[1] Pazyar, N.; Yaghoobi, R.; Rafiee, E.; Mehrabian, A.; Feily, A. Skin wound healing and phytomedicine: A review. Ski. Pharmacol. Physiol. 2014, 27, 303–310. [CrossRef] [PubMed]
[2] Daeschlein, G. Antimicrobial and antiseptic strategies in wound management Int. Wound J. 2013, 10, 9–14. [CrossRef] [PubMed]
[3] Serra, R.; Ielapi, N.; Barbetta, A.; de Franciscis, S. Skin tears and risk factors assessment: A systematic review on evidence-based medicine. Int. Wound J. 2018, 15, 38–42. [CrossRef] [PubMed]
[4] Howell-Jones, R.S.; Wilson, M.J.; Hill, K.E.; Howard, A.J.; Price, P.E.; Thomas, D.W. A review of the microbiology, antibiotic usage and resistance in chronic skin wounds. J. Antimicrob. Chemother. 2005, 55, 143–149. [CrossRef]
[5] Lazarus, G.S.; Cooper, D.M.; Knighton, D.R.; Margolis, D.J.; Percoraro, R.E.; Rodeheaver, G.; Robson, M.C. Definitions and guidelines for assessment of wounds and evaluation of healing. Wound Repair Regen. 1994, 2, 165–170. [CrossRef]
[6] Guo, S.; Dipietro, L.A. Factors affecting wound healing. J. Dent. Res. 2010, 89, 219–229. [CrossRef]
[7] Rodrigues, M.; Kosaric, N.; Bonham, C.A.; Gurtner, G.C. Wound Healing: A Cellular Perspective. Physiol. Rev. 2019, 99, 665–706. [CrossRef]
[8] Wilkinson, H.N.; Hardman, M.J. Wound healing: Cellular mechanisms and pathological outcomes. Open Biol. 2020, 10, 200223. [CrossRef]
[9] Velnar, T.; Bailey, T.; Smrkolj, V. The wound healing process: An overview of the cellular and molecular mechanisms. J. Int. Med. Res. 2009, 37, 1528–1542. [CrossRef]
[10] Abd Jalil, M.A.; Kasmuri, A.R.; Hadi, H. Stingless bee honey, the natural wound healer: A review. Ski. Pharmacol. Physiol. 2017, 30, 66–75. [CrossRef]
[11] Baron, J.M.; Glatz, M.; Proksch, E. Optimal Support of Wound Healing: New Insights. Dermatology 2020, 236, 593–600. [CrossRef] [PubMed]
[12] Rippa, A.L.; Kalabusheva, E.P.; Vorotelyak, E.A. Regeneration of Dermis: Scarring and Cells Involved. Cells 2019, 8, 607. [CrossRef]
[13] Broughton, G.; Janis, J.E.; Attinger, C.E. Wound healing: An overview. Plast. Reconstr. Surg. 2006, 117, 1e-S-32e-S. [CrossRef] [PubMed]
[14] Haalboom, M. Chronic Wounds: Innovations in Diagnostics and Therapeutics. Curr. Med. Chem. 2018, 25, 5772–5781. [CrossRef]
[15] Wilkins, R.G.; Unverdorben, M. Wound cleaning and wound healing: A concise review. Adv. Ski. Wound Care 2013, 26, 160–163. [CrossRef]
[16] Negut, I.; Grumezescu, V.; Grumezescu, A.M. Treatment strategies for infected wounds. Molecules 2018, 23, 2392. [CrossRef]
[17] Enioutina, E.Y.; Salis, E.R.; Job, K.M.; Gubarev, M.I.; Krepkova, L.V.; Sherwin, C.M.T. Herbal Medicines: Challenges in the modern world. Part 5. status and current directions of complementary and alternative herbal medicine worldwide. Expert Rev. Clin. Pharmacol. 2017, 10, 327–338. [CrossRef] [PubMed]
[18] Quave, C.L. Wound Healing with Botanicals: A Review and Future Perspectives. Curr. Dermatol. Rep. 2018, 7, 287–295. [CrossRef]
[19] Zhang, Y.; Yuan, H.; Kang, J.; Xie, H.; Long, X.; Qi, L.; Xie, C.; Gong, G. Clinical study for external washing by traditional Chinese medicine in the treatment of multiple infectious wounds of diabetic foot: Study protocol clinical trial (SPIRIT compliant). Medicine 2020, 99, e19841. [CrossRef]
