Volume 29, Issue 134 (May & June 2021)                   J Adv Med Biomed Res 2021, 29(134): 152-160 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Nuoroozi G, Omidi M, Rajabibazl M, Hoseinpoor R. Synergistic Effects of Graphene Oxide and Vascular Endothelial Growth Factor Immobilized in Polycaprolactone Nanofiber as a Candidate for Diabetic Wound Healing. J Adv Med Biomed Res 2021; 29 (134) :152-160
URL: http://journal.zums.ac.ir/article-1-6041-en.html
1- Dept. of Clinical Biochemistry, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
2- Protein Research Center, Shahid Beheshti University, Tehran, Iran
3- Dept. of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran , rajabibazl_m@yahoo.com
4- Dept. of Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract:   (135490 Views)

   Background & Objective: The combination of two or more therapeutic agents and their synergetic impacts can be therapeutically effective against multifactorial diseases, such as diabetic foot ulcers. This study demonstrates the application of a nanofiber-based drug delivery system with a controlled release of the growth factor. Various studies have shown that vascular endothelial growth factor (VEGF) stimulates angiogenesis via the VEGF signaling pathway and graphene oxide (GO) has been reported to possess antibacterial property. Therefore, VEGF and GO are hypothesized to have wound-healing effects when used synergistically.
 Materials & Methods:  In this study, VEGF was purified and verified by western blotting. GO and polycaprolactone (PCL) were prepared by electrospinning and were characterized by scanning electron microscope. Next, VEGF was immobilized by EDC/NHS linker in PCL-GO. Staphylococcus aureus and Escherichia coli were used to evaluate the antibacterial property of GO. Biodegradation and other release properties of the nanofibers were assessed. Moreover, the nanofibers were studied for cell viability and gene expression using human umbilical vein endothelial cells.
 Results:  The re-analysis of the protein-protein interaction network from the GO database confirmed the centrality of the nitric oxide synthase 3 (eNOS) showing its effects on the expression of other proteins. In addition, the PCL-GO nanofiber loaded with VEGF was studied for the expression of the eNOS gene in the VEGF signaling pathway. It was observed that PCL-GO-VEGF led to an increased expression of the eNOS gene in two weeks.
 Conclusion:   Based on the observed antibacterial property and angiogenesis influence, PCL-GO-VEGF can be considered as a candidate to promote diabetic wound healing.

 
 
Full-Text [PDF 682 kb]   (150749 Downloads) |   |   Full-Text (HTML)  (3177 Views)  

Based on the observed antibacterial property and angiogenesis influence, PCL-GO-VEGF can be considered as a candidate to promote diabetic wound healing.


Type of Study: Original Research Article | Subject: Bionanotechnology
Received: 2020/05/31 | Accepted: 2020/10/4 | Published: 2020/12/30

