1. A method for treating or preventing metastasis in a subject having cancer, said method comprising administering to said subject a lipocalin 2 compound, or a fragment or derivative thereof, that has lipocalin 2 biological activity, wherein said administering is for a time and in an amount sufficient to treat or prevent said metastasis in said subject.
2. The method of claim 1, wherein said lipocalin 2 compound is a lipocalin 2 polypeptide or fragment thereof.
3. The method of claim 2, wherein said lipocalin 2 polypeptide comprises a sequence substantially identical to the amino acid sequence of SEQ ID NO:2 or SEQ ID NO:4.
4. The method of claim 3, wherein said lipocalin 2 polypeptide comprises the sequence of SEQ ID NO:2 or SEQ ID NO:4.
5. The method of claim 4, wherein said lipocalin 2 polypeptide consists of the amino acid sequence of SEQ ID NO:2 or SEQ ID NO: 4.
6. The method of claim 1, wherein said lipocalin 2 compound binds a siderophore.
7. The method of claim 1, wherein said lipocalin 2 compound transports iron.
8. The method of claim 1, wherein said lipocalin 2 biological activity is the reversal or inhibition of epithelial to mesechymal transition.
9. The method of claim 1, wherein said lipocalin 2 compound binds to a lipocalin 2 receptor.
10. The method of claim 1, wherein said lipocalin 2 compound decreases phosphorylation of E-cadherin, increases E-cadherin biological activity, or inhibits ras-MAPK signaling.
11. The method of claim 1, wherein lipocalin 2 compound increases E-cadherin expression.
12. The method of claim 1, further comprising administering a siderophore.
13. The method of claim 12, wherein said siderophore is selected from the group consisting of bacterial catecholate-type ferric siderophores, enterochelin, carboxymycobactin, aminochelin, desferrioxamine, aerobactin, arthrobactin, schizokinen, foroxymithine, pseudobactins, neoenactin, photobactin, ferrichrome, hemin, achromobactin, achromobactin, and rhizobactin.
14. The method of claim 12, wherein said siderophore is in a complex with said lipocalin 2 compound.
15. The method of claim 1, further comprising administering iron or an iron replacement.
16. (canceled)
17. The method of claim 15, wherein said iron or iron replacement is in a complex with said lipocalin 2 compound either directly or indirectly.
18. The method of claim 17, wherein said iron or iron replacement is in a complex with said lipocalin 2 compound prior to administering to said subject.
19. The method of claim 1, wherein said lipocalin 2 compound is a nucleic acid molecule encoding a lipocalin 2 polypeptide that has lipocalin 2 biological activity.
20-22. (canceled)
23. The method of claim 1, wherein said cancer is from an epithelial cell solid tumor.
24. The method of claim 23, wherein said epithelial cell solid tumor is a cancer selected from the group consisting of gastrointestinal cancer, colon cancer, breast cancer, prostate cancer, renal cancer, lung cancer, melanoma, ovarian cancer, pancreatic cancer, head and neck cancer, and liver cancer.
25. The method of claim 1, wherein the cancer is metastatic and said method is used to treat said metastasis.
26. The method of claim 1, wherein the cancer is at risk of becoming metastatic.
27. The method of claim 1, wherein the subject is at risk for cancer or cancer metastasis.
28. The method of claim 1, further comprising administering to said subject an additional cancer therapy selected from the group consisting of surgery, radiation therapy, chemotherapy, differentiating therapy, and immune therapy.
29-31. (canceled)
32. A kit for the treatment or prevention of metastasis in a subject having, or at risk of developing, a metastatic cancer, said kit comprising a lipocalin 2 compound and instructions for the use of said lipocalin 2 compound for the treatment or prevention of said metastatic cancer.
33. The kit of claim 32, further comprising at least one additional compound selected from the group consisting of a chemotherapeutic agent, an angiogenesis inhibitor, or an anti-proliferative compound.
34. A method for reducing or inhibiting angiogenesis in a subject in need thereof, said method comprising administering to said subject a lipocalin 2 compound, wherein said administering is for a time and in an amount sufficient to reduce or inhibit said angiogenesis.
35-51. (canceled)
52-53. (canceled)
54. A method of diagnosing metastatic disease or a propensity to develop a metastatic disease in a subject having or at risk of having cancer, said method comprising the steps of:
(a) determining the level of a lipocalin 2 polypeptide, nucleic acid molecule, or fragments thereof, in a sample from said subject; and
(b) comparing said level in (a) to a normal reference level of lipocalin 2 polypeptide, nucleic acid molecule, or fragment thereof; wherein an alteration in said subject levels relative to said normal reference level is diagnostic of a metastatic disease or a propensity to develop a metastatic disease in said subject.
55-57. (canceled)
58. The method of claim 54, wherein said method is used to monitor the metastatic health of a subject having or at risk of having cancer.
59-69. (canceled)
70. A method for treating or preventing fibrosis in a subject having a fibrotic disorder, said method comprising administering to said subject a lipocalin 2 compound, wherein said administering is for a time and in an amount sufficient to prevent or reduce the occurrence of said fibrosis.
71-77. (canceled)
The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.
1. A method of preparing microparticles, comprising:
dissolving an active agent in a first solvent to form an active agent solution;
dissolving a polymer in a second solvent to form a polymer solution;
blending the active agent solution and the polymer solution to form an organic phase;
combining the organic phase and an aqueous phase in a first static mixer to form an emulsion, the emulsion forming an outflow of the first static mixer;
combining the outflow of the first static mixer and a first portion of a starting volume of an extraction liquid for extracting the first and second solvents from the emulsion in a second static mixer; and
combining an outflow of the second static mixer with a second portion of the extraction liquid to extract the first and second solvents from the emulsion.
2. The method of claim 1, wherein the step of combining the outflow of the second static mixer with the second portion of the extraction liquid comprises:
allowing the outflow of the second static mixer to flow into a vessel containing the second portion of the extraction liquid.
3. The method of claim 1, wherein the step of combining the outflow of the second static mixer with the second portion of the extraction liquid comprises:
combining the outflow of the second static mixer and the second portion of the extraction liquid in a third static mixer.
4. The method of claim 3, further comprising:
allowing an outflow of the third static mixer to flow into a vessel.
5. The method of claim 4, further comprising:
continuing the step of combining the outflow of the second static mixer and the second portion of the extraction liquid in the third static mixer until the organic phase is depleted; and
transferring a remainder of the starting volume of the extraction liquid to the vessel.
6. The method of claim 1, wherein the step of combining the outflow of the second static mixer with the second portion of the extraction liquid comprises:
combining the outflow of the second static mixer and the second portion of the extraction liquid in a third static mixer and repeating this combining step until the starting volume of the extraction liquid is depleted.
7. A method of preparing microparticles, comprising:
dissolving an active agent and a polymer in a solvent to form an organic phase;
combining the organic phase and an aqueous phase in a first static mixer to form an emulsion, the emulsion forming an outflow of the first static mixer;
combining the outflow of the first static mixer and a first portion of a starting volume of an extraction liquid for extracting the solvent from the emulsion in a second static mixer; and
combining an outflow of the second static mixer with a second portion of the extraction liquid to extract the solvent from the emulsion.
8. The method of claim 7, wherein the step of combining the outflow of the second static mixer with the second portion of the extraction liquid comprises:
allowing the outflow of the second static mixer to flow into a vessel containing the second portion of the extraction liquid.