Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos
Autor(a) principal: | |
---|---|
Data de Publicação: | 2016 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFSCAR |
Texto Completo: | https://repositorio.ufscar.br/handle/ufscar/7547 |
Resumo: | Many pharmaceutical solids are able to adopt more than one crystalline form, and this property is called polymorphism. Currently 80-90% of the drugs are marketed as in solid forms and a very common problem is the low solubility of these drugs, particularly in aqueous media. Depending on how a drug crystallizes, its physical and chemical properties can be changed, which may also result in changes in its solubility. Before this problem the crystals engineering appears as a strategy to improve the properties of the solid state related to the efficacy of the drugs through the development of new crystalline forms. Multicomponent molecular crystals can be prepared from supramolecular synthons forming approach by crystallization methods involving the optimization of conditions for the formation of these novel crystalline forms. In this context, this study aimed to use the solid state NMR for study of supramolecular chemistry the three antiparasitic drugs (secnidazole, albendazole and mebendazole) and one antiretroviral (tenofovir disoproxil fumarate) using a set of one-dimensional techniques (CP-TOSS, CP-NQS and CP-PI) for the carbon-13 and nitrogen-15 nucleus as well as two-dimensional (1Hx13C FSLG HETCOR). Solid state NMR was used as the primary analytical tool for characterizing the crystalline forms obtained in this study, as in the prior characterization of Active Pharmaceutical Ingredient (APIs) used as raw material, being demonstrated the applicability of this technique in the analysis of new formulations. The data obtained were of great importance in the study of these solid dosage forms which can contribute to the structural study of dosage forms, identify polymorphic forms of drugs, detect phase transitions in both API as in commercial samples and check for interactions molecular (intramolecular and intermolecular) by means of two-dimensional NMR. In this work it was shown that this technique is configured as an important tool for the characterization of new polymorphs but they certainly should be applied in conjunction with other techniques in order to take advantage of the complementarity provided when different techniques are used in combination. This work intends to consolidate the use of NMR in the solid state in Brazil as a tool for the characterization of the crystalline forms of drugs and also for the analysis of drugs, which has been few explored so far. |
id |
SCAR_ed39cf3f9b3ae26ce644098c97f7f91b |
---|---|
oai_identifier_str |
oai:repositorio.ufscar.br:ufscar/7547 |
network_acronym_str |
SCAR |
network_name_str |
Repositório Institucional da UFSCAR |
repository_id_str |
4322 |
spelling |
Xavier, Tatielih Pardim de OliveiraVenâncio, Tiagohttp://lattes.cnpq.br/4438399441102990http://lattes.cnpq.br/430731200189098596bee820-3ae5-4a36-a13f-eb61c5f51b952016-09-27T20:04:16Z2016-09-27T20:04:16Z2016-03-15XAVIER, Tatielih Pardim de Oliveira. Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos. 2016. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2016. Disponível em: https://repositorio.ufscar.br/handle/ufscar/7547.https://repositorio.ufscar.br/handle/ufscar/7547Many pharmaceutical solids are able to adopt more than one crystalline form, and this property is called polymorphism. Currently 80-90% of the drugs are marketed as in solid forms and a very common problem is the low solubility of these drugs, particularly in aqueous media. Depending on how a drug crystallizes, its physical and chemical properties can be changed, which may also result in changes in its solubility. Before this problem the crystals engineering appears as a strategy to improve the properties of the solid state related to the efficacy of the drugs through the development of new crystalline forms. Multicomponent molecular crystals can be prepared from supramolecular synthons forming approach by crystallization methods involving the optimization of conditions for the formation of these novel crystalline forms. In this context, this study aimed to use the solid state NMR for study of supramolecular chemistry the three antiparasitic drugs (secnidazole, albendazole and mebendazole) and one antiretroviral (tenofovir disoproxil fumarate) using a set of one-dimensional techniques (CP-TOSS, CP-NQS and CP-PI) for the carbon-13 and nitrogen-15 nucleus as well as two-dimensional (1Hx13C FSLG HETCOR). Solid state NMR was used as the primary analytical tool for characterizing the crystalline forms obtained in this study, as in the prior characterization of Active Pharmaceutical Ingredient (APIs) used as raw material, being demonstrated the applicability of this technique in the analysis of new formulations. The data obtained were of great importance in the study of these solid dosage forms which can contribute to the structural study of dosage forms, identify polymorphic forms of drugs, detect phase transitions in both API as in commercial samples and check for interactions molecular (intramolecular and intermolecular) by means of two-dimensional NMR. In this work it was shown that this technique is configured as an important tool for the characterization of new polymorphs but they certainly should be applied in conjunction