Please use this identifier to cite or link to this item: https://cuir.car.chula.ac.th/handle/123456789/63753
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dc.contributor.advisorSupason Wanichwecharungruang-
dc.contributor.authorSunatda Arayachukeat-
dc.contributor.otherChulalongkorn University. Faculty of Science-
dc.date.accessioned2019-10-09T08:13:03Z-
dc.date.available2019-10-09T08:13:03Z-
dc.date.issued2009-
dc.identifier.urihttp://cuir.car.chula.ac.th/handle/123456789/63753-
dc.descriptionThesis (M.Sc)--Chulalongkorn University, 2009en_US
dc.description.abstractIn this work, encapsulation of all-trans retinyl acetate was investigated using appropriate polymer. The result showed that ATRA-encapsulated poly(ethylene glycol)-4-methoxycinnamoylphthaloylchitosan (PCPLC) nanoparticles gave the particle size of 113.2 ± 27.1 nm. The encapsulation efficiency was 77.9 ± 2.5% at ATRA loading of 21.06 ± 0.1%. The stability study under light-proof condition and when exposed to 45.9 J/cm2 of UVA radiation indicated ~40% and ~36% higher stability of the encapsulated ATRA over free ATRA, respectively. Penetration study with Franz diffusion cell revealed that the encapsulated particles could not transdermally penetrate across the baby mouse skin. Further investigation using confocal fluorescent laser scanning microscope indicated that hair follicle was the skin penetrating route of the particles. In addition, the accumulated particles at the hair follicles released ATRA out into the surrounding tissue.en_US
dc.description.abstractalternativeIn this work, encapsulation of all-trans retinyl acetate was investigated using appropriate polymer. The result showed that ATRA-encapsulated poly(ethylene glycol)-4-methoxycinnamoylphthaloylchitosan (PCPLC) nanoparticles gave the particle size of 113.2 ± 27.1 nm. The encapsulation efficiency was 77.9 ± 2.5% at ATRA loading of 21.06 ± 0.1%. The stability study under light-proof condition and when exposed to 45.9 J/cm2 of UVA radiation indicated ~40% and ~36% higher stability of the encapsulated ATRA over free ATRA, respectively. Penetration study with Franz diffusion cell revealed that the encapsulated particles could not transdermally penetrate across the baby mouse skin. Further investigation using confocal fluorescent laser scanning microscope indicated that hair follicle was the skin penetrating route of the particles. In addition, the accumulated particles at the hair follicles released ATRA out into the surrounding tissue.en_US
dc.language.isoenen_US
dc.publisherChulalongkorn Universityen_US
dc.rightsChulalongkorn Universityen_US
dc.subjectNanoencapsulationen_US
dc.subjectนาโนเอนแคปซูเลชันen_US
dc.titleStability enhancement of all-trans retinyl acetate through Nanoencapsulationen_US
dc.title.alternativeการเพิ่มความเสถียรภาพของออล-ทรานส์เรทินิลแอซีเทตด้วยนาโนเอ็นแคปซูเลชัen_US
dc.typeThesisen_US
dc.degree.nameMaster of Scienceen_US
dc.degree.levelMaster's Degreeen_US
dc.degree.disciplinePetrochemistry and Polymer Scienceen_US
dc.degree.grantorChulalongkorn Universityen_US
dc.email.advisorSupason.P@Chula.ac.th-
Appears in Collections:Sci - Theses

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