Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound
Previously, we have developed collagen type I scaffolds including microparticles of gelatin-collagen type I (SGC) that are able to control the release of a hydroglycolic extract of the Calendula officinalis flower. The main goal of the present work was to carry out the preclinical evaluation of SGC...
- Autores:
-
Millán, Diana
Jimenez, Ronald
Nieto, L. E.
Linero, Itali M.
Laverde, M.
Fontanilla, Marta Raquel
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2016
- Institución:
- Universidad El Bosque
- Repositorio:
- Repositorio U. El Bosque
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.unbosque.edu.co:20.500.12495/3535
- Acceso en línea:
- http://hdl.handle.net/20.500.12495/3535
http://dx.doi.org/10.1007/s13346-015-0265-8
https://repositorio.unbosque.edu.co
- Palabra clave:
- Colágeno tipo I
Copolímero de ácido poliláctico-ácido poliglicólico
Plantas medicinales
Collagen type I
Scaffolds
Gelatin-collagenmicroparticles
- Rights
- openAccess
- License
- Acceso abierto
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oai:repositorio.unbosque.edu.co:20.500.12495/3535 |
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UNBOSQUE2 |
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Repositorio U. El Bosque |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
dc.title.translated.spa.fl_str_mv |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
title |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
spellingShingle |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound Colágeno tipo I Copolímero de ácido poliláctico-ácido poliglicólico Plantas medicinales Collagen type I Scaffolds Gelatin-collagenmicroparticles |
title_short |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
title_full |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
title_fullStr |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
title_full_unstemmed |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
title_sort |
Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin wound |
dc.creator.fl_str_mv |
Millán, Diana Jimenez, Ronald Nieto, L. E. Linero, Itali M. Laverde, M. Fontanilla, Marta Raquel |
dc.contributor.author.none.fl_str_mv |
Millán, Diana Jimenez, Ronald Nieto, L. E. Linero, Itali M. Laverde, M. Fontanilla, Marta Raquel |
dc.subject.decs.spa.fl_str_mv |
Colágeno tipo I Copolímero de ácido poliláctico-ácido poliglicólico Plantas medicinales |
topic |
Colágeno tipo I Copolímero de ácido poliláctico-ácido poliglicólico Plantas medicinales Collagen type I Scaffolds Gelatin-collagenmicroparticles |
dc.subject.keywords.spa.fl_str_mv |
Collagen type I Scaffolds Gelatin-collagenmicroparticles |
description |
Previously, we have developed collagen type I scaffolds including microparticles of gelatin-collagen type I (SGC) that are able to control the release of a hydroglycolic extract of the Calendula officinalis flower. The main goal of the present work was to carry out the preclinical evaluation of SGC alone or loaded with the C. officinalis extract (SGC-E) in a lagomorph model of full-thickness skin wound. A total of 39 rabbits were distributed in three groups, of 13 animals each. The first group was used to compare wound healing by secondary intention (control) with wound healing observed when wounds were grafted with SGC alone. Comparison of control wounds with wounds grafted with SGC-E was performed in the second group, and comparison of wounds grafted with SGC with wounds grafted with SGC-E was performed in the third group. Clinical follow-ups were carried in all animals after surgery, and histological and histomorphometric analyses were performed on tissues taken from the healed area and healthy surrounding tissue. Histological and histomorphometric results indicate that grafting of SGC alone favors wound healing and brings a better clinical outcome than grafting SGC-E. In vitro collagenase digestion data suggested that the association of the C. officinalis extract to SGC increased the SGC-E cross-linking, making it difficult to degrade and affecting its biocompatibility. |
publishDate |
2016 |
dc.date.issued.none.fl_str_mv |
2016 |
dc.date.accessioned.none.fl_str_mv |
2020-07-16T16:13:26Z |
dc.date.available.none.fl_str_mv |
2020-07-16T16:13:26Z |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.local.none.fl_str_mv |
Artículo de revista |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.driver.none.fl_str_mv |
info:eu-repo/semantics/article |
format |
http://purl.org/coar/resource_type/c_6501 |
dc.identifier.issn.none.fl_str_mv |
