The effect of chrysin–curcumin-loaded nanofibres on the wound-healing process in male rats

References

• Mohammadi Z, Sharif Zak M, Majdi H, et al. The effect of chrysin-loaded nanofiber on wound healing process in male rat. Chem Biol Drug Des. 2017;90:1106–1114.
   PubMed Web of Science ®Google Scholar
• Tan L, Hou Z, Gao Y. Efficacy of combined treatment with vacuum sealing drainage and recombinant human epidermal growth factor for refractory wounds in the extremities and its effect on serum levels of IL-6, TNF-α and IL-2. Exp Ther Med. 2018;15:288–294.
   PubMed Web of Science ®Google Scholar
• Victor-Vega C, Desai A, Montesinos MC, et al. Adenosine A2A receptor agonists promote more rapid wound healing than recombinant human platelet-derived growth factor (Becaplermin gel). Inflammation. 2002;26:19–24.
   PubMed Web of Science ®Google Scholar
• Braverman B, McCarthy RJ, Ivankovich AD, et al. Effect of helium-neon and infrared laser irradiation on wound healing in rabbits. Lasers Surg Med. 1989;9:50–58.
   PubMed Web of Science ®Google Scholar
• Kloth LC. Electrical stimulation for wound healing: A review of evidence from in vitro studies, animal experiments, and clinical trials. Int J Low Extrem Wounds. 2005;4:23–44.
   PubMedGoogle Scholar
• Bloch W, Huggel K, Sasaki T, et al. The angiogenesis inhibitor endostatin impairs blood vessel maturation during wound healing. FASEB J. 2000;14:2373–2376.
   PubMed Web of Science ®Google Scholar
• Hunt TK. Vitamin A and wound healing. J Am Acad Dermatol. 1986;15:817–821.
   PubMed Web of Science ®Google Scholar
• Kaplan B, Gonul B, Dincer S, Dincer Kaya FN, et al. Relationships between tensile strength, ascorbic acid, hydroxyproline, and zinc levels of rabbit full-thickness incision wound healing. Surg Today. 2004;34:747–751.
   PubMed Web of Science ®Google Scholar
• Cross KJ, Mustoe TA. Growth factors in wound healing. Surg Clin North Am. 2003;83:531–545.
   PubMed Web of Science ®Google Scholar
• Tejada S, Manayi A, Daglia M, et al. Wound healing effect of curcumin: a review. Curr Pharm Biotechnol 2016; 17: 1002-1007.
   Web of Science ®Google Scholar
• Firooz A, Bouzari N, Mojtahed F, et al. Topical immunotherapy with diphencyprone in the treatment of extensive and/or long-lasting alopecia areata. J Eur Acad Dermatol Venereol. 2005;19:393–394.
   PubMed Web of Science ®Google Scholar
• Pazoki-Toroudi H, Nilforoushzadeh MA, Ajami M, et al. Combination of azelaic acid 5% and clindamycin 2% for the treatment of acne vulgaris. Cutan Ocul Toxicol. 2011;30:286–291.
   PubMed Web of Science ®Google Scholar
• Toroudi HP, Rahgozar M, Bakhtiarian A, et al. Potassium channel modulators and indomethacin-induced gastric ulceration in rats. Scand J Gastroenterol. 1999;34:962–966.
   PubMed Web of Science ®Google Scholar
• Lee DS, Sinno S, Khachemoune A. Honey and wound healing: An overview. Am J Clin Dermatol. 2011;12:181–190.
   PubMed Web of Science ®Google Scholar
• Broughton G, Janis JE, Attinger CE. The basic science of wound healing. Plast Reconstr Surg. 2006;117:12S–34S.
   PubMed Web of Science ®Google Scholar
• Martin P. Wound healing-aiming for perfect skin regeneration. Science. 1997;276:75–81.
