Cited by 63Bone Tissue Engineering Materialsbiodegradable polymer synthesis and propertiesElectrospun Nanofibers in Biomedical Applications

Osteoblasts and fibroblasts attachment to poly(3-hydroxybutyric acid-co-3-hydrovaleric acid) (PHBV) film and electrospun scaffolds

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Kaniuk, Łukasz, Krysiak, Zuzanna J., Metwally, Sara, Stachewicz, Urszula·2020·Materials Science and Engineering: C

Abstract

The cellular response is the most crucial in vitro research. Materials' biocompatibility is determined based on cell proliferation and growth. Moreover, the topography of the scaffold surface is the key to enhance cell attachment and anchoring that importantly control further tissue development. Individual cell types have specific preferences regarding the type of surface and its geometry. In our research, we used poly(3-hydroxybutyric acid-co-3-hydrovaleric acid) PHBV to produce two types of substrate: a 3D structure of electrospun fibers and 2D flat films. The PHBV products were morphologically characterized by scanning electron microscopy (SEM). The cytocompatibility was evaluated with cell viability and proliferation using two different types of cells: human osteoblast-like cells (MG-63) and NIH 3 T3 murine fibroblast cells. The behaviour of both cell types was compared on the similar PHBV fiber scaffolds and films using two types of polystyrene (PS) based substrate for the cell culture study: unmodified PS that is not favourable for the attachment of cells and on tissue culture polystyrene (TCPS) plates, which are chemically modify to enhance cells attachment. The results clearly showed high biocompatibility of PHBV as both types of cells showed similar proliferation. These results indicated that PHBV scaffolds are suitable for the development of multifunctional substrates facilitating the growth of different types of tissue regardless of the 3D and 2D designed structures for regeneration purposes.

