US2017196811A1PendingUtilityA1

Core-shell particle formulation for delivering multiple therapeutic agents

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Assignee: KOYAKUTTY MANZOORPriority: Feb 21, 2012Filed: Jun 30, 2016Published: Jul 13, 2017
Est. expiryFeb 21, 2032(~5.6 yrs left)· nominal 20-yr term from priority
A61K 9/1647A61K 31/506A61K 31/436A61K 31/337A61K 9/1658A61K 9/1652A61K 47/48876A61K 31/44A61K 9/1635A61K 9/167A61K 31/704A61K 47/6931A61K 47/6939A61K 47/6927A61K 9/5153A61K 9/5161A61K 9/5169A61K 47/6935A61K 47/6933A61K 45/06A61K 9/5138A61K 9/5192A61K 31/437
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Claims

Abstract

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.

Claims

exact text as granted — not AI-modified
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(lactic-co-glycolic acid); 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 serum albumin;   wherein the core and the shell each comprise one or more therapeutic agents;   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 or EGFR.   
     
     
         2 . The formulation of  claim 1 , wherein the one or more therapeutic agents of the core comprise doxorubicin and the one or more therapeutic agents of the shell comprise sorafenib. 
     
     
         3 . The formulation of  claim 1 , wherein the one or more therapeutic agents of the core comprise sorafenib and the one or more therapeutic agents of the shell comprise doxorubicin. 
     
     
         4 . The formulation of  claim 1 , wherein the one or more therapeutic agents of the core comprise dasatinib and the one or more therapeutic agents of the shell comprise sorafenib. 
     
     
         5 . The formulation of  claim 1 , wherein the one or more therapeutic agents of the core comprise sorafenib and the one or more therapeutic agents of the shell comprise dasatinib. 
     
     
         6 . The formulation of  claim 1 , wherein the core is of average size ≦500 nm. 
     
     
         7 . The formulation of  claim 1 , wherein the shell is of average thickness ≦200 nm. 
     
     
         8 . The formulation of  claim 1 , wherein the therapeutic agents are configured to be delivered from the shell and core sequentially. 
     
     
         9 . The formulation of  claim 1 , wherein the therapeutic agents are configured to be delivered from the shell and core simultaneously. 
     
     
         10 . 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 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 or EGFR.   
     
     
         11 . The formulation of  claim 10 , wherein the one or more therapeutic agents of the core comprise doxorubicin and the one or more therapeutic agents of the shell comprise sorafenib. 
     
     
         12 . The formulation of  claim 10 , wherein the one or more therapeutic agents of the core comprise sorafenib and the one or more therapeutic agents of the shell comprise doxorubicin. 
     
     
         13 . The formulation of  claim 10 , wherein the one or more therapeutic agents of the core comprise dasatinib and the one or more therapeutic agents of the shell comprise sorafenib. 
     
     
         14 . The formulation of  claim 10 , wherein the one or more therapeutic agents of the core comprise sorafenib and the one or more therapeutic agents of the shell comprise dasatinib. 
     
     
         15 . The formulation of  claim 10 , wherein the core is of average size ≦500 nm. 
     
     
         16 . The formulation of  claim 10 , wherein the shell is of average thickness ≦200 nm. 
     
     
         17 . The formulation of  claim 10 , wherein the therapeutic agents are configured to be delivered from the shell and core sequentially. 
     
     
         18 . The formulation of  claim 10 , wherein the therapeutic agents are configured to be delivered from the shell and core simultaneously.

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