[20] Gendrisch, F.; Haarhaus, B.; Krieger, N.; Quirin, K.W.; Schempp, C.M.; Wölfle, U. The Effect of Herbal Medicinal Products on Psoriasis-Like Keratinocytes. Biomolecules 2021, 11, 3. [CrossRef] [PubMed]
[21] Lone, A.H.; Ahmad, T.; Anwar, M.; Sofi, G. Clinical efficacy and safety of a pharmacopial polyherbal Unani formulation in pityriasis versicolor: A comparative randomized single-blind study. J. Altern. Complement. Med. 2012, 18, 978–982. [CrossRef] [PubMed]
[22] Olisova, O.Y.; Snarskaya, E.S.; Gladko, V.V.; Burova, E.P. Russian traditional medicine in dermatology. Clin. Dermatol. 2018, 36, 325–337. [CrossRef] [PubMed]
[23] McEwen, S.A.; Collignon, P.J. Antimicrobial Resistance: A One Health Perspective. Microbiol. Spectr. 2018, 6, 521–547. [CrossRef] [PubMed]
[24] Huemer, M.; Mairpady Shambat, S.; Brugger, S.D.; Zinkernagel, A.S. Antibiotic resistance and persistence-Implications for human health and treatment perspectives. EMBO Rep. 2020, 21, e51034. [CrossRef]
[25] Sen, C.K. Human Wounds and Its Burden: An Updated Compendium of Estimates. Adv. Wound Care 2019, 8, 39–48. [CrossRef]
[26] Thomford, N.E.; Senthebane, D.A.; Rowe, A.; Munro, D.; Seele, P.; Maroyi, A.; Dzobo, K. Natural Products for Drug Discovery in the 21st Century: Innovations for Novel Drug Discovery. Int. J. Mol. Sci. 2018, 19, 6. [CrossRef]
[27] Hoffmann, J.; Gendrisch, F.; Schempp, C.M.; Wölfle, U. New Herbal Biomedicines for the Topical Treatment of Dermatological Disorders. Biomedicines 2020, 8, 2. [CrossRef]
[28] Katiyar, C.; Gupta, A.; Kanjilal, S.; Katiyar, S. Drug discovery from plant sources: An integrated approach. Ayu 2012, 33, 10–19.[CrossRef]
[29] Lautié, E.; Russo, O.; Ducrot, P.; Boutin, J.A. Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes. Front. Pharmacol. 2020, 11, 397. [CrossRef]
[30] Apel, L.; Lorenz, P.; Urban, S.; Sauer, S.; Spring, O.; Stintzing, F.C.; Kammerer, D.R. Phytochemical characterization of different yarrow species (Achillea sp.) and investigations into their antimicrobial activity. Z. Naturforsch. C 2021, 76, 55–65. [CrossRef]
[31] Nemeth, E.; Bernath, J. Biological activities of yarrow species (Achillea spp.). Curr. Pharm. Des. 2008, 14, 3151–3167. [CrossRef][PubMed]
[32] Tadic´, V.; Arsic´, I.; Zvezdanovic´, J.; Zugic´, A.; Cvetkovic´, D.; Pavkov, S. The estimation of the traditionally used yarrow (Achilleamillefolium L. Asteraceae) oil extracts with anti-inflamatory potential in topical application. J. Ethnopharmacol. 2016, 199, 138–148. [CrossRef] [PubMed]
[33] Ayoobi, F.; Shamsizadeh, A.; Fatemi, I.; Vakilian, A.; Allahtavakoli, M.; Hassanshahi, G.; Moghadam-Ahmadi, A. Bio-effectiveness of the main flavonoids of Achillea millefolium in the pathophysiology of neurodegenerative disorders—A review. Iran. J. Basic Med. Sci. 2017, 20, 604–612. [CrossRef] [PubMed]
[34] Strze˛pek-Gomółka, M.; Gaweł-Be˛ben, K.; Kukula-Koch, W. Achillea species as sources of active phytochemicals for dermatological and cosmetic applications. Oxid. Med. Cell. Longev. 2021, 2021. [CrossRef]
