Alkaline phosphatase formulations
US-12048735-B2 · Jul 30, 2024 · US
US10034903B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10034903-B2 |
| Application number | US-201313952711-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 29, 2013 |
| Priority date | Jul 27, 2012 |
| Publication date | Jul 31, 2018 |
| Grant date | Jul 31, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
To provide a bacterium-based microrobot which can be specifically targeted to cancer in vivo, the present invention provides a drug delivery system for cancer tissue, comprising a bacterium, and a microbead encapsulated with at least one drug, wherein biotin is bound to a surface of the bacterium and a surface of the microbead is coated with streptavidin.
Opening claim text (preview).
What is claimed is: 1. A drug delivery system for cancer tissue, comprising at least a mutant bacterium lack of an ability to synthesize guanosine 5′-diphosphate 3′-diphosphate (ppGpp), and a microbead encapsulating at least a drug, wherein at least a biotin is bound to a surface of the bacterium and a surface of the microbead is coated with streptavidin, and wherein the bacterium is bound to the microbead through an interaction between the biotin and the streptavidin, wherein the diameter of the microbead is 1 to 5 μm. 2. The drug delivery system of claim 1 , the bacterium is Salmonella, Clostridium, Bifidobacterium, E. coli, Yersinia enterocohtica, Listeria monocytogenies, Mycoplasma hominis , or Streptococcus. 3. The drug delivery system of claim 1 , wherein the cancer is any one selected from the group consisting of liver cancer, colorectal cancer, cervical cancer, renal cancer, gastric cancer, prostate cancer, breast cancer, brain tumor, lung cancer, uterine cancer, colon cancer, bladder cancer, hematologic malignancy and pancreatic cancer. 4. The drug delivery system of claim 1 , wherein the drug is a marker gene, a chemical material, a peptide, a polypeptide, a nucleic acid, carbohydrate or lipid. 5. The drug delivery system of claim 4 , wherein, the marker gene is a gene encoding a fluorescence protein or a luminescence protein, or a gene encoding a marker for nuclear medicine or MRI imaging comprising thymidine kinase of herpes simplex virus, a dopamine receptor, a somatostatin receptor, a sodium-iodide transporter, an iron receptor, a transferrin receptor, ferritin or an iron transporter (magA). 6. The drug delivery system of claim 4 , wherein, the chemical material is at least one selected from doxorubicin, epirubicin, cisplatin, carboplatin, oxaliplatin, paclitaxel, docetaxel, 5-fluorouracil, cytarabine, gemcitabine, pentostatin, methotrexate, 7-ethyl-10-hydroxycamptothecin, trimetrexate, vinblastine, vincristine and dexamethasone. 7. The drug delivery system of claim 1 , wherein, the microbead is produced by using a biodegradable/biocompatible polymer material. 8. The drug delivery system of claim 7 , wherein, the biodegradable/biocompatible polymer material is one or more selected from chitosan, a salt and a derivative thereof; dextran and a derivative thereof; gum acacia; tragacanthin; hyaluronic acid, a salt and a derivative thereof; pectin, a salt and a derivative thereof; alginic acid, a salt and a derivative thereof; agar; galactomannan, a salt and a derivative thereof; xanthan, a salt and a derivative thereof; β-cyclodextrin, a salt and a derivative thereof; amylose (water soluble starch), a salt and a derivative thereof; glycol chitosan, a salt and a derivative thereof; carboxylmethyl cellulose (CMC), a salt and a derivative thereof; hydroxyethyl cellulose (HEC), a salt and a derivative thereof; hyroxypropyl methyl cellulose (HPMC), a salt and a derivative thereof; methyl cellulose, a salt and a derivative thereof; cellulose acetate phthalate, a salt and a derivative thereof; gelatin, a salt and a derivative thereof; promaine sulfate; poly(β-hydroxyethyl methacrylate) (PHEMA); polyacrylamide (PA); polyvunyl alcohol (PVA); polyacrylic acid (PAA); polyethylene gylcol (PEG); poly(ethylene oxide-b-propylene oxide) (PER-PPO); and polylyasine. 9. A pharmaceutical composition for treating cancer, comprising: (a) a pharmaceutically effective dose of the drug delivery system set forth in claim 1 ; and (b) a pharmaceutically acceptable carrier, wherein the drug delivery system comprises a drug for treating cancer. 10. A composition for imaging cancer, comprising: (a) the drug delivery system set forth in claim 1 ; and (b) a pharmaceutically acceptable carrier. 11. A pharmaceutical composition for treating cancer, comprising: (a) a pharmaceutically effective dose of the drug delivery system set forth in claim 2 ; and (b) a pharmaceutically acceptable carrier, wherein the drug delivery system comprises a drug for treating cancer. 12. A pharmaceutical composition for treating cancer, comprising: (a) a pharmaceutically effective dose of the drug delivery system set forth in claim 3 ; and (b) a pharmaceutically acceptable carrier, wherein the drug delivery system comprises a drug for treating cancer. 13. A pharmaceutical composition for treating cancer, comprising: (a) a pharmaceutically effective dose of the drug delivery system set forth in claim 5 ; and (b) a pharmaceutically acceptable carrier, wherein the drug delivery system comprises a drug for treating cancer. 14. A pharmaceutical composition for treating cancer, comprising: (a) a pharmaceutically effective dose of the drug delivery system set forth in claim 8 ; and (b) a pharmaceutically acceptable carrier, wherein the drug delivery system comprises a drug for treating cancer.
Cells, viruses, ghosts, red blood cells, viral vectors, used for imaging or diagnosis in vivo · CPC title
Microparticle, microcapsule, microbubble, microsphere, microbead, i.e. having a size or diameter higher or equal to 1 micrometer · CPC title
Methine dyes, e.g. cyanine dyes · CPC title
Antineoplastic agents · CPC title
Conjugates being cells, cell fragments, viruses, ghosts, red blood cells or viral vectors · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.