Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.

Detalhes bibliográficos
Ano de defesa: 2024
Autor(a) principal: Melo, Luciana Aleixo dos Santos de lattes
Orientador(a): Bandeira, Maria Fulgência Costa Lima lattes
Banca de defesa: Vasconcellos, Marne Carvalho de, Fujimoto, Luciana Botinelly Mendonça, Sampaio, Fábio Correia, Toda, Carina
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal do Amazonas
Programa de Pós-Graduação: Programa de Pós-graduação em Inovação Farmacêutica
Departamento: Faculdade de Ciências Farmacêuticas
País: Brasil
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://tede.ufam.edu.br/handle/tede/10595
Resumo: Libidibia ferrea L. (jucá) has demonstrated promising therapeutic results in anti-inflammatory and healing, antimicrobial, analgesic and antipyretic properties. The present study performed physicochemical quality control and evaluated the healing activity in oral ulcers induced under topical therapy with Libidibia ferrea L. orabase ointment in rats with diabetes mellitus. For this purpose, Study 1 was carried out - “in vitro”: centrifugation tests, pH, density, rheological behavior, microbiological evaluation for research of contaminants and pathogenic microorganisms and organoleptic characteristics, under the physical storage conditions and experimental periods; and Study 2 - “in vivo”: healing action of the ointment on oral ulcers of rats with diabetes mellitus, divided into 5 groups: negative control - normosystem rats (G1), positive control - diabetic rats (G2), positive control - triamcinolone (G3), jucá group (G4) and orabase group (G5), through histopathological analysis, collagenesis, immunohistochemistry for IL-1, TNF-a, TGF-b and CD31, on days 01, 05 and 10 after ulcerative induction. In study 1, discrete separation of the oily phase without precipitates was observed under the conditions tested; in the pH test, there was a significant difference between the conditions tested, with the refrigerator showing a significant difference in relation to the air conditioning and TAC, presenting the most stable pH (±6.56); the density was stable during the 12 months; in terms of viscosity, the ointment was of the pseudoplastic/plastic type; the microbiological evaluation did not demonstrate the presence of contaminants; there were no color changes, with a strong and aromatic odor and the presence of shine and smooth consistency, and absence of granulations. Study 2 demonstrated differences in the values of ulcer sizes as well as their reduction during the evaluated period. Groups G1 and G4 were those that presented the smallest ulcer sizes at the end of the experiment, 5.26 cm and 6.42 cm, respectively. Evaluating the body weight of the rats, it was observed that G1 (7.84) presented weight gain in all periods and G4 on days 05 (2.75) and 10 (4.45), as well as group G5 (6.60) on day 10. Histopathologically, there was no significant difference in ulcer scores on days 01 and 05 in all groups (score 4). However, on day 10 there was a significant difference between groups G1 (2.75) and G5 (3.62), with no such difference existing in the other groups. The best results for total collagen activity (22.11 and 19.77), type I (14.80 and 13.91) and type III (7.31 and 5.85) were observed between groups G1 and G4 after 10 days. Histopathologically, there was no significant difference in ulcerative scores on days 01 and 05 in all groups (score 4). However, on day 10 there was a significant difference between groups G1 (2.75) and G5 (3.62), with no such difference in the other groups. The best results for total collagen activity (22.11 and 19.77), type I (14.80 and 13.91) and type III (7.31 and 5.85) were observed between groups G1 and G4 after 10 days. Immunohistochemical analysis demonstrated delayed healing associated with high levels of IL- 1, mainly in group G3 (741.20). When evaluating TNF-a, a decrease was observed in all groups, except in G1 (11.33) and G3 (50.20) where there were no significant changes. On day 05, all groups had an increase in TGF-b, with the exception of group G5 (9.50), and a significant increase was also noted in groups G2 (181.67), G3 (119.20) and G4 (24.33) on day 10. Finally, when evaluating CD31, none of the groups showed statistical differences on day 05, however, on day 10, those that expressed the most were groups G4 (130.33) and G5 (150.00). Based on the results presented, the formulation showed physical-chemical stability in all storage conditions and time tested, with better results when stored in the refrigerator, as well as effectiveness in tissue repair, suggesting the indication of the healing activity of the proposed phytotherapeutic formulation when used for the treatment of oral ulcers in diabetic rats.