[35] Pain, S.; Altobelli, C.; Boher, A.; Cittadini, L.; Favre-Mercuret, M.; Gaillard, C.; Sohm, B.; Vogelgesang, B.; André-Frei, V. Surface rejuvenating effect of Achillea millefolium extract. Int. J. Cosmet. Sci. 2011, 33, 535–542. [CrossRef]
[36] Ali, S.I.; Gopalakrishnan, B.; Venkatesalu, V. Pharmacognosy, Phytochemistry and Pharmacological Properties of Achillea millefolium L.: A Review. Phyther. Res. 2017, 31, 1140–1161. [CrossRef]
[37] Sonawane, S.K.; Gokhale, J.S.; Mulla, M.Z.; Kandu, V.R.; Patil, S. A comprehensive overview of functional and rheological properties of Aloe vera and its application in foods. J. Food Sci. Technol. 2021, 58, 1217–1226. [CrossRef]
[38] Guo, X.; Mei, N. Aloe vera: A review of toxicity and adverse clinical effects. J. Environ. Sci. HealthPart C 2016, 34, 77–96. [CrossRef]
[39] Atherton, P. Aloe vera: Magic or medicine? Nurs. Stand. 1998, 12, 49–52. [CrossRef]
[40] Salehi, B.; Albayrak, S.; Antolak, H.; Kre˛giel, D.; Pawlikowska, E.; Sharifi-Rad, M.; Uprety, Y.; Tsouh Fokou, P.V.; Yousef, Z.; Amiruddin Zakaria, Z.; et al. Aloe Genus Plants: From Farm to Food Applications and Phytopharmacotherapy. Int. J. Mol. Sci. 2018, 19, 2843. [CrossRef]
[41] Rahman, S.; Carter, P.; Bhattarai, N. Aloe vera for Tissue Engineering Applications. J. Funct. Biomater. 2017, 8, 6. [CrossRef][PubMed]
[42] Goetz, P. Aloe vera. Phytotherapie 2019, 17, 352–356. [CrossRef]
[43] Burusapat, C.; Supawan, M.; Pruksapong, C.; Pitiseree, A.; Suwantemee, C. Topical Aloe vera gel for accelerated wound healing of split-thickness skin graft donor sites: A double-blind, randomized, controlled trial and systematic review. Plast. Reconstr. Surg. 2018, 142, 217–226. [CrossRef] [PubMed]
[44] Hekmatpou, D.; Mehrabi, F.; Rahzani, K.; Aminiyan, A. The effect of Aloe vera clinical trials on prevention and healing of skin wound: A systematic review. Iran. J. Med. Sci. 2019, 44, 1–9.
[45] Meza-Valle, K.Z.; Saucedo-Acuña, R.A.; Tovar-Carrillo, K.L.; Cuevas-González, J.C.; Zaragoza-Contreras, E.A.; Melgoza-Lozano,
[46] J. Characterization and topical study of Aloe vera hydrogel on wound-healing process. Polymers 2021, 13, 3958. [CrossRef]
[47] Vogler, B.K.; Ernst, E. Aloe vera: A systematic review of its clinical effectiveness. Br. J. Gen. Pract. 1999, 49, 823–828. [PubMed]
[48] Gupta, S.C.; Patchva, S.; Aggarwal, B.B. Therapeutic roles of curcumin: Lessons learned from clinical trials. AAPS J. 2013, 15, 195–218. [CrossRef]
[49] Vollono, L. Potential of Curcumin in Skin Disorders. Nutrients 2019, 11, 2169. [CrossRef]
[50] Kotha, R.R.; Luthria, D.L. Curcumin: Biological, pharmaceutical, nutraceutical, and analytical aspects. Molecules 2019, 24, 2930. [CrossRef]
[51] Yen, Y.H. Curcumin accelerates cutaneous wound healing via multiple biological actions: The involvement of TNF-α, MMP-9,
[52] α-SMA, and collagen. Int. Wound J. 2018, 15, 605–617. [CrossRef]
[53] Dosoky, N.S.; Setzer, W.N. Chemical Composition and Biological Activities of Essential Oils of Curcuma Species. Nutrients 2018, 10, 1196.
