Methods and compositions for oral pharmaceutical therapy
It now has been found that oral administration of pharmaceutical agents, including N-methylol transfer agents such as Taurolidine may be used to provide efficacious blood plasma concentration of the agents for treatment of diseases by providing release of the active agent into the duodenum or jejunum of a patient and/or at a pH of about 5.4 to about 6.5. Embodiments of the invention therefore provide oral dosage forms, compositions and methods for administration of pharmaceutical agents to the duodenum or jejunum of a patient, and/or which release at a pH of about 5.4 to about 6.5.
1. A method of achieving a blood, serum, or plasma level in a subject of at least about 4 μg/mL of an N-methylol transfer agent comprising taurolidine, taurultam, a derivative of taurolidine or taurultam, or a combination thereof, comprising administering to said subject a capsule comprising the N-methylol transfer agent and a pharmaceutically acceptable targeted release carrier, said targeted release carrier providing an efficacious blood, serum or plasma level of said N-methylol transfer agent in said subject, after oral administration of said capsule, to treat a disease in said subject, wherein, after said oral administration, said carrier
(a) carries said agent substantially intact through said subject's stomach and releases said agent into said subject's duodenum or jejunum, wherein said agent enters the subject's bloodstream through said duodenum or jejunum,
(b) releases said agent at a pH of about 5.4 to about 6.5, wherein said agent enters the subject's bloodstream, or
(c) both.
2. The method of claim 1 , wherein said disease is a neoplastic disease.
3. The method of claim 2 , wherein said neoplastic disease is selected from the group consisting of a carcinoma, a sarcoma and a lymphoma.
4. The method of claim 2 , wherein said neoplastic disease is selected from the group consisting of colon cancer, rectal cancer, colo-rectal cancer, ovarian cancer, breast cancer, prostate cancer, lung cancer, mesothelioma, melanoma, renal cancer, liver cancer, pancreatic cancer, gastric cancer, esophageal cancer, urinary bladder cancer, cervical cancer, cardiac cancer, gall bladder cancer, skin cancer, bone cancer, a head cancer, a neck cancer, a central nervous system cancer, glioma, glioblastoma, neuroblastoma, astrocytoma, carcinomatous meningitis, leukemia, lymphoma, lymphosarcoma, adenocarcinoma, fibrosarcoma, and metastases thereof.
5. The method of claim 1 , wherein said an infectious disease.
6. The method of claim 5 , wherein said infectious disease is due to a bacterial or fungal infection.
7. The method of claim 5 , wherein said infectious disease is due to Stenotrophomonas maltophilia.
8. The method of claim 2 further comprising administering a corticosteroid to said subject.
9. The method of claim 1 , wherein said agent is released at a pH of 5.5 or higher.
10. The method of claim 1 , wherein said N-methylol transfer agent is selected from the group consisting of Taurolidine, Taurultam, 1183B (cyclo-taurolidine), N-methylol taurinamide and any combination thereof.
11. The method of claim 1 , wherein said N-methylol transfer agent is Taurolidine, Taurultam, or a mixture thereof.
12. The method of claim 1 , wherein said targeted release carrier comprises an enteric coating.
13. The method of claim 12 , wherein said enteric coating comprises a co-polymer of methacrylic acid and methyl acetate or methacrylic acid and ethyl acrylate.
14. The method of claim 1 , said dosage achieves a blood, serum or plasma level of said N-methylol transfer agent within a range of about 4 μg/mL to 80 μg/mL.
15. The method of claim 1 , said dosage achieves a blood, serum or plasma level of said N-methylol transfer agent of at least about 20 μg/mL.
16. The method of claim 1 , wherein said dosage achieves a blood, serum or plasma level of said N-methylol transfer agent of at least about 10 μg/mL to 20 μg/mL.