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Abstrakty
This study demonstrates the comparison in the method of fabrication and thus evaluates the potential of psyllium husk powder and gelatin-based composite microporous scaffolds for tissue engineering applications. The scaffold is being prepared in three different ratios of 50:50, 75:25 and 100 (w/w of psyllium husk powder and gelatin, respectively) by employing a suitable cross-linking agent, EDC-NHS, followed drying. We have demonstrated the use and outcomes of two different methods of scaffold drying, i.e., vacuum desiccation along with liquid nitrogen dip and lyophilization. It was concluded from the SEM micrographs that the scaffolds dried under vacuum accompanied with liquid nitrogen exposure exhibited less porous architecture when compared to those prepared using a lyophilizer, that resulted in pores in the range of 60-110 μm. Scaffolds fabricated using the former technique lost porosity and sponge-like characteristics of a scaffold. In spite of the above fact, water retaining capacity and stability in the cell culture of such scaffolds is significant, nearly 40-50% of its initial dry weight. Cell culture experiments support the potential of the scaffolds prepared from different methods of fabrication for its cytocompatibility and suitability for cell growth and proliferation for a substantial duration. Erosion in the porous design of the scaffolds was observed after 14 days via SEM micrographs. It was inferred that freeze-drying is a better technique than vacuum desiccation for scaffold preparation. The present investigation has been conducted keeping in mind the importance of drying a scaffold. Scaffold drying is a necessary step to increase its shelf-life, makes it easy to transport and much importantly, controlling the pore size of the scaffold.
Czasopismo
Rocznik
Tom
Strony
2--6
Opis fizyczny
Bibliogr. 30 poz., zdj.
Twórcy
autor
- Tissue Engineering and Biomicrofluidics Laboratory, School of Biomedical Engineering, Indian Institute of Technology, Banaras Hindu University, Varanasi, India
autor
- Tissue Engineering and Biomicrofluidics Laboratory, School of Biomedical Engineering, Indian Institute of Technology, Banaras Hindu University, Varanasi, India
autor
- Tissue Engineering and Biomicrofluidics Laboratory, School of Biomedical Engineering, Indian Institute of Technology, Banaras Hindu University, Varanasi, India
Bibliografia
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- [2] P. Zhao, H. Gu, H. Mi, C. Rao, J. Fu, L. Turng: Fabrication of scaffolds in tissue engineering: A review. Front. Mech. Eng. 13(1) (2018) 107-119.
- [3] B.P. Chan, K.W. Leong: Scaffolding in tissue engineering: ge-neral approaches and tissue-specific considerations. Eur Spine J 17(4) (2008) 467-479.
- [4] F.J. O’Brien: Biomaterials & scaffolds for tissue engineering. Materials Today 14(3) (2011) 88-95.
- [5] H. Zhang, L. Zhou, W. Zhang: Control of Scaffold Degradation in Tissue Engineering: A Review. Tissue Engineering Part B: Reviews 20(5) (2014) 492-502.
- [6] E. Carletti, A. Motta, C. Migliaresi: Scaffolds for tissue engineering and 3D cell culture. Methods Mol. Biol. 695 (2011) 17-39.
- [7] A. Sionkowska: Biopolymeric nanocomposites for potential biomedical applications. Polymer International 65(10) (2016) 1123-1131.
- [8] D.M. Mehta, P.K. Shelat, P.B. Parejiya, A.J. Patel, B. Barot: Inve-stigations of Plantago ovata husk powder as a disintegrating agent for development of famotidine tablets. Int J Pharm Sci Nanotechnol 4(2) (2011) 1412-1417.
- [9] M.A. Hussain, G. Muhammad, I. Jantan, S.N.A. Bukhari: Psyllium Arabinoxylan: A Versatile Biomaterial for Potential Medicinal and Pharmaceutical Applications. Polymer Reviews 56(1) (2016) 1-30.
- [10] A.O. Elzoghby: Gelatin-based nanoparticles as drug and gene delivery systems: Reviewing three decades of research. Journal of Controlled Release 172 (3) (2013) 1075-1091.
- [11] N. Davidenko et al.: Evaluation of cell binding to collagen and gelatin: a study of the effect of 2D and 3D architecture and surface chemistry. J Mater Sci Mater Med 27(10) 2016.