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  1. T.P. Kunzler, T. Drobek, M. Schuler, N.D. Spencer, Systematic study of osteoblast and fibroblast response to roughness by means of surface-morphology gradients, Biomaterials 28 (2007) 2175-2182, https://doi.org/10.1016/j.biomaterials.2007. 01.019. · DOI
  2. P. Kuppan, K.S. Vasanthan, D. Sundaramurthi, U.M. Krishnan, S. Sethuraman, Development of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) fibers for skin tissue engineering: effects of topography, mechanical, and chemical stimuli, Biomacromolecules 12 (2011) 3156-3165, https://doi.org/10.1021/bm200618w. · DOI
  3. L. Amaro, D.M. Correia, T. Marques-Almeida, P.M. Martins, L. Pérez, J.L. Vilas, G. Botelho, S. Lanceros-Mendez, C. Ribeiro, Tailored biodegradable and electro- active poly(Hydroxybutyrate-co-hydroxyvalerate) based morphologies for tissue engineering applications, Int. J. Mol. Sci. 19 (2018), https://doi.org/10.3390/ ijms19082149. · DOI
  4. M. Kouhi, M. Fathi, M.P. Prabhakaran, M. Shamanian, S. Ramakrishna, Poly L ly- sine-modified PHBV based nanofibrous scaffolds for bone cell mineralization and osteogenic differentiation, Appl. Surf. Sci. 457 (2018) 616-625, https://doi.org/10. 1016/j.apsusc.2018.06.239. · DOI
  5. J. Lim, M. You, J. Li, Z. Li, Emerging bone tissue engineering via Polyhydroxyalkanoate (PHA)-based scaffolds, Mater. Sci. Eng. C 79 (2017) 917-929, https://doi.org/10.1016/j.msec.2017.05.132. · DOI
  6. M. Liu, X.P. Duan, Y.M. Li, D.P. Yang, Y.Z. Long, Electrospun nanofibers for wound healing, Mater. Sci. Eng. C 76 (2017) 1413-1423, https://doi.org/10.1016/j.msec. 2017.03.034. · DOI
  7. G. Mutlu, S. Calamak, K. Ulubayram, E. Guven, Curcumin-loaded electrospun PHBV nanofibers as potential wound-dressing material, Journal of Drug Delivery Science and Technology 43 (2018) 185-193, https://doi.org/10.1016/j.jddst.2017.09.017. · DOI
  8. J. Yuan, Z.C. Xing, S.W. Park, J. Geng, I.K. Kang, J. Shen, W. Meng, K.J. Shim, I.S. Han, J.C. Kim, Fabrication of PHBV/keratin composite nanofibrous mats for biomedical applications, Macromol. Res. 17 (2009) 850-855, https://doi.org/10. 1007/BF03218625. · DOI
  9. K.E.M. Benders, P.R. van Weeren, S.F. Badylak, D.B.F. Saris, W.J.A. Dhert, J. Malda, Extracellular matrix scaffolds for cartilage and bone regeneration, Trends Biotechnol. 31 (2013) 169-176, https://doi.org/10.1016/j.tibtech.2012.12.004. · DOI
  10. S.N. Gorodzha, A.R. Muslimov, D.S. Syromotina, A.S. Timin, N.Y. Tcvetkov, K.V. Lepik, A.V. Petrova, M.A. Surmeneva, D.A. Gorin, G.B. Sukhorukov, R.A. Surmenev, A comparison study between electrospun polycaprolactone and piezoelectric poly(3-hydroxybutyrate-co-3-hydroxyvalerate) scaffolds for bone tissue engineering, Colloids Surf. B: Biointerfaces 160 (2017) 48-59, https://doi. org/10.1016/j.colsurfb.2017.09.004. · DOI
  11. R. Zine, M. Sinha, Nanofibrous poly(3-hydroxybutyrate-co-3-hydroxyvalerate)/ collagen/graphene oxide scaffolds for wound coverage, Mater. Sci. Eng. C 80 (2017) 129-134, https://doi.org/10.1016/j.msec.2017.05.138. · DOI
  12. U. Stachewicz, P.K. Szewczyk, A. Kruk, A.H. Barber, A. Czyrska-Filemonowicz, Pore shape and size dependence on cell growth into electrospun fiber scaffolds for tissue engineering: 2D and 3D analyses using SEM and FIB-SEM tomography, Mater. Sci. Eng. C 95 (2019) 397-408, https://doi.org/10.1016/j.msec.2017.08.076. · DOI
  13. U. Stachewicz, T. Qiao, S.C.F. Rawlinson, F.V. Almeida, W.Q. Li, M. Cattell, A.H. Barber, 3D imaging of cell interactions with electrospun PLGA nanofiber membranes for bone regeneration, Acta Biomater. 27 (2015) 88-100, https://doi. org/10.1016/j.actbio.2015.09.003. · DOI
  14. S. Agarwal, J.H. Wendorff, A. Greiner, Use of electrospinning technique for bio- medical applications, Polymer 49 (2008) 5603-5621, https://doi.org/10.1016/j. polymer.2008.09.014. · DOI
  15. S. Metwally, J.E. Karbowniczek, P.K. Szewczyk, M.M. Marzec, Single-step approach to tailor surface chemistry and potential on electrospun PCL fibers for tissue en- gineering application, Adv. Mater. Interfaces 1801211 (2018) 1-12, https://doi. org/10.1002/admi.201801211. · DOI
  16. P.K. Szewczyk, S. Metwally, J.E. Karbowniczek, M.M. Marzec, E. Stodolak, A. Gruszczynski, A. Bernasik, U. Stachewicz, Surface potential controlled cells proliferation and collagen mineralization on electrospun polyvinylidene fluoride (PVDF) fibers scaffolds for bone regeneration, ACS Biomaterials Science & Engineering (2018), https://doi.org/10.1021/acsbiomaterials.8b01108. · DOI
  17. B. Veleirinho, D.S. Coelho, P.F. Dias, M. Maraschin, R.M. Ribeiro-do-Valle, J.A. Lopes-da-Silva, Nanofibrous poly(3-hydroxybutyrate-co-3-hydroxyvalerate)/ chitosan scaffolds for skin regeneration, Int. J. Biol. Macromol. 51 (2012) 343-350, https://doi.org/10.1016/j.ijbiomac.2012.05.023. · DOI
  18. W. Zhu, L. Qian, J.G. Shen, Biosynthesis, biodegradation, and application of poly(3- hydroxybutyrate) and its copolymers -natural polyesters produced by diazotrophic bacteria, Physical Review D 44 (1991) 2762-2767, https://doi.org/10.1103/ PhysRevD.44.2762. · DOI
  19. W. Amass, A. Amass, B. Tighe, A review of biodegradable polymers: uses, current developments in the synthesis and characterization of biodegradable polyesters, blends of biodegradable polymers and recent advances in biodegradation studies, Polym. Int. 47 (1998) 89-144, https://doi.org/10.1002/(SICI)1097- 0126(1998100)47:2<89::AID-PI86>3.0.CO;2-F. · DOI
  20. M. Avella, E. Martuscelli, M. Raimo, Properties of blends and composites based on poly(3-hydroxy)butyrate (PHB) and poly(3-hydroxybutyrate-hydroxyvalerate) (PHBV) copolymers, J. Mater. Sci. 35 (2000) 523-545, https://doi.org/10.1023/ A:1004740522751. · DOI · Paper page
  21. M. Kouhi, M.P. Prabhakaran, M. Shamanian, M. Fathi, M. Morshed, S. Ramakrishna, Electrospun PHBV nanofibers containing HA and bredigite nanoparticles: fabrica- tion, characterization and evaluation of mechanical properties and bioactivity, Compos. Sci. Technol. 121 (2015) 115-122, https://doi.org/10.1016/j. compscitech.2015.11.006. · DOI