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spelling Bandeira, Maria Fulgência Costa Limahttp://lattes.cnpq.br/6480337217516258Conde, Nikeila Chacon de Oliveirahttp://lattes.cnpq.br/5598893517284033Vasconcellos, Marne Carvalho deFujimoto, Luciana Botinelly MendonçaSampaio, Fábio CorreiaToda, Carinahttp://lattes.cnpq.br/0487583887584405Melo, Luciana Aleixo dos Santos de2025-01-13T21:36:08Z2024-04-23MELO, Luciana Aleixo dos Santos de. Efeito reparador tecidual de uma pomada orabase de Libidibia ferrea L. para o tratamento de úlceras da cavidade bucal em ratos diabéticos. 2024. 132 f. Tese (Doutorado em Inovação Farmacêutica) - Universidade Federal do Amazonas, Manaus (AM), 2024.https://tede.ufam.edu.br/handle/tede/10595Libidibia ferrea L. (jucá) has demonstrated promising therapeutic results in anti-inflammatory and healing, antimicrobial, analgesic and antipyretic properties. The present study performed physicochemical quality control and evaluated the healing activity in oral ulcers induced under topical therapy with Libidibia ferrea L. orabase ointment in rats with diabetes mellitus. For this purpose, Study 1 was carried out - “in vitro”: centrifugation tests, pH, density, rheological behavior, microbiological evaluation for research of contaminants and pathogenic microorganisms and organoleptic characteristics, under the physical storage conditions and experimental periods; and Study 2 - “in vivo”: healing action of the ointment on oral ulcers of rats with diabetes mellitus, divided into 5 groups: negative control - normosystem rats (G1), positive control - diabetic rats (G2), positive control - triamcinolone (G3), jucá group (G4) and orabase group (G5), through histopathological analysis, collagenesis, immunohistochemistry for IL-1, TNF-a, TGF-b and CD31, on days 01, 05 and 10 after ulcerative induction. In study 1, discrete separation of the oily phase without precipitates was observed under the conditions tested; in the pH test, there was a significant difference between the conditions tested, with the refrigerator showing a significant difference in relation to the air conditioning and TAC, presenting the most stable pH (±6.56); the density was stable during the 12 months; in terms of viscosity, the ointment was of the pseudoplastic/plastic type; the microbiological evaluation did not demonstrate the presence of contaminants; there were no color changes, with a strong and aromatic odor and the presence of shine and smooth consistency, and absence of granulations. Study 2 demonstrated differences in the values of ulcer sizes as well as their reduction during the evaluated period. Groups G1 and G4 were those that presented the smallest ulcer sizes at the end of the experiment, 5.26 cm and 6.42 cm, respectively. Evaluating the body weight of the rats, it was observed that G1 (7.84) presented weight gain in all periods and G4 on days 05 (2.75) and 10 (4.45), as well as group G5 (6.60) on day 10. Histopathologically, there was no significant difference in ulcer scores on days 01 and 05 in all groups (score 4). However, on day 10 there was a significant difference between groups G1 (2.75) and G5 (3.62), with no such difference existing in the other groups. The best results for total collagen activity (22.11 and 19.77), type I (14.80 and 13.91) and type III (7.31 and 5.85) were observed between groups G1 and G4 after 10 days. Histopathologically, there was no significant difference in ulcerative scores on days 01 and 05 in all groups (score 4). However, on day 10 there was a significant difference between groups G1 (2.75) and G5 (3.62), with no such difference in the other groups. The best results for total collagen activity (22.11 and 19.77), type I (14.80 and 13.91) and type III (7.31 and 5.85) were observed between groups G1 and G4 after 10 days. Immunohistochemical analysis demonstrated delayed healing associated with high levels of IL- 1, mainly in group G3 (741.20). When evaluating TNF-a, a decrease was observed in all groups, except in G1 (11.33) and G3 (50.20) where there were no significant changes. On day 05, all groups had an increase in TGF-b, with the exception of group G5 (9.50), and a significant increase was also noted in groups G2 (181.67), G3 (119.20) and G4 (24.33) on day 10. Finally, when evaluating CD31, none of the groups showed statistical differences on day 05, however, on day 10, those that expressed the most were groups G4 (130.33) and G5 (150.00). Based on the results presented, the formulation showed physical-chemical stability in all storage conditions and time tested, with better results when stored in the refrigerator, as well as effectiveness in tissue repair, suggesting the indication of the healing activity of the proposed phytotherapeutic formulation when used for the treatment of oral ulcers in diabetic rats.A Libidibia ferrea L. (jucá) tem demonstrado resultados promissores terapêuticos antiinflamatório e cicatrizante, antimicrobiano, analgésico e antitérmico. O presente estudo realizou o controle de qualidade físico-químico e avaliou a atividade cicatrizante em úlceras orais induzidas sob a terapia tópica com pomada orabase de Libidibia ferrea L. em ratos portadores de diabetes mellitus. Para tal, realizou-se o Estudo 1 - “in vitro”: testes de centrifugação, pH, densidade, comportamento reológico, avaliação microbiológica para pesquisa de contaminantes e microrganismos patogênicos e características organolépticas, nas condições físicas de armazenamento e os períodos experimentais; e o Estudo 2 - “in vivo”: ação cicatrizante da pomada em úlceras orais de ratos portadores de diabetes mellitus, divididos em 5 grupos: controle negativo – ratos normossistêmicos (G1), controle positivo – ratos diabéticos (G2), controle positivo - triancinolona (G3), grupo jucá (G4) e grupo orabase (G5), através da análise histopatológica, colagênese, imuno-histoquímica para IL-1, TNF-a, TGF-b e CD31, nos dias 01, 05 e 10 pós indução ulcerativa. No estudo 1, observou-se discreta separação de fase oleosa sem precipitados nas condições testadas; no teste de pH houve diferença significativa entre as condições testadas sendo que a geladeira apresentou diferença significativa em relação ao Ar condicionado e TAC, apresentando o pH mais estável (±6,56); a densidade apresentou estabilidade durante os 12 meses; na viscosidade a pomada foi do tipo pseudoplástico/plástico; a avaliação microbiológica não demonstrou presença de contaminantes; não houve alterações de cor, com odor forte e aromático e presença de brilho e consistência lisa, ausência de granulações. O estudo 2 demonstrou diferenças nos valores dos tamanhos ulcerativos bem como sua redução durante o período avaliado. Os grupos G1 e G4 foram os que apresentaram os menores tamanhos ulcerativos no final do experimento, 5,26 cm e 6,42 cm, respectivamente. Avaliando o peso corporal dos ratos observou-se que o G1 (7,84) apresentou ganho de peso em todos os períodos e o G4 nos dias 05 (2,75) e 10 (4,45), bem como o grupo G5 (6,60) no dia 10. Histopalogicamente, não houve diferença significativa nos escores ulcerativos nos dias 01 e 05 em todos os grupos (score 4). Entretanto, no dia 10 houve diferença significativa entre os grupos G1 (2,75) e G5 (3,62), não existindo esta diferença nos demais grupos. Pôde-se observar entre os grupos G1 e G4 os melhores resultados para atividade de colágeno total (22,11 e 19,77), tipo I (14,80 e 13,91) e tipo III (7,31 e 5,85) depois dos 10 dias. A análise imunohistoquímica demonstrou um retardo da cicatrização associado a elevados níveis de IL-1, principalmente no grupo G3 (741,20). Ao avaliar o TNF-a, observou a diminuição em todos os grupos, excetuando no G1 (11,33) e G3 (50,20) que não houve mudanças significativas. No dia 05 que todos os grupos tiveram um aumento de TGF-b, com exceção do grupo G5 (9,50), nota-se ainda um aumento significativo nos grupos G2 (181,67), G3 (119,20) e G4 (24,33) no dia 10. Por fim, ao avaliar o CD31, nenhum dos grupos apresentaram diferenças estatísticas no dia 05, contudo no dia 10 os que mais expressaram foram os grupos G4 (130,33) e G5 (150,00). Com bases nos resultados apresentados, a formulação apresentou estabilidade físico-química em todas as condições de armazenamento e tempo testados, com melhores resultados no armazenamento em geladeira, bem