- [12] S. Gorgieva, T. Vuherer, V. Kokol: Autofluorescence-aided assessment of integration and μ-structuring in chitosan/gelatin bilayer membranes with rapidly mineralized interface in relevance to guided tissue regeneration. Materials Science and Engineering: C 93 (2018) 226-241.
- [13] S. Gorgieva, J. Štrancar, V. Kokol: Evaluation of surface/interface-related physicochemical and microstructural properties of gelatin 3D scaffolds, and their influence on fibroblast growth and morphology. Journal of Biomedical Materials Research Part A 102(11) (2014) 3986-3997.
- [14] S. Gorgieva, L. Girandon, V. Kokol: Mineralization potential of cellulose-nanofibrils reinforced gelatine scaffolds for promoted calcium deposition by mesenchymal stem cells. Materials Science and Engineering: C 73 (2017) 478-489.
- [15] S. Gorgieva, M. Modic, B. Dovgan, M. Kaisersberger-Vincek, V. Kokol: Plasma-Activated Polypropylene Mesh-Gelatin Scaffold Composite as Potential Implant for Bioactive Hernia Treatment. Plasma Processes and Polymers 12(3) (2015) 237-251.
- [16] M. Nikkhah, M. Akbari, A. Paul, A. Memic, A. Dolatshahi-Pirouz, A. Khademhosseini: Gelatin-Based Biomaterials For Tissue Engineering And Stem Cell Bioengineering, in Biomaterials from Nature for Advanced Devices and Therapies, Wiley-Blackwell (2016) 37-62.
- [17] F. Zhang et al.: Fabrication of gelatin-hyaluronic acid hybrid scaffolds with tunable porous structures for soft tissue engineering. Int. J. Biol. Macromol. 48(3) (2011) 474-481.
- [18] S.-N. Park, J.-C. Park, H.O. Kim, M.J. Song, H. Suh: Characterization of porous collagen/hyaluronic acid scaffold modified by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide cross-linking. Biomaterials 23(4) (2002) 1205-1212.
- [19] T.-W. Wang, M. Spector: Development of hyaluronic acid--based scaffolds for brain tissue engineering. Acta Biomaterialia 5(7) (2009) 2371-2384.
- [20] J.M. Lee, H.H.L. Edwards, C.A. Pereira, S.I. Samii: Crosslinking of tissue-derived biomaterials in 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC). J Mater Sci: Mater Med 7(9) (1996) 531-541.
- [21] K. Jarquín-Yáñez et al.: Structural Effect of Different EDC Crosslinker Concentration in Gelatin- Hyaluronic Acid Scaffolds. Journal of Bioengineering & Biomedical Science 6(2) (2016) 1-6.
- [22] B. Kaczmarek, A. Sionkowska, J. Kozlowska, A.M. Osyczka: New composite materials prepared by calcium phosphate precipitation in chitosan/collagen/hyaluronic acid sponge cross-linked by EDC/NHS. International Journal of Biological Macromolecules 107 (2018) 247-253.
- [23] N. Zhu, X. Che: Biofabrication of Tissue Scaffolds, in Advances in Biomaterials Science and Biomedical Applications, R. Pignatello, Ed. InTech (2013).
- [24] W.-Y. Yeong, C.-K. Chua, K.-F. Leong, M. Chandrasekaran, M.-W. Lee: Comparison of drying methods in the fabrication of collagen scaffold via indirect rapid prototyping. J. Biomed. Mater. Res. Part B Appl. Biomater. 82(1) (2007) 260-266.
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- [26] S. Poddar et al.: Fabrication and Cytocompatibility Evaluation of Psyllium Husk (Isabgol)/Gelatin Composite Scaffolds, Appl Biochem Biotechnol (2019). https://doi.org/10.1007/s12010-019-02958-7
- [27] N. Varshney et al.: Culturing melanocytes and fibroblasts within three-dimensional macroporous PDMS scaffolds: towards skin dressing material, Cytotechnology 71(1) (2019) 287-303.
- [28] G. Nireesha, L. Divya, C. Sowmya, N. Venkateshan, M.N. Babu, V. Lavakumar: Lyophilization/Freeze Drying - An Review. International Journal of Novel Trends in Pharmaceutical Sciences 3(4) (2013).
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Uwagi
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2019).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-11f5824a-3895-4196-a428-14283e028aa1