Show source-provided references
1. International Diabetes Federation (2023, October 17). IDF Diabetes Atlas. 10th ed. Available online: https://www.diabetesatlas.org.
4. World Health Organization (2023). Key Facts About Diabetes. Diabetes 2022, WHO.
5. Sanapalli, B.K.R., Yele, V., Singh, M.K., Thaggikuppe Krishnamurthy, P., and Karri, V.V.S.R. (2021). Preclinical models of diabetic wound healing: A critical review. Biomed. Pharmacother., 142.
10.1016/j.biopha.2021.111946 ↗6. Patel, S., Srivastava, S., Singh, M.R., and Singh, D. (2019). Mechanistic insight into diabetic wounds: Pathogenesis, molecular targets and treatment strategies to pace wound healing. Biomed. Pharmacother., 112.
10.1016/j.biopha.2019.108615 ↗9. Awasthi, A., Gulati, M., Kumar, B., Kaur, J., Vishwas, S., Khursheed, R., Porwal, O., Alam, A., Kr, A., and Corrie, L. (2022). Recent Progress in Development of Dressings Used for Diabetic Wounds with Special Emphasis on Scaffolds. BioMed Res. Int., 2022.
10.1155/2022/1659338 ↗12. Nolan, V.C., Harrison, J., Wright, J.E.E., and Cox, J.A.G. (2020). Clinical Significance of Manuka and Medical-Grade Honey for Antibiotic-Resistant Infections: A Systematic Review. Antibiotics, 9.
10.3390/antibiotics9110766 ↗13. Antibacterial performance and in vivo diabetic wound healing of curcumin loaded gum tragacanth/poly(ε-caprolactone) electrospun nanofibers
10.1016/j.msec.2016.08.032 ↗15. Activity of Polish unifloral honeys against pathogenic bacteria and its correlation with colour, phenolic content, antioxidant capacity and other parameters
10.1111/lam.12541 ↗16. Herman, A., and Herman, A.P. (2023). Herbal Products and Their Active Constituents for Diabetic Wound Healing-Preclinical and Clinical Studies: A Systematic Review. Pharmaceutics, 15.
10.3390/pharmaceutics15010281 ↗17. Therapeutic Properties of Honey for the Management of Wounds; Is There a Role in the Armamentarium of Diabetic Foot Ulcer Treatment? Results From in vitro and in vivo Studies
10.1177/15347346211026819 ↗18. Biological properties and therapeutic activities of honey in wound healing: A narrative review and meta-analysis
10.1016/j.jtv.2015.12.002 ↗21. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9(th) edition
10.1016/j.diabres.2019.107843 ↗26. A new in vivo model using a dorsal skinfold chamber to investigate microcirculation and angiogenesis in diabetic wounds
27. Current scenario of traditional medicines in management of diabetic foot ulcers: A review
10.4239/wjd.v14.i1.1 ↗28. Prevalence of Peripheral Arterial Disease in Diabetic Foot Ulcer Patients and its Impact in Limb Salvage
10.1177/15347346211027063 ↗32. Microvascular and Macrovascular Disease and Risk for Major Peripheral Arterial Disease in Patients with Type 2 Diabetes
10.2337/dc16-0588 ↗35. Honey-induced macrophage stimulation: AP-1 and NF-κB activation and cytokine production are unrelated to LPS content of honey
10.1016/j.intimp.2013.09.014 ↗36. Cellular and molecular mechanisms of repair in acute and chronic wound healing
10.1111/bjd.13954 ↗37. Novel nano-insulin formulation modulates cytokine secretion and remodeling to accelerate diabetic wound healing
10.1016/j.nano.2018.08.013 ↗39. Antibiofilm efficacy of honey and bee-derived defensin-1 on multispecies wound biofilm
10.1099/jmm.0.000227 ↗40. Dalton, T., Dowd, S.E., Wolcott, R.D., Sun, Y., Watters, C., Griswold, J.A., and Rumbaugh, K.P. (2011). An in vivo polymicrobial biofilm wound infection model to study interspecies interactions. PLoS ONE, 6.
10.1371/journal.pone.0027317 ↗43. Decreased Macrophage Number and Activation Lead to Reduced Lymphatic Vessel Formation and Contribute to Impaired Diabetic Wound Healing
10.2353/ajpath.2007.060018 ↗44. Camel milk peptide improves wound healing in diabetic rats by orchestrating the redox status and immune response
10.1186/s12944-015-0136-9 ↗45. Levels of macrophage migration inhibitory factor and glucocorticoids in chronic wound patients and their potential interactions with impaired wound endothelial progenitor cell migration
10.1111/j.1524-475X.2012.00817.x ↗46. Fibroblasts derived from chronic diabetic ulcers differ in their response to stimulation with EGF, IGF-I, bFGF and PDGF-AB compared to controls
10.1078/0171-9335-00228 ↗48. Induction of Keratinocyte Growth Factor Expression Is reduced and Delayed During Wound Healing in the Genetically Diabetic Mouse
10.1111/1523-1747.ep12395564 ↗49. Stachura, A., Khanna, I., Krysiak, P., Paskal, W., and Włodarski, P. (2022). Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review. Int. J. Mol. Sci., 23.