como uma efetividade no reparo tecidual, sugerindo a indicação da atividade cicatricial da formulação fitoterápica proposta quando utilizada para tratamento de úlceras orais em ratos diabéticos.Submitted by Luciana Melo (meloaleixoluciana@hotmail.com) on 2024-10-11T21:20:24Z No. of bitstreams: 5 Tese final - Luciana Aleixo dos S. de Melo.pdf: 251359871 bytes, checksum: 14ec5b41d11658729ba6771a934e6c7c (MD5) Carta_encaminhamento_Luciana_Aleixo_S_de_Melo_assinado.pdf: 189399 bytes, checksum: a6c934e3c95f3f7a7fb847db7650b598 (MD5) ata assinada.pdf: 466672 bytes, checksum: 1a0effe192ce4d5a19421ee155ef64c8 (MD5) Ficha catalográfica.pdf: 1989 bytes, checksum: 398f3e0884c3fa61f3d9d6be956a7015 (MD5) Declaração de nada consta biblioteca.pdf: 4738 bytes, checksum: 2e097f7ca9cdc6d191909fe48cfcc6c2 (MD5)Approved for entry into archive by PPGIF Inovação Farmacêutica (ppgif@ufam.edu.br) on 2024-10-29T15:22:04Z (GMT) No. of bitstreams: 5 Tese final - Luciana Aleixo dos S. de Melo.pdf: 251359871 bytes, checksum: 14ec5b41d11658729ba6771a934e6c7c (MD5) Carta_encaminhamento_Luciana_Aleixo_S_de_Melo_assinado.pdf: 189399 bytes, checksum: a6c934e3c95f3f7a7fb847db7650b598 (MD5) ata assinada.pdf: 466672 bytes, checksum: 1a0effe192ce4d5a19421ee155ef64c8 (MD5) Ficha catalográfica.pdf: 1989 bytes, checksum: 398f3e0884c3fa61f3d9d6be956a7015 (MD5) Declaração de nada consta biblioteca.pdf: 4738 bytes, checksum: 2e097f7ca9cdc6d191909fe48cfcc6c2 (MD5)Rejected by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br), reason: 1) Sugere-se verificar e corrigir a paginação do documento - As folhas começam a ser contadas a partir da folha de rosto, mas não são numeradas. 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Deve-se entrar direto pelos nomes dos docentes. on 2024-10-31T21:35:41Z (GMT)Submitted by Luciana Melo (meloaleixoluciana@hotmail.com) on 2024-11-25T21:34:39Z No. of bitstreams: 5 Carta_encaminhamento_Luciana_Aleixo_S_de_Melo_assinado.pdf: 189399 bytes, checksum: a6c934e3c95f3f7a7fb847db7650b598 (MD5) ata assinada.pdf: 466672 bytes, checksum: 1a0effe192ce4d5a19421ee155ef64c8 (MD5) Declaração de nada consta biblioteca.pdf: 4738 bytes, checksum: 2e097f7ca9cdc6d191909fe48cfcc6c2 (MD5) Tese final - Luciana Aleixo dos S. de Melo - corrigido.pdf: 251401559 bytes, checksum: ba233898c03180020468e3192afbd816 (MD5) Ficha catalográfica.pdf: 1946 bytes, checksum: 7a4e98b5187903fc31bee5304b03f2ea (MD5)Approved for entry into archive by PPGIF Inovação Farmacêutica (ppgif@ufam.edu.br) on 2024-11-27T15:50:57Z (GMT) No. of bitstreams: 5 Carta_encaminhamento_Luciana_Aleixo_S_de_Melo_assinado.pdf: 189399 bytes, checksum: a6c934e3c95f3f7a7fb847db7650b598 (MD5) ata assinada.pdf: 466672 bytes, checksum: 1a0effe192ce4d5a19421ee155ef64c8 (MD5) Declaração de nada consta biblioteca.pdf: 4738 bytes, checksum: 2e097f7ca9cdc6d191909fe48cfcc6c2 (MD5) Tese final - Luciana Aleixo dos S. de Melo - corrigido.pdf: 251401559 bytes, checksum: ba233898c03180020468e3192afbd816 (MD5) Ficha catalográfica.pdf: 1946 bytes, checksum: 7a4e98b5187903fc31bee5304b03f2ea (MD5)Rejected by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br), reason: 1) A Ficha catalográfica precisa de ajustes: a) Inserir corretamente, nos seus devidos campos, Nome e sobrenome. 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dc.title.eng.fl_str_mv Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
title Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
spellingShingle Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
Melo, Luciana Aleixo dos Santos de
Boca - Úlceras orais - Tratamento
Matéria médica vegetal
CIENCIAS DA SAUDE: FARMACIA
CIENCIAS DA SAUDE: ODONTOLOGIA
Cicatrização
Fitoterapia
Úlceras orais
Libidibia ferrea
Diabetes Mellitus
title_short Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
title_full Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
title_fullStr Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
title_full_unstemmed Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
title_sort Efeito reparador tecidual de uma pomada orabase de extrato de Libidibia ferrea L. para tratamento de úlceras da cavidade bucal em ratos diabéticos.