[54] [CrossRef] [PubMed]
[55] Bhagavathula, N.; Warner, R.L.; DaSilva, M.; McClintock, S.D.; Barron, A.; Aslam, M.N.; Johnson, K.J.; Varani, J. A combination of curcumin and ginger extract improves abrasion wound healing in corticosteroid-impaired hairless rat skin. Wound Repair Regen. 2009, 17, 360–366. [CrossRef]
[56] Banaee, M.; Soleimany, V.; Nematdoost Haghi, B. Therapeutic effects of marshmallow (Althaea officinalis L.) extract on plasma biochemical parameters of common carp infected with Aeromonas hydrophila. Vet. Res. Forum 2017, 8, 145–153. [PubMed]
[57] Bonaterra, G.A.; Bronischewski, K.; Hunold, P.; Schwarzbach, H.; Heinrich, E.U.; Fink, C.; Aziz-Kalbhenn, H.; Müller, J.; Kinscherf, R. Anti-inflammatory and Anti-oxidative Effects of Phytohustil® and Root Extract of Althaea officinalis L. on Macrophages in vitro. Front. Pharmacol. 2020, 11, 290. [CrossRef] [PubMed]
[58] Sadighara, P.; Gharibi, S.; Moghadam Jafari, A.; Jahed Khaniki, G.; Salari, S. The antioxidant and Flavonoids contents of Althaea officinalis L. flowers based on their color. Avicenna J. Phytomed. 2012, 2, 113–117. Available online: http://www.ncbi.nlm.nih.gov/ pubmed/25050239 (accessed on 21 January 2023).
[59] Rheder, D.T.; Guilger, M.; Bilesky-José, N.; Germano-Costa, T.; Pasquoto-Stigliani, T.; Gallep, T.B.B.; Grillo, R.; Carvalho, C.D.S.; Fraceto, L.F.; Lima, R. Synthesis of biogenic silver nanoparticles using Althaea officinalis as reducing agent: Evaluation of toxicity and ecotoxicity. Sci. Rep. 2018, 8, 12397. [CrossRef] [PubMed]
[60] Rezaei, M.; Dadgar, Z.; Noori-Zadeh, A.; Mesbah-Namin, S.A.; Pakzad, I.; Davodian, E. Evaluation of the antibacterial activity of the Althaea officinalis L. leaf extract and its wound healing potency in the rat model of excision wound creation. Avicenna J. Phytomed. 2015, 5, 105–112.
[61] Nicolaus, C.; Junghanns, S.; Hartmann, A.; Murillo, R.; Ganzera, M.; Merfort, I. In vitro studies to evaluate the wound healing properties of Calendula officinalis extracts. J. Ethnopharmacol. 2017, 196, 94–103. [CrossRef]
[62] Cruceriu, D.; Balacescu, O.; Rakosy, E. Calendula officinalis: Potential Roles in Cancer Treatment and Palliative Care. Integr. Cancer Ther. 2018, 17, 1068–1078. [CrossRef]
[63] Mehta, D.; Rastogi, P.; Kumar, A.; Chaudhary, A.K. Review on Pharmacological Update: Calendula Officinalis Linn. Inventi 2012,2012, 195–203.
[64] Preethi, K.C.; Kuttan, R. Wound healing activity of flower extract of Calendula officinalis. J. Basic Clin. Physiol. Pharmacol. 2009, 20, 73–80. [CrossRef] [PubMed]
[65] Faizi, N.; Kazmi, S. Universal health coverage—There is more to it than meets the eye. J. Fam. Med. Prim. Care 2017, 6, 169–170. [CrossRef] [PubMed]
[66] Chauhan, R.; Singh, S.; Kumar, V.; Kumar, A.; Kumari, A.; Rathore, S.; Kumar, R.; Singh, S. A Comprehensive Review on Biology, Genetic Improvement, Agro and Process Technology of German Chamomile (Matricaria chamomilla L.). Plants 2021, 11, 29. [CrossRef] [PubMed]
[67] Qasem, A.; Assaggaf, H.; Montesano, D.; Khalil, Z.; Al-Mijalli, S.H.; Baaboua, A.E.; El Omari, N.; El Menyiy, N.; Bakrim, S.; Sheikh, R.A.; et al. Determination of Chemical Compounds and Investigation of Biological Properties of Matricaria chamomilla Essential Oils, Honey, and Their Mixture. Molecules 2022, 27, 5850. [CrossRef] [PubMed]
[68] Singh, O.; Khanam, Z.; Misra, N.; Srivastava, M.K. Chamomile (Matricaria chamomilla L.): An overview. Pharmacogn. Rev. 2011, 5, 82–95.[CrossRef]
[69] Duarte, C.M.E.; Quirino, M.R.S.; PatrocÃnio, M.C.; Anbinder, A.L. Effects of Chamomilla recutita (L.) on oral wound healing in rats.
