Malignant wound – The influence of oil components in flubendazole-loaded nanoemulsions in A549 lung cancer xenograft-bearing mice
Malignant wounds (MWs) affect up to 15% of advanced stage cancer patients, causing detrimental effects such as tissue deformity and extreme malodor, affecting the social and psychological quality of life of these patients. Although treating MW is mandatory to prevent infections and reduce wound heal...
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Published in: | Journal of drug delivery science and technology Vol. 78; p. 103963 |
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Elsevier B.V
01-12-2022
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Abstract | Malignant wounds (MWs) affect up to 15% of advanced stage cancer patients, causing detrimental effects such as tissue deformity and extreme malodor, affecting the social and psychological quality of life of these patients. Although treating MW is mandatory to prevent infections and reduce wound healing time, this disease has often been overlooked by researchers. For the first time, we propose a new alternative MW treatment for oral administration using high-oil-content flubendazole (FLZ) loaded in nanoemulsions, prepared by the d-phase emulsification process. We performed in vivo tests on the A549 xenograft murine model and compared FLZ in suspension, drug-free nanoemulsion, FLZ-loaded nanoemulsion containing oil derived from linoleic acid, and FLZ-loaded nanoemulsion containing mixture of oils. Mice treated by gavage three times a week with FLZ in suspension, drug-free nanoemulsion, and FLZ-loaded nanoemulsion with mixed oil, presented MW emergence in 20–40% of the cases at different time intervals and extents. However, mice treated with FLZ-loaded nanoemulsion containing only the oil derived from linoleic acid presented MW emergence in 0% of cases, even after 80 days of treatment. Thus, we observed a positive synergy between the drug FLZ and the oil derived from linoleic acid in the treatment of MW. Discussions on the mechanism of action of this oil and the drug are intensively described in this article. We present such FLZ-loaded nanoemulsion as a promising prevention and treatment solution for greater patient compliance and lower adverse effects.
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•Malignant wound (MW) is one of the most complex and difficult disease to treat, but it is often undervalued.•Nanoemulsions were prepared by the d-Phase Emulsification Method at 25 ± 0.5 °C.•Oral administration of nanoemulsion loaded with flubendazole and linoleic acid-derived oil did not show the presence of MW.•The comparison between the different preparations showed distinct results in the percentage of occurrence and time of MW. |
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AbstractList | Malignant wounds (MWs) affect up to 15% of advanced stage cancer patients, causing detrimental effects such as tissue deformity and extreme malodor, affecting the social and psychological quality of life of these patients. Although treating MW is mandatory to prevent infections and reduce wound healing time, this disease has often been overlooked by researchers. For the first time, we propose a new alternative MW treatment for oral administration using high-oil-content flubendazole (FLZ) loaded in nanoemulsions, prepared by the d-phase emulsification process. We performed in vivo tests on the A549 xenograft murine model and compared FLZ in suspension, drug-free nanoemulsion, FLZ-loaded nanoemulsion containing oil derived from linoleic acid, and FLZ-loaded nanoemulsion containing mixture of oils. Mice treated by gavage three times a week with FLZ in suspension, drug-free nanoemulsion, and FLZ-loaded nanoemulsion with mixed oil, presented MW emergence in 20–40% of the cases at different time intervals and extents. However, mice treated with FLZ-loaded nanoemulsion containing only the oil derived from linoleic acid presented MW emergence in 0% of cases, even after 80 days of treatment. Thus, we observed a positive synergy between the drug FLZ and the oil derived from linoleic acid in the treatment of MW. Discussions on the mechanism of action of this oil and the drug are intensively described in this article. We present such FLZ-loaded nanoemulsion as a promising prevention and treatment solution for greater patient compliance and lower adverse effects.
