Core-shell particle formulation for delivering multiple therapeutic agents

US9402918B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9402918-B2
Application numberUS-201414465521-A
CountryUS
Kind codeB2
Filing dateAug 21, 2014
Priority dateFeb 21, 2012
Publication dateAug 2, 2016
Grant dateAug 2, 2016

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A core-shell particle formulation for delivering multiple therapeutic agents is disclosed. More particularly, core-shell particle formulation configured to independently release therapeutic agents from the core and the shell. Moreover, the core-shell particle bearing therapeutic agents enables treatment against the diseases such as cancer, inflammatory and auto-immune diseases.

First claim

Opening claim text (preview).

What is claimed is: 1. A core-shell particle formulation for delivering multiple therapeutic agents comprising: one or more polymers forming a core, wherein the one or more polymers forming the core comprise poly vinyl alcohol; and one or more proteins forming a shell encapsulating the core to form a particle formulation, wherein the one or more proteins forming the shell comprise protamine; wherein the core and the shell each comprise one or more therapeutic agents, wherein the one or more therapeutic agents of the core comprise doxorubicin and the one or more therapeutic agents of the shell comprise sorafenib; wherein the particle formulation is configured to independently release the therapeutic agents from the core and the shell; and wherein the therapeutic agents are configured to be delivered by active targeting, wherein the active targeting is done by conjugating the core-shell formulation with transferrin ligand. 2. The formulation of claim 1 , wherein the core is of average size ≦500 nm. 3. The formulation of claim 1 , wherein the shell is of average thickness ≦200 nm. 4. The formulation of claim 1 , wherein the therapeutic agents of the core and shell further comprise one or more small molecule kinase inhibitors or chemotherapeutic drugs. 5. The formulation of claim 1 , wherein the shell comprises one or both of hydrophilic and hydrophobic therapeutic agents. 6. The formulation of claim 1 , wherein the one or more polymers forming the core further comprise poly glycolic acid, poly(lactic-co-glycolic acid), glycolide/trimethylene carbonate copolymers, poly-lactides, poly-L lactide, poly-DL-lactide, L-lactide/DL-lactide copolymers, lactide/tetramethyl-glycolide copolymers, poly-caprolactone, poly-valerolacton, poly-hydroxy butyrate, poly-hydroxyvalerate, polyvinylpyrrolidone, or polyethyleneimine and lactide/trimethylene carbonate copolymers. 7. The formulation of claim 1 , wherein the one or more proteins forming the shell further comprise human serum albumin, bovine serum albumin, protamine, transferrin, lactoferrin, fibrinogen, or gelatin. 8. The formulation of claim 4 , wherein the small molecule kinase inhibitor is chosen from the group consisting of inhibitors of tyrosine kinase, epidermal growth factor receptor inhibitors, vascular endothelial growth factor receptor inhibitors, platelet derived growth factor receptor inhibitors, fibroblast growth factor receptor inhibitors, Rous sarcoma oncogene/Breakpoint cluster region/Abl inhibitors, insulin-like growth factor 1 receptor inhibitors, FLT-3 inhibitors, HER-2 inhibitors, c-Kit inhibitors, c-Met inhibitors, ALK inhibitors, ETA receptor inhibitors, HIF inhibitors, Syk inhibitors, Tie2 kinase inhibitors, vascular disrupting agents, cell cycle/check point inhibitors, polo-like kinase inhibitors, cyclin dependent kinase inhibitors, topoisomerase inhibitors, microtubule inhibitors, antimetabolites, telomerase inhibitors, DNA replication inhibitors, RNA replication inhibitors, dihydrofolate reductase inhibitors, HDAC inhibitors, Bcl-2 inhibitors, TNF-a inhibitors, p53 inhibitors, PARP inhibitors, MAPK inhibitors, PI3K/Akt/mTOR inhibitors, integrase inhibitors, protease inhibitors, Wnt/Hedgehog/Notch inhibitors, Jak/STAT inhibitors, PKC inhibitors, TGF-P inhibitors, antioxidant inhibitors, and combinations thereof. 9. The formulation of claim 4 , wherein the chemotherapeutic drug is chosen from the group consisting of aminoglutethimide, amsacrine, anastrozole, asparaginase, bcg, bicalutamide, bleomycin, buserelin, busulfan, campothecin, capecitabine, carboplatin, carmustine, chlorambucil, cisplatin, cladribine, clodronate, colchicine, cyclophosphamide, cyproterone, cytarabine, dacarbazine, dactinomycin, daunorubicin, dienestrol, diethylstilbestrol, docetaxel, dasatinib, epirubicin, estradiol, estramustine, etoposide, exemestane, filgrastim, fludarabine, fludrocortisone, fluorouracil, fluoxymesterone, flutamide, gemcitabine, genistein, goserelin, hydroxyurea, idarubicin, ifosfamide, imatinib, interferon, irinotecan, letrozole, leucovorin, leuprolide, levamisole, lomustine, mechlorethamine, medroxyprogesterone, megestrol, melphalan, mercaptopurine, mesna, methotrexate, mitomycin, mitotane, mitoxantrone, nilutamide, nocodazole, octreotide, oxaliplatin, paclitaxel, pamidronate, pentostatin, plicamycin, porfimer, procarbazine, raltitrexed, rituximab, streptozocin, suramin, tamoxifen, temozolomide, teniposide, testosterone, thioguanine, thiotepa, titanocene dichloride, topotecan, trastuzumab, tretinoin, vinblastine, vincristine, vindesine, vinorelbine and combinations thereof. 10. The formulation of claim 1 , wherein the therapeutic agents are configured to be delivered from the shell and core sequentially. 11. The formulation of claim 1 , wherein the therapeutic agents are configured to be delivered from the shell and core simultaneously.

Assignees

Inventors

Classifications

  • Polysaccharides, e.g. alginate, chitosan, cellulose derivatives; Cyclodextrin · CPC title

  • Human Necessities · mapped topic

  • Processes · CPC title

  • A61K9/167Primary

    with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface (with further drug-free outer coating A61K9/5073) · CPC title

  • the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9402918B2 cover?
A core-shell particle formulation for delivering multiple therapeutic agents is disclosed. More particularly, core-shell particle formulation configured to independently release therapeutic agents from the core and the shell. Moreover, the core-shell particle bearing therapeutic agents enables treatment against the diseases such as cancer, inflammatory and auto-immune diseases.
Who is the assignee on this patent?
Koyakutty Manzoor, Chandran Parwathy, P R Archana, and 2 more
What technology area does this patent fall under?
Primary CPC classification A61K9/167. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Aug 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).