Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae)
| Ano de defesa: | 2017 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | , |
| Tipo de documento: | Dissertação |
| Tipo de acesso: | Acesso aberto |
| Idioma: | por |
| Instituição de defesa: |
Universidade Estadual da Paraíba
|
| Programa de Pós-Graduação: |
Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF
|
| Departamento: |
Pró-Reitoria de Pós-Graduação e Pesquisa - PRPGP
|
| País: |
BR
|
| Palavras-chave em Português: | |
| Palavras-chave em Inglês: | |
| Área do conhecimento CNPq: | |
| Link de acesso: | https://repositorio.uepb.edu.br/handle/123456789/75541 |
Resumo: | The present work describes the first phytochemical studies, biological evaluation and physical-chemical characterization of Apodanthera congestiflora Cogn roots. This cucurbitacea popularly known as ―cabeça de negro‖ is cited in ethnobotanical studies for its analgesic, anti-inflammatory, depurative, antiparasitic and antimicrobial activities. The preparation of an aqueous extract by decoction (EAN-Ac) and others by accelerated extraction with the solvents hexane, acetate and ethanol (FH-Ac, FA-Ac, FE-Ac) was carried out. The vegetal drug (DV-Ac) and EAN-Ac were submitted to quality control through traditional pharmacopoeial methods and instrumental techniques. Both were within the parameters recommended by the official compendia. The extracts underwent a preliminary phytochemical evaluation, demonstrating the presence of saponins, polysaccharides and alkaloids. Specifically, EAN-Ac and FA-Ac presented quantification of polyphenols, flavonoids and tannins. In the evaluation of the biological activity and phytochemical prospecting the bioguided study model was followed, guided by the anti-inflammatory activity. EAN-AC-Ac and FA-Ac exhibited anti-inflammatory activity. The latter also presented antimicrobial activity against strains of S. aureus and C. albicans and presented a considerable toxicological potential. The FA-Ac was selected and isolated (through chromatographic techniques) and identified by spectroscopic techniques (IV, 1H and 13C) 2 esterified phenolic acids, 2- propenoic acid ferulate, 3- (4- hydroxy-3-methoxyphenyl) decyl ester (Ac-1) and p cinnamate 2-propenoic acid, 3- (4-hydroxyphenyl) decyl ester (Ac-2). In addition to the latter, 3 glycosylated triterpenoids of the norcucurbitacin class were purified: 29-nor 1,2,3,4,5,10-dehydro-25-O-acetyl-2-O-β-D-glucopyranosyl-3 , 16α, 20 (R) -trihydroxy 11,22-dioxocurbite-6.23, diene (Ac-3), known as Cayaponoside A; (R) -trihydroxy 11,22-dihydro-25-O-acetyl-2-O-β-D-glucopyranosyl-3,16α, 20β- (Ac-4), known as Fevicordine A and 19-norcolesta-1,3,5,10-6-tetraene-11,22-dione, 2- (β-D glucopyranosyl) -6- 3, 16, 20,25-tetrahydroxy-4,9,14-trimethyl- (9β, 16α), known as Cayaponoside C. The phenolic esters isolated in the present study are already widely known in the literature, but the triterpenes obtained belong to a class with few studies described and, in general, the isolation of these chemical compounds is pioneer in the mentioned species. In addition, the EAN-AC-Ac, obtained by decoction, did not present evidence of toxicity, inferring that A. congestiflora is safe for use by the population in the form of decoction, but with the proper criterion, since it presents in its constitution active principles potentially toxic. |
| id |
UEPB-2_635a83ada2d2a7b742e2f4c7c91dc7f1 |
|---|---|
| oai_identifier_str |
oai:repositorio.uepb.edu.br:123456789/75541 |
| network_acronym_str |
UEPB-2 |
| network_name_str |
Repositório Institucional da Universidade Estadual da Paraíba (UEPB) |
| repository_id_str |
|
| spelling |