[70] Med. Oral Patol. Oral Cir. Bucal 2011, 16, 716–721. [CrossRef]
[71] Shokrollahi, M.; Bahrami, S.H.; Nazarpak, M.H.; Solouk, A. Multilayer nanofibrous patch comprising chamomile loaded carboxyethyl chitosan/poly(vinyl alcohol) and polycaprolactone as a potential wound dressing. Int. J. Biol. Macromol. 2020, 147, 547–559. [CrossRef]
[72] Grattapaglia, D.; Kirst, M. Eucalyptus applied genomics: From gene sequences to breeding tools. New Phytol. 2008, 179, 911–929.[CrossRef]
[73] Ping, L.; Xie, Z.Q. Effects of introducing Eucalyptus on indigenous biodiversity. Yingyong Shengtai Xuebao J. Appl. Ecol. 2009, 20, 1765–1774.
[74] Vuong, Q.V.; Chalmers, A.C.; Jyoti Bhuyan, D.; Bowyer, M.C.; Scarlett, C.J. Botanical, phytochemical, and anticancer properties of the Eucalyptus species. Chem. Biodivers. 2015, 12, 907–924. [CrossRef]
[75] Mulyaningsih, S.; Sporer, F.; Zimmermann, S.; Reichling, J.; Wink, M. Synergistic properties of the terpenoids aromadendrene and 1,8-cineole from the essential oil of Eucalyptus globulus against antibiotic-susceptible and antibiotic-resistant pathogens. Phytomedicine 2010, 17, 1061–1066. [CrossRef] [PubMed]
[76] Alam, P.; Shakeel, F.; Anwer, M.K.; Foudah, A.I.; Alqarni, M.H. Wound healing study of Eucalyptus essential oil containing nanoemulsion in rat model. J. Oleo Sci. 2018, 67, 957–968. [CrossRef] [PubMed]
[77] Mumtaz, R.; Zubair, M.; Khan, M.A.; Muzammil, S.; Siddique, M.H. Extracts of Eucalyptus alba Promote Diabetic Wound Healing by Inhibiting α-Glucosidase and Stimulating Cell Proliferation. Evid. Based Complement. Altern. Med. 2022, 2022, 4953105. [CrossRef] [PubMed]
[78] Al-Obaidi, J.R.; Halabi, M.F.; AlKhalifah, N.S.; Asanar, S.; Al-Soqeer, A.A.; Attia, M.F. A review on plant importance, biotechno- logical aspects, and cultivation challenges of jojoba plant. Biol. Res. 2017, 50, 25. [CrossRef]
[79] Sturtevant, D.; Lu, S.; Zhou, Z.W.; Shen, Y.; Wang, S.; Song, J.M.; Zhong, J.; Burks, D.J.; Yang, Z.Q.; Yang, Q.Y.; et al. The genome of jojoba (Simmondsia chinensis): A taxonomically isolated species that directs wax ester accumulation in its seeds. Sci. Adv. 2020, 6, eaay3240. [CrossRef]
[80] Zhang, G.; Xie, F.; Sun, Y.; Yu, X.; Xiao, Z.; Fang, R.; Li, J.; Li, Q.; Du, L.; Jin, Y. Inhalable jojoba oil dry nanoemulsion powders for the treatment of lipopolysaccharide-or H2O2-induced acute lung injury. Pharmaceutics 2021, 13, 486. [CrossRef]
[81] Ranzato, E.; Martinotti, S.; Burlando, B. Wound healing properties of jojoba liquid wax: An in vitro study. J. Ethnopharmacol. 2011,134, 443–449. [CrossRef]
[82] Gad, H.A.; Roberts, A.; Hamzi, S.H.; Gad, H.A.; Touiss, I.; Altyar, A.E.; Kensara, O.A.; Ashour, M.L. Jojoba oil: An updated comprehensive review on chemistry, pharmaceutical uses, and toxicity. Polymers 2021, 13, 1711. [CrossRef]
[83] Samuelsen, A.B. The traditional uses, chemical constituents and biological activities of Plantago major L. A review. J. Ethnopharmacol.2000, 71, 1–21. [CrossRef]