  22. B. Veleirinho, R.M. Ribeiro-Do-Valle, J.A. Lopes-Da-Silva, Processing conditions and characterization of novel electrospun poly (3-hydroxybutyrate-co-hydro- xyvalerate)/chitosan blend fibers, Mater. Lett. 65 (2011) 2216-2219, https://doi. org/10.1016/j.matlet.2011.04.058. · DOI
  23. I. Unalan, O. Colpankan, A.Z. Albayrak, C. Gorgun, A.S. Urkmez, Biocompatibility of plasma-treated poly(3-hydroxybutyrate-co-3-hydroxyvalerate) nanofiber mats modified by silk fibroin for bone tissue regeneration, Mater. Sci. Eng. C 68 (2016) 842-850, https://doi.org/10.1016/j.msec.2016.07.054. · DOI
  24. C. Lei, H. Zhu, J. Li, J. Li, X. Feng, J. Chen, Preparation and characterization of polyhydroxybutyrate-co-hydroxyvalerate/silk fibroin nanofibrous scaffolds for skin tissue engineering, Anasthesiologie Und Intensivmedizin 57 (2016) 147-151, https://doi.org/10.1002/pen. · DOI
  25. A.S.G. Curtis, J.V. Forrester, C. McInnes, F. Lawrie, Adhesion of cells to polystyrene surfaces, J. Cell Biol. 97 (1983) 1500-1506, https://doi.org/10.1016/b978-0-12- 469050-9.50008-9. · DOI
  26. M.J. Lerman, J. Lembong, S. Muramoto, G. Gillen, J.P. Fisher, The evolution of polystyrene as a cell culture material, Tissue Eng. B Rev. 24 (2018) 359-372, https://doi.org/10.1089/ten.teb.2018.0056. · DOI
  27. J.G. Steele, C.L. McFarland, B. Ann Dalton, G. Johnson, M.D.M. Evans, C. Rolfe Howlett, P. Anne Underwood, Attachment of human bone cells to tissue culture polystyrene and to unmodified polystyrene: the effect of surface chemistry upon initial cell attachment, J. Biomater. Sci. Polym. Ed. 5 (1994) 245-257, https://doi. org/10.1163/156856293X00339. · DOI
  28. A. Klinder, J. Markhoff, A. Jonitz-Heincke, P. Sterna, A. Salamon, R. Bader, Comparison of different cell culture plates for the enrichment of non-adherent human mononuclear cells, Experimental and Therapeutic Medicine (2019) 2004-2012, https://doi.org/10.3892/etm.2019.7204. · DOI
  29. P.K. Szewczyk, D.P. Ura, S. Metwally, J. Knapczyk-Korczak, M. Gajek, M.M. Marzec, A. Bernasik, U. Stachewicz, Roughness and fiber fraction dominated wetting of electrospun fiber-based porous meshes, Polymers 11 (2018), https://doi.org/10. 3390/polym11010034. · DOI
  30. D.P. Ura, J.E. Karbowniczek, P.K. Szewczyk, S. Metwally, M. Kopyściański, U. Stachewicz, Cell integration with electrospun PMMA nanofibers, microfibers, ribbons, and films: a microscopy study, Bioengineering 6 (2019) 41, https://doi. org/10.3390/bioengineering6020041. · DOI
  31. U. Stachewicz, R.J. Bailey, H. Zhang, C.A. Stone, C.R. Willis, A.H. Barber, Wetting hierarchy in oleophobic 3D electrospun nanofiber networks, ACS Appl. Mater. Interfaces 7 (2015) 16645-16652, https://doi.org/10.1021/acsami.5b04272. · DOI
  32. H.W. Tong, M. Wang, Electrospinning of fibrous polymer scaffolds using positive voltage or negative voltage: a comparative study, Biomed. Mater. 5 (2010), https:// doi.org/10.1088/1748-6041/5/5/054110. · DOI
  33. K. Sombatmankhong, N. Sanchavanakit, P. Pavasant, P. Supaphol, Bone scaffolds from electrospun fiber mats of poly(3-hydroxybutyrate), poly(3-hydroxybutyrate- co-3-hydroxyvalerate) and their blend, Polymer 48 (2007) 1419-1427, https://doi. org/10.1016/j.polymer.2007.01.014. · DOI
  34. S.K. Rajaraman, M. Jainu, G. Dhakshinamoorthy, Ocimum basilicum L. essential oil coated biomaterial surfaces prevent bacterial adhesion and biofilm growth, Asian Journal of Pharmaceutical and Clinical Research 9 (2016).
  35. M. Thukkaram, S. Sitaram, S.K. Kannaiyan, G. Subbiahdoss, Antibacterial efficacy of iron-oxide nanoparticles against biofilms on different biomaterial surfaces, International Journal of Biomaterials 2014 (2014), https://doi.org/10.1155/2014/ 716080. · DOI
  36. P.K. Szewczyk, S. Metwally, Z.J. Krysiak, Ł. Kaniuk, J.E. Karbowniczek, U. Stachewicz, Enhanced osteoblasts adhesion and collagen formation on biomi- metic polyvinylidene fluoride (PVDF) films for bone regeneration, Biomed. Mater. 14 (2019) 65006, https://doi.org/10.1088/1748-605X/ab3c20. · DOI
  37. A.I. Teixeira, G.A. Abrams, P.J. Bertics, C.J. Murphy, P.F. Nealey, Epithelial contact guidance on well-defined micro-and nanostructured substrates, J. Cell Sci. 116 (2003) 1881-1892, https://doi.org/10.1038/jid.2014.371. · DOI · Paper page
  38. M. Chrzanowska-Wodnicka, K. Burridge, Rho-stimulated contractility drives the formation of stress fibers and focal adhesions, J. Cell Biol. 133 (1996) 1403-1415, https://doi.org/10.1083/jcb.133.6.1403. · DOI
  39. K. Anselme, M. Bigerelle, B. Noel, E. Dufresne, D. Judas, A. Iost, P. Hardouin, Qualitative and quantitative study of human osteoblast adhesion on materials with various surface roughnesses, J. Biomed. Mater. Res. 49 (2000) 155-166, https:// doi.org/10.1002/(SICI)1097-4636(200002)49:2<155::AID-JBM2>3.0.CO;2-J. · DOI
  40. S. Migita, K. Araki, Effect of nanometer scale surface roughness of titanium for osteoblast function, AIMS Bioengineering 4 (2017) 162-170, https://doi.org/10. 3934/bioeng.2017.1.162. · DOI
  41. Y.C. Kuo, R. Rajesh, Nerve growth factor-loaded heparinized cationic solid lipid nanoparticles for regulating membrane charge of induced pluripotent stem cells during differentiation, Mater. Sci. Eng. C 77 (2017) 680-689, https://doi.org/10. 1016/j.msec.2017.03.303. · DOI
  42. T. Dvir, B.P. Timko, D.S. Kohane, R. Langer, Nanotechnological strategies for en- gineering complex tissues, Nat. Nanotechnol. 6 (2011) 13-22, https://doi.org/10. 1038/nnano.2010.246. · DOI · Paper page
  43. J. Li, X. Mou, J. Qiu, S. Wang, D. Wang, D. Sun, W. Guo, D. Li, A. Kumar, X. Yang, A. Li, H. Liu, Surface charge regulation of osteogenic differentiation of mesench- ymal stem cell on polarized ferroelectric crystal substrate, Advanced Healthcare Materials 4 (2015) 998-1003, https://doi.org/10.1002/adhm.201500032. · DOI