2026-03-12T10:53:26Z2017-09-06PEREIRA, Helimarcos Nunes. Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae). 2017. 146f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF) - Universidade Estadual da Paraíba, Campina Grande, 2022.https://repositorio.uepb.edu.br/handle/123456789/7554124004014014P8The present work describes the first phytochemical studies, biological evaluation and physical-chemical characterization of Apodanthera congestiflora Cogn roots. This cucurbitacea popularly known as ―cabeça de negro‖ is cited in ethnobotanical studies for its analgesic, anti-inflammatory, depurative, antiparasitic and antimicrobial activities. The preparation of an aqueous extract by decoction (EAN-Ac) and others by accelerated extraction with the solvents hexane, acetate and ethanol (FH-Ac, FA-Ac, FE-Ac) was carried out. The vegetal drug (DV-Ac) and EAN-Ac were submitted to quality control through traditional pharmacopoeial methods and instrumental techniques. Both were within the parameters recommended by the official compendia. The extracts underwent a preliminary phytochemical evaluation, demonstrating the presence of saponins, polysaccharides and alkaloids. Specifically, EAN-Ac and FA-Ac presented quantification of polyphenols, flavonoids and tannins. In the evaluation of the biological activity and phytochemical prospecting the bioguided study model was followed, guided by the anti-inflammatory activity. EAN-AC-Ac and FA-Ac exhibited anti-inflammatory activity. The latter also presented antimicrobial activity against strains of S. aureus and C. albicans and presented a considerable toxicological potential. The FA-Ac was selected and isolated (through chromatographic techniques) and identified by spectroscopic techniques (IV, 1H and 13C) 2 esterified phenolic acids, 2- propenoic acid ferulate, 3- (4- hydroxy-3-methoxyphenyl) decyl ester (Ac-1) and p cinnamate 2-propenoic acid, 3- (4-hydroxyphenyl) decyl ester (Ac-2). In addition to the latter, 3 glycosylated triterpenoids of the norcucurbitacin class were purified: 29-nor 1,2,3,4,5,10-dehydro-25-O-acetyl-2-O-β-D-glucopyranosyl-3 , 16α, 20 (R) -trihydroxy 11,22-dioxocurbite-6.23, diene (Ac-3), known as Cayaponoside A; (R) -trihydroxy 11,22-dihydro-25-O-acetyl-2-O-β-D-glucopyranosyl-3,16α, 20β- (Ac-4), known as Fevicordine A and 19-norcolesta-1,3,5,10-6-tetraene-11,22-dione, 2- (β-D glucopyranosyl) -6- 3, 16, 20,25-tetrahydroxy-4,9,14-trimethyl- (9β, 16α), known as Cayaponoside C. The phenolic esters isolated in the present study are already widely known in the literature, but the triterpenes obtained belong to a class with few studies described and, in general, the isolation of these chemical compounds is pioneer in the mentioned species. In addition, the EAN-AC-Ac, obtained by decoction, did not present evidence of toxicity, inferring that A. congestiflora is safe for use by the population in the form of decoction, but with the proper criterion, since it presents in its constitution active principles potentially toxic.O presente trabalho descreve os primeiros estudos fitoquímicos, avaliação biológica e caracterização físico-química das raízes da Apodanthera congestiflora Cogn. Essa cucurbitácea conhecida popularmente como cabeça de negro é citada em estudos etnobotânicos pelas suas atividades analgésica, anti-inflamatória, depurativa, antiparasitária e antimicrobiana. Foi realizada a preparação de um extrato aquoso por decocção (EAN-Ac) e outros por extração acelerada com os solventes hexano, acetato e etanol (FH-Ac, FA-Ac, FE-Ac). A droga vegetal (DV-Ac) e o EAN-Ac foram submetidos ao controle de qualidade através de métodos farmacopeicos tradicionais e por técnicas