Isomerization of fatty acids: A cellular barrier mechanism in nanotechnology?
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| Autores: | , , |
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| Formáid: | artículo |
| Fecha de Publicación: | 2017 |
| Cur Síos: | This work is a kinetic study of the coupling reaction of 2-mercaptoethanol with methyl undecenoate and with methyl oleate through " click " chemistry. Reversibility and reactivity of each system were followed through Fourier Transform Infrared Spectroscopy and ATR conversion (FTIR-ATR) and Nuclear Magnetic Resonance Spectroscopy (1 H NMR). It was proved that the addition of thiol to the alkene may be reversible, that it depends on factors such as the structure of the alkene and the concentration of thiol or photoinitiator, but that it is mainly affected by the isomerization process in fatty acids and the reactivity of each configuration (cis or trans). It was concluded that under our " click " chemical experimental conditions, the cis form of methyl oleate is more reactive than the trans form. Finally, the plausibility of applying this process in nanotechnology is discussed as a cellular barrier mechanism to avoid internalization of toxic nanoparticles |
| País: | Repositorio UNA |
| Institiúid: | Universidad Nacional de Costa Rica |
| Repositorio: | Repositorio UNA |
| Teanga: | Inglés |
| OAI Identifier: | oai:https://repositorio.una.ac.cr:11056/17411 |
| Rochtain Ar Líne: | http://hdl.handle.net/11056/17411 |
| Access Level: | acceso abierto |
| Palabra clave: | ISOMERIZATION ÁCIDOS GRASOS THIYL RADICALS CELULAR MEMBRANE NANOTECNOLOGÍA |