The objective of this work was to assess the potential effect of bone marrow mast cells (BMMCs) on burn wound healing in rats. We included 45 male rats into three groups of 15 animals each: CNTRL group: We treated the burn wounds with normal saline (0.1 ml). TRTMENT group: In this group, the burn wounds were treated with bone marrow mast cells (1× 106/ml). SSD (Positive control) group: In this group, the wounds were treated with silver sulfadiazine 1% ointment. Wound area reduction measurements, histopathological studies, and biochemical assessments levels showed significant differences between rats in TRTMENT group in comparison with other groups (p < 0.05). Accelerated repair of the wounds in TRTMENT group showed that local application of BMMCs could be taken into consideration in burn wound healing.
Jeschke MG, van Baar ME, Choudhry, M A, Chung K K, Gibran N S, Logsetty, S. Burn injury. Nature Reviews. Disease Primers. 2020: 6(1): 11. doi: 10.1038/s41572-020-0145-5
Stone IR, Natesan S, Kowalczewski CJ, Mangum LH, Clay NE, Clohessy RM, Carlsson AH, Tassin, DH, Chan RK, Rizzo JA, Christy RJ. Advancements in regenerative strategies through the continuum of burn care. Frontiers in Pharmacology. 2018; 9: 672. doi: 10.3389/fphar.2018.00672
Leclerc T, Thepenier C, Jault P, Bey E, Peltzer J, Trouillas M, Duhamel P, Bargues L, Prat M, Bonderriter M, Lataillade JJ. Cell therapy of burns. Cell Proliferation. 2011; 44 (Suppl 1): 48–54. doi: 10.1111/j.1365-2184.2010.00727.x
Zhang X, Xing H, Zhao Y, Ma Z. Pharmaceutical dispersion techniques for dissolution and bioavailability enhancement of poorly water-soluble drugs. Pharmaceutics. 2018; 10(3): 74. doi: 10.3390/pharmaceutics10030074
Carsin H, Ainaud P, Le Bever H, Rives J, Lakhel A, Stephanazzi J, Lambert F, Perrot J. Cultured epithelial autografts in extensive burn coverage of severely traumatized patients: a five year single‐center experience with 30 patients. Burns. 2000; 26: 379–387. doi: 10.1016/s0305-4179(99)00143-6
Srivastava S, Mishra S, Dewangan J, Divakar A, Gupta N, Kalleti N, Mugale MN, Kumar S, Sharma S, Rath SK. Safety assessment of the pharmacological excipient, diethylene glycol monoethyl ether (DEGEE), using in vitro and in vivo systems. Daru. 2019; 27(1): 219–231. doi: 10.1007/s40199-019-00264-5
van Eeden CM, Liebenberg W, du Preez JL, de Villiers MM. Solvent and surfactant enhanced solubilization, stabilization, and degradation of amitraz. Journal of environmental science and health. Part. B, Pesticides, Food Contaminants, and Agricultural Wastes. 2044; 39(1): 33–51. doi: 10.1081/pfc-120027437
Singhal M, Baumgartner A, Turunen E, van Veen B, Hirvonen J, Peltonen L. Nanosuspensions of a poorly soluble investigational molecule ODM-106: Impact of milling bead diameter and stabilizer concentration. International Journal of Pharmaceutics. 2020; 587: 119636. doi: 10.1016/j.ijpharm.2020.119636
Ahmadi Tehrani A, Omranpoor MM, Vatanara A, Seyedabadi M, Ramezani V. Formation of nanosuspensions in bottom-up approach: theories and optimization. Daru. 2019; 27(1): 451–473. doi: 10.1007/s40199-018-00235-2
Zhao M, Lee SH, Song JG, Kim HY, Han HK. Enhanced oral absorption of sorafenib via the layer-by-layer deposition of a pH-sensitive polymer and glycol chitosan on the liposome. International Journal of Pharmaceutic. 2018; 544(1): 14–20. doi: 10.1016/j.ijpharm.2018.04.020
Kato Y, Onishi H, Machida,Y. Application of chitin and chitosan derivatives in the pharmaceutical field. Current Pharmaceutical Biotechnology. 2003; 4(5): 303–309. doi: 10.2174/1389201033489748
Brey Gil VS, Brey Gil CS, Goulart G, Oréfice RL. Multi-drug hybrid delivery systems with distinct release profiles based on gelatin/collagen containing vesicles derived from block copolymers. International Journal of Biological Macromolecules. 2019; 139: 967–974. doi: 10.1016/j.ijbiomac.2019.08.056
Sadeghinia A, Soltani S, Aghazadeh M, Khalilifard J, Davaran, S. Design and fabrication of clinoptilolite-nanohydroxyapatite/chitosan-gelatin composite scaffold and evaluation of its effects on bone tissue engineering. Journal of Biomedical Materials Research. Part A. 2020; 108(2): 221–233. doi: 10.1002/jbm.a.36806
Cheng YH, Ko YC, Chang YF, Huang SH, Liu CJ. Thermosensitive chitosan-gelatin-based hydrogel containing curcumin-loaded nanoparticles and latanoprost as a dual-drug delivery system for glaucoma treatment. Experimental Eye Research. 2019; 179: 179–187. doi: 10.1016/j.exer.2018.11.017
Farnia P, Mollaei, S , Bahrami A, Ghassempour A, Velayati AA, Ghanavi J. Improvement of curcumin solubility by polyethylene glycol/chitosan-gelatin nanoparticles (CUR-PEG/CS-G-nps). Biomedical Research. 2016; 27 (3): 659-665.
