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Preparation and Characterization of a Lutein Solid Dispersion to Improve Its Solubility and Stability

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dc.contributor.authorLim, C.-
dc.contributor.authorKang, J.K.-
dc.contributor.authorJung, C.E.-
dc.contributor.authorSim, T.-
dc.contributor.authorHer, J.-
dc.contributor.authorKang, K.-
dc.contributor.authorLee, E.S.-
dc.contributor.authorYoun, Y.S.-
dc.contributor.authorChoi, H.-G.-
dc.contributor.authorOh, K.T.-
dc.date.accessioned2023-03-08T10:51:09Z-
dc.date.available2023-03-08T10:51:09Z-
dc.date.issued2021-06-02-
dc.identifier.issn1530-9932-
dc.identifier.issn1522-1059-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/62364-
dc.description.abstractLutein has been used as a dietary supplement for the treatment of eye diseases, especially age-related macular degeneration. For oral formulations, we investigated lutein stability in artificial set-ups mimicking different physiological conditions and found that lutein was degraded over time under acidic conditions. To enhance the stability of lutein upon oral intake, we developed enteric-coated lutein solid dispersions (SD) by applying a polymer, hydroxypropyl methylcellulose acetate succinate (HPMCAS-LF), through a solvent-controlled precipitation method. The SD were characterized in crystallinity, morphology, and drug entrapment. In the dissolution profile of lutein SD, a F80 formulation showed resistance toward the acidic environment under simulated gastric conditions while exhibiting a bursting drug release under simulated intestinal conditions. Our results highlight the potential use of HPMCAS-LF as an effective matrix to enhance lutein bioavailability during oral delivery and to provide novel insights into the eye-care supplement industry, with direct benefits for the health of patients. Graphical abstract: [Figure not available: see fulltext.]. © 2021, American Association of Pharmaceutical Scientists.-
dc.language영어-
dc.language.isoENG-
dc.publisherSpringer Science and Business Media Deutschland GmbH-
dc.titlePreparation and Characterization of a Lutein Solid Dispersion to Improve Its Solubility and Stability-
dc.typeArticle-
dc.identifier.doi10.1208/s12249-021-02036-4-
dc.identifier.bibliographicCitationAAPS PharmSciTech, v.22, no.5-
dc.description.isOpenAccessN-
dc.identifier.wosid000765803400001-
dc.identifier.scopusid2-s2.0-85107152944-
dc.citation.number5-
dc.citation.titleAAPS PharmSciTech-
dc.citation.volume22-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorabsorption-
dc.subject.keywordAuthorbioavailability-
dc.subject.keywordAuthordegradation-
dc.subject.keywordAuthorlutein-
dc.subject.keywordAuthororal drug delivery-
dc.subject.keywordAuthorpH sensitivity-
dc.subject.keywordAuthorsolid dispersion-
dc.subject.keywordAuthorstability-
dc.subject.keywordPlushydroxypropylmethylcellulose acetate succinate-
dc.subject.keywordPlusmethylcellulose-
dc.subject.keywordPluspolymer-
dc.subject.keywordPlussolvent-
dc.subject.keywordPlusxanthophyll-
dc.subject.keywordPlusbioavailability-
dc.subject.keywordPlusdrug release-
dc.subject.keywordPlusdrug stability-
dc.subject.keywordPlushigh performance liquid chromatography-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusprocedures-
dc.subject.keywordPlussolubility-
dc.subject.keywordPlussynthesis-
dc.subject.keywordPlusX ray diffraction-
dc.subject.keywordPlusBiological Availability-
dc.subject.keywordPlusChromatography, High Pressure Liquid-
dc.subject.keywordPlusDrug Liberation-
dc.subject.keywordPlusDrug Stability-
dc.subject.keywordPlusHumans-
dc.subject.keywordPlusLutein-
dc.subject.keywordPlusMethylcellulose-
dc.subject.keywordPlusPolymers-
dc.subject.keywordPlusSolubility-
dc.subject.keywordPlusSolvents-
dc.subject.keywordPlusX-Ray Diffraction-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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