Building Porous Biopolymeric Microstructures for Controlled Drug Delivery Devices Using Selective Laser Sintering

2006 ◽  
Vol 31 (5-6) ◽  
pp. 483-489 ◽  
Author(s):  
K. F. Leong ◽  
C. K. Chua ◽  
W. S. Gui ◽  
Verani
Author(s):  
Gean V. Salmoria ◽  
Priscila Klauss ◽  
Carlos R. M. Roesler ◽  
Luiz Alberto Kanis

Selective laser sintering (SLS) is a rapid prototype process that creates objects, layer by layer, using infrared laser beams to process powder materials [1–8]. In recent years, the SLS process has shown great prominence in the medical field, and several researchers have conducted studies showing a wide diversity of materials and applications, such as the manufacture of porous drug delivery devices (DDDs) [9–12].


2012 ◽  
Vol 7 (2) ◽  
pp. 107-115 ◽  
Author(s):  
G.V. Salmoria ◽  
P. Klauss ◽  
K. Zepon ◽  
L.A. Kanis ◽  
C.R.M. Roesler ◽  
...  

Author(s):  
K F Leong ◽  
K K S Phua ◽  
C K Chua ◽  
Z H Du ◽  
K O M Teo

New techniques in solid freeform fabrication (SFF) have prompted research into methods of manufacturing and controlling porosity. The strategy of this research is to integrate computer aided design (CAD) and the SFF technique of selective laser sintering (SLS) to fabricate porous polymeric matrix drug delivery devices (DDDs). This study focuses on the control of the porosity of a matrix by manipulating the SLS process parameters of laser beam power and scan speed. Methylene blue dye is used as a drug model to infiltrate the matrices via a degassing method; visual inspection of dye penetration into the matrices is carried out. Most notably, the laser power matrices show a two-stage penetration process. The matrices are sectioned along the XZ planes and viewed under scanning electron microscope (SEM). The morphologies of the samples reveal a general increase in channel widths as laser power decreases and scan speed increases. The fractional release profiles of the matrices are determined by allowing the dye to diffuse out in vitro within a controlled environment. The results show that laser power and scan speed matrices deliver the dye for 8-9 days and have an evenly distributed profile. Mercury porosimetry is used to analyse the porosity of the matrices. Laser power matrices show a linear relationship between porosity and variation in parameter values. However, the same relationship for scan speed matrices turns out to be rather inconsistent. Relationships between the SLS parameters and the experimental results are developed using the fractional release rate equation for the infinite slab porous matrix DDD as a basis for correlation.


Author(s):  
Dennis Cherian ◽  
Samuel Lienemann ◽  
Tobias Abrahamsson ◽  
Nara Kim ◽  
Magnus Berggren ◽  
...  

Abstract Implantable electronically controlled drug delivery devices can provide precision theraputic treatments by highly spatiotemporally controlled delivery. Iontronic delivery devices rely on the movement of ions rather than liquid, and can therefore achieve electronically controlled precision delivery in a compact setting without disturbing the microenvironment within the tissue with fluid flow. For maximum precision, the delivery device needs to be closely integrated into the tissue, which is challenging due to the mechanical mismatch between the soft tissue and the harder devices. Here we address this challenge by developing a soft and stretchable iontronic delivery device. By formulating an ink based on an in-house synthesized hyperbranched polyelectrolyte, water dispersed polyurethane, and a thickening agent, a viscous ink is developed for stencil patterning of soft ion exchange membranes. We use this ink for developing soft and stretchable delivery devices, which are characterized both in the relaxed and stretched state. We find that their functionality is preserved up to 100 % strain, with small variations in resistance due to the strain. Finally, we develop a skin patch to demonstrate the outstanding conformability of the developed device. The presented technology is attractive for future soft implantable delivery devices, and the stretchable ion exchange membranes may also find applications within wearable energy devices.


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