Bamrungsap S, Zhao Z, Chen T, Wang L, Li C, Fu T, Tan W. Nanotechnology in therapeutics: a focus on nanoparticles as a drug delivery system. Nanomedicine. 2012; 7(8): 1253–1271. doi: 10.2217/nnm.12.87
Qiu Z, Kwon AH, Kamiyama Y. Effects of plasma fibronectin on the healing of full-thickness skin wounds in streptozotocin-induced diabetic rats. The Journal of Surgical Research. 2007; 138(1): 64–70. doi: 10.1016/j.jss.2006.06.034
Taghavifar S, Afroughi F,Saadati Keyvan M. Curcumin nanoparticles improved diabetic wounds infected with methicillin-resistant Staphylococcus aureus sensitized with HAMLET. The International Journal of Lower Extremity Wounds. 2022; 21(2): 141-153. doi: 10.1177/1534734620933079
Guo S, Fang Q, Chen L, Yu M, Chen Y, Li N, Han C, Hu X. Locally activated mitophagy contributes to a "built-in" protection against early burn-wound progression in rats. Life Sciences. 2021; 276: 119095. doi: 10.1016/j.lfs.2021.119095
Kassem A, Ayoub GM, Malaeb L. Antibacterial activity of chitosan nano-composites and carbon nanotubes: a review. The Science of the Total Environment. 2019; 668: 566–576. doi: 10.1016/j.scitotenv.2019.02.446
Stoica AE, Chircov C, Grumezescu AM. Nanomaterials for wound dressings: an up-to-date overview. Molecules. 2020; 25(11): 2699. doi: 10.3390/molecules25112699
Kallel I, Hadrich B, Gargouri B, Chaabane A, Lassoued S, Gdoura R, Bayoudh A, Ben Messaoud E. Optimization of cinnamon (Cinnamomum zeylanicum blume) essential oil extraction: evaluation of antioxidant and antiproliferative effects. Evidence-Based Complementary and Alternative Medicine: eCAM. 2019, 6498347. doi: 10.1155/2019/6498347
Aziz Z, Abdul Rasool Hassan B. The effects of honey compared to silver sulfadiazine for the treatment of burns: a systematic review of randomized controlled trials. Burns. 2017; 43(1): 50–57. doi: 10.1016/j.burns.2016.07.004
Patrulea V, Ostafe V, Borchard G, Jordan O. Chitosan as a starting material for wound healing applications. European Journal of Pharmaceutics and Biopharmaceutics. 2015; 97(Pt B): 417–426. doi: 10.1016/j.ejpb.2015.08.004
Diegelmann RF, Evans MC. Wound healing: an overview of acute, fibrotic and delayed healing. Frontiers in Bioscience. 2004; 9: 283–289. doi: 10.2741/1184
Marchete R, Oliveira S, Bagne L, Silva JIS, Valverde AP, Aro AA, Figueira MM, Fronza M, Bressam TM, Goes VFF, Gaspari de Gaspi FO, Dos Santos GMT, Andrade TAM. Anti-inflammatory and antioxidant properties of Alternanthera brasiliana improve cutaneous wound healing in rats. Inflammopharmacology. 2021; 29(5): 1443–1458. doi: 10.1007/s10787-021-00862-3
Chen D, Hao H, Fu X, Han W. Insight into reepithelialization: how do mesenchymal stem cells perform? Stem Cells International. 2016; 2016: 6120173. doi: 10.1155/2016/6120173
Samdavid Thanapaul R, Ranjan A, Manikandan SK, Nadar M. Efficacy of Lobelia alsinoides Lam ethanolic extract on a third-degree burn: An experimental study on rats. Dermatologic Therapy. 2020; 33(6): e14242. doi: 10.1111/dth.14242
Ladhani HA, Yowler CJ, Claridge JA. Burn wound colonization, infection, and sepsis. Surgical Infections. 2021; 22(1): 44–48. doi: 10.1089/sur.2020.346
Gibson-Corley KN, Olivier AK, Meyerholz,D K. Principles for valid histopathologic scoring in research. Veterinary Pathology. 2013; 50(6): 1007–1015. doi: 10.1177/0300985813485099
Mousazadeh,S. , Amniattalab,A. and Mohammadi,R. (2024). Evaluation of Potential Effect of Bone Marrow Mast Cells on Burn Wound Healing in Rat. Iranian Journal of Veterinary Surgery, 19(2), 82-88. doi: 10.30500/ivsa.2024.446910.1392
MLA
Mousazadeh,S. , , Amniattalab,A. , and Mohammadi,R. . "Evaluation of Potential Effect of Bone Marrow Mast Cells on Burn Wound Healing in Rat", Iranian Journal of Veterinary Surgery, 19, 2, 2024, 82-88. doi: 10.30500/ivsa.2024.446910.1392
HARVARD
Mousazadeh S., Amniattalab A., Mohammadi R. (2024). 'Evaluation of Potential Effect of Bone Marrow Mast Cells on Burn Wound Healing in Rat', Iranian Journal of Veterinary Surgery, 19(2), pp. 82-88. doi: 10.30500/ivsa.2024.446910.1392
CHICAGO
S. Mousazadeh, A. Amniattalab and R. Mohammadi, "Evaluation of Potential Effect of Bone Marrow Mast Cells on Burn Wound Healing in Rat," Iranian Journal of Veterinary Surgery, 19 2 (2024): 82-88, doi: 10.30500/ivsa.2024.446910.1392
VANCOUVER
Mousazadeh S., Amniattalab A., Mohammadi R. Evaluation of Potential Effect of Bone Marrow Mast Cells on Burn Wound Healing in Rat. Iran J Vet Surg, 2024; 19(2): 82-88. doi: 10.30500/ivsa.2024.446910.1392