Publication:
Cetyl palmitate-based NLC for topical delivery of Coenzyme Q<inf>10</inf>- Development, physicochemical characterization and in vitro release studies

dc.contributor.authorVeerawat Teeranachaideekulen_US
dc.contributor.authorEliana B. Soutoen_US
dc.contributor.authorVaraporn B. Junyapraserten_US
dc.contributor.authorRainer H. Mülleren_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherFreie Universitat Berlinen_US
dc.date.accessioned2018-08-24T01:40:58Z
dc.date.available2018-08-24T01:40:58Z
dc.date.issued2007-08-01en_US
dc.description.abstractIn the present study, nanostructured lipid carriers (NLC) composed of cetyl palmitate with various amounts of caprylic/capric triacylglycerols (as liquid lipid) were prepared and Coenzyme Q10(Q10) has been incorporated in such carriers due to its high lipophilic character. A nanoemulsion composed solely of liquid lipid was prepared for comparison studies. By photon correlation spectroscopy a mean particle size in the range of 180-240 nm with a narrow polydispersity index (PI) lower than 0.2 was obtained for all developed formulations. The entrapment efficiency was 100% in all cases. The increase of oil loading did not affect the mean particle size of NLC formulations. NLC and nanoemulsion, stabilized by the same emulsifier, showed zeta potential values in the range -40/-50 mV providing a good physical stability of the formulations. Scanning electron microscopy studies revealed NLC of disc-like shape. With respect to lipid polymorphism, a decrease in the ordered structure of NLC was observed with the increase of both oil and Q10loadings, allowing therefore high accommodation for Q10within the NLC. Using static Franz diffusion cells, the in vitro release studies demonstrated that Q10-loaded NLC possessed a biphasic release pattern, in comparison to Q10-loaded nanoemulsions comprising similar composition of which a nearly constant release was observed. The NLC release patterns were defined by an initial fast release in comparison to the release of NE followed by a prolonged release, which was dependent on the oil content. © 2007 Elsevier B.V. All rights reserved.en_US
dc.identifier.citationEuropean Journal of Pharmaceutics and Biopharmaceutics. Vol.67, No.1 (2007), 141-148en_US
dc.identifier.doi10.1016/j.ejpb.2007.01.015en_US
dc.identifier.issn09396411en_US
dc.identifier.other2-s2.0-34250893864en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/24149
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34250893864&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleCetyl palmitate-based NLC for topical delivery of Coenzyme Q<inf>10</inf>- Development, physicochemical characterization and in vitro release studiesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34250893864&origin=inwarden_US

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