   PubMed Web of Science ®Google Scholar
• Reinders Y, Felthaus O, Brockhoff G, et al. Impact of platelet-rich plasma on viability and proliferation in wound healing processes after external radiation. IJMS. 2017;18:1819.
   Web of Science ®Google Scholar
• Edwards R, Harding KG. Bacteria and wound healing. Curr Opin Infect Dis. 2004;17:91–96.
   PubMed Web of Science ®Google Scholar
• Browne AC, Vearncombe M, Sibbald RG. High bacterial load in asymptomatic diabetic patients with neurotrophic ulcers retards wound healing after application of Dermagraft. Ostomy Wound Manage. 2001;47:44–49.
   PubMedGoogle Scholar
• Shivakumar M, Ramalingam S, Natarajan D. Larvicidal potential of some India medicinal plant extracts against Aedes aegypti (L). Asian J Pharm Clin Res. 2013;6: 77-80.
   Google Scholar
• Veer V, Gopalakrishnan R. Herbal insecticides, repellents and biomedicines: effectiveness and commercialization. New Delhi, India: Springer; 2016.
   Google Scholar
• Mukhtar MD, Sani A, Yakasai AA. Cytotoxicity of fractions of Pistia stratiotes l. On larvae of Culex mosquito and A. salina. Anim Res Int. 2004;1; 95-99.
   Google Scholar
• Karou SD, Savadogo A, Canini A, et al. Antibacterial activity of alkaloids from Sida acuta. Afr J Biotechnol. 2006;5; 195-200.
   Google Scholar
• Chelela B, Chacha M, Matemu A. Larvicidal potential of wild mushroom extracts against Culex quinquefasciatus Say, Aedes aegypti and Anopheles gambiae Giles S.S. Am J Res Commun. 2014;2:2325–4076.
   Google Scholar
• Mandal S, DebMandal M, Pal NK, et al. Antibacterial activity of honey against clinical isolates of Escherichia coli, Pseudomonas aeruginosa and Salmonella enterica serovar Typhi. Asian Pacific J Trop Med. 2010;3:961–964.
   Web of Science ®Google Scholar
• Willix DJ, Molan PC, Harfoot CG. A comparison of the sensitivity of wound-infecting species of bacteria to the antibacterial activity of manuka honey and other honey. J Appl Bacteriol. 1992;73:388–394.
   PubMedGoogle Scholar
• Al-Waili N, Salom K, Al-Ghamdi AA. Honey for wound healing, ulcers, and burns; data supporting its use in clinical practice. ScientificWorldJ. 2011;11:766–787.
   PubMed Web of Science ®Google Scholar
• Mostafavi, E. Soltantabar, P. Webster, TJ. Nanotechnology and picotechnology: A new arena for translational medicine. In: Biomaterials in translational medicine. Academic Press; 2019. p. 191–212.
   Google Scholar
• Cho H, Yun CW, Park WK, et al. Modulation of the activity of pro-inflammatory enzymes, COX-2 and iNOS, by chrysin derivatives. Pharmacol Res. 2004;49:37–43.
   PubMed Web of Science ®Google Scholar
• Fonseca SF, Padilha NB, Thurow S, et al. Ultrasound-promoted copper-catalyzed synthesis of bis-arylselanyl chrysin derivatives with boosted antioxidant and anticancer activities. Ultrason Sonochem. 2017;39:827–836.
   PubMed Web of Science ®Google Scholar
• Asadi N, Annabi N, Mostafavi E, et al. Synthesis, characterization and in vitro evaluation of magnetic nanoparticles modified with PCL-PEG-PCL for controlled delivery of 5FU. Artif Cells Nanomed Biotechnol. 2018;46:938–945.
   PubMed Web of Science ®Google Scholar
• Munin A, Edwards-Lévy F. Encapsulation of natural polyphenolic compounds; a review. Pharmaceutics. 2011;3:793–829.
