Flexible Drug Delivery Chip, its Fabrication Method and Uses Thereof

Abstract

Nanodevice and method for in vivo monitoring and release of drugs are provided. The disclosed nanodevice is characterized in having a drug-loaded nanosphere that is capable of releasing the encapsulated drugs upon magnetically stimulation. The nanodevice may also be used as a contrast agent for in vivo imaging and monitoring the concentration and distribution of the released drugs and/or active compounds injected separately into a target site of a subject.

1 . A method of fabricating a drug-containing cell, comprising:
 providing a flexible substrate;   constructing a drug-containing reservoir by forming a plurality of side walls on the flexible substrate to define a drug-containing volume thereon, wherein at least one side of the drug-containing volume is not sealed by the plurality of side walls;   electrophoretically depositing a first layer of drug-containing nanoparticles on the flexible substrate in the drug-containing volume,   forming a layer of metal on the first layer of drug-containing nanoparticles by sputter deposition; and   electrophoretically depositing a second layer of drug-containing nanoparticles on the metal layer.   
     
     
         2 . The method of  claim 1 , wherein the electrophoretic deposition is performed by steps of:
 providing an electrophoretic deposition cell, which comprises:
 a colloidal suspension containing about 0.01-30% by weight of drug-containing nanoparticles; and 
 a pair of electrodes; 
   immersing the flexible substrate having constructed thereon the drug-containing reservoir in the colloidal suspension in the electrophoretic deposition cell; and   applying a voltage of about 1-50 V to the pair of electrodes for a period of about 1-30 min or until the layer of drug-containing nanoparticles has a thickness of at least 0.1 μm.   
     
     
         3 . The method of  claim 2 , wherein the colloidal suspension is prepared by suspending the drug-containing nanoparticles in a diluting medium selected from the group consisting of water, a C 1-6  alcohol, glycol, glycerin, dimethyl sulfoxide and a combination thereof. 
     
     
         4 . The method of  claim 1 , wherein a gap of about 0.5 cm to about 5 cm is formed between the pair of electrodes. 
     
     
         5 . The method of  claim 1 , wherein the electrophoretic deposition is carried out at a temperature ranges from about −10° C. to about 70° C. 
     
     
         6 . The method of  claim 1 , wherein the metal is selected form the group consisting of Au, Ag, Pt, and Ta. 
     
     
         7 . The method of  claim 1 , wherein the plurality of side walls are made of a biocompatible material that is selected from the group consisting of collagen, polyvinylchloride (PVC), polylactide, polyethylene glycol, polycaprolactone (PCL), polycolide, polydioxanone, and derivatives and copolymers thereof. 
     
     
         8 . The method of  claim 1 , wherein the flexible substrate is made of a material selected from the group consisting of polyethylene terephthalate (PET), polyethylene, ethylene-vinyl acetate, polyimides, polyamides, polyethylene naphthalate (PEN), polyimide (PI) and polyaryletheretherketone (PEEK). 
     
     
         9 . The method of  claim 1 , wherein each of the drug-containing nanoparticles comprises a magnetic iron oxide-containing core and a silicon dioxide shell, and a drug is encapsulated within the magnetic iron oxide-containing core. 
     
     
         10 . The method of  claim 9 , wherein the drug is ethosuximide.