Formulation and Evaluation of Topical Delivery Diosgenin Emulgel for Diabetic Wounds

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Authors

  • Department of Pharmacognosy, Poona College of Pharmacy, Bharati Vidyapeeth (Deemed to be University), Pune - 411038, Maharashtra ,IN
  • Department of Pharmacognosy, Poona College of Pharmacy, Bharati Vidyapeeth (Deemed to be University), Pune - 411038, Maharashtra ,IN
  • Department of Pharmaceutics, Poona College of Pharmacy, Bharati Vidyapeeth (Deemed to be University), Pune - 411038, Maharashtra ,IN
  • Department of Pharmacology, Poona College of Pharmacy, Bharati Vidyapeeth (Deemed to be University), Pune - 411038, Maharashtra ,IN
  • Department of Pharmacognosy, Poona College of Pharmacy, Bharati Vidyapeeth (Deemed to be University), Pune - 411038, Maharashtra ,IN

DOI:

https://doi.org/10.18311/ti/2024/v31i1/35423

Keywords:

Diosgenin, Emulgel, Excision Wound Model, Streptozotocin (STZ)

Abstract

A variety of cellular processes work together in a highly coordinated manner to facilitate a complex and dynamic process of wound healing ensuring the efficient restoration of injured tissue. Diosgenin, a plant sterol saponin is primarily found in various plants. The aim of this research was to create an emulgel containing Diosgenin and examine its effects on wound healing in diabetic rats with excision wounds. Histopathological findings further supported the efficacy of the emulgel and results indicate that the application of Diosgenin Emulgel (DE) shows an effective approach for healing of diabetic wounds. The objective of the research stands to explore the possibility of formulation development and wound-healing capabilities of DE. The study evaluated the wound healing effects of the DE in Streptozotocin-induced (STZ) (55 mg/kg) given by intraperitoneal route diabetes and control group. The emulgel was topically applied to assess its effectiveness in promoting wound healing. The application of DE on the rat wounds resulted in a notable wound closure within a 21-day period and significant epithelization was observed with p < 0.001. The study concluded that the formulation demonstrated remarkable effectiveness in promoting the functional recovery of diabetic wounds.

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Published

2024-02-28

How to Cite

Lanjekar, D., Salunke, M., Mali, A., Muthal, A., & Shinde, V. (2024). Formulation and Evaluation of Topical Delivery Diosgenin Emulgel for Diabetic Wounds. Toxicology International, 31(1), 111–119. https://doi.org/10.18311/ti/2024/v31i1/35423
Received 2023-10-25
Accepted 2024-01-31
Published 2024-02-28

 

References

Burgess JL, Wyant WA, Abujamra BA, Kirsner RS, Jozic I. Diabetic wound-healing science. Medicina. 2021; 57:1072- 95. https://doi.org/10.3390/medicina57101072 DOI: https://doi.org/10.3390/medicina57101072

Redondo MJ, Hagopian WA, Oram R, Steck AK, Vehik K, Weedon M. The clinical consequences of heterogeneity within and between different diabetes types. Diabetologia, Springer. 2020; 63:2040-8. https://doi.org/10.1007/s00125- 020-05211-7 DOI: https://doi.org/10.1007/s00125-020-05211-7

Dong J, Chen L, Jayaswal N, Meghani I, Zhang W, Veves A. Mast cells in diabetes and diabetic wound healing. Israel Deaconess Foot Center JB. 2020; 37:4519-37. https://doi. org/10.1007/s12325-020-01499-4 DOI: https://doi.org/10.1007/s12325-020-01499-4

Deng L, Du C, Song P, Chen T, Rui S, Armstrong DG, Deng W. The role of oxidative stress and antioxidants in diabetic wound healing. Oxidative Medicine and Cellular Longevity. Hindawi Limited. 2021; 1-11. https://doi. org/10.1155/2021/8852759 DOI: https://doi.org/10.1155/2021/8852759

Bodas K, Shinde V. Healing of wounds: A detailed review on models, biomarkers, biochemical and other wound assessment parameters. International Journal of All Research Education and Scientific Methods (IJARESM). 2021; 9(3):2069-85.