[84] Aioub, A.A.A.; Zuo, Y.; Aioub, A.A.A.; Hu, Z. Biochemical and phytoremediation of Plantago major L. to protect tomato plants from the contamination of cypermethrin pesticide. Environ. Sci. Pollut. Res. Int. 2021, 28, 43992–44001. [CrossRef] [PubMed]
[85] Kizi, K.S.A. Pharmacological Properties of Plantago Major L. and Its Active Constituents. Int. J. Med. Sci. Public Health Res. 2022, 3, 9–12. [CrossRef]
[86] Najafian, Y.; Hamedi, S.S.; Kaboli Farshchi, M.; Feyzabadi, Z. Plantago major in Traditional Persian Medicine and modern phytotherapy: A narrative review. Electron. Physician 2018, 10, 6390–6399. [CrossRef]
[87] Keshavarzi, A.; Montaseri, H.; Akrami, R.; Moradi Sarvestani, H.; Khosravi, F.; Foolad, S.; Zardosht, M.; Zareie, S.; Saharkhiz, M.J.; Shahriarirad, R. Therapeutic Efficacy of Great Plantain (Plantago major L.) in the Treatment of Second-Degree Burn Wounds: A Case-Control Study. Int. J. Clin. Pract. 2022, 2022, 4923277. [CrossRef]
[88] Thome, R.G.; Santos, H.B.D.; Santos, F.V.D.; Oliveira, R.J.D.S.; De Camargos, L.F.; Pereira, M.N.; Longatti, T.R.; Souto, C.M.; Franco, C.S.; De Oliveira Aquino Schüffner, R.; et al. Evaluation of healing wound and genotoxicity potentials from extracts hydroalcoholic of Plantago major and Siparuna guianensis. Exp. Biol. Med. 2012, 237, 1379–1386. [CrossRef] [PubMed]
[89] Zubair, M.; Nybom, H.; Lindholm, C.; Brandner, J.M.; Rumpunen, K. Promotion of wound healing by Plantago major L. leaf extracts—Ex-vivo experiments confirm experiences from traditional medicine. Nat. Prod. Res. 2016, 30, 622–624. [CrossRef] [PubMed]
[90] Wang, G.W.; Qin, J.J.; Cheng, X.R.; Shen, Y.H.; Shan, L.; Jin, H.Z.; Zhang, W.D. Inula sesquiterpenoids: Structural diversity, cytotoxicity and anti-tumor activity. Expert Opin. Investig. Drugs 2014, 23, 317–345. [CrossRef] [PubMed]
[91] Sun, C.P.; Jia, Z.L.; Huo, X.K.; Tian, X.G.; Feng, L.; Wang, C.; Zhang, B.J.; Zhao, W.Y.; Ma, X.C. Medicinal Inula Species: Phytochemistry, Biosynthesis, and Bioactivities. Am. J. Chin. Med. 2021, 49, 315–358. [CrossRef]
[92] Tavares, W.R.; Seca, A.M. Inula L. secondary metabolites against oxidative stress-related human diseases. Antioxidants 2019, 8, 122. [CrossRef]
[93] El Yaagoubi, O.M.; Lahmadi, A.; Bouyahya, A.; Filali, H.; Samaki, H.; El Antri, S.; Aboudkhil, S. Antitumor Effect of Inula viscosa Extracts on DMBA-Induced Skin Carcinoma Are Mediated by Proteasome Inhibition. Biomed. Res. Int. 2021, 2021, 6687589. [CrossRef]
[94] Kurz, H.; Karygianni, L.; Argyropoulou, A.; Hellwig, E.; Skaltsounis, A.L.; Wittmer, A.; Vach, K.; Al-Ahmad, A. Antimicrobial effects of Inula viscosa extract on the in situ initial oral biofilm. Nutrients 2021, 13, 4029. [CrossRef]
[95] Bar-Shalom, R.; Bergman, M.; Grossman, S.; Azzam, N.; Sharvit, L.; Fares, F. Inula viscosa Extract Inhibits Growth of Colorectal Cancer Cells in vitro and in vivo through Induction of Apoptosis. Front. Oncol. 2019, 9, 227. [CrossRef] [PubMed]