author Melo, Luciana Aleixo dos Santos de
author_facet Melo, Luciana Aleixo dos Santos de
author_role author
dc.contributor.advisor1.fl_str_mv Bandeira, Maria Fulgência Costa Lima
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/6480337217516258
dc.contributor.advisor-co1.fl_str_mv Conde, Nikeila Chacon de Oliveira
dc.contributor.advisor-co1Lattes.fl_str_mv http://lattes.cnpq.br/5598893517284033
dc.contributor.referee1.fl_str_mv Vasconcellos, Marne Carvalho de
dc.contributor.referee2.fl_str_mv Fujimoto, Luciana Botinelly Mendonça
dc.contributor.referee3.fl_str_mv Sampaio, Fábio Correia
dc.contributor.referee4.fl_str_mv Toda, Carina
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0487583887584405
dc.contributor.author.fl_str_mv Melo, Luciana Aleixo dos Santos de
contributor_str_mv Bandeira, Maria Fulgência Costa Lima
Conde, Nikeila Chacon de Oliveira
Vasconcellos, Marne Carvalho de
Fujimoto, Luciana Botinelly Mendonça
Sampaio, Fábio Correia
Toda, Carina
dc.subject.por.fl_str_mv Boca - Úlceras orais - Tratamento
Matéria médica vegetal
topic Boca - Úlceras orais - Tratamento
Matéria médica vegetal
CIENCIAS DA SAUDE: FARMACIA
CIENCIAS DA SAUDE: ODONTOLOGIA
Cicatrização
Fitoterapia
Úlceras orais
Libidibia ferrea
Diabetes Mellitus
dc.subject.cnpq.fl_str_mv CIENCIAS DA SAUDE: FARMACIA
CIENCIAS DA SAUDE: ODONTOLOGIA
dc.subject.user.por.fl_str_mv Cicatrização
Fitoterapia
Úlceras orais
Libidibia ferrea
Diabetes Mellitus
description Libidibia ferrea L. (jucá) has demonstrated promising therapeutic results in anti-inflammatory and healing, antimicrobial, analgesic and antipyretic properties. The present study performed physicochemical quality control and evaluated the healing activity in oral ulcers induced under topical therapy with Libidibia ferrea L. orabase ointment in rats with diabetes mellitus. For this purpose, Study 1 was carried out - “in vitro”: centrifugation tests, pH, density, rheological behavior, microbiological evaluation for research of contaminants and pathogenic microorganisms and organoleptic characteristics, under the physical storage conditions and experimental periods; and Study 2 - “in vivo”: healing action of the ointment on oral ulcers of rats with diabetes mellitus, divided into 5 groups: negative control - normosystem rats (G1), positive control - diabetic rats (G2), positive control - triamcinolone (G3), jucá group (G4) and orabase group (G5), through histopathological analysis, collagenesis, immunohistochemistry for IL-1, TNF-a, TGF-b and CD31, on days 01, 05 and 10 after ulcerative induction. In study 1, discrete separation of the oily phase without precipitates was observed under the conditions tested; in the pH test, there was a significant difference between the conditions tested, with the refrigerator showing a significant difference in relation to the air conditioning and TAC, presenting the most stable pH (±6.56); the density was stable during the 12 months; in terms of viscosity, the ointment was of the pseudoplastic/plastic type; the microbiological evaluation did not demonstrate the presence of contaminants; there were no color changes, with a strong and aromatic odor and the presence of shine and smooth consistency, and absence of granulations. Study 2 demonstrated differences in the values of ulcer sizes as well as their reduction during the evaluated period. Groups G1 and G4 were those that presented the smallest ulcer sizes at the end of the experiment, 5.26 cm and 6.42 cm, respectively. Evaluating the body weight of