with other techniques in order to take advantage of the complementarity provided when different techniques are used in combination. This work intends to consolidate the use of NMR in the solid state in Brazil as a tool for the characterization of the crystalline forms of drugs and also for the analysis of drugs, which has been few explored so far.Muitos sólidos farmacêuticos são capazes de adotar mais de uma forma cristalina, sendo esta propriedade denominada polimorfismo. Atualmente 80-90% dos fármacos são comercializados na forma sólida e um problema muito frequente é a baixa solubilidade destas drogas, principalmente em meio aquoso. Dependendo da forma como um fármaco se cristaliza, as suas propriedades físico-químicas podem ser alteradas, o que também poderá implicar em alterações em sua solubilidade. Diante desta problemática a engenharia de cristais surge como uma estratégia para aperfeiçoar as propriedades do estado sólido relacionada à eficácia dos fármacos, por meio do desenvolvimento de novas formas cristalinas. Cristais moleculares multicomponentes podem ser preparados a partir da abordagem de formação de sintões supramoleculares por meio de métodos de cristalização que envolve a otimização de condições favoráveis para a formação dessas novas formas cristalinas. Neste contexto este trabalho teve como objetivo utilizar a RMN no estado sólido para estudar a química supramolecular de três fármacos antiparasitários (secnidazol, albendazol e mebendazol) e um antirretroviral (tenofovir disoproxil fumarato) utilizando um conjunto de técnicas unidimensionais (CP-TOSS, CP-NQS e CP-PI) para os núcleos de carbono-13 e nitrogênio-15, e também bidimensionais (1Hx13C FSLG-HETCOR). A RMN em estado sólido foi utilizada como principal ferramenta analítica na caracterização das formas cristalinas obtidas neste estudo, assim como na caracterização prévia dos Insumos Farmacêuticos Ativos (do inglês, APIs) utilizados como matéria prima, sendo demonstrada a aplicabilidade desta técnica na análise de novas formulações. Os dados obtidos mostraram-se de grande relevância no estudo de sólidos farmacêuticos sendo possível contribuir para o estudo estrutural de formas farmacêuticas, identificar formas polimórficas de fármacos, averiguar transições de fases tanto nos API quanto em amostras comerciais e verificar a presença de interações moleculares (intermolecular e intramolecular) por meio de RMN bidimensional. Neste trabalho foi mostrado que esta técnica se configura como uma importante ferramenta para a caracterização de novos polimorfos, mas que certamente deve ser aplicada em conjunto com outras técnicas de forma a aproveitar a complementaridade oferecida quando diferentes técnicas são utilizadas em xiii conjunto. Com este trabalho pretende-se consolidar no país o uso da RMN no estado sólido como uma ferramenta para a caracterização de fármacos e também para a análise de medicamentos, que tem sido pouco explorada até o momento.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)porUniversidade Federal de São CarlosCâmpus São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarRessonância Magnética Nuclear(RMN) no estado sólidoPolimorfismoQuímica SupramolecularCIENCIAS EXATAS E DA TERRAEmprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacosUSE OF SOLID STATE NMR. IN STUDY OF SUPRAMOLECULAR COMPLEXES OF PHARMACEUTICALinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisOnline600600ddf43a40-427f-4e12-b8a9-941dca760bf8info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINALTeseTPOX.pdfTeseTPOX.pdfapplication/pdf4435169https://repositorio.ufscar.br/bitstream/ufscar/7547/1/TeseTPOX.pdf2f1dbd61f15be162aa3a7103c86917a1MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81957https://repositorio.ufscar.br/bitstream/ufscar/7547/2/license.txtae0398b6f8b235e40ad82cba6c50031dMD52TEXTTeseTPOX.pdf.txtTeseTPOX.pdf.txtExtracted texttext/plain170645https://repositorio.ufscar.br/bitstream/ufscar/7547/3/TeseTPOX.pdf.txte5a98ab85d196c891349eb2e826fc939MD53THUMBNAILTeseTPOX.pdf.jpgTeseTPOX.pdf.jpgIM Thumbnailimage/jpeg10333https://repositorio.ufscar.br/bitstream/ufscar/7547/4/TeseTPOX.pdf.jpg2c08de44de8d5d957252d782ea0feb8cMD54ufscar/75472023-09-18 18:30:54.961oai:repositorio.ufscar.br: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Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-09-18T18:30:54Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false |
dc.title.por.fl_str_mv |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos |
dc.title.alternative.eng.fl_str_mv |
USE OF SOLID STATE NMR. IN STUDY OF SUPRAMOLECULAR COMPLEXES OF PHARMACEUTICAL |
title |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos |
spellingShingle |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos Xavier, Tatielih Pardim de Oliveira Ressonância Magnética Nuclear(RMN) no estado sólido Polimorfismo Química Supramolecular CIENCIAS EXATAS E DA TERRA |
title_short |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos |
title_full |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos |
title_fullStr |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos |
title_full_unstemmed |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos |
title_sort |
Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos |
author |
Xavier, Tatielih Pardim de Oliveira |
author_facet |
Xavier, Tatielih Pardim de Oliveira |
author_role |
author |
dc.contributor.authorlattes.por.fl_str_mv |