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Sorted by citations

Authors
Kaniuk, Ł., Krysiak, Z. J., Metwally, S., & Stachewicz, U.
Affiliations
AGH University of Krakow (PL)
Corresponding author
Stachewicz, Urszula
Venue
Materials Science and Engineering: C
Publisher
Elsevier BV
Published
2020-05
Volume
110
Pages
110668
ISSN
0928-4931 (ISSN-L)
OpenAlex
W3000277234
Cited by
63
References
1
Citations by year
2026: 1 · 2025: 7 · 2024: 12 · 2023: 12 · 2022: 13 · 2021: 14 · 2020: 4
FWCI
3.31
Type
journal article
Language
en
Open access
Locations
  • Materials Science and Engineering C (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • Foundation for Polish Science
  • European Union (POIR.04.04.00-00- 4571/18-00)
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
  • Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
  • Physical Sciences › Materials Science › Biomaterials › Electrospun Nanofibers in Biomedical Applications
Keywords
poly(3-hydroxybutyrate-co-3-hydroxyvalerate), electrospun scaffolds, cell attachment, osteoblasts, fibroblasts, biocompatibility, MG-63 cells, NIH3T3 cells, surface topography, tissue culture polystyrene, polystyrene substrate, cell proliferation, tissue regeneration
MeSH terms
Polyhydroxybutyrates, Animals, Cell Survival, Fibroblasts, Osteoblasts, Polyesters, Surface Properties, Tissue Engineering, NIH 3T3 Cells, Cell Shape, Cell Proliferation, Mice, Tissue Scaffolds

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