the rats, it was observed that G1 (7.84) presented weight gain in all periods and G4 on days 05 (2.75) and 10 (4.45), as well as group G5 (6.60) on day 10. Histopathologically, there was no significant difference in ulcer scores on days 01 and 05 in all groups (score 4). However, on day 10 there was a significant difference between groups G1 (2.75) and G5 (3.62), with no such difference existing in the other groups. The best results for total collagen activity (22.11 and 19.77), type I (14.80 and 13.91) and type III (7.31 and 5.85) were observed between groups G1 and G4 after 10 days. Histopathologically, there was no significant difference in ulcerative scores on days 01 and 05 in all groups (score 4). However, on day 10 there was a significant difference between groups G1 (2.75) and G5 (3.62), with no such difference in the other groups. The best results for total collagen activity (22.11 and 19.77), type I (14.80 and 13.91) and type III (7.31 and 5.85) were observed between groups G1 and G4 after 10 days. Immunohistochemical analysis demonstrated delayed healing associated with high levels of IL- 1, mainly in group G3 (741.20). When evaluating TNF-a, a decrease was observed in all groups, except in G1 (11.33) and G3 (50.20) where there were no significant changes. On day 05, all groups had an increase in TGF-b, with the exception of group G5 (9.50), and a significant increase was also noted in groups G2 (181.67), G3 (119.20) and G4 (24.33) on day 10. Finally, when evaluating CD31, none of the groups showed statistical differences on day 05, however, on day 10, those that expressed the most were groups G4 (130.33) and G5 (150.00). Based on the results presented, the formulation showed physical-chemical stability in all storage conditions and time tested, with better results when stored in the refrigerator, as well as effectiveness in tissue repair, suggesting the indication of the healing activity of the proposed phytotherapeutic formulation when used for the treatment of oral ulcers in diabetic rats.
publishDate 2024
dc.date.issued.fl_str_mv 2024-04-23
dc.date.accessioned.fl_str_mv 2025-01-13T21:36:08Z
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dc.identifier.citation.fl_str_mv MELO, Luciana Aleixo dos Santos de. Efeito reparador tecidual de uma pomada orabase de Libidibia ferrea L. para o tratamento de úlceras da cavidade bucal em ratos diabéticos. 2024. 132 f. Tese (Doutorado em Inovação Farmacêutica) - Universidade Federal do Amazonas, Manaus (AM), 2024.
dc.identifier.uri.fl_str_mv https://tede.ufam.edu.br/handle/tede/10595
identifier_str_mv MELO, Luciana Aleixo dos Santos de. Efeito reparador tecidual de uma pomada orabase de Libidibia ferrea L. para o tratamento de úlceras da cavidade bucal em ratos diabéticos. 2024. 132 f. Tese (Doutorado em Inovação Farmacêutica) - Universidade Federal do Amazonas, Manaus (AM), 2024.
url https://tede.ufam.edu.br/handle/tede/10595
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dc.relation.department.fl_str_mv -8773172453627126821
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dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by-nc-nd/4.0/
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dc.publisher.none.fl_str_mv Universidade Federal do Amazonas
dc.publisher.program.fl_str_mv Programa de Pós-graduação em Inovação Farmacêutica
dc.publisher.initials.fl_str_mv UFAM
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade Federal do Amazonas
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