OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações do UNICENTRO |
Texto Completo: | http://tede.unicentro.br:8080/jspui/handle/jspui/676 |
Resumo: | Tamoxifen and curcumin are compounds widely studied for the treatment of cancer, tamoxifen is already used in breast cancer, but it has several side effects. Many studies report the activity of curcumin in cancer, but it has low bioavailability. Therefore, the combination of these compounds and encapsulation in nanoparticles are promising strategy for the treatment of cancer, which can increase the antitumor activity, reduce side effects of tamoxifen and increase the bioavailability of curcumin, as well as providing a controlled release. In this study poly (lactic acid) nanoparticles containing curcumin, tamoxifen citrate (CTAM) and the combination of these compounds were obtained by the method of emulsification-solvent evaporation (O/W). To calculate the encapsulation efficiency an analytical method by high performance liquid chromatography to quantify curcumin and CTAM at the same time was developed, this method was validated and showed linearity, specificity, precision, accuracy and robustness. The encapsulation efficiency was similar for curcumin and CTAM when encapsulated together or alone, with approximately 57% for CTAM and 92% for curcumin. The nanoparticles had spherical morphology, with a size next to 190 nm, the zeta potential was -16 mV to CTAM nanoparticles, -26 mV to curcumin nanoparticles and -17 mV for curcumin-CTAM nanoparticles. The size, zeta potential and polydispersity index were stable for 90 days. The nanoparticles obtained were also analyzed by infrared spectroscopy, differential scanning calorimetry and thermogravimetry. The in vitro release in 120 hours was 57% for curcumin and 49% for CTAM in curcumin-CTAM nanoparticle, 45% for CTAM nanoparticle and 61% for curcumin nanoparticles. Evaluating the cytotoxic activity against red blood cells, it was observed a decrease in hemolysis of CTAM when associated with curcumin, when encapsulated both compounds showed low hemolysis in 96 hours, while the drug in free form showed 100% hemolysis in 24 hours. In the cytotoxicity against melanoma cells (B16-F10) nanoparticles containing curcumin-CTAM showed an additive effect compared to the nanoparticles of the isolated compounds. |
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Khalil, Najeh Maissarhttp://lattes.cnpq.br/8578241611510102077.888.939-43http://lattes.cnpq.br/1666222584872959DALPOSSO, LORIANGELA MARCELI2017-06-07T12:32:41Z2015-04-29DALPOSSO, LORIANGELA MARCELI. OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA. 2015. 97 f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - Mestrado / Associação Ampla com UEPG) - Universidade Estadual do Centro-Oeste, Guarapuava - PR.http://tede.unicentro.br:8080/jspui/handle/jspui/676Tamoxifen and curcumin are compounds widely studied for the treatment of cancer, tamoxifen is already used in breast cancer, but it has several side effects. Many studies report the activity of curcumin in cancer, but it has low bioavailability. Therefore, the combination of these compounds and encapsulation in nanoparticles are promising strategy for the treatment of cancer, which can increase the antitumor activity, reduce side effects of tamoxifen and increase the bioavailability of curcumin, as well as providing a controlled release. In this study poly (lactic acid) nanoparticles containing curcumin, tamoxifen citrate (CTAM) and the combination of these compounds were obtained by the method of emulsification-solvent evaporation (O/W). To calculate the encapsulation efficiency an analytical method by high performance liquid chromatography to quantify curcumin and CTAM at the same time was developed, this method was validated and showed linearity, specificity, precision, accuracy and robustness. The encapsulation efficiency was similar for curcumin and CTAM when encapsulated together or alone, with approximately 57% for CTAM and 92% for curcumin. The nanoparticles had spherical morphology, with a size next to 190 nm, the zeta potential was -16 mV to CTAM nanoparticles, -26 mV to curcumin nanoparticles and -17 mV for curcumin-CTAM nanoparticles. The size, zeta potential and polydispersity index were stable for 90 days. The nanoparticles obtained were also analyzed by infrared spectroscopy, differential scanning calorimetry and thermogravimetry. The in vitro release in 120 hours was 57% for curcumin and 49% for CTAM in curcumin-CTAM nanoparticle, 45% for CTAM nanoparticle and 61% for curcumin nanoparticles. Evaluating