Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10362/121299 |
Resumo: | UIDB/50006/2020 POCI-01-0145-FEDER?007265 PTDC/QUI-QOR/32406/2017 MAR-02.01.01-FEAMP-0042 |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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7160 |
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Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studiesBioavailabilityCytotoxicityIonic liquids & organic saltsIsoniazidTuberculosisPharmaceutical ScienceSDG 3 - Good Health and Well-beingUIDB/50006/2020 POCI-01-0145-FEDER?007265 PTDC/QUI-QOR/32406/2017 MAR-02.01.01-FEAMP-0042Tuberculosis is one of the ten causes of morbidity and mortality worldwide caused by Mycobacterium tuberculosis complex. Some of the anti-tuberculosis drugs used in clinic studies, despite being effective for the treatment of tuberculosis, present serious adverse effects as well as poor bioavailability, stability, and drug-resistance problems. Thus, it is important to develop approaches that could provide shorter drug regimens, preventing drug resistance, toxicity of the antibiotics, and improve their bioavailability. Herein, we reported the use of organic salts based on the isoniazid drug, which can act as an organic cation combined with suitable organic anions such as alkylsulfonate-based (mesylate, R or S-Camphorsulfonate), carboxylate-based (glycolate, vanylate) and sacharinate. The synthesis, characterization, and cytotoxicity studies comparing with the original isoniazid drug have been performed. The possibility to explore dicationic salts seems promising in order to improve original bioavailability, and promote the elimination of polymorphic forms as well as higher stability, which are relevant characteristics that the pharmaceutical industry pursues.LAQV@REQUIMTEDQ - Departamento de QuímicaRUNSantos, FilipaBranco, Luís C.Duarte, Ana Rita C.2021-07-19T22:17:57Z2020-10-102020-10-10T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article15application/pdfhttp://hdl.handle.net/10362/121299eng1999-4923PURE: 32646123https://doi.org/10.3390/pharmaceutics12100952info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T05:03:31Zoai:run.unl.pt:10362/121299Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:44:33.331995Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies |
title |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies |
spellingShingle |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies Santos, Filipa Bioavailability Cytotoxicity Ionic liquids & organic salts Isoniazid Tuberculosis Pharmaceutical Science SDG 3 - Good Health and Well-being |
title_short |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies |
title_full |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies |
title_fullStr |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies |
title_full_unstemmed |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies |
title_sort |
Organic salts based on isoniazid drug: Synthesis, bioavailability and cytotoxicity studies |
author |
Santos, Filipa |
author_facet |
Santos, Filipa Branco, Luís C. Duarte, Ana Rita C. |
author_role |
author |
author2 |
Branco, Luís C. Duarte, Ana Rita C. |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
LAQV@REQUIMTE DQ - Departamento de Química RUN |
dc.contributor.author.fl_str_mv |
Santos, Filipa Branco, Luís C. Duarte, Ana Rita C. |
dc.subject.por.fl_str_mv |
Bioavailability Cytotoxicity Ionic liquids & organic salts Isoniazid Tuberculosis Pharmaceutical Science SDG 3 - Good Health and Well-being |
topic |
Bioavailability Cytotoxicity Ionic liquids & organic salts Isoniazid Tuberculosis Pharmaceutical Science SDG 3 - Good Health and Well-being |
description |
UIDB/50006/2020 POCI-01-0145-FEDER?007265 PTDC/QUI-QOR/32406/2017 MAR-02.01.01-FEAMP-0042 |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-10-10 2020-10-10T00:00:00Z 2021-07-19T22:17:57Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10362/121299 |
url |
http://hdl.handle.net/10362/121299 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1999-4923 PURE: 32646123 https://doi.org/10.3390/pharmaceutics12100952 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
15 application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799138053259788288 |