Metallosomes for biomedical applications by mixing molybdenum carbonyl metallosurfactants and phospholipids
Marín-García, M. and Benseny-Cases, N. and Camacho, M. and Perrie, Y. and Suades, J. and Barnadas-Rodríguez, R. (2018) Metallosomes for biomedical applications by mixing molybdenum carbonyl metallosurfactants and phospholipids. Dalton Transactions. ISSN 1477-9226 (https://doi.org/10.1039/c8dt01584h)
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Abstract
New supramolecular systems have been prepared by mixing molybdenum organometallic metallosurfactants M(CO)5L and M(CO)4L2 {L = Ph2P(CH2)6SO3Na} with the phospholipid phosphatidylcholine. The analysis of the resulting supramolecular structures using dynamic light scattering and cryo-transmission electron microscopy has shown the formation of different aggregates depending on the metallosurfactant/phospholipid ratio, as well as a significantly different behaviour between the two studied metallosurfactants. Mixed vesicles, with properties very similar to liposomes, can be obtained with both compounds, and are called metallosomes. The formation of the mixed aggregates has also been studied by microfluidics using MeOH and EtOH as organic solvents, and it has been observed that the size of the aggregates is strongly dependent on the organic solvent used. In order to analyse the viability of these mixed systems as CO Releasing Molecules (CORMs) for biomedical applications, the CO release was studied by FT-IR spectroscopy, showing that they behave as photo-CORMs with visible and ultraviolet light. Toxicity studies of the different mixed aggregate systems have shown that metallosomes exhibit a very low toxicity, similar to liposomes that do not contain metallosurfactants, which is well below the results observed for pure metallosurfactants. Micro-FTIR microscopy using synchrotron radiation has shown the presence of metallosurfactants in cells. The results of this study show the influence of the length of the hydrocarbon chain on the properties of these mixed systems, compared with previously reported data.
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Item type: Article ID code: 64668 Dates: DateEvent28 June 2018Published28 June 2018Published Online15 June 2018AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 04 Jul 2018 09:21 Last modified: 11 Nov 2024 12:02 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/64668