Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo

ABSTRACT: Cutaneous leishmaniasis (CL) is classified as a neglected tropical disease by the World Health Organization. As the standard drugs for the treatment of this disease suffer from severeunwanted effects, new effective and safe therapeutic options are required. In our previous work, Arnica tin...

Full description

Autores:
Robledo Restrepo, Sara María
Jürgens, Franziska M.
Schmidt, Thomas J.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/44293
Acceso en línea:
https://hdl.handle.net/10495/44293
Palabra clave:
Arnica
Lactonas
Lactones
Leishmaniasis Cutánea
Leishmaniasis, Cutaneous
Helenalina
Helenalin
https://id.nlm.nih.gov/mesh/D018650
https://id.nlm.nih.gov/mesh/D007783
https://id.nlm.nih.gov/mesh/D016773
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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dc.title.spa.fl_str_mv Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
title Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
spellingShingle Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
Arnica
Lactonas
Lactones
Leishmaniasis Cutánea
Leishmaniasis, Cutaneous
Helenalina
Helenalin
https://id.nlm.nih.gov/mesh/D018650
https://id.nlm.nih.gov/mesh/D007783
https://id.nlm.nih.gov/mesh/D016773
title_short Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
title_full Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
title_fullStr Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
title_full_unstemmed Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
title_sort Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo
dc.creator.fl_str_mv Robledo Restrepo, Sara María
Jürgens, Franziska M.
Schmidt, Thomas J.
dc.contributor.author.none.fl_str_mv Robledo Restrepo, Sara María
Jürgens, Franziska M.
Schmidt, Thomas J.
dc.contributor.researchgroup.spa.fl_str_mv Programa de Estudio y Control de Enfermedades Tropicales (PECET)
dc.subject.decs.none.fl_str_mv Arnica
Lactonas
Lactones
Leishmaniasis Cutánea
Leishmaniasis, Cutaneous
topic Arnica
Lactonas
Lactones
Leishmaniasis Cutánea
Leishmaniasis, Cutaneous
Helenalina
Helenalin
https://id.nlm.nih.gov/mesh/D018650
https://id.nlm.nih.gov/mesh/D007783
https://id.nlm.nih.gov/mesh/D016773
dc.subject.proposal.spa.fl_str_mv Helenalina
Helenalin
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D018650
https://id.nlm.nih.gov/mesh/D007783
https://id.nlm.nih.gov/mesh/D016773
description ABSTRACT: Cutaneous leishmaniasis (CL) is classified as a neglected tropical disease by the World Health Organization. As the standard drugs for the treatment of this disease suffer from severeunwanted effects, new effective and safe therapeutic options are required. In our previous work, Arnica tincture showed promising antileishmanial effects in vitro and in vivo. For the potential treatment of human CL patients with Arnica tincture, data on the pharmacokinetic properties of the bioactive, antileishmanial compounds (the sesquiterpene lactone (STL) helenalin and its derivatives) are needed. Therefore, we studied the in vivo absorption of the bioactive compounds after the dermal application of Arnica tincture in rats. Moreover, we analyzed the blood plasma, urine, and feces of the animals by ultra-high-performance liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS). Although the majority (84%) of the applied STLs (1.0 mg) were absorbed, the concentrations in the plasma, urine, and feces were below the limit of detection (0.3 ng/mL) in the samples for UHPLC-HRMS analysis. This result may be explained by extensive metabolism and slow permeation accompanied by the accumulation of STLs in the skin, as described in our previous work. Accordingly, the plasma concentration of STLs after the topical application of Arnica tincture was very far from a dose where toxicity could be expected. Additionally, tests for corrosive or irritant activity as well as acute and repeated-dose dermal toxicity did not show any positive results after the administration of the amounts of Arnica tincture that would be needed for the treatment of CL. Consequently, in the treatment of CL patients with Arnica tincture, no toxic effects are expected, other than the known sensitization potential of the STLs.
publishDate 2022
dc.date.issued.none.fl_str_mv 2022
dc.date.accessioned.none.fl_str_mv 2025-01-21T20:05:33Z
dc.date.available.none.fl_str_mv 2025-01-21T20:05:33Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Jürgens FM, Robledo SM, Schmidt TJ. Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo. Pharmaceutics. 2022 Nov 4;14(11):2379. doi: 10.3390/pharmaceutics14112379.
