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Enzymatic production process of capric acid-rich structured lipids: Development of formulation as a new therapeutic approach.
Miotti, Rodney H; do Amaral, Stephanie R; Freitas, Amanda Noli; Bento, Heitor B S; de Carvalho, Ana Karine F; Primo, Fernando L; de Paula, Ariela V.
Afiliação
  • Miotti RH; Department of Bioprocess Engineering and Biotechnology, São Paulo State University (UNESP), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil.
  • do Amaral SR; Department of Bioprocess Engineering and Biotechnology, São Paulo State University (UNESP), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil.
  • Freitas AN; Department of Bioprocess Engineering and Biotechnology, São Paulo State University (UNESP), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil.
  • Bento HBS; Department of Bioprocess Engineering and Biotechnology, São Paulo State University (UNESP), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil.
  • de Carvalho AKF; Department of Basic and Environmental Sciences, Engineering School of Lorena, University of São Paulo, Lorena, Brazil.
  • Primo FL; Department of Bioprocess Engineering and Biotechnology, São Paulo State University (UNESP), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil.
  • de Paula AV; Department of Bioprocess Engineering and Biotechnology, São Paulo State University (UNESP), School of Pharmaceutical Sciences, Araraquara, São Paulo, Brazil. Electronic address: ariela.veloso@unesp.br.
Int J Biol Macromol ; 257(Pt 2): 128641, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38061520
ABSTRACT
The present work reports an optimization of the synthesis of MLM-type (medium, long, medium) structured lipids (SL) through an acidolysis reaction of grape seed oil with capric acid catalyzed by Rhizopus oryzae lipase immobilized. At first, tests were carried out by preparing the biocatalysts using enzyme loadings (0.15 to 1 g of enzymatic powder) for each gram of support. Enzyme loading was used 0.3 g of enzymatic powder, and hydrolytic activity of 1860 ± 23.4 IU/g was reached. Optimized conditions determined by the Central Composite Rotatable Design (CCRD) revealed that the acidolysis reaction reached approximately 59 % incorporation degree (%ID) after 24 h, in addition to the fact that the biocatalyst could maintain the incorporation degree in five consecutive cycles. From this high incorporation degree, cell viability assays were performed with murine fibroblast cell lines and human cervical adenocarcinoma cell lines. Concerning the cytotoxicity assays, the concentration of MLM-SL to 1.75 and 2 % v/v were able to induce cell death in 56 % and 64 % of adenocarcinoma cells, respectively. Human cervical adenocarcinoma cells showed greater sensitivity to the induction of cell death when using emulsions with MLM-SL > 1.75 % v/v compared to emulsions with lower content indicating a potential for combating carcinogenic cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenocarcinoma / Ácidos Decanoicos Limite: Animals / Humans Idioma: En Revista: Int J Biol Macromol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenocarcinoma / Ácidos Decanoicos Limite: Animals / Humans Idioma: En Revista: Int J Biol Macromol Ano de publicação: 2024 Tipo de documento: Article