Subscribe to RSS
DOI: 10.1055/s-0042-1755550
Novel Application of 3D Scaffolds of Poly(E-Caprolactone)/Graphene as Osteoinductive Properties in Bone Defect
Abstract
Objective Scaffolds provided a surface on which cells could attach, proliferate, and differentiate. Nowadays, bone tissue engineering offers hope for treating bone cancer. Poly(e-caprolactone) (PCL)/graphene have capability as an osteogenic and regenerative therapy. It could be used to produce bone tissue engineering scaffolds. The purpose of this study was to investigate the ability of PCL/graphene to enhance the osteoinductive mechanism.
Materials and Methods The PCL/graphene scaffold was developed utilizing a particulate-leaching process and cultured with osteoblast-like cells MG63 at 0.5, 1.5, and 2.5 wt% of graphene. We evaluated the porosity, pore size, migratory cells, and cell attachment of the scaffold.
Statistical Analysis Data was expressed as the mean ± standard error of the mean and statistical analyses were performed using one-way analysis of variance and Tukey's post hoc at a level of p-value < 0.05.
Results Porosity of scaffold with various percentage of graphene was nonsignificant (p > 0.05). There were differences in the acceleration of cell migration following wound closure between groups at 24 hours (p < 0.01) and 48 hours (p < 0.00). Adding the graphene on the scaffolds enhanced migration of osteoblast cells culture and possibility to attach. Graphene on 2.5 wt% exhibited good characteristics over other concentrations.
Conclusion This finding suggests that PCL/graphene composites may have potential applications in bone tissue engineering.
Authors' Contributions
H.S.B. reports all support for study design, collection of data, data analysis/interpretation, writing of the manuscript, and revision of the manuscript.
S.A. reports all support for data analysis/interpretation, writing of the manuscript, and revision of the manuscript.
N.A.S. reports support for collection of data and writing of the manuscript.
Y.-K.S. reports all support for study design, writing of the manuscript, and revision of the manuscript.
M.T. reports all support for data analysis/interpretation and writing of the manuscript.
Publication History
Article published online:
09 November 2022
© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India
-
References
- 1 Cheng A, Schwartz Z, Kahn A. et al. Advances in porous scaffold design for bone and cartilage tissue engineering and regeneration. Tissue Eng Part B Rev 2019; 25 (01) 14-29
- 2 Wang W, Huang B, Byun JJ, Bártolo P. Assessment of PCL/carbon material scaffolds for bone regeneration. J Mech Behav Biomed Mater 2019; 93: 52-60
- 3 Cheng X, Wan Q, Pei X. Graphene family materials in bone tissue regeneration: perspectives and challenges. Nanoscale Res Lett 2018; 13 (01) 289
- 4 Ren J, Zhang XG, Chen Y. Graphene accelerates osteoblast attachment and biomineralization. Carbon Lett 2017; 22: 42-47
- 5 Wu DT, Munguia-Lopez JG, Cho YW. et al. Polymeric scaffolds for dental, oral, and craniofacial regenerative medicine. Molecules 2021; 26 (22) 7043
- 6 Zhang K, Fan Y, Dunne N, Li X. Effect of microporosity on scaffolds for bone tissue engineering. Regen Biomater 2018; 5 (02) 115-124
- 7 Secor EB, Santos MHD, Wallace SG, Bradshaw NP, Hersam MC. Tailoring the porosity and microstructure of printed graphene electrodes via polymer phase inversion. J Phys Chem C 2018; 122: 13745-13750
- 8 Sattar T. Current review on synthesis, composites and multifunctional properties of graphene. Top Curr Chem (Cham) 2019; 377 (02) 10
- 9 Hutmacher DW. Scaffolds in tissue engineering bone and cartilage. Biomaterials 2000; 21 (24) 2529-2543
- 10 Prasadh S, Suresh S, Wong R. Osteogenic potential of graphene in bone tissue engineering scaffolds. Materials (Basel) 2018; 11 (08) 1430
