Method of making, and the use of cytotoxic agents containing elemental selenium
Pharmaceutical compositions containing elemental selenium (Se(0)), Se(0)-carrier conjugates, a chromophore photoproduct, fluorescent conjugates of the chromophore photoproduct and carrier molecules, or a mixture thereof are disclosed. Methods of using the pharmaceutical compositions such as inducing cell death are also disclosed. Further disclosed are methods of making the pharmaceutical compositions and components thereof.
1. A composition comprising:
elemental selenium (Se(0)) particles having a diameter of 0.4 to 1 nanometer; and a
pharmaceutically acceptable delivering medium.
2. The composition of claim 1 , further comprising:
a carrier molecule that can be internalized by a living cell wherein the carrier molecule forms a conjugate with one or more Se(0) particles.
3. The composition of claim 2 , wherein the carrier molecule is selected from the group consisting of proteins, glycoproteins and lipoproteins.
4. The composition of claim 2 , wherein the carrier molecule is selected from the group consisting of albumin, high density lipoprotein, low density lipoprotein and very low density lipoprotein.
5. The composition of claim 1 , wherein the elemental selenium (Se(0)) particles can form a Se(0) colloid in a dispersion medium.
6. A composition comprising:
elemental selenium (Se(0)) particles having a diameter of 0.4 to 1 nanometer;
a target cell-specific carrier molecule that can be internalized by a living cell wherein the carrier molecule forms a conjugate with one or more Se(0) particles; and
a pharmaceutically acceptable delivering medium.
7. A pharmaceutical composition comprising:
elemental selenium (Se(0)) particles having a diameter of 0.4 to 1 nanometer;
a target cell-specific carrier molecule that can be internalized by a living target cell wherein the carrier molecule is albumin and forms a conjugate with one or more Se(0) particles; and
a pharmaceutically acceptable delivering medium.
8. A composition comprising:
elemental selenium (Se(0)) particles having a diameter of 0.4 to 1 nanometer;
a target cell-specific carrier molecule that can be internalized by a living target cell selected from the group consisting of a cancer cell, an immune cell responsible for an autoimmune disorder, an alloreactive lymphocyte responsible for graft-versus-host disease or a rejection reaction, a parasite and a parasitized blood cell, wherein the carrier molecule forms a conjugate with one or more Se(0) particles; and
a pharmaceutically acceptable delivering medium.
9. The composition of claim 8 , wherein the living target cell is a cancer cell.
10. A method for generating Se(0) comprising the steps of:
providing a photosensitizing selone dye;
exposing the dye to light of a suitable wavelength in the presence of molecular oxygen; and
purifying Se(0).
11. The method of claim 10 , wherein the photosensitizing selone dye is selected from the group consisting of a selenomerocyanine dye and a selenooxonol dye.
12. The method of claim 11 , wherein the selenomerocyanine dye is selected from the group consisting of MC54, MC55, MC56 and MC57.
13. The method of claim 10 , wherein Se(0) is colloidal Se(0).
14. The method of claim 10 , wherein the light of suitable wavelength is generated by light-emitting diodes (LED).
15. A method for treating a human or nonhuman subject having cancer comprising the step of:
administering a composition that comprises a pharmaceutically effective amount of Se(0) particles having a diameter of 0.4 to 1 nanometers and a carrier molecule that can be internalized by a cancer cell, wherein the carrier molecule is albumin, and forms a conjugate with one or more Se(0) particles, to the human or non-human subject.
16. The method of claim 15 , wherein the Se(0) particles can form a Se(0) colloid in a dispersion medium.
17. A method for sensitizing a cell to a cytotoxic agent wherein the cell is resistant to the cytotoxic agent due to the presence of intracellular glutathione, the method comprising of:
treating the cell, or a human or nonhuman subject having the cell, with a composition that comprises Se(0) particles having a diameter of 0.4 to 1 nanometers and a carrier molecule that can be internalized by the cell and forms a conjugate with one or more Se(0) particles, wherein the cell becomes susceptible to the killing by an otherwise ineffective amount of the cytotoxic agent.