dc.creatorFernandez Ruocco, Maria Julieta
dc.creatorSiri, Macarena
dc.creatorIgartúa, Daniela
dc.creatorPrieto, Maria Jimena
dc.creatorAlonso, Silvia del Valle
dc.creatorChiaramoni, Nadia Silvia
dc.date.accessioned2019-05-31T00:46:24Z
dc.date.accessioned2022-10-14T22:46:42Z
dc.date.available2019-05-31T00:46:24Z
dc.date.available2022-10-14T22:46:42Z
dc.date.created2019-05-31T00:46:24Z
dc.date.issued2013-03
dc.identifierFernandez Ruocco, Maria Julieta; Siri, Macarena; Igartúa, Daniela; Prieto, Maria Jimena; Alonso, Silvia del Valle; et al.; Lipid-polymer membranes as carriers for L-tryptophan: molecular and metabolic properties; Scientific Research; Open Journal of Medicinal Chemistry; 3; 1; 3-2013; 31-33
dc.identifier2164-3121
dc.identifierhttp://hdl.handle.net/11336/77442
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4315664
dc.description.abstractPolymerized 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-glyc- ero-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 stud- ied 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 meta- bolic activity of the Caco-2 cell line was also studied. Cytotoxic effects were low in the presence of polymerized lipo- somes, rendering a maximum percentage of cell death of 30%. In summary, this work stresses the relevance of nonspe- cific 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 pro- posed to be applied in human health.
dc.languageeng
dc.publisherScientific Research
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.scirp.org/journal/PaperInformation.aspx?PaperID=29497
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.4236/ojmc.2013.31005
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectLIPOPOLYMERS
dc.subjectL-TRYPTOPHAN
dc.subjectDRUG DELIVERY
dc.titleLipid-polymer membranes as carriers for L-tryptophan: molecular and metabolic properties
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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