Wilkinson HN, Hardman MJ. Wound healing: Cellular mechanisms and pathological outcomes. Open Biology. Royal Society Publishing. 2020; 10:200-23. https://doi. org/10.1098/rsob.200223 DOI: https://doi.org/10.1098/rsob.200223

Raziyeva K, Kim Y, Zharkinbekov Z, Kassymbek K, Jimi S, Saparov A. Immunology of acute and chronic wound healing. Biomolecules. 2021; 11:700-24. https://doi. org/10.3390/biom11050700 DOI: https://doi.org/10.3390/biom11050700

Al Sadoun H. Macrophage phenotypes in normal and diabetic wound healing and therapeutic interventions. Cells. 2022; 11:2430-57. https://doi.org/10.3390/cells11152430 DOI: https://doi.org/10.3390/cells11152430

Alam W, Hasson J, Reed M. Clinical approach to chronic wound management in older adults. Journal of the American Geriatrics Society. 2021; 69:2327-34. https://doi. org/10.1111/jgs.17177 DOI: https://doi.org/10.1111/jgs.17177

Liang Y, Li M, Yang Y, Qiao L, Xu H, Guo B. pH/Glucose dual responsive metformin release hydrogel dressings with adhesion and self-healing via dual-dynamic bonding for athletic diabetic foot wound healing. ACS Nano. 2022; 16(2):3194-207. https://doi.org/10.1021/acsnano.1c11040 DOI: https://doi.org/10.1021/acsnano.1c11040

Prasetyono TOH. General concept of wound healing, revisited. Med J Indones. 2009; 18:208-16. https://doi. org/10.13181/mji.v18i3.364 DOI: https://doi.org/10.13181/mji.v18i3.364

Zhou X, Ruan Q, Ye Z, Chu Z, Xi M, Li M, Hu W, Guo X, Yao P. Resveratrol accelerates wound healing by attenuating oxidative stress-induced impairment of cell proliferation and migration. Burns. 2021; 47(1):133-9. https://doi. org/10.1016/j.burns.2020.10.016 DOI: https://doi.org/10.1016/j.burns.2020.10.016

Arya P, Munshi M, Kumar P. Diosgenin: Chemistry, extraction, quantification and health benefits. Food Chemistry Advances. 2023; 2:100170. https://doi. org/10.1016/j.focha.2022.100170 DOI: https://doi.org/10.1016/j.focha.2022.100170

Varghese R, Shinde V. Therapeutic potential of novel phyto-medicine from natural origin for accelerated wound healing. International Journal of Pharmacognosy. 2021; 8(1):14-24.

Tariq M, Tahir HM, Butt SA, Ali S, Ahmad AB, Raza C, Summer M, Hassan A, Nadeem J. Silk-derived formulations for accelerated wound healing in diabetic mice. Peer J. 2021; 9:1-18. https://doi.org/10.7717/peerj.10232 DOI: https://doi.org/10.7717/peerj.10232

Bodas KS, Bagul CD, Shinde VM. Evaluation of wound healing effect of Mallotus philippensis (Lam.) Mull Arg by in silico multitargets directed for multiligand approach. In Silico Pharmacol. 2022; 10(1):1-19. https://doi.org/10.1007/ s40203-022-00134-0 DOI: https://doi.org/10.1007/s40203-022-00134-0

Parama D, Boruah M, Yachna K, Rana V, Banik K, Harsha C, Thakur K, Dutta U, Arya A, Mao X, Ahn K, Kunnumakkara A. Diosgenin, a steroidal saponin, and its analogs: Effective therapies against different chronic diseases. Life Sciences. 2020; 260-87. https://doi.org/10.1016/j.lfs.2020.118182 DOI: https://doi.org/10.1016/j.lfs.2020.118182

Okonogi S, Riangjanapatee P. Physicochemical characterization of lycopene-loaded nanostructured lipid carrier formulations for topical administration. Int J Pharm. 2015; 478(2):726-35. https://doi.org/10.1016/j. ijpharm.2014.12.002 DOI: https://doi.org/10.1016/j.ijpharm.2014.12.002

Ambala R, Vemula SK. Formulation and characterization of ketoprofen emulgels. J Appl Pharm Sci. 2015; 5(7):112-7. https://doi.org/10.7324/JAPS.2015.50717 DOI: https://doi.org/10.7324/JAPS.2015.50717

Nazir R, Pandey DK, Pandey B, Kumar V, Dwivedi P, Khampariya A, Dey A, Malik T. Optimization of diosgenin extraction from Dioscorea deltoidea tubers using response surface methodology and artificial neural network modeling. PLoS One. 2021; 16:1-19. https://doi. org/10.1371/journal.pone.0253617 DOI: https://doi.org/10.1371/journal.pone.0253617

Khan BA, Ullah S, Khan MK, Alshahrani SM, Braga VA. Formulation and evaluation of Ocimum basilicum-based emulgel for wound healing using an animal model. Saudi Pharm J. 2020; 28(12):1842-50. https://doi.org/10.1016/j. jsps.2020.11.011 DOI: https://doi.org/10.1016/j.jsps.2020.11.011

