionalized scaffolds. Bacterial metabolic activity and morphology were monitored via the Resazurin assay and microscopic approaches. The presence of ZnO evidently decreased the metabolic activity of bacteria and led to impaired cell morphology. The results from this study have led to the conclusion that the combination of fs laser-structured surface topography and ZnO could yield a potential antimicrobial interface for implants in bone tissue engineering. Full article
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19 pages, 8907 KiB  
Article
Fibronectin Conformations after Electrodeposition onto 316L Stainless Steel Substrates Enhanced Early-Stage Osteoblasts’ Adhesion but Affected Their Behavior
by Séverine Alfonsi, Pithursan Karunathasan, Ayann Mamodaly-Samdjee, Keerthana Balathandayutham, Sarah Lefevre, Anamar Miranda, Olivier Gallet, Damien Seyer and Mathilde Hindié
J. Funct. Biomater. 2024, 15(1), 5; https://0-doi-org.brum.beds.ac.uk/10.3390/jfb15010005 - 21 Dec 2023
Viewed by 1426
Abstract
The implantation of metallic orthopedic prostheses is increasingly common due to an aging population and accidents. There is a real societal need to implement new metal implants that combine durability, good mechanical properties, excellent biocompatibility, as well as affordable costs. Since the functionalization [...] Read more.
The implantation of metallic orthopedic prostheses is increasingly common due to an aging population and accidents. There is a real societal need to implement new metal implants that combine durability, good mechanical properties, excellent biocompatibility, as well as affordable costs. Since the functionalization of low-cost 316L stainless steel substrates through the successive electrodeposition of a polypyrrole film (PPy) and a calcium phosphate deposit doped with silicon was previously carried out by our labs, we have also developed a bio-functional coating by electrodepositing or oxidating of fibronectin (Fn) coating. Fn is an extracellular matrix glycoprotein involved in cell adhesion and differentiation. Impacts of either electrodeposition or oxidation on the structure and functionality of Fn were first studied. Thus, electrodeposition is the technique that permits the highest deposition of fibronectin, compared to adsorption or oxidation. Furthermore, electrodeposition seems to strongly modify Fn conformation by the formation of intermingled long fibers, resulting in changes to the accessibility of the molecular probes tested (antibodies directed against Fn whole molecule and Fn cell-binding domain). Then, the effects of either electrodeposited Fn or oxidized Fn were validated by the resulting pre-osteoblast behavior. Electrodeposition reduced pre-osteoblasts’ ability to remodel Fn coating on supports because of a partial modification of Fn conformation, which reduced accessibility to the cell-binding domain. Electrodeposited Fn also diminished α5 integrin secretion and clustering along the plasma membrane. However, the N-terminal extremity of Fn was not modified by electrodeposition as demonstrated by Staphylococcus aureus attachment after 3 h of culture on a specific domain localized in this region. Moreover, the number of pre-osteoblasts remains stable after 3 h culture on either adsorbed, oxidized, or electrodeposited Fn deposits. In contrast, mitochondrial activity and cell proliferation were significantly higher on adsorbed Fn compared with electrodeposited Fn after 48 h culture. Hence, electro-deposited Fn seems more favorable to pre-osteoblast early-stage behavior than during a longer culture of 24 h and 48 h. The electrodeposition of matrix proteins could be improved to maintain their bio-activity and to develop this promising, fast technique to bio-functionalize metallic implants. Full article
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18 pages, 7377 KiB  
Article
Nanostructured Porous Silicon for Bone Tissue Engineering: Kinetics of Particle Degradation and Si-Controlled Release
by Naveen Fatima, Hamideh Salehi, Eduardo J. Cueto-Díaz, Alban Desoutter, Frédéric Cuisinier, Frédérique Cunin and Pierre-Yves Collart-Dutilleul
J. Funct. Biomater. 2023, 14(10), 493; https://0-doi-org.brum.beds.ac.uk/10.3390/jfb14100493 - 30 Sep 2023
Viewed by 1708
Abstract
Nanostructured porous silicon (pSi) is a synthetic silicon-based material. Its biocompatibility and bioresorbability in body fluids make pSi an appealing biomaterial for tissue engineering, with surfaces characteristics facilitating human cell adhesion and differentiation. The resorption kinetics of such porous biomaterials is crucial for [...] Read more.