[96] Wang, Z.; Geng, L.; Chen, Z.; Lin, B.; Zhang, M.; Zheng, S. In vivo therapeutic potential of Inula racemosa in hepatic ischemia– reperfusion injury following orthotopic liver transplantation in male albino rats. AMB Express 2017, 7, 211. [CrossRef] [PubMed]
[97] Bouwmeester, H. Dissecting the pine tree green chemical factory. J. Exp. Bot. 2019, 70, 4–6. [CrossRef] [PubMed]
[98] Mumm, R.; Hilker, M. Direct and indirect chemical defence of pine against folivorous insects. Trends Plant Sci. 2006, 11, 351–358. [CrossRef] [PubMed]
[99] Tümen, I˙.; Akkol, E.K.; Tas¸tan, H.; Süntar, I.; Kurtca, M. Research on the Antioxidant, Wound Healing, and Anti-Inflammatory Activities and the Phytochemical Composition of Maritime Pine (Pinus Pinaster Ait). J. Ethnopharmacol. 2018, 211, 235–246. [CrossRef] [PubMed]
[100] Wang, C.; Shang, H.; Cui, W.; Zhou, F.; Zhang, S.; Wang, X.; Gao, P.; Wei, K.; Zhu, R. Pine pollen polysaccharides promote cell proliferation and accelerate wound healing by activating the JAK2-STAT3 signaling pathway. Int. J. Biol. Macromol. 2022, 210, 579–587. [CrossRef]
[101] Süntar, I.; Tumen, I.; Ustün, O.; Keles¸, H.; Küpeli Akkol, E. Appraisal on the wound healing and anti-inflammatory activities of the essential oils obtained from the cones and needles of Pinus species by in vivo and in vitro experimental models. J. Ethnopharmacol. 2012, 139, 533–540. [CrossRef]
[102] Park, J.Y.; Lee, Y.K.; Lee, D.S.; Yoo, J.E.; Shin, M.S.; Yamabe, N.; Kim, S.N.; Lee, S.; Kim, K.H.; Lee, H.J.; et al. Abietic acid isolated from pine resin (Resina Pini) enhances angiogenesis in HUVECs and accelerates cutaneous wound healing in mice. Elsevier Ireland Ltd. J. Ethnopharmacol. 2017, 203, 279–287. [CrossRef]
[103] Ferreira-Santos, P.; Zanuso, E.; Genisheva, Z.; Rocha, C.M.R.; Teixeira, J.A. Green and sustainable valorization of bioactive phenolic compounds from Pinus by-products. Molecules 2020, 25, 2931. [CrossRef]
[104] Dou, Q.P. Tea in Health and Disease. Nutrients 2019, 11, 929. [CrossRef]
[105] Musial, C.; Kuban-Jankowska, A.; Gorska-Ponikowska, M. Beneficial Properties of Green Tea Catechins. Int. J. Mol. Sci. 2020, 21, 1744. [CrossRef] [PubMed]
[106] Hayakawa, S.; Ohishi, T.; Miyoshi, N.; Oishi, Y.; Nakamura, Y.; Isemura, M. Anti-Cancer Effects of Green Tea Epigallocatchin-3- Gallate and Coffee Chlorogenic Acid. Molecules 2020, 25, 4553. [CrossRef] [PubMed]
[107] Hayat, K.; Iqbal, H.; Malik, U.; Bilal, U.; Mushtaq, S. Tea and Its Consumption: Benefits and Risks. Crit. Rev. Food Sci. Nutr. 2015, 55, 939–954. [CrossRef] [PubMed]
[108] Chu, C.; Deng, J.; Man, Y.; Qu, Y. Green Tea Extracts Epigallocatechin-3-Gallate for Different Treatments. Biomed Res. Int. 2017, 2017, 5615647. [CrossRef] [PubMed]