   PubMedGoogle Scholar
• Mat Nor MS, Manan Z, Mustaffa A, et al. Solubility prediction of flavonoids using new developed UNIFAC-based model. Chem Eng Trans. 2017;56: 799-804.
   Google Scholar
• Rahmani Del Bakhshayesh A, Mostafavi E, Alizadeh E, et al. Fabrication of three-dimensional scaffolds based on nano-biomimetic collagen hybrid constructs for skin tissue engineering. ACS Omega. 2018;3:8605–8611.
   PubMed Web of Science ®Google Scholar
• Hafezi F, Gatzioufas Z, Angunawela R, et al. Absence of IL-6 prevents corneal wound healing after deep excimer laser ablation in vivo. Eye (Lond). 2018;32:156–157.
   PubMed Web of Science ®Google Scholar
• Lin ZQ, Kondo T, Ishida Y, et al. Essential involvement of IL-6 in the skin wound-healing process as evidenced by delayed wound healing in IL-6-deficient mice. J Leukoc Biol. 2003;73:713–721.
   PubMed Web of Science ®Google Scholar
• Kunkemoeller B, Kyriakides TR. Redox signaling in diabetic wound healing regulates extracellular matrix deposition. Antioxid Redox Signal. 2017;27:823–838.
   PubMed Web of Science ®Google Scholar
• Vaalamo M, Leivo T, Saarialho-Kere U. Differential expression of tissue inhibitors of metalloproteinases (TIMP-1, -2, -3, and -4) in normal and aberrant wound healing. Hum Pathol. 1999;30:795–802.
   PubMed Web of Science ®Google Scholar
• A Abd El-Aleem S, Muftah AA, B Jude E. Immunohistochemical characterization of the inflammatory responses in wound healing and the use of the subcutaneous polyvinyl alcohol (PVA) sponge implantation for evaluation of the healing process. J Cytol Histol. 2018;09: 519.
   Google Scholar
• Shi HP, Most D, Efron DT, et al. The role of iNOS in wound healing. Surgery 2001;130:225–229.
   PubMed Web of Science ®Google Scholar
• Ellies LG, Hingorani DV, Lippert CN, et al. Impact of MMP-2 and MMP-9 activation on wound healing. Tumor Growth and RACPP Cleavage. BioRxiv . 2018: 327791.
   Google Scholar
• Wysocki AB, Staiano-Coico L, Grinnell F. Wound fluid from chronic leg ulcers contains elevated levels of metalloproteinases MMP-2 and MMP-9. J Invest Dermatol. 1993;101:64–68.
   PubMed Web of Science ®Google Scholar
• Akira S, Kishimoto T. IL-6 and NF-IL6 in acute-phase response and viral infection. Immunol Rev. 1992;127:25–50.
   PubMed Web of Science ®Google Scholar
• Xue M, Jackson CJ. Extracellular matrix reorganization during wound healing and its impact on abnormal scarring. Adv Wound Care (New Rochelle). 2015;4:119–136.
   PubMed Web of Science ®Google Scholar
• Badr G, Hozzein WN, Badr BM, et al. Bee venom accelerates wound healing in diabetic mice by suppressing activating transcription factor-3 (ATF-3) and inducible nitric oxide synthase (iNOS)-mediated oxidative stress and recruiting bone marrow-derived endothelial progenitor cells. J Cell Physiol. 2016;231:2159–2171.
   PubMed Web of Science ®Google Scholar
• Javedan G, Shidfar F, Davoodi SH, et al. Conjugated linoleic acid rat pretreatment reduces renal damage in ischemia/reperfusion injury: unraveling antiapoptotic mechanisms and regulation of phosphorylated mammalian target of rapamycin. Mol Nutr Food Res. 2016;60:2665–2677.
   PubMed Web of Science ®Google Scholar
• Mehrjerdi FZ, Aboutaleb N, Pazoki-Toroudi H, et al. The protective effect of remote renal preconditioning against hippocampal ischemia reperfusion injury: role of KATP channels. J Mol Neurosci. 2015;57:554–560.