the cytotoxic activity against red blood cells, it was observed a decrease in hemolysis of CTAM when associated with curcumin, when encapsulated both compounds showed low hemolysis in 96 hours, while the drug in free form showed 100% hemolysis in 24 hours. In the cytotoxicity against melanoma cells (B16-F10) nanoparticles containing curcumin-CTAM showed an additive effect compared to the nanoparticles of the isolated compounds.O tamoxifeno e a curcumina são compostos amplamente estudados para o tratamento do câncer, sendo que o tamoxifeno já é utilizado no câncer de mama, mas apresenta diversos efeitos colaterais. Vários estudos relatam a atividade da curcumina nesse tipo de câncer, porém ela apresenta uma baixa biodisponibilidade. Dessa forma, a associação desses compostos e a encapsulação em nanopartículas são estratégias promissoras para o tratamento do câncer, resultando em um potencial aumento da atividade antitumoral, diminuição dos efeitos indesejáveis do tamoxifeno e aumento da biodisponibilidade da curcumina, além de proporcionar uma liberação controlada. Neste trabalho foram obtidas nanopartículas de poli (ácido láctico) contendo curcumina, citrato de tamoxifeno (CTAM) e curcumina-CTAM pelo método de emulsificação-evaporação do solvente (O/A). Para calcular a eficiência de encapsulação dos sistemas obtidos, foi desenvolvida uma metodologia analítica por cromatografia líquida de alta eficiência para quantificação de curcumina e CTAM simultaneamente, esse método foi validado e apresentou linearidade, especificidade, precisão, exatidão e robustez. A eficiência de encapsulação foi de aproximadamente 57% para o CTAM e 92% para curcumina. As nanopartículas apresentaram morfologia esférica, com tamanho próximo a 190 nm, o potencial zeta para as nanopartículas de CTAM foi de -16 mV, para as nanopartículas de curcumina -26 mV e para as nanopartículas de curcumina-CTAM -17 mV. O tamanho, índice de polidispersão e o potencial zeta ficaram estáveis durante 90 dias. As nanopartículas obtidas também foram analisadas por espectroscopia na região do infravermelho, calorimetria exploratória diferencial e termogravimetria. Na liberação in vitro em 120 horas a liberação foi de 57% para a curcumina e 49% para o tamoxifeno na nanopartícula de curcumina-CTAM e de 45% para nanopartícula de CTAM e 61% para a nanopartículas de curcumina. Avaliando a atividade citotóxica sobre hemácias, foi possível observar uma diminuição da hemólise do CTAM quando associado com a curcumina, em nanopartículas ambos os compostos apresentaram uma baixa hemólise mesmo no tempo de 96 horas, enquanto as drogas na forma livre apresentaram valores próximos a 100% de hemólise em 24 horas. Na citotoxicidade sobre células de melanoma da linhagem B16-F10, as nanopartículas contendo curcumina-CTAM mostraram um efeito aditivo em relação às nanopartículas contendo os compostos isolados.Submitted by Fabiano Jucá (fjuca@unicentro.br) on 2017-06-07T12:32:41Z No. of bitstreams: 1 LORIANGELA MARCELI DALPOSSO.pdf: 2651877 bytes, checksum: e75ee225c807527b9621a717d7d056bf (MD5)Made available in DSpace on 2017-06-07T12:32:41Z (GMT). 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dc.title.por.fl_str_mv |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA |
title |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA |
spellingShingle |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA DALPOSSO, LORIANGELA MARCELI Nanopartículas Poli (ácido láctico) Citotoxicidade Curcumina Tamoxifeno Nanoparticles Poly (lactic acid) Cytotoxicity Curcumin Tamoxifen CIENCIAS DA SAUDE::FARMACIA |
title_short |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA |
title_full |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA |
title_fullStr |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA |
title_full_unstemmed |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA |
title_sort |
OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA |
author |
DALPOSSO, LORIANGELA MARCELI |
author_facet |
DALPOSSO, LORIANGELA MARCELI |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Khalil, Najeh Maissar |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/8578241611510102 |
dc.contributor.authorID.fl_str_mv |
077.888.939-43 |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/1666222584872959 |
dc.contributor.author.fl_str_mv |
DALPOSSO, LORIANGELA MARCELI |
contributor_str_mv |
Khalil, Najeh Maissar |
dc.subject.por.fl_str_mv |
Nanopartículas Poli (ácido láctico) Citotoxicidade Curcumina Tamoxifeno |
topic |
