Logo do repositório

Comparative analysis of bacterial and microalgal natural astaxanthin: Part II — Biocompatibility, bioaccessibility, encapsulation, mutagenicity, and aquatic toxicity

dc.contributor.authorMussagy, Cassamo U.
dc.contributor.authorGini, Ana L.R. [UNESP]
dc.contributor.authorScarim, Cauê B. [UNESP]
dc.contributor.authorDuarte, Jonatas L. [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorMilitão, Gabriely F.G.
dc.contributor.authordos Santos, Amanda [UNESP]
dc.contributor.authorLima, Nayara P.
dc.contributor.authorRibeiro, Isabela S.
dc.contributor.authorHaminiuk, Charles W.I.
dc.contributor.authorFarias, Fabiane O.
dc.contributor.authorde A. Umbuzeiro, Gisela
dc.contributor.authorPessoa, Adalberto
dc.date.accessioned2026-05-11T19:11:15Z
dc.date.issued2025-10-01
dc.description.abstractAstaxanthin (AXT) is a potent antioxidant with applications in food, pharmaceutical, and cosmetic industries. While Haematococcus pluvialis (a microalga) is the only natural AXT source approved for human use, bacterial alternatives such as Paracoccus carotinifaciens are gaining attention for their sustainable production potential. This study, Part II of a comparative research analysis between AXT from H. pluvialis and P. carotinifaciens, explores key aspects of biocompatibility, bioaccessibility, encapsulation performance, mutagenicity, and aquatic toxicity. The HET-CAM confirmed that both AXT sources are non-irritant. In vitro digestion revealed that H. pluvialis AXT undergoes greater solubilization in the gastric phase but experiences higher losses in the intestinal phase, while P. carotinifaciens AXT demonstrates better retention. Nanoemulsions of both extracts showed high encapsulation efficiency (99 %) and colloidal stability, with bacterial AXT forming smaller, more stable droplets. Ames mutagenicity assays with five Salmonella strains showed no evidence of mutagenic activity. Additionally, no acute toxicity was observed in Daphnia similis, even at the highest tested concentrations. These findings reinforce the safety and functionality of both microbial AXT sources, supporting P. carotinifaciens as a promising alternative for future nutraceutical and pharmaceutical applications.
dc.description.affiliationLaboratorio de Desarrollo de Bioprocesos Sostenibles (Labisost), Escuela de Agronomía, Facultad de Ciencias Agronómicas y de los Alimentos, Pontificia Universidad Católica de Valparaíso, Casilla 4-D, Quillota, 2260000, Chile
dc.description.affiliationSão Paulo State University (UNESP), School of Pharmaceutical Sciences, Department of Drugs and Medicines, Araraquara, 14800-903, São Paulo, Brazil
dc.description.affiliationUniversidade Estadual de Campinas (UNICAMP), School of Medical Sciences, Department of Pharmacology, Campinas, 13083-888, São Paulo, Brazil
dc.description.affiliationSão Paulo State University (UNESP), School of Pharmaceutical Sciences, Department of Bioprocess Engineering and Biotechnology, Araraquara 14800-903, São Paulo, Brazil
dc.description.affiliationLaboratório de Biotecnologia, Departamento Acadêmico de Química e Biologia (DAQBi), Universidade Tecnológica Federal do Paraná, Sede Ecoville, Curitiba, Paraná, 81280-340, Brazil
dc.description.affiliationGraduate Program of Food Engineer, Department of Chemical Engineering, Polytechnique Center, Federal University of Paraná, Curitiba, PR, Brazil
dc.description.affiliationUniversidade Estadual de Campinas (UNICAMP), School of Technology, Limeira, São Paulo, Brazil
dc.description.affiliationDepartment of Pharmaceutical-Biochemical Technology, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil
dc.description.affiliationUnespSão Paulo State University (UNESP), School of Pharmaceutical Sciences, Department of Drugs and Medicines, Araraquara, 14800-903, São Paulo, Brazil
dc.description.affiliationUnespSão Paulo State University (UNESP), School of Pharmaceutical Sciences, Department of Bioprocess Engineering and Biotechnology, Araraquara 14800-903, São Paulo, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1193544543
dc.identifier.dimensionspub.1193544543
dc.identifier.doi10.1016/j.algal.2025.104343
dc.identifier.issn2211-9264
dc.identifier.orcid0000-0003-2907-5826
dc.identifier.orcid0000-0003-2643-810X
dc.identifier.orcid0000-0002-2540-6395
dc.identifier.orcid0000-0002-7276-3686
dc.identifier.orcid0000-0002-6698-0545
dc.identifier.orcid0000-0003-2512-1928
dc.identifier.orcid0000-0003-0945-5856
dc.identifier.orcid0000-0002-1841-3589
dc.identifier.orcid0000-0002-1432-9427
dc.identifier.orcid0000-0002-0223-1393
dc.identifier.orcid0000-0002-5268-8690
dc.identifier.urihttps://hdl.handle.net/11449/323682
dc.publisherElsevier
dc.relation.ispartofAlgal Research; v. 91; p. 104343
dc.rights.accessRightsAcesso restritopt
dc.rights.sourceRightsclosed
dc.sourceDimensions
dc.titleComparative analysis of bacterial and microalgal natural astaxanthin: Part II — Biocompatibility, bioaccessibility, encapsulation, mutagenicity, and aquatic toxicity
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

Arquivos