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
Main Authors: Yukuyama, Megumi Nishitani, Guimaraes, Lara Mendes Ferreira, Segovia, Rafael Scheliga, Lameu, Claudiana, de Araujo, Gabriel Lima Barros, Löbenberg, Raimar, de Souza, Aline, Henostroza, Mirla Anali Bazán, Folchini, Beatriz Rabelo, Peroni, Camilla Midori, Miyagi, Mariana Yasue Saito, Oliveira, Isabela Fernandes, Alvarenga, José Fernando Rinaldi, Fiamoncini, Jarlei, Bou-Chacra, Nádia Araci
Format: Journal Article
Language:English
Published: 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. [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.
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
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  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
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  givenname: Rafael Scheliga
  orcidid: 0000-0001-8450-6030
  surname: Segovia
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  organization: Department of Biochemistry - Chemistry Institute, University of São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP, Brazil
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  givenname: Claudiana
  surname: Lameu
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  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
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  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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CitedBy_id crossref_primary_10_1016_j_ijpharm_2022_122554
crossref_primary_10_1016_j_jddst_2023_105017
crossref_primary_10_1007_s11864_023_01172_2
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Keywords d-phase emulsification
Flubendazole
Lung cancer
Malignant wound
Nanoemulsion
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Snippet Malignant wounds (MWs) affect up to 15% of advanced stage cancer patients, causing detrimental effects such as tissue deformity and extreme malodor, affecting...
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SubjectTerms d-phase emulsification
Flubendazole
Lung cancer
Malignant wound
Nanoemulsion
Title Malignant wound – The influence of oil components in flubendazole-loaded nanoemulsions in A549 lung cancer xenograft-bearing mice
URI https://dx.doi.org/10.1016/j.jddst.2022.103963
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