   PubMed Web of Science ®Google Scholar
• Habibey R, Ajami M, Ebrahimi SA, et al. Nitric oxide and renal protection in morphine-dependent rats. Free Radic Biol Med. 2010;49:1109–1118.
   PubMed Web of Science ®Google Scholar
• Arabian M, Aboutaleb N, Soleimani M, et al. Role of morphine preconditioning and nitric oxide following brain ischemia reperfusion injury in mice. Iran J Basic Med Sci. 2015;18:14–21.
   PubMed Web of Science ®Google Scholar
• Mellor LF, Huebner P, Cai S, et al. Fabrication and evaluation of electrospun, 3D-bioplotted, and combination of electrospun/3D-bioplotted scaffolds for tissue engineering applications. Biomed Res Int. 2017;2017:6956794.
   PubMed Web of Science ®Google Scholar
• Saghati, S, Akbarzadeh, A, Del Bakhshayesh, A, et al. Electrospinning and 3D Printing: Prospects for Market Opportunity. Electrospinning 2018;136–155.
   Google Scholar
• Mei L, Wang Y, Tong A, et al. Facile electrospinning of an efficient drug delivery system. Expert Opin Drug Deliv. 2016;13:741–753.
   PubMed Web of Science ®Google Scholar
• Mei L, Fan R, Li X, et al. Nanofibers for improving the wound repair process: the combination of a grafted chitosan and an antioxidant agent. Polym Chem. 2017;8:1664–1671.
   Web of Science ®Google Scholar
• Kamble P, Sadarani B, Majumdar A, et al. Nanofiber based drug delivery systems for skin: A promising therapeutic approach. J Drug Deliv Sci Technol. 2017;41:124–133.
   Web of Science ®Google Scholar
• Kishimoto T, Akira S, Taga T. Interleukin-6 and its receptor: A paradigm for cytokines. Science. 1992;258:593–597.
   PubMed Web of Science ®Google Scholar
• Natsume M, Tsuji H, Harada A, et al. Attenuated liver fibrosis and depressed serum albumin levels in carbon tetrachloride-treated IL-6-deficient mice. J Leukoc Biol. 1999;66:601–608.
   PubMed Web of Science ®Google Scholar
• Romano M, Sironi M, Toniatti C, et al. Role of IL-6 and its soluble receptor in induction of chemokines and leukocyte recruitment. Immunity. 1997;6:315–325.
   PubMed Web of Science ®Google Scholar
• Salo T, Mäkelä M, Kylmäniemi M, et al. Expression of matrix metalloproteinase-2 and -9 during early human wound healing. Lab Invest. 1994;70:176–182.
   PubMed Web of Science ®Google Scholar
• Caley MP, Martins VLC, O'Toole EA. Metalloproteinases and wound healing. Adv Wound Care (New Rochelle). 2015;4:225–234.
   PubMed Web of Science ®Google Scholar
• Ravanti L, Toriseva M, Penttinen R, et al. Expression of human collagenase-3 (MMP-13) by fetal skin fibroblasts is induced by transforming growth factor beta via p38 mitogen-activated protein kinase. FASEB J. 2001;15: 1098-1100.
   Web of Science ®Google Scholar
• Nwomeh BC, Liang HX, Diegelmann RF, et al. Dynamics of the matrix metalloproteinases MMP-1 and MMP-8 in acute open human dermal wounds. Wound Repair Regen. 1998;6:127–134.
   PubMedGoogle Scholar
• Hartenstein B, Dittrich BT, Stickens D, et al. Epidermal development and wound healing in matrix metalloproteinase 13-deficient mice. J Invest Dermatol. 2006;126:486–496.
   PubMed Web of Science ®Google Scholar
• Park JE, Barbul A. Understanding the role of immune regulation in wound healing. The Am J Surg. 2004;187:S11–S16.
   PubMed Web of Science ®Google Scholar