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dc.date.accessioned 2020-05-20T17:08:53Z
dc.date.available 2020-05-20T17:08:53Z
dc.date.issued 2013-03
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/96392
dc.description.abstract Polymerized liposomes encapsulating L-tryptophan were studied with the aim to characterize them as drug delivery systems for the treatment of several metabolic diseases that need an increased systemic L-tryptophan concentration, polymerized liposomes were obtained by UV irradiation of vesicles containing 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (DC8,9PC) and 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) in a 1:1 molar ratio, in the presence of 10 and 50 mol% of L-tryptophan (respect to total lipid concentration). Polymerization efficiency was studied spectrophotometrically. Also, bilayer packing at the polar head region was followed with the Merocyanine 540 (MC540) and specific interactions in the lipopolymers were studied by FTIR. High L-tryptophan concentrations (50 mol% respect to total lipid concentration) induced a higher amount of six- and nine-unit polymers. This phenomenon was induced because the L-tryptophan located outside the lipid membrane was included in it during the polymerization process and was thus responsible for the better accommodate of the polar head region. This was not possible with the lower amount of L-tryptophan (10 mol%). The stability of lipopolymers with different amounts of L-tryptophan was studied through release profiles. Polymerized liposomes with 50 mol% of L-tryptophan were able to retain around 80% of the amino acid after 24 hours, whereas those with 10 mol % of the amino acid were able to retain 20%. The metabolic activity of the Caco-2 cell line was also studied. Cytotoxic effects were low in the presence of polymerized liposomes, rendering a maximum percentage of cell death of 30%. In summary, this work stresses the relevance of nonspecific drug-polymerized membrane binding on L-tryptophan pharmacological interaction with possible pharmaceutical applications in liposomal drug delivery. Moreover, the absence of significant cytotoxic effects allows the system proposed to be applied in human health. en
dc.format.extent 31-33 es
dc.language en es
dc.subject Lipopolymers es
dc.subject L-tryptophan es
dc.subject Drug delivery es
dc.title Lipid-polymer membranes as carriers for L-tryptophan
dc.type Articulo es
sedici.identifier.uri https://ri.conicet.gov.ar/11336/77442 es
sedici.identifier.uri https://www.scirp.org/journal/PaperInformation.aspx?PaperID=29497 es
sedici.identifier.other http://dx.doi.org/10.4236/ojmc.2013.31005 es
sedici.identifier.other hdl:11336/77442 es
sedici.identifier.issn 2164-3121 es
sedici.title.subtitle Molecular and metabolic properties es
sedici.creator.person Fernández Ruocco, María Julieta es
sedici.creator.person Siri, Macarena es
sedici.creator.person Igartúa, Daniela Edith es
sedici.creator.person Prieto, María Jimena es
sedici.creator.person Alonso, Silvia del Valle es
sedici.creator.person Chiaramoni, Nadia Silvia es
sedici.subject.materias Ciencias Médicas es
sedici.subject.materias Ingeniería es
sedici.description.fulltext true es
mods.originInfo.place Instituto Multidisciplinario de Biología Celular es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution 4.0 International (CC BY 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Open Journal of Medicinal Chemistry es
sedici.relation.journalVolumeAndIssue vol. 3, no. 1 es


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Creative Commons Attribution 4.0 International (CC BY 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution 4.0 International (CC BY 4.0)