Arsenoplatin anti-cancer agents
US-2017355722-A1 · Dec 14, 2017 · US
US9592300B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9592300-B2 |
| Application number | US-45064006-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 9, 2006 |
| Priority date | Jun 9, 2005 |
| Publication date | Mar 14, 2017 |
| Grant date | Mar 14, 2017 |
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The present invention provides methods utilizing redox-active surfactants to provide electrochemical control over polymer interactions. In one embodiment, the invention is directed to a transfection method using a redox-active transfection agent that preferentially promotes transfection dependent on the oxidation state of the transfection agent. Accordingly, certain methods according to the invention provide spatial and/or temporal control of cell transfection.
Opening claim text (preview).
What is claimed is: 1. A method of controlling the aggregation of polymers by contact with redox active surfactants, comprising the step of contacting a polymer with a redox-active surfactant that is a cationic lipid transformable between oxidation states, wherein transforming the cationic lipid between oxidation states results in a change in charge density of said cationic lipid and the aggregation of the polymer is controlled by the oxidation state of said cationic lipid. 2. The method according to claim 1 wherein said polymer and redox-active surfactant are present in solution. 3. The method according to claim 1 wherein said redox-active surfactant bears a ferrocenyl moiety. 4. The method according to claim 1 wherein said polymer is a biopolymer. 5. The method according to claim 1 wherein said polymer is a nucleic acid, protein, polysaccharide, or derivative thereof. 6. A method for transfecting a cell, comprising the steps of: (a) providing a redox active transfection agent in the form of a lipoplex between a nucleic acid and a redox active cationic lipid that is transformable between: (i) a first oxidation state that facilitates transfection of cells; and (ii) a second oxidation state that is less effective at transfecting cells, wherein transforming the cationic lipid between said first and second oxidation states results in a change in charge density of said cationic lipid; and (b) contacting a cell with the redox-active transfection agent in which the cationic lipid is in said first oxidation state to facilitate transfection of the cell with the nucleic acid. 7. The method according to claim 6 further comprising the step of transforming the redox-active transfection agent to said first oxidation state. 8. The method according to claim 7 wherein the transforming step is carried out by applying an electrochemical potential to said redox-active transfection agent. 9. The method according to claim 8 wherein said electrochemical potential is provided by an electrode. 10. The method according to claim 7 wherein the transforming step is carried out by the transfer of electrons between said redox-active transfection agent and an electron donor/acceptor molecule. 11. The method according to claim 7 wherein the transforming step is carried out by exposure of the redox-active transfection agent to an oxidative/reductive environment of a tissue. 12. The method according to claim 11 wherein said tissue is a cancerous tissue. 13. The method according to claim 7 wherein the transforming step is spatially-controlled whereby said cell is selectively-transfected relative to a population of cells. 14. The method according to claim 7 wherein the transforming step is temporally-controlled whereby said cell is transfected at a predetermined time. 15. The method according to claim 6 wherein said method is carried out in vitro. 16. The method according to claim 6 wherein said method is carried out in vivo. 17. The method according to claim 6 wherein said redox-active cationic lipid further comprises a ferrocenyl moiety. 18. The method according to claim 6 wherein said redox-active transfection agent possesses an oxidation potential between about −2V to about +5V (vs. SCE). 19. A method for transfecting cells comprising steps of: (a) providing a molecule containing a ferrocenyl moiety; and (b) contacting a cell with a nucleic acid in the presence of the molecule containing the ferrocenyl moiety to facilitate transfection of the cell with the nucleic acid.
Iron group metal compounds · CPC title
characterised by an aspect of the 'non-active' part of the composition delivered, e.g. wherein such 'non-active' part is not delivered simultaneously with the 'active' part of the composition · CPC title
wherein the non-active part clearly interacts with the delivered nucleic acid · CPC title
containing heavy metals, e.g. hemin, hematin, melarsoprol · CPC title
using microencapsulation, e.g. using {amphiphile} liposome vesicle · CPC title
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