instrumentais. Ambos se mostraram dentro dos parâmetros preconizados pelos compêndios oficiais. Os extratos passaram por uma avaliação fitoquímica preliminar, demonstrando a presença de saponinas, polissacarídeos e alcaloides e, especificamente, o EAN-Ac e o FA-Ac apresentaram na quantificação teores significativos de polifenóis, flavonoides e taninos. Na avaliação da atividade biológica e prospecção fitoquímica foi seguido o modelo de estudo bioguiado, norteado pela atividade anti-inflamatória. O EAN-AC-Ac e o FA-Ac exibiram atividade anti inflamatória. Esse último também apresentou atividade antimicrobiana frente às cepas de S. aureus e C. albicans e apresentou um potencial toxicológico considerável. Diante disso, o FA-Ac foi selecionado e dele foram isolados (através de técnicas cromatográficas) e identificados através de técnicas espectroscópicas (IV, RMN 1H e 13C) 2 ácidos fenólicos esterificados, o ferulato 2-ácido propenóico, 3-(4-hidroxi-3- metoxifenil) decil éster (Ac-1) e o p-cinamato 2-ácido propenóico, 3-(4-hidroxifenil)- decil éster (Ac-2). Além desses últimos, foram purificados 3 triterpenoides glicosilados da classe das norcucurbitacinas: o 29-nor-1, 2, 3, 4, 5,10- dehidro-25- O- acetil- 2- O- β D- glicopiranosil-3,16 α, 20 (R)- trihidroxi-11,22-dioxocurbita- 6,23, dieno (Ac-3), conhecido como Cayaponosídeo A; o 29-nor-1, 2, 3, 4, 5,10-dehidro-25-O- acetil-2-O β-D-glicopiranosil-3,16 α, 20 (R)-trihidroxi-11, 22-dioxocurbita- 6- eno (Ac-4), conhecido como Fevicordina A e o 19-norcolesta-1, 3, 5, 10-6-tetraeno-11,22-diona, 2- (β-D-glicopiranosil)-3, 16, 20,25-tetrahidroxi-4, 9,14-trimetil-(9 β, 16 α), conhecido por Cayaponosídeo C. Os ésteres fenólicos isolados no presente estudo já são conhecidos amplamente na literatura, mas os triterpenos obtidos pertencem a uma classe com poucos estudos descritos e, de forma geral, o isolamento desses compostos químicos é pioneiro na referida espécie. Além disso, o EAN-AC-Ac, obtido por decocção, não apresentou evidências de toxicidade, inferindo que A. congestiflora é segura para o uso pela população na forma de decocto, mas com o devido critério, pois apresenta em sua constituição princípios ativos potencialmente tóxicos.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfUniversidade Estadual da ParaíbaPrograma de Pós-Graduação em Ciências Farmacêuticas - PPGCFUEPBBRPró-Reitoria de Pós-Graduação e Pesquisa - PRPGPPró-Reitoria de Pós-Graduação e Pesquisa - PRPGPAnti-inflammatory activityCucurbitaceaeCIENCIAS DA SAUDEAtividade anti-inflmatóriaCucurbitaceaePlantas medicinaisEstudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae)info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisTôrres, Maria da Conceição de MenezesPortela, Alyne da SilvaAlves, Harley da SilvaPereira, Helimarcos Nunesinfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da Universidade Estadual da Paraíba (UEPB)instname:Universidade Estadual da Paraíba (UEPB)instacron:UEPBORIGINALDS_Helimarcos_Nunes_Pereira.pdfDS_Helimarcos_Nunes_Pereiraapplication/pdf7468189https://repositorio.uepb.edu.br/bitstreams/88af4cd6-9ca5-48a7-86ad-6b087943fe34/download8f840db1ff834304bbbd1a07ddfffbf6MD51trueAnonymousREADLICENSElicense.txttext/plain1960https://repositorio.uepb.edu.br/bitstreams/fb1402ff-4d5f-468b-aa0f-beca90eb168d/download6052ae61e77222b2086e666b7ae213ceMD52falseAnonymousREADTHUMBNAILDS_Helimarcos_Nunes_Pereira.pdf.jpgDS_Helimarcos_Nunes_Pereira.pdf.jpgGenerated Thumbnailimage/jpeg2892https://repositorio.uepb.edu.br/bitstreams/6736be41-148e-4c11-a88d-086f967a378f/download33ddf6bc098b2597383884ec4d103bb4MD53falseAnonymousREAD123456789/755412026-05-06T11:51:55.695255Zopen.accessoai:repositorio.uepb.edu.br:123456789/75541https://repositorio.uepb.edu.brRepositório InstitucionalPUBhttp://dspace.bc.uepb.edu.br/oai/requestsibuepb@setor.uepb.edu.bropendoar:2026-05-06T11:51:55Repositório Institucional da Universidade Estadual da Paraíba (UEPB) - Universidade Estadual da Paraíba (UEPB)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 |
