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Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing

This study aimed to develop novel topical formulations based on a natural component (0.5% of Siberian pine essential oil) and to assess its wound-healing capacity through macroscopic, histopathological, and biochemical examination. The phytochemical profile of Pinus sibirica essential oil (PSEO) and...

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Autores principales: Nikolic, Milica, Andjic, Marijana, Bradic, Jovana, Kocovic, Aleksandar, Tomovic, Marina, Samanovic, Andjela Milojevic, Jakovljevic, Vladimir, Veselinovic, Mirjana, Capo, Ivan, Krstonosic, Veljko, Kladar, Nebojsa, Petrovic, Anica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610429/
https://www.ncbi.nlm.nih.gov/pubmed/37896197
http://dx.doi.org/10.3390/pharmaceutics15102437
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author Nikolic, Milica
Andjic, Marijana
Bradic, Jovana
Kocovic, Aleksandar
Tomovic, Marina
Samanovic, Andjela Milojevic
Jakovljevic, Vladimir
Veselinovic, Mirjana
Capo, Ivan
Krstonosic, Veljko
Kladar, Nebojsa
Petrovic, Anica
author_facet Nikolic, Milica
Andjic, Marijana
Bradic, Jovana
Kocovic, Aleksandar
Tomovic, Marina
Samanovic, Andjela Milojevic
Jakovljevic, Vladimir
Veselinovic, Mirjana
Capo, Ivan
Krstonosic, Veljko
Kladar, Nebojsa
Petrovic, Anica
author_sort Nikolic, Milica
collection PubMed
description This study aimed to develop novel topical formulations based on a natural component (0.5% of Siberian pine essential oil) and to assess its wound-healing capacity through macroscopic, histopathological, and biochemical examination. The phytochemical profile of Pinus sibirica essential oil (PSEO) and rheological analysis and safety potential of formulations were determined. The wound-healing effect was evaluated on an excision wound model in diabetic Wistar albino rats randomly divided into the following groups topically treated with (1) untreated, (2) 1% silver sulfadiazine, (3) ointment base, (4) gel base, (5) PSEO ointment, and (6) PSEO gel. Formulations containing PSEO were stable and safe for skin application. Three weeks of treatment with both PSEO formulations (ointment and gel) led to a significant reduction in wound size (98.14% and 96.28%, respectively) and a remarkably higher level of total hydroxyproline content (9.69 µg/mg and 7.26 µg/mg dry tissue, respectively) relative to the control group (65.97%; 1.81 µg/mg dry tissue). These findings were in correlation with histopathological results. Topically applied PSEO formulations were associated with a significant reduction in most of the measured pro-oxidants and enhanced activity of the antioxidant defense system enzymes (p < 0.05). Our findings showed that gel and ointment with PSEO demonstrated significant wound-repairing capabilities in the excision wound model.
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spelling pubmed-106104292023-10-28 Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing Nikolic, Milica Andjic, Marijana Bradic, Jovana Kocovic, Aleksandar Tomovic, Marina Samanovic, Andjela Milojevic Jakovljevic, Vladimir Veselinovic, Mirjana Capo, Ivan Krstonosic, Veljko Kladar, Nebojsa Petrovic, Anica Pharmaceutics Article This study aimed to develop novel topical formulations based on a natural component (0.5% of Siberian pine essential oil) and to assess its wound-healing capacity through macroscopic, histopathological, and biochemical examination. The phytochemical profile of Pinus sibirica essential oil (PSEO) and rheological analysis and safety potential of formulations were determined. The wound-healing effect was evaluated on an excision wound model in diabetic Wistar albino rats randomly divided into the following groups topically treated with (1) untreated, (2) 1% silver sulfadiazine, (3) ointment base, (4) gel base, (5) PSEO ointment, and (6) PSEO gel. Formulations containing PSEO were stable and safe for skin application. Three weeks of treatment with both PSEO formulations (ointment and gel) led to a significant reduction in wound size (98.14% and 96.28%, respectively) and a remarkably higher level of total hydroxyproline content (9.69 µg/mg and 7.26 µg/mg dry tissue, respectively) relative to the control group (65.97%; 1.81 µg/mg dry tissue). These findings were in correlation with histopathological results. Topically applied PSEO formulations were associated with a significant reduction in most of the measured pro-oxidants and enhanced activity of the antioxidant defense system enzymes (p < 0.05). Our findings showed that gel and ointment with PSEO demonstrated significant wound-repairing capabilities in the excision wound model. MDPI 2023-10-09 /pmc/articles/PMC10610429/ /pubmed/37896197 http://dx.doi.org/10.3390/pharmaceutics15102437 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nikolic, Milica
Andjic, Marijana
Bradic, Jovana
Kocovic, Aleksandar
Tomovic, Marina
Samanovic, Andjela Milojevic
Jakovljevic, Vladimir
Veselinovic, Mirjana
Capo, Ivan
Krstonosic, Veljko
Kladar, Nebojsa
Petrovic, Anica
Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing
title Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing
title_full Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing
title_fullStr Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing
title_full_unstemmed Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing
title_short Topical Application of Siberian Pine Essential Oil Formulations Enhance Diabetic Wound Healing
title_sort topical application of siberian pine essential oil formulations enhance diabetic wound healing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610429/
https://www.ncbi.nlm.nih.gov/pubmed/37896197
http://dx.doi.org/10.3390/pharmaceutics15102437
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