Nanostructured porous silicon (pSi) is a synthetic silicon-based material. Its biocompatibility and bioresorbability in body fluids make pSi an appealing biomaterial for tissue engineering, with surfaces characteristics facilitating human cell adhesion and differentiation. The resorption kinetics of such porous biomaterials is crucial for in vivo bone regeneration, in order to adapt biomaterial resorption to tissue formation, and to control the release of loaded bioactive molecules. We investigated pSi as a bioactive scaffold for bone tissue engineering, with an emphasis on kinetics of pSi resorption and silicon release. PSi particles and chips were fabricated from crystalline silicon, and functionalized by oxidation and chemical grafting of amine groups to mimic biological structures. Materials resorption over time was investigated with Raman spectroscopy, infrared spectroscopy, and Scanning Electron Microscopy. Silicon release was followed by mass spectrometry. Particle degradation and inclusion in newly formed bone were studied in vivo. The in vitro experiments revealed that non-oxidized pSi had an accelerated initial dissolution in ddH2O and an inhibition of initial Si release in SBF. This high reactivity also led to transformation towards amorphous non-resorbable silica when incubated in SBF. PSi resorption started immediately with a maximal dissolution in the first 24 h. Later, the dissolution rate decreased over time. In comparison, the resorption process of oxidized pSi seemed delayed, but more continuous. This delayed dissolution increased the bioactivity and stability, leading to enhanced bone formation in vivo. Delayed pSi degradation provided a constant surge of silicic acid over time and promoted bone regeneration, demonstrating the high potential of pSi for bone tissue engineering: Oxidized pSi were almost completely resorbed after 2 months of healing, with remaining partially dissolved particles surrounded by newly formed bone. On the contrary, non-oxidized particles were still obviously present after 2 months with limited bone regeneration. This delayed resorption is consistent with the in vitro observations in SBF, and particles’ transformation towards silica. Full article
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15 pages, 10647 KiB  
Article
Cryo-Electrospinning Generates Highly Porous Fiber Scaffolds Which Improves Trabecular Meshwork Cell Infiltration
by Devon J. Crouch, Carl M. Sheridan, Julia G. Behnsen, Raechelle A. D’Sa and Lucy A. Bosworth
J. Funct. Biomater. 2023, 14(10), 490; https://0-doi-org.brum.beds.ac.uk/10.3390/jfb14100490 - 22 Sep 2023
Cited by 1 | Viewed by 1626
Abstract
Human trabecular meshwork is a sieve-like tissue with large pores, which plays a vital role in aqueous humor outflow. Dysfunction of this tissue can occur, which leads to glaucoma and permanent vision loss. Replacement of trabecular meshwork with a tissue-engineered device is the [...] Read more.
Human trabecular meshwork is a sieve-like tissue with large pores, which plays a vital role in aqueous humor outflow. Dysfunction of this tissue can occur, which leads to glaucoma and permanent vision loss. Replacement of trabecular meshwork with a tissue-engineered device is the ultimate objective. This study aimed to create a biomimetic structure of trabecular meshwork using electrospinning. Conventional electrospinning was compared to cryogenic electrospinning, the latter being an adaptation of conventional electrospinning whereby dry ice is incorporated in the fiber collector system. The dry ice causes ice crystals to form in-between the fibers, increasing the inter-fiber spacing, which is retained following sublimation. Structural characterization demonstrated cryo-scaffolds to have closer recapitulation of the trabecular meshwork, in terms of pore size, porosity, and thickness. The attachment of a healthy, human trabecular meshwork cell line (NTM5) to the scaffold was not influenced by the fabrication method. The main objective was to assess cell infiltration. Cryo-scaffolds supported cell penetration deep within their structure after seven days, whereas cells remained on the outer surface for conventional scaffolds. This study demonstrates the suitability of cryogenic electrospinning for the close recapitulation of trabecular meshwork and its potential as a 3D in vitro model and, in time, a tissue-engineered device. Full article
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