| dc.title.none.fl_str_mv |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) |
| title |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) |
| spellingShingle |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) Pereira, Helimarcos Nunes Anti-inflammatory activity Cucurbitaceae CIENCIAS DA SAUDE Atividade anti-inflmatória Cucurbitaceae Plantas medicinais |
| title_short |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) |
| title_full |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) |
| title_fullStr |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) |
| title_full_unstemmed |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) |
| title_sort |
Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae) |
| author |
Pereira, Helimarcos Nunes |
| author_facet |
Pereira, Helimarcos Nunes |
| author_role |
author |
| dc.contributor.referee1.fl_str_mv |
Tôrres, Maria da Conceição de Menezes |
| dc.contributor.referee2.fl_str_mv |
Portela, Alyne da Silva |
| dc.contributor.advisor1.fl_str_mv |
Alves, Harley da Silva |
| dc.contributor.author.fl_str_mv |
Pereira, Helimarcos Nunes |
| contributor_str_mv |
Tôrres, Maria da Conceição de Menezes Portela, Alyne da Silva Alves, Harley da Silva |
| dc.subject.eng.fl_str_mv |
Anti-inflammatory activity Cucurbitaceae |
| topic |
Anti-inflammatory activity Cucurbitaceae CIENCIAS DA SAUDE Atividade anti-inflmatória Cucurbitaceae Plantas medicinais |
| dc.subject.cnpq.fl_str_mv |
CIENCIAS DA SAUDE |
| dc.subject.por.fl_str_mv |
Atividade anti-inflmatória Cucurbitaceae Plantas medicinais |
| description |
The present work describes the first phytochemical studies, biological evaluation and physical-chemical characterization of Apodanthera congestiflora Cogn roots. This cucurbitacea popularly known as ―cabeça de negro‖ is cited in ethnobotanical studies for its analgesic, anti-inflammatory, depurative, antiparasitic and antimicrobial activities. The preparation of an aqueous extract by decoction (EAN-Ac) and others by accelerated extraction with the solvents hexane, acetate and ethanol (FH-Ac, FA-Ac, FE-Ac) was carried out. The vegetal drug (DV-Ac) and EAN-Ac were submitted to quality control through traditional pharmacopoeial methods and instrumental techniques. Both were within the parameters recommended by the official compendia. The extracts underwent a preliminary phytochemical evaluation, demonstrating the presence of saponins, polysaccharides and alkaloids. Specifically, EAN-Ac and FA-Ac presented quantification of polyphenols, flavonoids and tannins. In the evaluation of the biological activity and phytochemical prospecting the bioguided study model was followed, guided by the anti-inflammatory activity. EAN-AC-Ac and FA-Ac exhibited anti-inflammatory activity. The latter also presented antimicrobial activity against strains of S. aureus and C. albicans and presented a considerable toxicological potential. The FA-Ac was selected and isolated (through chromatographic techniques) and identified by spectroscopic techniques (IV, 1H and 13C) 2 esterified phenolic acids, 2- propenoic acid ferulate, 3- (4- hydroxy-3-methoxyphenyl) decyl ester (Ac-1) and p cinnamate 2-propenoic acid, 3- (4-hydroxyphenyl) decyl ester (Ac-2). In addition to the latter, 3 glycosylated triterpenoids of the norcucurbitacin class were purified: 