[109] Xu, F.W.; Lv, Y.L.; Zhong, Y.F.; Xue, Y.N.; Wang, Y.; Zhang, L.Y.; Hu, X.; Tan, W.Q. Beneficial effects of green tea EGCG on skin wound healing: A comprehensive review. Molecules 2021, 26, 6123. [CrossRef]
[110] Xing, L.; Zhang, H.; Qi, R.; Tsao, R.; Mine, Y. Recent Advances in the Understanding of the Health Benefits and Molecular Mechanisms Associated with Green Tea Polyphenols. J. Agric. Food Chem. 2019, 67, 1029–1043. [CrossRef]
[111] Shahrahmani, H.; Kariman, N.; Jannesari, S.; Rafieian-Kopaei, M.; Mirzaei, M.; Ghalandari, S.; Shahrahmani, N.; Mardani, G. The effect of green tea ointment on episiotomy pain and wound healing in primiparous women: A randomized, double-blind, placebo-controlled clinical trial. Phyther. Res. 2018, 32, 522–530. [CrossRef] [PubMed]
[112] Chen, G.; He, L.; Zhang, P.; Zhang, J.; Mei, X.; Wang, D.; Zhang, Y.; Ren, X.; Chen, Z. Encapsulation of green tea polyphenol nanospheres in PVA/alginate hydrogel for promoting wound healing of diabetic rats by regulating PI3K/AKT pathway. Mater. Sci. Eng. C 2020, 110, 110686. [CrossRef]
[113] Saeed, M.; Naveed, M.; BiBi, J.; Kamboh, A.A.; Arain, M.A.; Shah, Q.A.; Alagawany, M.; El-Hack, M.E.; Abdel-Latif, M.A.; Yatoo, M.; et al. The Promising Pharmacological Effects and Therapeutic/Medicinal Applications of Punica granatum, L. (Pomegranate) as a Functional Food in Humans and Animals. Recent Pat. Inflamm. Allergy Drug Discov. 2018, 12, 24–38. [CrossRef]
[114] Magangana, T.P.; Makunga, N.P.; Fawole, O.A.; Opara, U.L. Processing Factors Affecting the Phytochemical and Nutritional Properties of Pomegranate (Punica Granatum L.) Peel Waste: A Review. Molecules 2020, 25, 4690. [CrossRef]
[115] Fourati, M.; Smaoui, S.; Hlima, H.B.; Elhadef, K.; Braïek, O.B.; Ennouri, K.; Mtibaa, A.C.; Mellouli, L. Bioactive Compounds and Pharmacological Potential of Pomegranate (Punica granatum) Seeds—A Review. Plant Foods Hum. Nutr. 2020, 75, 477–486. [CrossRef] [PubMed]
[116] Zhang, L.; Yang, R.; Hu, Y.; Yang, Y.; Zhang, X.; He, B.; Shen, Z.; Yang, J.; Chen, P. Promoting effect of pomegranate peel extract on second-degree burn wound-healing through VEGF-A and TGF-β1 regulation. Burns 2022, 48, 639–648. [CrossRef] [PubMed]
[117] Lukiswanto, B.S.; Miranti, A.; Sudjarwo, S.A.; Primarizky, H.; Yuniarti, W.M. Evaluation of wound healing potential of pomegranate (Punica granatum) whole fruit extract on skin burn wound in rats (Rattus norvegicus). J. Adv. Vet. Anim. Res. 2019, 6, 202–207. [CrossRef] [PubMed]
[118] Nasiri, E.; Hosseinimehr, S.J.; Akbari, J.; Azadbakht, M.; Azizi, S. The Effects of Punica granatum Flower Extract on Skin Injuries Induced by Burn in Rats. Adv. Pharmacol. Sci. 2017, 2017, 3059745. [CrossRef] [PubMed]
[119] Hayouni, E.A.; Miled, K.; Boubaker, S.; Bellasfar, Z.; Abedrabba, M.; Iwaski, H.; Oku, H.; Matsui, T.; Limam, F.; Hamdi, M. Hydroalcoholic extract based-ointment from Punica granatum L. peels with enhanced in vivo healing potential on dermal wounds. Phytomedicine 2011, 18, 976–984. [CrossRef] [PubMed]