Charyulu NR, Joshi P, Dubey A, Shetty A. Emulgel: A boon for enhanced topical drug delivery. Journal of Young Pharmacists. 2021; 13(1):76-9. https://doi.org/10.5530/ jyp.2021.13.17 DOI: https://doi.org/10.5530/jyp.2021.13.17

Khan BA, Ali A, Hosny KM, Halwani AA, Almehmady AM, Iqbal M, Alharbi W, Abualsunun A, Bakhaidar R, Murshid S, Khan M. Carbopol emulgel loaded with ebastine for urticaria: Development, characterization, in vitro and in vivo evaluation. Drug Deliv. 2022; 29(1):52-61. https://doi. org/10.1080/10717544.2021.2015483 DOI: https://doi.org/10.1080/10717544.2021.2015483

Rahman M, Ahmad Bhat K, Ara T. Synthesis and antimicrobial activity of triazolyl analogs of diosgenin. The Journal of Phytopharmacology. 2017; 6(4):227-33. https:// doi.org/10.31254/phyto.2017.6405 DOI: https://doi.org/10.31254/phyto.2017.6405

Choudhry A, Akhtar N. Formulation, characterization of Quercus infectoria (Olivier) emulsions, and in vitro, in vivo evaluation as cosmeceutical formulation. J Cosmet Dermatol. 2023; 22(12):3480-90. https://doi.org/10.1111/jocd.15865 DOI: https://doi.org/10.1111/jocd.15865

Gottrup F, Ågren MS, Karlsmark T. Models for use in wound healing research: A survey focusing on in vitro and in vivo adult soft tissue. Wound Repair and Regeneration. 2000; 8(2):83- 96. https://doi.org/10.1046/j.1524-475x.2000.00083.x DOI: https://doi.org/10.1046/j.1524-475x.2000.00083.x

Masson-Meyers DS, Andrade TAM, Caetano GF, Guimaraes FR, Leite MN, Leite SN, Frade MAC. Experimental models and methods for cutaneous wound healing assessment. Int J Exp Pathol. 2020; 101(1-2):21-37. https://doi.org/10.1111/ iep.12346 DOI: https://doi.org/10.1111/iep.12346

Cross SE, Naylor L, Coleman RA, Teo TC. An experimental model to investigate the dynamics of wound contraction. British journal of plastic surgery. 1995; 48(4):189-97. https://doi.org/10.1016/0007-1226(95)90001-2 DOI: https://doi.org/10.1016/0007-1226(95)90001-2

Franz MG, Smith PD, Wachtel TL, Wright TE, Kuhn MA, Ko F, Robson MC. Fascial incisions heal faster than skin: A new model of abdominal wall repair. Surgery. 2001; 129(2):203-8. https://doi.org/10.1067/msy.2001.110220 DOI: https://doi.org/10.1067/msy.2001.110220

Dorsett-Martin WA. Rat models of skin wound healing: A review. Wound Repair Regen. 2004; 12(6):591-9. https:// doi.org/10.1111/j.1067-1927.2004.12601.x DOI: https://doi.org/10.1111/j.1067-1927.2004.12601.x

Jung DH, Park HJ, Byun HE, Park YM, Kim TW, Kim BO, Um SH, Pyo S. Diosgenin inhibits macrophagederived inflammatory mediators through downregulation of CK2, JNK, NF-κB, and AP-1 activation. International Immunopharmacology. 2010; 10(9):1047-54. https://doi. org/10.1016/j.intimp.2010.06.004 DOI: https://doi.org/10.1016/j.intimp.2010.06.004

Leite SN, Leite MN, Caetano GF, Ovidio PP, Junior AA, Frade MA. Phototherapy improves wound healing in rats subjected to a high-fat diet. Lasers in Medical Science. 2015; 30:1481-8. https://doi.org/10.1007/s10103-015-1745-2 DOI: https://doi.org/10.1007/s10103-015-1745-2

Fisman EZ, Motro M, Tenenbaum A. Cardiovascular diabetology in the core of a novel interleukins classification: The bad, the good and the aloof. Cardiovascular Diabetology. 2003; 2(1):1-0. https://doi.org/10.1186/1475-2840-1-2 DOI: https://doi.org/10.1186/1475-2840-1-2

Ku CM, Lin JY. The anti-inflammatory effects of 27 selected terpenoid compounds were tested through modulating Th1/Th2 cytokine secretion profiles using murine primary splenocytes. Food Chemistry. 2013; 141(2):1104-13. https:// doi.org/10.1016/j.foodchem.2013.04.044 DOI: https://doi.org/10.1016/j.foodchem.2013.04.044