Effect of Hydrogel Containing Achyrocline satureioides (Asteraceae) Extract-Loaded Nanoemulsions on Wound Healing Activity
(Lam.) DC extract-loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte proliferation. We carried out the first in vivo investigation of the wound healing activity of a hydrogel containing extract-loaded nanoemulsions. We prepared hydrogels by add...
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Published in | Pharmaceutics Vol. 14; no. 12; p. 2726 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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06.12.2022
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Abstract | (Lam.) DC extract-loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte proliferation. We carried out the first in vivo investigation of the wound healing activity of a hydrogel containing
extract-loaded nanoemulsions. We prepared hydrogels by adding the gelling agent (Carbopol
Ultrez) to extract-loaded nanoemulsions (~250 nm in diameter) obtained by spontaneous emulsification. The final flavonoid content in formulation was close to 1 mg/mL, as estimated by ultra-fast liquid chromatography. Permeation/retention studies using porcine ear skin showed that flavonoids reached deeper layers of pig ear skin when it was damaged (up to 3.2 µg/cm² in the dermis), but did not reach the Franz-type diffusion cell receptor fluid. For healing activity, we performed a dorsal wound model using Wistar rats, evaluating the lesion size, anti-inflammatory markers, oxidative damage, and histology. We found that extract-loaded formulations promoted wound healing by increasing angiogenesis by ~20%, reducing inflammation (tumor necrosis factor α) by ~35%, decreasing lipid damage, and improving the re-epithelialization process in lesions. In addition, there was an increase in the number of blood vessels and hair follicles for wounds treated with the formulation compared with the controls. Our findings indicate that the proposed formulation could be promising in the search for better quality healing and tissue reconstruction. |
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AbstractList | Achyrocline satureioides (Lam.) DC extract–loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte proliferation. We carried out the first in vivo investigation of the wound healing activity of a hydrogel containing A. satureioides extract–loaded nanoemulsions. We prepared hydrogels by adding the gelling agent (Carbopol® Ultrez) to extract-loaded nanoemulsions (~250 nm in diameter) obtained by spontaneous emulsification. The final flavonoid content in formulation was close to 1 mg/mL, as estimated by ultra-fast liquid chromatography. Permeation/retention studies using porcine ear skin showed that flavonoids reached deeper layers of pig ear skin when it was damaged (up to 3.2 µg/cm² in the dermis), but did not reach the Franz-type diffusion cell receptor fluid. For healing activity, we performed a dorsal wound model using Wistar rats, evaluating the lesion size, anti-inflammatory markers, oxidative damage, and histology. We found that extract-loaded formulations promoted wound healing by increasing angiogenesis by ~20%, reducing inflammation (tumor necrosis factor α) by ~35%, decreasing lipid damage, and improving the re-epithelialization process in lesions. In addition, there was an increase in the number of blood vessels and hair follicles for wounds treated with the formulation compared with the controls. Our findings indicate that the proposed formulation could be promising in the search for better quality healing and tissue reconstruction. Achyrocline satureioides (Lam.) DC extract–loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte proliferation. We carried out the first in vivo investigation of the wound healing activity of a hydrogel containing A. satureioides extract–loaded nanoemulsions. We prepared hydrogels by adding the gelling agent (Carbopol ® Ultrez) to extract-loaded nanoemulsions (~250 nm in diameter) obtained by spontaneous emulsification. The final flavonoid content in formulation was close to 1 mg/mL, as estimated by ultra-fast liquid chromatography. Permeation/retention studies using porcine ear skin showed that flavonoids reached deeper layers of pig ear skin when it was damaged (up to 3.2 µg/cm² in the dermis), but did not reach the Franz-type diffusion cell receptor fluid. For healing activity, we performed a dorsal wound model using Wistar rats, evaluating the lesion size, anti-inflammatory markers, oxidative damage, and histology. We found that extract-loaded formulations promoted wound healing by increasing angiogenesis by ~20%, reducing inflammation (tumor necrosis factor α) by ~35%, decreasing lipid damage, and improving the re-epithelialization process in lesions. In addition, there was an increase in the number of blood vessels and hair follicles for wounds treated with the formulation compared with the controls. Our findings indicate that the proposed formulation could be promising in the search for better quality healing and tissue reconstruction. (Lam.) DC extract-loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte proliferation. We carried out the first in vivo investigation of the wound healing activity of a hydrogel containing extract-loaded nanoemulsions. We prepared hydrogels by adding the gelling agent (Carbopol Ultrez) to extract-loaded nanoemulsions (~250 nm in diameter) obtained by spontaneous emulsification. The final flavonoid content in formulation was close to 1 mg/mL, as estimated by ultra-fast liquid chromatography. Permeation/retention studies using porcine ear skin showed that flavonoids reached deeper layers of pig ear skin when it was damaged (up to 3.2 µg/cm² in the dermis), but did not reach the Franz-type diffusion cell receptor fluid. For healing activity, we performed a dorsal wound model using Wistar rats, evaluating the lesion size, anti-inflammatory markers, oxidative damage, and histology. We found that extract-loaded formulations promoted wound healing by increasing angiogenesis by ~20%, reducing inflammation (tumor necrosis factor α) by ~35%, decreasing lipid damage, and improving the re-epithelialization process in lesions. In addition, there was an increase in the number of blood vessels and hair follicles for wounds treated with the formulation compared with the controls. Our findings indicate that the proposed formulation could be promising in the search for better quality healing and tissue reconstruction. |
