References
- 1. R. G. Frykberg and J. Banks, Challenges in the treatment of chronic wounds, Adv. Wound Care4 (2015) 560–582; https://doi.org/10.1089/wound.2015.0635
- 2. T. Shipperley, C. Martin and B. Healthcare, The physiology of wound healing : an emergency response, Surg. 35 (2011) 8–10; http://www.sciencedirect.com/science/article/pii/S0263931917301369
- 3. K. Kaplani, S. Koutsi, V. Armenis, F. G. Skondra, N. Karantzelis, S. Champeris Tsaniras and S. Taraviras, Wound healing related agents: Ongoing research and perspectives, Adv. Drug Deliv. Rev. (2018); https://doi.org/10.1016/j.addr.2018.02.007
- 4. Y.-K. Wu, N.-C. Cheng and C.-M. Cheng, Biofilms in chronic wounds: pathogenesis and diagnosis, Trends Biotechnol. 37 (2019) 505–517; https://doi.org/10.1016/j.tibtech.2018.10.011
- 5. R. J. Reiter, D.-X. Tan, L. Fuentes-Broto and M. Luciano, Chapter 8 – Melatonin: A multitasking molecule, Progress in Brain Res.181 (2010) 127–151; https://doi.org/10.1016/S0079-6123(08)81008-4
- 6. R. Hardeland, A. T. Slominski, R. M. Slominski, R. J. Reiter, M. A. Zmijewski and R. Paus, Melatonin: A cutaneous perspective on its production, metabolism, and functions, J. Invest. Dermatol.138 (2018) 490–499; https://doi.org/10.1016/j.jid.2017.10.025
- 7. A. Crooke, A. Guzman-Aranguez, A. Mediero, P. Alarma-Estrany, G. Carracedo, T. Pelaez, A. Peral and J. Pintor, Effect of melatonin and analogues on corneal wound healing: involvement of Mt2 melatonin receptor, Curr. Eye Res.40 (2015) 56–65; https://doi.org/10.3109/02713683.2014.914540
- 8. R. Song, L. Ren, H. Ma, R. Hu, H. Gao, L. Wang, X. Chen, Z. Zhao and J. Liu, Melatonin promotes diabetic wound healing in vitro by regulating keratinocyte activity, Am. J. Transl. Res.8 (2016) 4682–4693.
- 9. R. Murali, P. Thanikaivelan and K. Cheirmadurai, Melatonin in functionalized biomimetic constructs promotes rapid tissue regeneration in Wistar albino rats, J. Mater. Chem. B4 (2016) 5850; https://doi.org/10.1039/c6tb01221c.
- 10. I. Garcia-Orue, J. L. Pedraz, R. M. Hernandez and M. Igartua, Nanotechnology-based delivery systems to release growth factors and other endogenous molecules for chronic wound healing, J. Drug Deliv. Sci. Technol.42 (2017) 2–17; https://doi.org/10.1016/j.jddst.2017.03.002
- 11. J. Pardeike, A. Hommoss and R. H. Müller, Lipid nanoparticles (SLN, NLC) in cosmetic and pharmaceutical dermal products, Int. J. Pharm.366 (2009) 170–184; https://doi.org/10.1016/j.ijpharm.2008.10.003
- 12. G. Gainza, M. Pastor, J. J. Aguirre, S. Villullas, J. L. Pedraz, R. M. Hernandez and M. Igartua, A novel strategy for the treatment of chronic wounds based on the topical administration of rhEGF-loaded lipid nanoparticles: In vitro bioactivity and in vivo effectiveness in healing-impaired db/db mice, J. Control. Release185 (2014) 51–61; https://doi.org/10.1016/j.jconrel.2014.04.032
- 13. N. Karimi, B. Ghanbarzadeh, H. Hamishehkar, B. Mehramuz and H. S. Kafil, Antioxidant, antimicrobial and physicochemical properties of turmeric extract-loaded nanostructured lipid carrier (NLC), Colloid. Interface Sci. Commun.22 (2018) 18–24; https://doi.org/10.1016/j.colcom.2017.11.006
- 14. F. Saporito, G. Sandri, M. C. Bonferoni, S. Rossi, C. Boselli, A. I. Cornaglia, B. Mannucci, P. Grisoli, B. Vigani and F. Ferrari, Essential oil-loaded lipid nanoparticles for wound healing, Int. J. Nanomed.13 (2018) 175–186; https://doi.org/10.2147/IJN.S152529
- 15. Z. Ma, A. Garrido-Maestu and K. C. Jeong, Application, mode of action, and in vivo activity of chitosan and its micro- and nanoparticles as antimicrobial agents: A review, Carbohydr. Polym.176 (2017) 257–265; https://doi.org/10.1016/j.carbpol.2017.08.082
