Isoflavonoid compositions and methods for the treatment of cancer
US-2017342044-A1 · Nov 30, 2017 · US
US11723893B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11723893-B2 |
| Application number | US-202117193335-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 5, 2021 |
| Priority date | Nov 1, 2010 |
| Publication date | Aug 15, 2023 |
| Grant date | Aug 15, 2023 |
Opening claim text (preview).
What is claimed is: 1. A pharmaceutical composition comprising: i) d-cis-3-(4-hydroxyphenyl)-4-(4-hydroxyphenyl)-8-methylchroman-7-ol provided in at least 90% enantiomeric excess and ii) a cyclodextrin. 2. The pharmaceutical composition of claim 1 , wherein the cyclodextrin is selected from the group consisting of SAE-CD derivatives, SBE-α-CD, SBE-β-CD, SBE1-β-CD, SBE4-β-CD, SBE7-β-CD, SBE-γ-CD, hydroxypropyl-β-cyclodextrin, 2-HP-β-CD, hydroxyethyl-β-cyclodextrin, hydroxypropyl-γ-cyclodextrin, hydroxyethyl-γ-cyclodextrin, dihydroxypropyl-β-cyclodextrin, glucosyl-α-cyclodextrin, glucosyl-β-cyclodextrin, diglucosyl-β-cyclodextrin, maltosyl-α-cyclodextrin, maltosyl-β-cyclodextrin, maltosyl-γ-cyclodextrin, maltotriosyl-β-cyclodextrin, maltotriosyl-γ-cyclodextrin, dimaltosyl-β-cyclodextrin, methyl-β-cyclodextrin, and derivatives and/or combinations thereof. 3. The pharmaceutical composition of claim 1 , wherein the cyclodextrin is SBE7-β-CD. 4. The pharmaceutical composition of claim 1 , wherein the cyclodextrin has a concentration (w/v) ranging from about 0.001% to about 50%. 5. The pharmaceutical composition of claim 1 , wherein the composition further comprises water. 6. The pharmaceutical composition of claim 1 , wherein the composition further comprises one or more of lactose, dextrose, mannitol, a pH buffering agent, an antioxidant agent, a preservative agent, a tonicity adjuster, or a combination thereof. 7. The pharmaceutical composition of claim 1 , wherein the composition comprises d-cis-3-(4-hydroxyphenyl)-4-(4-hydroxyphenyl)-8-methylchroman-7-ol in an amount of about 0.2-50 mg/mL. 8. A method of treating cancer in an individual in need of cancer therapy, the method comprising administering to the individual a pharmaceutical composition comprising: —i) d-cis-3-(4-hydroxyphenyl)-4-(4-hydroxyphenyl)-8-methylchroman-7-ol provided in at least 90% enantiomeric excess and —ii) a cyclodextrin. 9. The method of claim 7 , wherein the pharmaceutical composition increases or induces sensitivity of the cancer to a chemotherapeutic agent, anti-cancer agent, or radiation therapy. 10. The method of claim 7 , wherein the cancer has lost sensitivity to a chemotherapeutic agent, anti-cancer agent, or radiation therapy. 11. The method of claim 7 , wherein the cancer is selected from the group consisting of bladder cancer, breast cancer, colon cancer, rectal cancer, endometrial cancer, kidney cancer, leukemia, lung cancer, melanoma, non-Hodgkin lymphoma, ovarian cancer, pancreatic cancer, prostate cancer, thyroid cancer, and cancers of the brain. 12. The method of claim 7 , wherein the cancer is human breast cancer or ovarian cancer.
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