Fabrication and characterization of chitosan‐gelatin blend nanofibers for skin tissue engineering
Abstract
Tissue engineering scaffolds produced by electrospinning feature a structural similarity to the natural extracellular matrix. Polymer blending is one of the effective methods to provide new and desirable biocomposites for tissue engineering applications. In this study chitosan was blended with gelatin and the effect of processing parameters of electrospinning and the solution properties of the polymer on the morphology of the fibers obtained were investigated. The morphology of the electrospun chitosan, gelatin and the chitosan‐gelatin blend were characterized using a scanning electron microscope (SEM). The miscibility of the blend was determined using a SEM, and differential scanning calorimetry (DSC) Fourier transform Infrared spectrometer (FTIR). Further the tensile properties of the blend nanofibers were studied and compared with chitosan and gelatin fibers. In this study we have been able to electrospin defect‐free chitosan, gelatin and chitosan‐gelatin blend nanofibers with smooth morphology and diameter ranging from 120 to 200 nm, 100 to 150 nm, and 120–220 nm, respectively by optimizing the process and solution parameters. Chitosan and gelatin formed completely miscible blends as evidenced from DSC and FTIR measurements. The tensile strength of the chitosan‐gelatin blend nanofibers (37.91 ± 4.42 MPa) was significantly higher than the gelatin nanofibers (7.23 ± 1.15 MPa) (p < 0.05) and comparable with that of normal human skin. Thus the novel chitosan‐gelatin blend nanofiber system has potential application in skin regeneration. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2010.
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Gelatin exhibits excellent biocompatibility and biodegradability.
“Gelatin, a high-molecular-weight natural protein obtained from the hydrolysis of collagen, exhibits excellent biocompatibility and biodegradability [227,228].”
From Liver tissue engineering using decellularized scaffolds: Current progress, challenges, and opportunities (2024) · cites this paper as [228]
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Hussein, K. H., Ahmadzada, B., Correa, J. C., Sultan, A., Wilken, S., Amiot, B., & Nyberg, S. L. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.06.001 · Cited by 28 · see citing works
“Gelatin, a high-molecular-weight natural protein obtained from the hydrolysis of collagen, exhibits excellent biocompatibility and biodegradability [227,228].”
Background
- Authors
- Dhandayuthapani, B., Krishnan, U. M., & Sethuraman, S.
- Affiliations
- SASTRA University (IN)
- Corresponding author
- Sethuraman, Swaminathan
- Venue
- Journal of Biomedical Materials Research Part B: Applied Biomaterials
- Publisher
- Wiley
- Published
- 2010-05-12
- Volume
- 94B
- Issue
- 1
- Pages
- 264-272
- ISSN
- 1552-4973 (ISSN-L)
- 1552-4981
- OpenAlex
- W2111040259
- Cited by
- 261
- References
- 0
- Citations by year
- 2026: 5 · 2025: 7 · 2024: 12 · 2023: 17 · 2022: 15 · 2021: 22 · 2020: 24 · 2019: 22 · 2018: 23 · 2017: 19 · 2016: 19 · 2015: 18 · 2014: 24 · 2013: 9 · 2012: 13
- FWCI
- 4.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Biomedical Materials Research Part B Applied Biomaterials (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Electrospun Nanofibers in Biomedical Applications
- Physical Sciences › Materials Science › Biomaterials › Silk-based biomaterials and applications
- Physical Sciences › Materials Science › Biomaterials › Nanocomposite Films for Food Packaging
- Keywords
- chitosan, gelatin, polymer blend nanofibers, electrospinning, skin tissue engineering, skin regeneration, tensile strength, blend miscibility, fiber morphology, extracellular matrix mimicry, biocomposites
- MeSH terms
- Biocompatible Materials, Calorimetry, Differential Scanning, Gelatin, Humans, Skin, Surface Properties, Tensile Strength, Spectroscopy, Fourier Transform Infrared, Tissue Engineering, Chitosan, Tissue Scaffolds, Electrochemical Techniques, Nanofibers
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