References
1. de Smet GH, Kroese LF, Menon AG, et al. Oxygen therapies and their effects on wound healing. Wound Repair Regenerat. 2017;25(4):591-608. [DOI:10.1111/wrr.12561] [PMID]
2. Tardáguila‐García A, García‐Morales E, García‐Alamino JM, Álvaro‐Afonso FJ, Molines‐Barroso RJ, Lázaro‐Martínez JL. Metalloproteinases in chronic and acute wounds: A systematic review and meta‐analysis. Wound Repair Regenerat. 2019;27(4):415-20. [DOI:10.1111/wrr.12717] [PMID]
3. Tahergorabi Z, Khazaei M. Imbalance of angiogenesis in diabetic complications: the mechanisms. Int J Prevent Med. 2012;3(12):827. [DOI:10.4103/2008-7802.104853] [PMID] [PMCID]
4. Bao P, Kodra A, Tomic-Canic M, Golinko MS, Ehrlich HP, Brem H. The role of vascular endothelial growth factor in wound healing. J Surg Res. 2009;153(2):347-58. [DOI:10.1016/j.jss.2008.04.023] [PMID] [PMCID]
5. Abhinand CS, Raju R, Soumya SJ, Arya PS, Sudhakaran PR. VEGF-A/VEGFR2 signaling network in endothelial cells relevant to angiogenesis. J Cell Communicat Signal. 2016;10(4):347-54. [DOI:10.1007/s12079-016-0352-8] [PMID] [PMCID]
6. Geng H, Song H, Qi J, Cui D. Sustained release of VEGF from PLGA nanoparticles embedded thermo-sensitive hydrogel in full-thickness porcine bladder acellular matrix. Nanoscale Res Lett. 2011;6(1):312. [DOI:10.1186/1556-276X-6-312] [PMID] [PMCID]
7. Briquez PS, Hubbell JA, Martino MM. Extracellular matrix-inspired growth factor delivery systems for skin wound healing. Adv Wound Care. 2015;4(8):479-89. [DOI:10.1089/wound.2014.0603] [PMID] [PMCID]
8. Wang Z, Lu WW, Zhen W, Yang D, Peng S. Novel biomaterial strategies for controlled growth factor delivery for biomedical applications. NPG Asia Materials. 2017;9(10):e435-e. [DOI:10.1038/am.2017.171]
9. Chen RR, Mooney DJ. Polymeric growth factor delivery strategies for tissue engineering. Pharmaceut Res. 2003;20(8):1103-12. [DOI:10.1023/A:1025034925152] [PMID]
10. Praveen G, Sreerekha P, Menon D, Nair SV, Chennazhi KP. Fibrin nanoconstructs: a novel processing method and their use as controlled delivery agents. Nanotechnol. 2012;23(9):095102. [DOI:10.1088/0957-4484/23/9/095102] [PMID]
11. Brannigan RP, Dove AP. Synthesis, properties and biomedical applications of hydrolytically degradable materials based on aliphatic polyesters and polycarbonates. Biomater Sci. 2017;5(1):9-21. [DOI:10.1039/C6BM00584E] [PMID]
12. Chen S, Li X, Yang Z, et al. A simple one-step modification of various materials for introducing effective multi-functional groups. Colloids and Surfaces B: Biointerfaces. 2014;113:125-33. [DOI:10.1016/j.colsurfb.2013.08.041] [PMID]
13. Dideikin AT, Vul AY. Graphene oxide and derivatives: the place in graphene family. Front Physics. 2019;6:149. [DOI:10.3389/fphy.2018.00149]
14. Mahmoudi N, Eslahi N, Mehdipour A, et al. Temporary skin grafts based on hybrid graphene oxide-natural biopolymer nanofibers as effective wound healing substitutes: pre-clinical and pathological studies in animal models. J Mater Sci Mater Med. 2017;28(5):73. [DOI:10.1007/s10856-017-5874-y] [PMID]
15. Lu B, Li T, Zhao H, et al. Graphene-based composite materials beneficial to wound healing. Nanoscale. 2012;4(9):2978-82. [DOI:10.1039/c2nr11958g] [PMID]
16. Khan MS, Abdelhamid HN, Wu H-F. Near infrared (NIR) laser mediated surface activation of graphene oxide nanoflakes for efficient antibacterial, antifungal and wound healing treatment. Colloids and Surfaces B: Biointerfaces. 2015;127:281-91. [DOI:10.1016/j.colsurfb.2014.12.049] [PMID]
17. Ebrahimizadeh W, Gargari SLMM, Javidan Z, Rajabibazl M. Production of novel VHH nanobody inhibiting angiogenesis by targeting binding site of VEGF. App Biochem Biotechnol. 2015;176(7):1985-95. [DOI:10.1007/s12010-015-1695-y] [PMID]
18. Afarideh B, Rajabibazl M, Omidi M, Yaghmaee B, Rahimpour A, Khodabakhshi R. Anticancer activity of graphene oxide/5-FU on CT26 Ds-Red adenocarcinoma cell line. Orient J Chem. 2018;34(4):2002-7. [DOI:10.13005/ojc/3404038]
19. Ul-Islam M, Khattak WA, Ullah MW, Khan S, Park JK. Synthesis of regenerated bacterial cellulose-zinc oxide nanocomposite films for biomedical applications. Cellulose. 2014;21(1):433-47. [DOI:10.1007/s10570-013-0109-y]
20. Bastian M, Heymann S, Jacomy M. Gephi: an open source software for exploring and manipulating networks. Third international AAAI conference on weblogs and social media; 2009.
21. Davis FM, Kimball A, Boniakowski A, Gallagher K. Dysfunctional wound healing in diabetic foot ulcers: new crossroads. Curr Diabet Report. 2018;18(1):2. [DOI:10.1007/s11892-018-0970-z] [PMID]
22. Masters KS. Covalent growth factor immobilization strategies for tissue repair and regeneration. Macromolec Biosci. 2011;11(9):1149-63. [DOI:10.1002/mabi.201000505] [PMID]
23. Han FY, Thurecht KJ, Whittaker AK, Smith MT. Bioerodable PLGA-based microparticles for producing sustained-release drug formulations and strategies for improving drug loading. Front Pharmacol. 2016;7:185. [DOI:10.3389/fphar.2016.00185] [PMID] [PMCID]
24. Borselli C, Ungaro F, Oliviero O, et al. Bioactivation of collagen matrices through sustained VEGF release from PLGA microspheres. J Biomed Mater Res A. 2010;92(1):94-102. [DOI:10.1002/jbm.a.32332] [PMID]
25. Szunerits S, Boukherroub R. Antibacterial activity of graphene-based materials. J Mater Chem B. 2016;4(43):6892-912. [DOI:10.1039/C6TB01647B] [PMID]

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2025 CC BY-NC 4.0 | Journal of Advances in Medical and Biomedical Research

Designed & Developed by : Yektaweb