Nanopartículas Poli (ácido láctico) Citotoxicidade Curcumina Tamoxifeno Nanoparticles Poly (lactic acid) Cytotoxicity Curcumin Tamoxifen CIENCIAS DA SAUDE::FARMACIA |
dc.subject.eng.fl_str_mv |
Nanoparticles Poly (lactic acid) Cytotoxicity Curcumin Tamoxifen |
dc.subject.cnpq.fl_str_mv |
CIENCIAS DA SAUDE::FARMACIA |
description |
Tamoxifen and curcumin are compounds widely studied for the treatment of cancer, tamoxifen is already used in breast cancer, but it has several side effects. Many studies report the activity of curcumin in cancer, but it has low bioavailability. Therefore, the combination of these compounds and encapsulation in nanoparticles are promising strategy for the treatment of cancer, which can increase the antitumor activity, reduce side effects of tamoxifen and increase the bioavailability of curcumin, as well as providing a controlled release. In this study poly (lactic acid) nanoparticles containing curcumin, tamoxifen citrate (CTAM) and the combination of these compounds were obtained by the method of emulsification-solvent evaporation (O/W). To calculate the encapsulation efficiency an analytical method by high performance liquid chromatography to quantify curcumin and CTAM at the same time was developed, this method was validated and showed linearity, specificity, precision, accuracy and robustness. The encapsulation efficiency was similar for curcumin and CTAM when encapsulated together or alone, with approximately 57% for CTAM and 92% for curcumin. The nanoparticles had spherical morphology, with a size next to 190 nm, the zeta potential was -16 mV to CTAM nanoparticles, -26 mV to curcumin nanoparticles and -17 mV for curcumin-CTAM nanoparticles. The size, zeta potential and polydispersity index were stable for 90 days. The nanoparticles obtained were also analyzed by infrared spectroscopy, differential scanning calorimetry and thermogravimetry. The in vitro release in 120 hours was 57% for curcumin and 49% for CTAM in curcumin-CTAM nanoparticle, 45% for CTAM nanoparticle and 61% for curcumin nanoparticles. Evaluating the cytotoxic activity against red blood cells, it was observed a decrease in hemolysis of CTAM when associated with curcumin, when encapsulated both compounds showed low hemolysis in 96 hours, while the drug in free form showed 100% hemolysis in 24 hours. In the cytotoxicity against melanoma cells (B16-F10) nanoparticles containing curcumin-CTAM showed an additive effect compared to the nanoparticles of the isolated compounds. |
publishDate |
2015 |
dc.date.issued.fl_str_mv |
2015-04-29 |
dc.date.accessioned.fl_str_mv |
2017-06-07T12:32:41Z |
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 |
DALPOSSO, LORIANGELA MARCELI. OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA. 2015. 97 f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - Mestrado / Associação Ampla com UEPG) - Universidade Estadual do Centro-Oeste, Guarapuava - PR. |
dc.identifier.uri.fl_str_mv |
http://tede.unicentro.br:8080/jspui/handle/jspui/676 |
identifier_str_mv |
DALPOSSO, LORIANGELA MARCELI. OBTENÇÃO, CARACTERIZAÇÃO E AVALIAÇÃO DA CITOTOXICIDADE DE NANOPARTÍCULAS DE POLI (ÁCIDO LÁCTICO) CONTENDO TAMOXIFENO E CURCUMINA. 2015. 97 f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - Mestrado / Associação Ampla com UEPG) - Universidade Estadual do Centro-Oeste, Guarapuava - PR. |
url |
http://tede.unicentro.br:8080/jspui/handle/jspui/676 |
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por |
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por |
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600 600 600 600 |
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6997636413449754996 |
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2075167498588264571 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Estadual do Centro-Oeste |
dc.publisher.program.fl_str_mv |
Programa de Pós-Graduação em Ciências Farmacêuticas (Mestrado / Associação Ampla com UEPG) |
dc.publisher.initials.fl_str_mv |
UNICENTRO |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Unicentro::Departamento de Farmácia |
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Universidade Estadual do Centro-Oeste |
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Biblioteca Digital de Teses e Dissertações do UNICENTRO |
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repository.name.fl_str_mv |
Biblioteca Digital de Teses e Dissertações do UNICENTRO - Universidade Estadual do Centro-Oeste (UNICENTRO) |
repository.mail.fl_str_mv |
repositorio@unicentro.br||fabianoqueiroz@yahoo.com.br |
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1811733811417841664 |