<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-28T13:47:52Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/40543" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/40543</identifier><datestamp>2026-02-03T11:33:24Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Castro Varela, Pablo Andrés</subfield>
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      <subfield code="a">Rubilar, Mónica</subfield>
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      <subfield code="a">Martínez-Férez, Antonio</subfield>
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      <subfield code="a">Fuentes-Ríos, David</subfield>
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      <subfield code="a">López-Romero, Juan Manuel</subfield>
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      <subfield code="a">Alarcón, Claudio</subfield>
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      <subfield code="a">Abdala-Díaz, Roberto Teófilo</subfield>
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      <subfield code="a">López-Figueroa, Félix</subfield>
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      <subfield code="c">2024-03-11</subfield>
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      <subfield code="a">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.</subfield>
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      <subfield code="a">Algal Research 79 (2024) 103473</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/40543</subfield>
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      <subfield code="a">10.1016/j.algal.2024.103473</subfield>
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      <subfield code="a">Nanotecnología</subfield>
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      <subfield code="a">Industria farmacéutica</subfield>
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      <subfield code="a">R-phycoerythrin alginate/shellac beads by external gelation: Process optimization and the effects of gastrointestinal digestion for nutraceutical applications.</subfield>
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