IP Library Granted Patent US 9,000,036
Granted Patent B2
US 9,000,036 · App. 13/959,484 · Granted Apr 7, 2015

Compositions and methods for targeting of treating neoplasms

Inventor: Baofa Yu (San Diego, CA)
Assignee: Baofa Yu
A61K47/48084A61K31/04A61K31/06A61K31/185A61K31/21A61K31/32A61K31/53A61K33/24A61K36/00A61K38/00A61K45/06A61K47/48061
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Quick Facts
Patent No.
US 9,000,036
App. No.
13/959,484
Granted
Apr 7, 2015
Kind
B2
Abstract

Methods for treating neoplasm, tumors and cancers, using one or more tumor treating drug carriers, haptens and anticancer drugs, alone or in combination with other antineoplastic agents or treatments, are provided. Also provided are compositions, and kits containing the composition for affecting the therapy.

Claims (20)

1. A method of treating a neoplasm in a mammal, comprising administering an effective amount of a conjugated complex, wherein the conjugated complex comprises:

a targeting compound; and

a chemical drug,

wherein said targeting compound is a non-covalently complexed to said chemical drug via a redox agent as a reactant.

2. The method of claim 1 , wherein said mammal is human.

3. The method of claim 1 , wherein said targeting compound is selected from the group consisting of a carrier capable of delivering an agent to a targeted tissue, Sodium Dimercaptosuccinate (III) (DMSA-III), Sodium Dimercaptosuccinate (V) (DMSA-V), Sodium Pyrophosphate and Stannous Chloride for Injection (PYP), Methylene Diphosphonate for Injection (MDP), polymerized albumin, Mercaptoacetyltriglycine, Pentetic Acid and Stannous Chloride (DTPA), Sodium Glucoheptonate and Stannous Chloride, L, L-Ethyl Cysteinate Dimer and Stannous Chloride (ECD), Exametazime (HMPAO), Etifenin and Stannous Chloride, Sodium Phytate and Stannous Chloride, Cu(MIBI) 4 BF 4 (MIBI), α-methyltyrosine, MIBI (2-methoxy isobutyl isonitrile), 2-nitroimidazole, monoclonal antibodies and monoclonal antibodies against neoplasm, and traditional Chinese drug extract selected from the group consisting of Bruceantin, Tetrandrine, thalicarpine and maytansine.

4. The method of claim 1 , wherein said chemical drug is selected from the group consisiting of cisplatin, carboplatin, calcium folinate, vincristine, methotrexate, fluorouracil, cytosine arabinoside (Ara-C), cyclophosphamide, epirubicin, doxorubicin rapid dissolution, mitomycin, etoposide, bleomycin A5.

5. The method of claim 1 , wherein the redox agent is selected from the group consisting of stannous chloride (SnCl 2 ), stannous sulfate (SnSO 3 ), stannous oxide (SnO), stannic oxide (SnO 2 ), sodium stannate (Na 2 SnO 3 ), sodium stannite (Na 2 SnO 2 ), stannic chloride (SnCl 4 ), thiostannate (SnS 3 ), and stannous sulfide (SnS).

6. The method of claim 1 , further comprising using an immune response potentiator.

7. The method of claim 6 , wherein the immune response potentiator is selected from the group consisting of Bacille Calmette-Guerin (BCG), Corynebacterium Parvum, Brucella abortus , glucan, levamisole, tilorone, an enzyme, and a nonvirulent virus.

8. The method of claim 7 , wherein the enzyme is selected from the group consisting of Vibrio cholera neuraminidase (VCN), Papain, β-Gal, and ConA.

9. The method of claim 1 , wherein said conjugated complex comprises two or more targeting compounds, a chemical drug formulated in a single pharmaceutical composition.

10. The method of claim 1 , wherein said conjugated complex comprises two or more chemical drugs, and a targeting compound formulated in a single pharmaceutical composition.

11. The method of claim 1 , wherein the conjugated complex further comprises an anti-neoplasm agent.

12. The method of claim 11 , wherein the anti-neoplasm agent is selected from the group consisting of an alkylating agent, an antimetabolite, a natural product, a platinum coordination complex, an anthracenedione, a substituted urea, a methylhydrazine derivative, an adrenocortical suppressant, a hormone, an antagonist, an anti-cancer polysaccharide, an herb extract and a traditional Chinese drug extract.

13. The method of claim 1 , wherein the neoplasm to be treated is selected from the group consisting of adrenal gland, anus, auditory nerve, bile ducts, bladder, bone, osseous metastastic, brain, breast, central nervous system, cervix, colon, ear, endometrium, esophagus, eye, eyelids, fallopian tube, gastrointestinal tract, head and neck, heart, kidney, larynx, liver, lung, mandible, mandibular condyle, maxilla, mouth, nasopharynx, nose, oral cavity, ovary, pancreas, parotid gland, penis, pinna, pituitary, prostate gland, rectum, retina, salivary glands, skin, small intestine, spinal cord, stomach, testes, thyroid, tonsil, urethra, uterus, vagina, vestibulocochlear nerve and vulva neoplasms, lymph and lymph node metastases of various cancers, and malignant lymphoma.

14. The method of claim 1 , wherein the neoplasm is a solid tumor.

15. The method of claim 1 , wherein the neoplasm is not a solid tumor.

16. The method of claim 14 , wherein the size of the solid tumor is larger than 10 8 cells.

17. The use of claim 1 , wherein the conjugated complex is administered to the neoplasm via intravenous injection, intratumoral injection, or direct injection.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Oct 18, 2016
From: KNOBBE, MARTENS, OLSON & BEAR, LLP
To: YU, BAOFA
Reel/Frame 040049/0632 →
SECURITY INTEREST Recorded Oct 13, 2015
From: YU, BAOFA
To: KNOBBE, MARTENS, OLSON & BEAR, LLP
Reel/Frame 036852/0476 →
Priority Claims (1)
CN 2006 1 0151437 · Sep 7, 2006 · national
Continuity (2)
Division 12440198
Related Publication 20140037695A1 · Feb 6, 2014