- 16. V. Patrulea, V. Ostafe, G. Borchard and O. Jordan, Chitosan as a starting material for wound healing applications, Eur. J. Pharm. Biopharm. (2015); https://doi.org/10.1016/j.ejpb.2015.08.004
- 17. M. Duvnjak Romić, M. Š. Klarić, J. Lovrić, I. Pepić, B. Cetina-Čižmek, J. Filipović-Grčić and A. Hafner, Melatonin-loaded chitosan/Pluronic® F127 microspheres as in situ forming hydrogel: An innovative antimicrobial wound dressing, Eur. J. Pharm. Biopharm.107 (2016) 67–79; https://doi.org/10.1016/j.ejpb.2016.06.013
- 18. M. Duvnjak Romić, D. Špoljarić, M. Š. Klarić, B. Cetina-Čižmek, J. Filipović-Grčić and A. Hafner, Melatonin loaded lipid enriched chitosan microspheres – Hybrid dressing for moderate exuding wounds, J. Drug Deliv. Sci. Technol. (2019); https://doi.org/10.1016/j.jddst.2019.05.004
- 19. B. N. Estevinho, F. Rocha, L. Santos and A. Alves, Microencapsulation with chitosan by spray drying for industry applications – A review, Trends Food Sci. Technol. 31 (2013) 138–155; https://doi.org/10.1016/j.tifs.2013.04.001
- 20. B. R. P. Cabral, P. M. de Oliveira, G. M. Gelfuso, T. de S. C. Quintão, J. A. Chaker, M. G. de O. Karnikowski and E. F. Gris, Improving stability of antioxidant compounds from Plinia cauliflora (jabuticaba) fruit peel extract by encapsulation in chitosan microparticles, J. Food Eng.238 (2018) 195–201; https://doi.org/10.1016/j.jfoodeng.2018.06.004
- 21. D. P. Gaspar, M. M. Gaspar, C. V. Eleutério, A. Grenha, M. Blanco, L. M. D. Gonçalves, P. Taboada, A. J. Almeida and C. Remunán-López, Microencapsulated solid lipid nanoparticles as a hybrid platform for pulmonary antibiotic delivery, Mol. Pharmaceutics14 (2017) 2977–2990; https://doi.org/10.1021/acs.molpharmaceut.7b00169
- 22. T. Wang, Q. Hu, M. Zhou, J. Xue and Y. Luo, Preparation of ultra-fine powders from polysaccharide-coated solid lipid nanoparticles and nanostructured lipid carriers by innovative nano spray drying technology, Int. J. Pharm.511 (2016) 219–222; https://doi.org/10.1016/j.ijpharm.2016.07.005
- 23. H. Salminen, J. Ankenbrand, B. Zeeb, G. Badolato Bönisch, C. Schäfer, R. Kohlus and J. Weiss, Influence of spray drying on the stability of food-grade solid lipid nanoparticles, Food Res. Int.119 (2018) 741–750; https://doi.org/10.1016/j.foodres.2018.10.056
- 24. D. G. Sami, H. H. Heiba and A. Abdellatif, Wound healing models: A systematic review of animal and non-animal models, Wound Med.24 (2019) 8–17; https://doi.org/10.1016/j.wndm.2018.12.001
- 25. A. Stunova and L. Vistejnova, Dermal fibroblasts – A heterogeneous population with regulatory function in wound healing, Cytokine Growth Factor Rev.39 (2018) 137–150; https://doi.org/10.1016/j.cytogfr.2018.01.003
- 26. I. Rubelj, Telomere Q-PNA-FISH – reliable results from stochastic signals, PLoS One9 (2014) e92559; https://doi.org/10.1371/journal.pone.0092559
- 27. F. Felice, Y. Zambito, E. Belardinelli, A. Fabiano, T. Santoni and R. Di Stefano, Effect of different chitosan derivatives on in vitro scratch wound assay: A comparative study, Int. J. Biol. Macromol.76 (2015) 236–241; https://doi.org/10.1016/j.ijbiomac.2015.02.041
- 28. A. D. Kulkarni, D. B. Bari, S. J. Surana and C. V Pardeshi, In vitro, ex vivo and in vivo performance of chitosan-based spray-dried nasal mucoadhesive microspheres of diltiazem hydrochloride, J. Drug Deliv. Sci. Technol.31 (2016) 108–117; https://doi.org/10.1016/j.jddst.2015.12.004
- 29. S. Demarger-Andre and A. Domard, Chitosan carboxylic acid salts in solution and in the solid state, Carbohydr. Polym.23 (1994) 211–219; https://doi.org/10.1016/0144-8617(94)90104-X
- 30. N. El Moussaoui and A. Bendriss, The influence of storage conditions on melatonin stability, Int. J. Eng. Res. Technol.3 (2014) 2243–2246.