Author | Marques, Magno da Silva Silveira, Tony Rodrigues, Jamile Lima Bassani, Valquiria Linck Dora, Cristiana Lima Batista, Matheus Monteiro Horn, Ana Paula Balestrin, Lucélia Albarello Carrasco, Mariana Corrêa Falkembach Fachel, Flávia Nathiely Silveira Teixeira, Helder Ferreira Back, Patrícia Inês Araújo, Gabriela de Moraes Soares Koester, Leticia Scherer |
AuthorAffiliation | 3 Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil 2 Programa de Pós-Graduação em Ciências Fisiológicas (PPGCF), Laboratório de Histologia, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande (FURG), Av. Itália, km 8, s/n, Rio Grande 96203-900, Rio Grande do Sul, Brazil 1 Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil |
AuthorAffiliation_xml | – name: 3 Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil – name: 1 Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil – name: 2 Programa de Pós-Graduação em Ciências Fisiológicas (PPGCF), Laboratório de Histologia, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande (FURG), Av. Itália, km 8, s/n, Rio Grande 96203-900, Rio Grande do Sul, Brazil |
Author_xml | – sequence: 1 givenname: Lucélia Albarello surname: Balestrin fullname: Balestrin, Lucélia Albarello organization: Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil – sequence: 2 givenname: Patrícia Inês surname: Back fullname: Back, Patrícia Inês organization: Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil – sequence: 3 givenname: Magno da Silva orcidid: 0000-0003-2451-1270 surname: Marques fullname: Marques, Magno da Silva organization: Programa de Pós-Graduação em Ciências Fisiológicas (PPGCF), Laboratório de Histologia, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande (FURG), Av. Itália, km 8, s/n, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 4 givenname: Gabriela de Moraes Soares surname: Araújo fullname: Araújo, Gabriela de Moraes Soares organization: Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 5 givenname: Mariana Corrêa Falkembach surname: Carrasco fullname: Carrasco, Mariana Corrêa Falkembach organization: Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 6 givenname: Matheus Monteiro orcidid: 0000-0001-5729-1214 surname: Batista fullname: Batista, Matheus Monteiro organization: Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 7 givenname: Tony orcidid: 0000-0001-8802-5701 surname: Silveira fullname: Silveira, Tony organization: Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 8 givenname: Jamile Lima surname: Rodrigues fullname: Rodrigues, Jamile Lima organization: Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 9 givenname: Flávia Nathiely Silveira orcidid: 0000-0002-0777-9497 surname: Fachel fullname: Fachel, Flávia Nathiely Silveira organization: Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil – sequence: 10 givenname: Leticia Scherer surname: Koester fullname: Koester, Leticia Scherer organization: Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil – sequence: 11 givenname: Valquiria Linck surname: Bassani fullname: Bassani, Valquiria Linck organization: Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil – sequence: 12 givenname: Ana Paula surname: Horn fullname: Horn, Ana Paula organization: Programa de Pós-Graduação em Ciências Fisiológicas (PPGCF), Laboratório de Histologia, Instituto de Ciências Biológicas, Universidade Federal do Rio Grande (FURG), Av. Itália, km 8, s/n, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 13 givenname: Cristiana Lima orcidid: 0000-0002-9198-437X surname: Dora fullname: Dora, Cristiana Lima organization: Programa de Pós-Graduação em Ciências da Saúde (PPGCS), Laboratório de Nanotecnologia, Faculdade de Medicina, Universidade Federal do Rio Grande (FURG), Rua Visconde de Paranaguá 102, Rio Grande 96203-900, Rio Grande do Sul, Brazil – sequence: 14 givenname: Helder Ferreira surname: Teixeira fullname: Teixeira, Helder Ferreira organization: Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, Rio Grande do Sul, Brazil |
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Keywords | nanoemulsion Achyrocline satureioides hydrogel healing activity |
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Snippet | (Lam.) DC extract-loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte proliferation. We carried out the... Achyrocline satureioides (Lam.) DC extract–loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte... Achyrocline satureioides (Lam.) DC extract–loaded nanoemulsions have demonstrated potential for wound healing, with promising effects on keratinocyte... |
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SubjectTerms | Achyrocline satureioides Animals Ethanol Flavonoids healing activity Herbal medicine hydrogel Hydrogels Injuries nanoemulsion Nanoemulsions Skin Triglycerides Wound healing |
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Title | Effect of Hydrogel Containing Achyrocline satureioides (Asteraceae) Extract-Loaded Nanoemulsions on Wound Healing Activity |
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