2190-3948 |
dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/20.500.12495/3535 |
dc.identifier.doi.none.fl_str_mv |
http://dx.doi.org/10.1007/s13346-015-0265-8 |
dc.identifier.instname.spa.fl_str_mv |
instname:Universidad El Bosque |
dc.identifier.reponame.spa.fl_str_mv |
reponame:Repositorio Institucional Universidad El Bosque |
dc.identifier.repourl.none.fl_str_mv |
https://repositorio.unbosque.edu.co |
identifier_str_mv |
2190-3948 instname:Universidad El Bosque reponame:Repositorio Institucional Universidad El Bosque |
url |
http://hdl.handle.net/20.500.12495/3535 http://dx.doi.org/10.1007/s13346-015-0265-8 https://repositorio.unbosque.edu.co |
dc.language.iso.none.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartofseries.spa.fl_str_mv |
Drug delivery and translational research, 2190-3948, Vol. 6, Nro. 1, 2016, p. 57-66 |
dc.relation.uri.none.fl_str_mv |
https://link.springer.com/article/10.1007%2Fs13346-015-0265-8 |
dc.rights.local.spa.fl_str_mv |
Acceso abierto |
dc.rights.accessrights.none.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 info:eu-repo/semantics/openAccess Acceso abierto |
dc.rights.creativecommons.none.fl_str_mv |
2016-02-01 |
rights_invalid_str_mv |
Acceso abierto http://purl.org/coar/access_right/c_abf2 2016-02-01 |
eu_rights_str_mv |
openAccess |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Springer Nature |
dc.publisher.journal.spa.fl_str_mv |
Drug delivery and translational research |
institution |
Universidad El Bosque |
bitstream.url.fl_str_mv |
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spelling |
Millán, DianaJimenez, RonaldNieto, L. E.Linero, Itali M.Laverde, M.Fontanilla, Marta Raquel2020-07-16T16:13:26Z2020-07-16T16:13:26Z20162190-3948http://hdl.handle.net/20.500.12495/3535http://dx.doi.org/10.1007/s13346-015-0265-8instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengSpringer NatureDrug delivery and translational researchDrug delivery and translational research, 2190-3948, Vol. 6, Nro. 1, 2016, p. 57-66https://link.springer.com/article/10.1007%2Fs13346-015-0265-8Preclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin woundPreclinical evaluation of collagen type I scaffolds, including gelatin-collagen microparticles and loaded with a hydroglycolic Calendula officinalis extract in a lagomorph model of full-thickness skin woundArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85Colágeno tipo ICopolímero de ácido poliláctico-ácido poliglicólicoPlantas medicinalesCollagen type IScaffoldsGelatin-collagenmicroparticlesPreviously, we have developed collagen type I scaffolds including microparticles of gelatin-collagen type I (SGC) that are able to control the release of a hydroglycolic extract of the Calendula officinalis flower. The main goal of the present work was to carry out the preclinical evaluation of SGC alone or loaded with the C. officinalis extract (SGC-E) in a lagomorph model of full-thickness skin wound. A total of 39 rabbits were distributed in three groups, of 13 animals each. The first group was used to compare wound healing by secondary intention (control) with wound healing observed when wounds were grafted with SGC alone. Comparison of control wounds with wounds grafted with SGC-E was performed in the second group, and comparison of wounds grafted with SGC with wounds grafted with SGC-E was performed in the third group. Clinical follow-ups were carried in all animals after surgery, and histological and histomorphometric analyses were performed on tissues taken from the healed area and healthy surrounding tissue. Histological and histomorphometric results indicate that grafting of SGC alone favors wound healing and brings a better clinical outcome than grafting SGC-E. In vitro collagenase digestion data suggested that the association of the C. officinalis extract to SGC increased the SGC-E cross-linking, making it difficult to degrade and affecting its biocompatibility.Acceso abiertohttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto2016-02-01LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.unbosque.edu.co/bitstreams/888ec06e-38d3-4830-9d90-99380fcab318/download8a4605be74aa9ea9d79846c1fba20a33MD52ORIGINALD. Millán ,RA Jiménez ,LE Nieto ,I. Linero_2016.pdfD. Millán ,RA Jiménez ,LE Nieto ,I. Linero_2016.pdfapplication/pdf16540894https://repositorio.unbosque.edu.co/bitstreams/bc12e380-a221-4bb0-b73d-551f68d33f28/download17c0149cd17daeeac9213bc6e65a1efeMD51THUMBNAILD. Millán ,RA Jiménez ,LE Nieto ,I. Linero_2016.pdf.jpgD. Millán ,RA Jiménez ,LE Nieto ,I. 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