10.3390/ijms23158621 ↗51. Differential expression and localization of insulin-like growth factors I and II in cutaneous wounds of diabetic and nondiabetic mice
52. Cutaneous Epithelial to Mesenchymal Transition Activator ZEB1 Regulates Wound Angiogenesis and Closure in a Glycemic Status-Dependent Manner
10.2337/db19-0202 ↗53. A comparison of two diabetic foot ulcer classification systems: The Wagner and the University of Texas wound classification systems
10.2337/diacare.24.1.84 ↗57. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections
10.1093/cid/cis346 ↗60. European Centre for Disease Prevention and Control (2009). The Bacterial Challenge: Time to Reach, European Medicines Agency.
61. O’Neill, J. (2014). Antimicrobial Resistance: Tackling a Crisis for the Health and Wealth of Nations, HM Government.
62. Synergistic Effects of Honey and Propolis toward Drug Multi-Resistant Staphylococcus Aureus, Escherichia Coli and Candida Albicans Isolates in Single and Polymicrobial Cultures
10.7150/ijms.4722 ↗64. An in vivo and in vitro investigation of the effect of Aloe vera gel ethanolic extract using animal model with diabetic foot ulcer
10.4103/0975-7406.135248 ↗65. Prospective randomized controlled study of a Chinese herbal medicine compound Tangzu Yuyang Ointment for chronic diabetic foot ulcers: A preliminary report
10.1016/j.jep.2010.10.040 ↗66. Evaluation of the topical spray containing extract and its efficacy on excision wounds in rats
10.1515/acph-2016-0018 ↗68. Phytochemicals-mediated production of hydrogen peroxide is crucial for high antibacterial activity of honeydew honey
10.1038/s41598-018-27449-3 ↗69. Yupanqui Mieles, J., Vyas, C., Aslan, E., Humphreys, G., Diver, C., and Bartolo, P. (2022). Honey: An Advanced Antimicrobial and Wound Healing Biomaterial for Tissue Engineering Applications. Pharmaceutics, 14.
10.3390/pharmaceutics14081663 ↗70. Identification and quantification of methylglyoxal as the dominant antibacterial constituent of Manuka (Leptospermum scoparium) honeys from New Zealand
10.1002/mnfr.200700282 ↗72. Brudzynski, K., and Sjaarda, C. (2014). Antibacterial Compounds of Canadian Honeys Target Bacterial Cell Wall Inducing Phenotype Changes, Growth Inhibition and Cell Lysis That Resemble Action of β-Lactam Antibiotics. PLoS ONE, 9.
10.1371/journal.pone.0106967 ↗73. Al-Kafaween, M.A., Alwahsh, M., Mohd Hilmi, A.B., and Abulebdah, D.H. (2023). Physicochemical Characteristics and Bioactive Compounds of Different Types of Honey and Their Biological and Therapeutic Properties: A Comprehensive Review. Antibiotics, 12.
10.3390/antibiotics12020337 ↗76. Kwakman, P.H.S., Velde, A.A.t., de Boer, L., Vandenbroucke-Grauls, C.M.J.E., and Zaat, S.A.J. (2011). Two Major Medicinal Honeys Have Different Mechanisms of Bactericidal Activity. PLoS ONE, 6.
10.1371/journal.pone.0017709 ↗77. Manuka honey inhibits cell division in methicillin-resistant Staphylococcus aureus
10.1093/jac/dkr340 ↗78. Brudzynski, K., Abubaker, K., and Wang, T. (2012). Powerful bacterial killing by buckwheat honeys is concentration-dependent, involves complete DNA degradation and requires hydrogen peroxide. Front. Microbiol., 3.
10.3389/fmicb.2012.00242 ↗80. Hussein, S.Z., Mohd Yusoff, K., Makpol, S., and Mohd Yusof, Y.A. (2013). Gelam Honey Attenuates Carrageenan-Induced Rat Paw Inflammation via NF-κB Pathway. PLoS ONE, 8.
10.1371/journal.pone.0072365 ↗85. Influence of honey-balm on the rate of scare formation during experimental burn wound healing in pigs
86. Manuka honey inhibits adhesion and invasion of medically important wound bacteria in vitro
10.2217/fmb.13.126 ↗91. Mode of action of hydrogen peroxide and other oxidizing agents: Differences between liquid and gas forms
10.1093/jac/dkq308 ↗92. Nolan, V.C., Harrison, J., and Cox, J.A.G. (2019). Dissecting the Antimicrobial Composition of Honey. Antibiotics, 8.
10.3390/antibiotics8040251 ↗93. Nachweis antibakterieller, hitze- und lichtempfindlicher Hemmungsstoffe (Inhibine) im Naturhonig (Blütenhonig)
10.1007/BF02178015 ↗95. The identification of inhibine, the antibacterial factor in honey, as hydrogen peroxide and its origin in a honey glucose-oxidase system
10.1016/0926-6569(63)90108-1 ↗96. Brudzynski, K., Abubaker, K., and Castle, A. (2011). Re-Examining the Role of Hydrogen Peroxide in Bacteriostatic and Bactericidal Activities of Honey. Front. Microbiol., 2.
10.3389/fmicb.2011.00213 ↗97. Topical application of honey for burn wound treatment—An overview
98. The Effect of Dilution on the Rate of Hydrogen Peroxide Production in Honey and Its Implications for Wound Healing
10.1089/10755530360623383 ↗99. Effect of hydrogen peroxide on antibacterial activities of Canadian honeys
10.1139/w06-086 ↗100. Use of hydrogen peroxide as a biocide: New consideration of its mechanisms of biocidal action
10.1093/jac/dks129 ↗