- 31. M. Friciu, T. Savji, S. Zaraa and G. Leclair, Evaluation of stability of melatonin in extemporaneously compounded oral suspensions, J. Pharm. Pract. Res.46 (2016) 28–33; https://doi.org/10.1002/jppr.1171
- 32. P. Linse and M. Malmsten, Temperature-dependent micellization in aqueous block copolymer solutions, Macromolecules25 (1992) 5434–5439; https://doi.org/10.1021/ma00046a048
- 33. A. Garcês, M. H. Amaral, J. M. Sousa Lobo and A. C. Silva, Formulations based on solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) for cutaneous use: A review, Eur. J. Pharm. Sci.112 (2018) 159–167; https://doi.org/10.1016/j.ejps.2017.11.023
- 34. B. M. Dulmovits and I. M. Herman, Microvascular remodeling and wound healing: A role for pericytes, Int. J. Biochem. Cell Biol.44 (2012) 1800–1812; https://doi.org/10.1016/j.biocel.2012.06.031
- 35. S. L. Percival, S. McCarty, J. A. Hunt, E. J. Woods, The effects of pH on wound healing, biofilms, and antimicrobial efficacy, Wound Rep. Reg.22 (2014) 174–186; https://doi.org/10.1111/wrr.12125
- 36. D. B. Friedman, D. L. Stauff, G. Pishchany, C. W. Whitwell, V. J. Torres and E. P. Skaar, Staphylococcus aureus redirects central metabolism to increase iron availability, PLoS Pathog.2 (2006) 0777–0789; https://doi.org/10.1371/journal.ppat.0020087
- 37. X. Chen, L. H. Peng, Y. H. Shan, N. Li, W. Wei, L. Yu, Q. M. Li, W. Q. Liang and J. Q. Gao, Astragaloside IV-loaded nanoparticle-enriched hydrogel induces wound healing and anti-scar activity through topical delivery, Int. J. Pharm.447 (2013) 171–181; https://doi.org/10.1016/j.ijpharm.2013.02.054
- 38. V. Kant, A. Gopal, D. Kumar, A. Gopalkrishnan, N. N. Pathak, N. P. Kurade, S. K. Tandan and D. Kumar, Topical pluronic F-127 gel application enhances cutaneous wound healing in rats, Acta Histochem.116 (2014) 5–13; https://doi.org/10.1016/j.acthis.2013.04.010
- 39. G. Soybir, C. Topuzlu, Ö. Odabaş, K. Dolay, A. Bilir and F. Köksoy, The effects of melatonin on angiogenesis and wound healing, Surg. Today. 33 (2003) 896–901; https://doi.org/10.1007/s00595-003-2621-3
- 40. I. Garcia-Orue, G. Gainza, P. Garcia-Garcia, F. B. Gutierrez, J. J. Aguirre, R. M. Hernandez, A. Delgado and M. Igartua, Composite nanofibrous membranes of PLGA/Aloe vera containing lipid nanoparticles for wound dressing applications, Int. J. Pharm. (2019); https://doi.org/10.1016/j.ijpharm.2018.12.010.
- 41. M. Ghodrati, M. R. Farahpour and H. Hamishehkar, Encapsulation of Peppermint essential oil in nanostructured lipid carriers: In-vitro antibacterial activity and accelerative effect on infected wound healing, Colloids Surfaces A Physicochem. Eng. Asp. (2019); https://doi.org/10.1016/j.colsurfa.2018.12.043