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      <dc:title>R-phycoerythrin alginate/shellac beads by external gelation: Process optimization and the effects of gastrointestinal digestion for nutraceutical applications.</dc:title>
      <dc:creator>Castro Varela, Pablo Andrés</dc:creator>
      <dc:creator>Rubilar, Mónica</dc:creator>
      <dc:creator>Martínez-Férez, Antonio</dc:creator>
      <dc:creator>Fuentes-Ríos, David</dc:creator>
      <dc:creator>López-Romero, Juan Manuel</dc:creator>
      <dc:creator>Alarcón, Claudio</dc:creator>
      <dc:creator>Abdala-Díaz, Roberto Teófilo</dc:creator>
      <dc:creator>López-Figueroa, Félix</dc:creator>
      <dc:subject>Nanotecnología</dc:subject>
      <dc:subject>Polímeros</dc:subject>
      <dc:subject>Industria farmacéutica</dc:subject>
      <dc:subject>Materiales compuestos</dc:subject>
      <dc:description>This study aimed to evaluate an alginate/shellac mixture as wall material to develop an aqueous phycoerythrin (R-PE) encapsulation system by external gelation and to determine the effect of encapsulation on the biological properties of R-PE released during simulated gastrointestinal digestion. The Taguchi method was implemented to formulate beads with a high R-PE encapsulation efficiency (EE). The effect of the variables: feeding flow (90 and&#xd;
20 mL h− 1), distance (5 and 10 cms), and CaCl2 (5 and 15 g L− 1) were optimized, and the bead size, sphericity factor (SF), and total R-PE content were characterized. Finally, the optimal alginate/shellac beads were subjected to in vitro dynamic gastrointestinal digestion. The results show that the beads formed under optimal conditions reached an EE value of 97.5 %. The CaCl2 concentration and feeding flow most affected the R-PE EE. The release&#xd;
of R-PE from alginate/shellac was affected at acid pH 1; however, the concentration was under 10 % of the total R-PE content showing promising targeting properties in terms of time and pH. The R-PE extracts and capsules were partially degraded in gastric and intestinal conditions; the mouth did not detect signals from the protein profile. The encapsulation of alginate/shellac led to higher R-PE contents at the end of digestion than non-encapsulated R-PE, suggesting a protective role. Significantly, from permeate streams, equivalent to the absorption of encapsulated R-PE, the bioavailability was 2.5 times higher than non-encapsulated R-PE. NMR results indicate the presence of R-PE and its methyl amino acids and oligosaccharides between 0.5 and 2.5 and 3.8–6.8 ppm, respectively. Cytotoxicity activity was observed for the R-PE extract on the HCT-116 human colon cancer cell line. The alginate/shellac as a wall material and ionic gelation technology used may determine the release of the R-PE pigment at an intestinal site and its antiproliferative effect on health.</dc:description>
      <dc:date>2025-10-31T10:02:59Z</dc:date>
      <dc:date>2025-10-31T10:02:59Z</dc:date>
      <dc:date>2024-03-11</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Algal Research 79 (2024) 103473</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/40543</dc:identifier>
      <dc:identifier>10.1016/j.algal.2024.103473</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>open access</dc:rights>
      <dc:publisher>Elsevier</dc:publisher>
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