http://lattes.cnpq.br/4307312001890985 |
dc.contributor.author.fl_str_mv |
Xavier, Tatielih Pardim de Oliveira |
dc.contributor.advisor1.fl_str_mv |
Venâncio, Tiago |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/4438399441102990 |
dc.contributor.authorID.fl_str_mv |
96bee820-3ae5-4a36-a13f-eb61c5f51b95 |
contributor_str_mv |
Venâncio, Tiago |
dc.subject.por.fl_str_mv |
Ressonância Magnética Nuclear(RMN) no estado sólido Polimorfismo Química Supramolecular |
topic |
Ressonância Magnética Nuclear(RMN) no estado sólido Polimorfismo Química Supramolecular CIENCIAS EXATAS E DA TERRA |
dc.subject.cnpq.fl_str_mv |
CIENCIAS EXATAS E DA TERRA |
description |
Many pharmaceutical solids are able to adopt more than one crystalline form, and this property is called polymorphism. Currently 80-90% of the drugs are marketed as in solid forms and a very common problem is the low solubility of these drugs, particularly in aqueous media. Depending on how a drug crystallizes, its physical and chemical properties can be changed, which may also result in changes in its solubility. Before this problem the crystals engineering appears as a strategy to improve the properties of the solid state related to the efficacy of the drugs through the development of new crystalline forms. Multicomponent molecular crystals can be prepared from supramolecular synthons forming approach by crystallization methods involving the optimization of conditions for the formation of these novel crystalline forms. In this context, this study aimed to use the solid state NMR for study of supramolecular chemistry the three antiparasitic drugs (secnidazole, albendazole and mebendazole) and one antiretroviral (tenofovir disoproxil fumarate) using a set of one-dimensional techniques (CP-TOSS, CP-NQS and CP-PI) for the carbon-13 and nitrogen-15 nucleus as well as two-dimensional (1Hx13C FSLG HETCOR). Solid state NMR was used as the primary analytical tool for characterizing the crystalline forms obtained in this study, as in the prior characterization of Active Pharmaceutical Ingredient (APIs) used as raw material, being demonstrated the applicability of this technique in the analysis of new formulations. The data obtained were of great importance in the study of these solid dosage forms which can contribute to the structural study of dosage forms, identify polymorphic forms of drugs, detect phase transitions in both API as in commercial samples and check for interactions molecular (intramolecular and intermolecular) by means of two-dimensional NMR. In this work it was shown that this technique is configured as an important tool for the characterization of new polymorphs but they certainly should be applied in conjunction with other techniques in order to take advantage of the complementarity provided when different techniques are used in combination. This work intends to consolidate the use of NMR in the solid state in Brazil as a tool for the characterization of the crystalline forms of drugs and also for the analysis of drugs, which has been few explored so far. |
publishDate |
2016 |
dc.date.accessioned.fl_str_mv |
2016-09-27T20:04:16Z |
dc.date.available.fl_str_mv |
2016-09-27T20:04:16Z |
dc.date.issued.fl_str_mv |
2016-03-15 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/doctoralThesis |
format |
doctoralThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
XAVIER, Tatielih Pardim de Oliveira. Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos. 2016. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2016. Disponível em: https://repositorio.ufscar.br/handle/ufscar/7547. |
dc.identifier.uri.fl_str_mv |
https://repositorio.ufscar.br/handle/ufscar/7547 |
identifier_str_mv |
XAVIER, Tatielih Pardim de Oliveira. Emprego da RMN no estado sólido em estudos de complexos supramoleculares de fármacos. 2016. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2016. Disponível em: https://repositorio.ufscar.br/handle/ufscar/7547. |
url |
https://repositorio.ufscar.br/handle/ufscar/7547 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.confidence.fl_str_mv |
600 600 |
dc.relation.authority.fl_str_mv |
ddf43a40-427f-4e12-b8a9-941dca760bf8 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Universidade Federal de São Carlos Câmpus São Carlos |
dc.publisher.program.fl_str_mv |
Programa de Pós-Graduação em Química - PPGQ |
dc.publisher.initials.fl_str_mv |
UFSCar |
publisher.none.fl_str_mv |
Universidade Federal de São Carlos Câmpus São Carlos |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFSCAR instname:Universidade Federal de São Carlos (UFSCAR) instacron:UFSCAR |
instname_str |
Universidade Federal de São Carlos (UFSCAR) |
instacron_str |
UFSCAR |
institution |
UFSCAR |
reponame_str |
Repositório Institucional da UFSCAR |
collection |
Repositório Institucional da UFSCAR |
bitstream.url.fl_str_mv |
https://repositorio.ufscar.br/bitstream/ufscar/7547/1/TeseTPOX.pdf https://repositorio.ufscar.br/bitstream/ufscar/7547/2/license.txt https://repositorio.ufscar.br/bitstream/ufscar/7547/3/TeseTPOX.pdf.txt https://repositorio.ufscar.br/bitstream/ufscar/7547/4/TeseTPOX.pdf.jpg |
bitstream.checksum.fl_str_mv |
2f1dbd61f15be162aa3a7103c86917a1 ae0398b6f8b235e40ad82cba6c50031d e5a98ab85d196c891349eb2e826fc939 2c08de44de8d5d957252d782ea0feb8c |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR) |
repository.mail.fl_str_mv |
|
_version_ |
1813715561939468288 |