29-nor 1,2,3,4,5,10-dehydro-25-O-acetyl-2-O-β-D-glucopyranosyl-3 , 16α, 20 (R) -trihydroxy 11,22-dioxocurbite-6.23, diene (Ac-3), known as Cayaponoside A; (R) -trihydroxy 11,22-dihydro-25-O-acetyl-2-O-β-D-glucopyranosyl-3,16α, 20β- (Ac-4), known as Fevicordine A and 19-norcolesta-1,3,5,10-6-tetraene-11,22-dione, 2- (β-D glucopyranosyl) -6- 3, 16, 20,25-tetrahydroxy-4,9,14-trimethyl- (9β, 16α), known as Cayaponoside C. The phenolic esters isolated in the present study are already widely known in the literature, but the triterpenes obtained belong to a class with few studies described and, in general, the isolation of these chemical compounds is pioneer in the mentioned species. In addition, the EAN-AC-Ac, obtained by decoction, did not present evidence of toxicity, inferring that A. congestiflora is safe for use by the population in the form of decoction, but with the proper criterion, since it presents in its constitution active principles potentially toxic. |
| publishDate |
2017 |
| dc.date.issued.fl_str_mv |
2017-09-06 |
| dc.date.accessioned.fl_str_mv |
2026-03-12T10:53:26Z |
| dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
| format |
masterThesis |
| status_str |
publishedVersion |
| dc.identifier.citation.fl_str_mv |
PEREIRA, Helimarcos Nunes. Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae). 2017. 146f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF) - Universidade Estadual da Paraíba, Campina Grande, 2022. |
| dc.identifier.uri.fl_str_mv |
https://repositorio.uepb.edu.br/handle/123456789/75541 |
| dc.identifier.capesdegreeprogramcode.none.fl_str_mv |
24004014014P8 |
| identifier_str_mv |
PEREIRA, Helimarcos Nunes. Estudo fitoquímico e atividade biológica das raízes de Apodanthera congestiflora Cogn. (Cucurbitaceae). 2017. 146f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF) - Universidade Estadual da Paraíba, Campina Grande, 2022. 24004014014P8 |
| url |
https://repositorio.uepb.edu.br/handle/123456789/75541 |
| dc.language.iso.fl_str_mv |
por |
| language |
por |
| dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
Universidade Estadual da Paraíba |
| dc.publisher.program.fl_str_mv |
Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF |
| dc.publisher.initials.fl_str_mv |
UEPB |
| dc.publisher.country.fl_str_mv |
BR |
| dc.publisher.department.fl_str_mv |
Pró-Reitoria de Pós-Graduação e Pesquisa - PRPGP Pró-Reitoria de Pós-Graduação e Pesquisa - PRPGP |
| publisher.none.fl_str_mv |
Universidade Estadual da Paraíba |
| dc.source.none.fl_str_mv |
reponame:Repositório Institucional da Universidade Estadual da Paraíba (UEPB) instname:Universidade Estadual da Paraíba (UEPB) instacron:UEPB |
| instname_str |
Universidade Estadual da Paraíba (UEPB) |
| instacron_str |
UEPB |
| institution |
UEPB |
| reponame_str |
Repositório Institucional da Universidade Estadual da Paraíba (UEPB) |
| collection |
Repositório Institucional da Universidade Estadual da Paraíba (UEPB) |
| bitstream.url.fl_str_mv |
https://repositorio.uepb.edu.br/bitstreams/88af4cd6-9ca5-48a7-86ad-6b087943fe34/download https://repositorio.uepb.edu.br/bitstreams/fb1402ff-4d5f-468b-aa0f-beca90eb168d/download https://repositorio.uepb.edu.br/bitstreams/6736be41-148e-4c11-a88d-086f967a378f/download |
| bitstream.checksum.fl_str_mv |
8f840db1ff834304bbbd1a07ddfffbf6 6052ae61e77222b2086e666b7ae213ce 33ddf6bc098b2597383884ec4d103bb4 |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 |
| repository.name.fl_str_mv |
Repositório Institucional da Universidade Estadual da Paraíba (UEPB) - Universidade Estadual da Paraíba (UEPB) |
| repository.mail.fl_str_mv |
sibuepb@setor.uepb.edu.br |
| _version_ |
1865082711576674304 |