- 11 Cappiello F, Casciaro B, Mangoni ML. A novel in vitro wound healing assay to evaluate cell migration. J Vis Exp 2018; (133) 56825
- 12 Grada A, Otero-Vinas M, Prieto-Castrillo F, Obagi Z, Falanga V. Research techniques made simple: analysis of collective cell migration using the wound healing assay. J Invest Dermatol 2017; 137 (02) e11-e16
- 13 Barateiro A, Fernandes A. Temporal oligodendrocyte lineage progression: in vitro models of proliferation, differentiation and myelination. Biochim Biophys Acta 2014; 1843 (09) 1917-1929
- 14 Fu X, Liu G, Halim A, Ju Y, Luo Q, Song AG. Mesenchymal stem cell migration and tissue repair. Cells 2019; 8 (08) 784
- 15 Cai S, Wu C, Yang W, Liang W, Yu H, Liu L. Recent advance in surface modification for regulating cell adhesion and behaviors. Nanotechnol Rev 2020; 9 (01) 971-989
- 16 Huang HY, Fan FY, Shen YK. et al. 3D poly-ε-caprolactone/graphene porous scaffolds for bone tissue engineering. Coll Surf A. 2020; 606: 1-9
- 17 Rötzer V, Hartlieb E, Winkler J. et al. Desmoglein 3-dependent signaling regulates keratinocyte migration and wound healing. J Invest Dermatol 2016; 136 (01) 301-310
- 18 Silva MJ, Gonçalves CP, Galvão KM, D'Alpino PHP, Nascimento FD. Synthesis and characterizations of a collagen-rich biomembrane with potential for tissue-guided regeneration. Eur J Dent 2019; 13 (03) 295-302
- 19 Ouyang P, Dong H, He X. et al. Hydromechanical mechanism behind the effect of pore size of porous titanium scaffolds on osteoblast response and bone ingrowth. Mater Des 2019; 183: 108151
- 20 Budi HS, Anitasari S, Ulfa NM. et al. Topical medicine potency of Musa paradisiaca var. sapientum (L.) kuntze as oral gel for wound healing: an in vitro, in vivo study. Eur J Dent 2022; Oct; 16 (04) 848-855
- 21 Zhu G, Zhang T, Chen M. et al. Bone physiological microenvironment and healing mechanism: basis for future bone-tissue engineering scaffolds. Bioact Mater 2021; 6 (11) 4110-4140
- 22 Gonzalez AC, Costa TF, Andrade ZA, Medrado AR. Wound healing - a literature review. An Bras Dermatol. 2016; 91 (05) 614-620
- 23 Wen JH, Choi O, Taylor-Weiner H. et al. Haptotaxis is cell type specific and limited by substrate adhesiveness. Cell Mol Bioeng 2015; 8 (04) 530-542
- 24 Nikolova MP, Chavali MS. Recent advances in biomaterials for 3D scaffolds: a review. Bioact Mater 2019; 4: 271-292
- 25 Du Z, Wang C, Zhang R, Wang X, Li X. Applications of graphene and its derivatives in bone repair: advantages for promoting bone formation and providing real-time detection, challenges and future prospects. Int J Nanomedicine 2020; 15: 7523-7551
- 26 Wu M, Zou L, Jiang L, Zhao Z, Liu J. Osteoinductive and antimicrobial mechanisms of graphene-based materials for enhancing bone tissue engineering. J Tissue Eng Regen Med 2021; 15 (11) 915-935
- 27 Aryaei A, Jayatissa AH, Jayasuriya AC. The effect of graphene substrate on osteoblast cell adhesion and proliferation. J Biomed Mater Res A 2014; 102 (09) 3282-3290
- 28 Padilha Fontoura C, Ló Bertele P, Machado Rodrigues M. et al. Comparative study of physicochemical properties and biocompatibility (L929 and MG63 Cells) of TiN coatings obtained by plasma nitriding and thin film deposition. ACS Biomater Sci Eng 2021; 7 (08) 3683-3695
- 29 Gibieža P, Petrikaitė V. The regulation of actin dynamics during cell division and malignancy. Am J Cancer Res 2021; 11 (09) 4050-4069
- 30 Tewari M, Pareek P, Kumar S. Correlating amino acid interaction with graphene-based materials regulating cell function. J Indian Inst Sci 2022; 102: 639-651
- 31 Matthews HK, Ganguli S, Plak K. et al. Oncogenic signaling alters cell shape and mechanics to facilitate cell division under confinement. Dev Cell 2020; 52 (05) 563-573.e3
- 32 Moutzouri AG, Athanassiou GM. Insights into the alteration of osteoblast mechanical properties upon adhesion on chitosan. BioMed Res Int 2014; 2014: 740726