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/44293
dc.identifier.doi.none.fl_str_mv 10.3390/pharmaceutics14112379
dc.identifier.eissn.none.fl_str_mv 1999-4923 1
identifier_str_mv Jürgens FM, Robledo SM, Schmidt TJ. Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo. Pharmaceutics. 2022 Nov 4;14(11):2379. doi: 10.3390/pharmaceutics14112379.
10.3390/pharmaceutics14112379
1999-4923 1
url https://hdl.handle.net/10495/44293
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Pharmaceutics
dc.relation.citationendpage.spa.fl_str_mv 13
dc.relation.citationissue.spa.fl_str_mv 11
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 14
dc.relation.ispartofjournal.spa.fl_str_mv Pharmaceutics
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dc.format.extent.spa.fl_str_mv 13 páginas
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dc.publisher.place.spa.fl_str_mv Basilea, Suiza
institution Universidad de Antioquia
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spelling Robledo Restrepo, Sara MaríaJürgens, Franziska M.Schmidt, Thomas J.Programa de Estudio y Control de Enfermedades Tropicales (PECET)2025-01-21T20:05:33Z2025-01-21T20:05:33Z2022Jürgens FM, Robledo SM, Schmidt TJ. Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In Vivo. Pharmaceutics. 2022 Nov 4;14(11):2379. doi: 10.3390/pharmaceutics14112379.https://hdl.handle.net/10495/4429310.3390/pharmaceutics141123791999-4923 1ABSTRACT: Cutaneous leishmaniasis (CL) is classified as a neglected tropical disease by the World Health Organization. As the standard drugs for the treatment of this disease suffer from severeunwanted effects, new effective and safe therapeutic options are required. In our previous work, Arnica tincture showed promising antileishmanial effects in vitro and in vivo. For the potential treatment of human CL patients with Arnica tincture, data on the pharmacokinetic properties of the bioactive, antileishmanial compounds (the sesquiterpene lactone (STL) helenalin and its derivatives) are needed. Therefore, we studied the in vivo absorption of the bioactive compounds after the dermal application of Arnica tincture in rats. Moreover, we analyzed the blood plasma, urine, and feces of the animals by ultra-high-performance liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS). Although the majority (84%) of the applied STLs (1.0 mg) were absorbed, the concentrations in the plasma, urine, and feces were below the limit of detection (0.3 ng/mL) in the samples for UHPLC-HRMS analysis. This result may be explained by extensive metabolism and slow permeation accompanied by the accumulation of STLs in the skin, as described in our previous work. Accordingly, the plasma concentration of STLs after the topical application of Arnica tincture was very far from a dose where toxicity could be expected. Additionally, tests for corrosive or irritant activity as well as acute and repeated-dose dermal toxicity did not show any positive results after the administration of the amounts of Arnica tincture that would be needed for the treatment of CL. Consequently, in the treatment of CL patients with Arnica tincture, no toxic effects are expected, other than the known sensitization potential of the STLs.COL001509913 páginasapplication/pdfengMDPIBasilea, Suizahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Evaluation of Pharmacokinetic and Toxicological Parameters of Arnica Tincture after Dermal Application In VivoArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArnicaLactonasLactonesLeishmaniasis CutáneaLeishmaniasis, CutaneousHelenalinaHelenalinhttps://id.nlm.nih.gov/mesh/D018650https://id.nlm.nih.gov/mesh/D007783https://id.nlm.nih.gov/mesh/D016773Pharmaceutics1311114PharmaceuticsPublicationORIGINALRobledoSara_2022_DermalHumanSTL.pdfRobledoSara_2022_DermalHumanSTL.pdfArtículo de investigaciónapplication/pdf1143334https://bibliotecadigital.udea.edu.co/bitstreams/229d04b4-6233-45ef-b1e7-60c3ea728916/downloadea4783f8abdc88c858eba489364b2c69MD51trueAnonymousREADRobledoSara_2022_Dermal_Human_Pharmacokinetic.epubRobledoSara_2022_Dermal_Human_Pharmacokinetic.epubArtículo de investigaciónapplication/epub+zip238604https://bibliotecadigital.udea.edu.co/bitstreams/8d137547-8a06-4d5b-859c-e42cdc8b64d1/download303fa5b3b314b546d7229859e2d75fe1MD54falseAnonymousREADCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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