3D printed oral solid dosage forms containing hydrochlorothiazide for controlled drug delivery
3D printed oral solid dosage forms containing hydrochlorothiazide for controlled drug delivery
  3D printing has been recently employed in the design and fabrication of medicine, aiming to improve their properties and release behavior. In the current work an oral solid dosage form was designed by Fused Deposition Modeling (FDM), using a custom built filament comprised of a water soluble polymer polyvinyl alcohol (PVA), mannitol and hydrochlorothiazide (HCTZ) as model drug and further co-formulated via Hot-Melt Extrusion (HME). This composition was printed as the inner part of a three-compartment hollow cylinder dosage form using a dual extrusion 3D FDM printer, whereas the outer parts of the formulation consisted of water-insoluble polylactic acid (PLA). The produced formulations were characterized by means of differential scanning calorimetry (DSC), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). Release studies were performed in pH 1.2 and 6.8 whereas four-dimensional X-ray micro focus Computed Tomography (4D-CT), was employed to visualize volumetric and morphological changes of the formulations during the dissolution procedure. The results showed that HCTZ was incorporated in the amorphous state. Dissolution studies demonstrated that HCTZ exhibited zero-order kinetics whereas 4D-CT revealed a bi-directional smooth and homogenous reduction of PVA further corroborating the dissolution studies. The results showed that FDM printing might be used to ‘fine tune’ the release of drug molecules.
  Fused Deposition Modeling, 3D printing, zero-order release, printed dosage form, 4D micro focus Computed Tomography (4D-CT)
  
  
  164-171
  
    
      Gioumouxouzis, Christos I.
      
        25c586af-3b71-4fe7-9815-53ddf6df2d8e
      
     
  
    
      Katsamenis, Orestis L.
      
        8553e7c3-d860-4b7a-a883-abf6c0c4b438
      
     
  
    
      Bouropoulos, Nikolaos
      
        fadadea1-2aa2-4cd9-a7e5-33ba790cd45f
      
     
  
    
      Fatouros, Dimitrios G.
      
        4a716c96-a8ba-4fbf-b3db-3b2a3a2794c4
      
     
  
  
   
  
  
    
    
  
    
    
  
    
      August 2017
    
    
  
  
    
      Gioumouxouzis, Christos I.
      
        25c586af-3b71-4fe7-9815-53ddf6df2d8e
      
     
  
    
      Katsamenis, Orestis L.
      
        8553e7c3-d860-4b7a-a883-abf6c0c4b438
      
     
  
    
      Bouropoulos, Nikolaos
      
        fadadea1-2aa2-4cd9-a7e5-33ba790cd45f
      
     
  
    
      Fatouros, Dimitrios G.
      
        4a716c96-a8ba-4fbf-b3db-3b2a3a2794c4
      
     
  
       
    
 
  
    
      
  
  
  
  
  
  
    Gioumouxouzis, Christos I., Katsamenis, Orestis L., Bouropoulos, Nikolaos and Fatouros, Dimitrios G.
  
  
  
  
   
    (2017)
  
  
    
    3D printed oral solid dosage forms containing hydrochlorothiazide for controlled drug delivery.
  
  
  
  
    Journal of Drug Delivery Science and Technology, 40, .
  
   (doi:10.1016/j.jddst.2017.06.008). 
  
  
   
  
  
  
  
  
   
  
    
    
      
        
          Abstract
          3D printing has been recently employed in the design and fabrication of medicine, aiming to improve their properties and release behavior. In the current work an oral solid dosage form was designed by Fused Deposition Modeling (FDM), using a custom built filament comprised of a water soluble polymer polyvinyl alcohol (PVA), mannitol and hydrochlorothiazide (HCTZ) as model drug and further co-formulated via Hot-Melt Extrusion (HME). This composition was printed as the inner part of a three-compartment hollow cylinder dosage form using a dual extrusion 3D FDM printer, whereas the outer parts of the formulation consisted of water-insoluble polylactic acid (PLA). The produced formulations were characterized by means of differential scanning calorimetry (DSC), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). Release studies were performed in pH 1.2 and 6.8 whereas four-dimensional X-ray micro focus Computed Tomography (4D-CT), was employed to visualize volumetric and morphological changes of the formulations during the dissolution procedure. The results showed that HCTZ was incorporated in the amorphous state. Dissolution studies demonstrated that HCTZ exhibited zero-order kinetics whereas 4D-CT revealed a bi-directional smooth and homogenous reduction of PVA further corroborating the dissolution studies. The results showed that FDM printing might be used to ‘fine tune’ the release of drug molecules.
         
      
      
        
          
            
  
    Text
 1-s2.0-S1773224717302721-main
     - Accepted Manuscript
   
  
  
    
  
 
          
            
          
            
           
            
           
        
        
       
    
   
  
  
  More information
  
    
      Accepted/In Press date: 12 June 2017
 
    
      e-pub ahead of print date: 13 June 2017
 
    
      Published date: August 2017
 
    
  
  
    
  
    
  
    
  
    
  
    
  
    
     
        Keywords:
        Fused Deposition Modeling, 3D printing, zero-order release, printed dosage form, 4D micro focus Computed Tomography (4D-CT)
      
    
  
    
     
        Organisations:
        Engineering Mats & Surface Engineerg Gp
      
    
  
    
  
  
  
    
  
  
        Identifiers
        Local EPrints ID: 411346
        URI: http://eprints.soton.ac.uk/id/eprint/411346
        
          
        
        
        
          ISSN: 1773-2247
        
        
          PURE UUID: 92793bb3-b6f4-4626-9af6-dfcdc45b6694
        
  
    
        
          
        
    
        
          
            
              
            
          
        
    
        
          
        
    
        
          
        
    
  
  Catalogue record
  Date deposited: 19 Jun 2017 16:31
  Last modified: 16 Mar 2024 05:27
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      Contributors
      
          
          Author:
          
            
            
              Christos I. Gioumouxouzis
            
          
        
      
        
      
          
          Author:
          
            
            
              Nikolaos Bouropoulos
            
          
        
      
          
          Author:
          
            
            
              Dimitrios G. Fatouros
            
          
        
      
      
      
    
  
   
  
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