[Display omitted]
•Malignant wound (MW) is one of the most complex and difficult disease to treat, but it is often undervalued.•Nanoemulsions were prepared by the d-Phase Emulsification Method at 25 ± 0.5 °C.•Oral administration of nanoemulsion loaded with flubendazole and linoleic acid-derived oil did not show the presence of MW.•The comparison between the different preparations showed distinct results in the percentage of occurrence and time of MW. |
ArticleNumber | 103963 |
Author | Folchini, Beatriz Rabelo Henostroza, Mirla Anali Bazán Segovia, Rafael Scheliga Lameu, Claudiana Guimaraes, Lara Mendes Ferreira de Souza, Aline Oliveira, Isabela Fernandes Yukuyama, Megumi Nishitani de Araujo, Gabriel Lima Barros Alvarenga, José Fernando Rinaldi Peroni, Camilla Midori Miyagi, Mariana Yasue Saito Bou-Chacra, Nádia Araci Fiamoncini, Jarlei Löbenberg, Raimar |
Author_xml | – sequence: 1 givenname: Megumi Nishitani orcidid: 0000-0002-6757-2084 surname: Yukuyama fullname: Yukuyama, Megumi Nishitani organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 2 givenname: Lara Mendes Ferreira orcidid: 0000-0003-1651-3719 surname: Guimaraes fullname: Guimaraes, Lara Mendes Ferreira organization: Department of Biochemistry - Chemistry Institute, University of São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP, Brazil – sequence: 3 givenname: Rafael Scheliga orcidid: 0000-0001-8450-6030 surname: Segovia fullname: Segovia, Rafael Scheliga organization: Department of Biochemistry - Chemistry Institute, University of São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP, Brazil – sequence: 4 givenname: Claudiana surname: Lameu fullname: Lameu, Claudiana email: claulameu@usp.br organization: Department of Biochemistry - Chemistry Institute, University of São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP, Brazil – sequence: 5 givenname: Gabriel Lima Barros orcidid: 0000-0001-7590-3587 surname: de Araujo fullname: de Araujo, Gabriel Lima Barros email: gabriel.araujo@usp.br organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 6 givenname: Raimar surname: Löbenberg fullname: Löbenberg, Raimar organization: Division of Pharmaceutical Sciences, Faculty of Pharmacy & Pharmaceutical Sciences, Katz Group-Rexall Centre for Pharmacy & Health Research, University of Alberta, 11361 - 87 Avenue, Room 3-142-K, Edmonton, AB, T6G 2E1, Canada – sequence: 7 givenname: Aline surname: de Souza fullname: de Souza, Aline organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 8 givenname: Mirla Anali Bazán surname: Henostroza fullname: Henostroza, Mirla Anali Bazán organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 9 givenname: Beatriz Rabelo surname: Folchini fullname: Folchini, Beatriz Rabelo organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 10 givenname: Camilla Midori surname: Peroni fullname: Peroni, Camilla Midori organization: Department of Biochemistry - Chemistry Institute, University of São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP, Brazil – sequence: 11 givenname: Mariana Yasue Saito orcidid: 0000-0002-1012-5777 surname: Miyagi fullname: Miyagi, Mariana Yasue Saito organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 12 givenname: Isabela Fernandes surname: Oliveira fullname: Oliveira, Isabela Fernandes organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 13 givenname: José Fernando Rinaldi surname: Alvarenga fullname: Alvarenga, José Fernando Rinaldi organization: Faculty of Pharmaceutical Sciences, Department of Food Science and Experimental Nutrition, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 14 givenname: Jarlei surname: Fiamoncini fullname: Fiamoncini, Jarlei organization: Faculty of Pharmaceutical Sciences, Department of Food Science and Experimental Nutrition, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil – sequence: 15 givenname: Nádia Araci surname: Bou-Chacra fullname: Bou-Chacra, Nádia Araci organization: Faculty of Pharmaceutical Sciences, Department of Pharmacy, University of Sao Paulo, Avenida Professor Lineu Prestes 508, Butantan, Sao Paulo, SP, Brazil |
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Copyright | 2022 Elsevier B.V. |
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Keywords | d-phase emulsification Flubendazole Lung cancer Malignant wound Nanoemulsion |
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